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Open Access Highly Accessed Research article

Comparative genomic analysis of four representative plant growth-promoting rhizobacteria in Pseudomonas

Xuemei Shen, Hongbo Hu, Huasong Peng, Wei Wang and Xuehong Zhang*

Author Affiliations

State Key Laboratory of Microbial Metabolism, School of Life Sciences and Biotechnology, Shanghai Jiao Tong University, 800 Dongchuan Road, Shanghai, 200240, People’s Republic of China

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BMC Genomics 2013, 14:271  doi:10.1186/1471-2164-14-271

The electronic version of this article is the complete one and can be found online at: http://www.biomedcentral.com/1471-2164/14/271


Received:16 March 2013
Accepted:16 April 2013
Published:22 April 2013

© 2013 Shen et al.; licensee BioMed Central Ltd.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Background

Some Pseudomonas strains function as predominant plant growth-promoting rhizobacteria (PGPR). Within this group, Pseudomonas chlororaphis and Pseudomonas fluorescens are non-pathogenic biocontrol agents, and some Pseudomonas aeruginosa and Pseudomonas stutzeri strains are PGPR. P. chlororaphis GP72 is a plant growth-promoting rhizobacterium with a fully sequenced genome. We conducted a genomic analysis comparing GP72 with three other pseudomonad PGPR: P. fluorescens Pf-5, P. aeruginosa M18, and the nitrogen-fixing strain P. stutzeri A1501. Our aim was to identify the similarities and differences among these strains using a comparative genomic approach to clarify the mechanisms of plant growth-promoting activity.

Results

The genome sizes of GP72, Pf-5, M18, and A1501 ranged from 4.6 to 7.1 M, and the number of protein-coding genes varied among the four species. Clusters of Orthologous Groups (COGs) analysis assigned functions to predicted proteins. The COGs distributions were similar among the four species. However, the percentage of genes encoding transposases and their inactivated derivatives (COG L) was 1.33% of the total genes with COGs classifications in A1501, 0.21% in GP72, 0.02% in Pf-5, and 0.11% in M18. A phylogenetic analysis indicated that GP72 and Pf-5 were the most closely related strains, consistent with the genome alignment results. Comparisons of predicted coding sequences (CDSs) between GP72 and Pf-5 revealed 3544 conserved genes. There were fewer conserved genes when GP72 CDSs were compared with those of A1501 and M18. Comparisons among the four Pseudomonas species revealed 603 conserved genes in GP72, illustrating common plant growth-promoting traits shared among these PGPR. Conserved genes were related to catabolism, transport of plant-derived compounds, stress resistance, and rhizosphere colonization. Some strain-specific CDSs were related to different kinds of biocontrol activities or plant growth promotion. The GP72 genome contained the cus operon (related to heavy metal resistance) and a gene cluster involved in type IV pilus biosynthesis, which confers adhesion ability.

Conclusions

Comparative genomic analysis of four representative PGPR revealed some conserved regions, indicating common characteristics (metabolism of plant-derived compounds, heavy metal resistance, and rhizosphere colonization) among these pseudomonad PGPR. Genomic regions specific to each strain provide clues to its lifestyle, ecological adaptation, and physiological role in the rhizosphere.

Keywords:
Plant growth-promoting rhizobacteria; Pseudomonad; Comparative genomics; Environmental adaptability; Rhizosphere colonization; Biocontrol activity

Background

Pseudomonas (sensu stricto) is a diverse genus that occupies many different niches and exhibits versatile metabolic capacity [1]. A number of pseudomonad strains function as plant growth-promoting rhizobacteria (PGPR). Such strains can protect plants from various soilborne pathogens and/or stimulate plant growth [2]. For example, Pseudomonas chlororaphis and Pseudomonas fluorescens are non-pathogenic biocontrol agents, while several strains of Pseudomonas aeruginosa and Pseudomonas stutzeri show strong plant growth-promoting activities. Some characteristic features associated with plant growth promotion have been studied at the molecular level. For example, effective PGPR show sufficient colonization of the rhizosphere [3,4]. Moreover, PGPR have certain biocontrol activities; for example, they can produce antibiotics that prevent infection by plant pathogens [2]. Such antibiotics include phenazine derivatives [5-7], pyoluteorin (Plt) [8,9], pyrrolnitrin (Prn) [10], hydrogen cyanide (HCN) [11], and so on. Some rhizobacteria directly promote plant growth in the absence of pathogens [12]. However, a comprehensive analysis of the characteristics of PGPR among different Pseudomonas species using a comparative genomics approach has not been reported yet.

Comparative genomics has emerged as a powerful tool to identify functionally important genomic elements [13-15]. As more and more genomic information becomes available, the development of genomic technologies can provide further insights into essential life processes [16]. As of March 2012, the complete genomic sequences of strains representing the following Pseudomonas species were available: the rhizobacteria P. fluorescens[14,17], P. stutzeri[18], and Pseudomonas putida[15,19,20], and the pathogens P. aeruginosa[21,22], Pseudomonas syringae[23], and Pseudomonas entomophila[24]. Genomic information for P. chlororaphis, which plays an important role in suppressing pathogens and stimulating plant growth [3,25-27], was first reported by our group [28].

P. chlororaphis GP72 (hereafter, GP72) was isolated from the rhizosphere of green pepper in China. This strain shows broad antagonistic activities [29]. It completely suppresses the phytopathogens Coletotrichum lagenarium, Pythium ultimum, Sclerotinia sclerotiorum, Fusarium oxysporum f. sp. cucumerinum, Carposina sasakii, and Rhizoctonia solani[7]. In vitro screening and in vivo genetic engineering experiments showed that GP72 can produce two phenazine derivatives, phenazine-1-carboxylic acid (PCA) and 2-hydroxyphenazine (2-OH-PHZ), which have strong fungicidal activities [30]. It also produces other secondary metabolites including HCN, indole-3-acetic acid (IAA), and siderophores, contributing to rhizosphere adaptability [7]. P. fluorescens Pf-5 (hereafter, Pf-5) was isolated from the rhizosphere of cotton and is able to suppress damping-off caused by P. ultimum[8]. As a well-recognized biocontrol agent, Pf-5 produces a spectrum of antibiotics including Prn, Plt, and 2,4-diacetylphloroglucinol (DAPG) [8,31], and two siderophores, pyoverdine (Pvd) and pyochelin (Pch). P. aeruginosa M18 (hereafter, M18) was isolated from the rhizosphere of sweet melon. It produces both PCA and Plt, which show strong antifungal activities [22,32], and it shows biocontrol activity in the rhizosphere niche [33]. Most P. aeruginosa strains are opportunistic pathogens, including the first-sequenced strain, P. aeruginosa PAO1 [21,34,35]. P. stutzeri A1501 (hereafter, A1501), which belongs to the nonfluorescent Pseudomonas group, was isolated from the rhizosphere of rice based on its nitrogen-fixation capacity [36,37]. A1501 has been commercialized for use as a crop inoculant in China. Genetic information for A1501 has provided insights into the mechanisms of its nitrogen-fixation ability and environmental adaptability, such as its ability to mineralize aromatic compounds [18,38].

To identify the shared characteristics of pseudomonad PGPR, we compared genomic information for GP72 with those of three other representative pseudomonad PGPR: the biological control agent Pf-5, the rhizobacterium M18, and the nitrogen-fixing strain A1501. There were 602 genes conserved among the four species. Comparison among these PGPR also revealed previously unknown common traits related to plant growth promotion. This comparative genomics analysis of different PGPR provides information about the genetic basis of diversity and adaptation. The results of this study also provide foundation knowledge to improve and exploit the plant growth-promoting activities of PGPR in agricultural applications via molecular techniques.

Results and discussion

General genome features and comparative genomics

The general features of the four PGPR genomes are summarized in Table 1. The assembled genome of GP72 had approximately 270-fold sequence coverage [28], with putative functions assigned to 83% of the genes. It is reasonable to assume that the vast majority of genes are important for cell metabolism. GP72, Pf-5, M18, and A1501 showed a wide range of genome sizes, ranging from 4.6 to 7.1 M, resulting in different numbers of protein-coding genes (Table 1). The genome sequences and additional information related to each predicted gene, such as gene product annotation, KEGG orthology, gene ontology, and predicted subcellular location are available on the IMG database (https://img.jgi.doe.gov/cgi-bin/er/main.cgi webcite) [39]. Predicted proteins were functionally categorized using the COGs database [40], and COGs categories were compared among the genomes of GP72, Pf-5, M18, and A1501 (Figure 1). The COGs showed similar distributions among the four strains, except for the COGs K and L, which were quite different in A1501 compared with the other strains. The percentage of genes with COG K annotations, representing transcription clusters, was lower in A1501 than in the other three strains, mainly because it contained a smaller proportion of genes encoding transcriptional regulators. COG L represents proteins with functions in replication, recombination, and repair. There were 50 genes encoding transposases and their inactivated derivatives in A1501 (approximately 1.33% of the total genes with COG annotations), compared with 0.21% in GP72, 0.02% in Pf-5, and 0.11% in M18. The large number of transposases in A1501 indicated that this strain would be more suitable for transposition, providing clues to the genetic diversity within this species and its adaptability to changes in growth conditions.

thumbnailFigure 1. Comparison of COG categories among four pseudomonad PGPR. Functional classifications provided by the COG database [40] were used for functional comparisons among the genomes of P. chlororaphis GP72, P. fluorescens Pf-5, P. aeruginosa M18, and P. stutzeri A1501. The ordinate axis indicates the percentage of genes in each COG functional category relative to the genes of all COG categories. Comparison was based on 22 COGs categories: RNA processing and modification (A), chromatin structure and dynamics (B), energy production and conversion (C), cell cycle control, cell division, chromosome partitioning (D), amino acid transport and metabolism (E), nucleotide transport and metabolism (F), carbohydrate transport and metabolism (G), coenzyme transport and metabolism (H), lipid transport and metabolism (I), translation, ribosomal structure and biogenesis (J), transcription (K), replication, recombination and repair (L), cell wall, membrane, envelope biogenesis (M), cell motility (N), posttranslational modification, protein turnover, chaperones (O), inorganic transport and metabolism (P), secondary metabolites biosynthesis, transport and catabolism (Q), general function prediction only (R), function unknown (S), signal transduction mechanisms (T), intracellular trafficking, secretion and vesicular transport (U), defense mechanisms (V).

Table 1. General genome features of the four studied pseudomonad PGPR

Global alignments provide a powerful tool to identify conserved and specific regions in the genome, which can reveal similar biological behaviors or adaptations to specific niches. We conducted BLASTN analysis using an online version of the Artemis Comparison Tool (WebACT) [41], comparing GP72, Pf-5, and M18 (Figure 2). We excluded A1501 from this analysis, since the alignment analysis showed very low synteny (data not shown). According to alignments at current assemblies, the extent of conservation of regions among the different species of Pseudomonas was difficult to visualize by ACT, mainly because of multiple chromosomal rearrangements. Nevertheless, the genomes of Pf-5 and GP72 showed many regions with conserved sequences and conserved gene order, except for 10 major inversions. BLAST atlas, which provides a quick overview of genomic regions of gene conservation across many genomes [42], was used to compare the reference genome of GP72 to the other three query genomes (Figure 3).

thumbnailFigure 2. Comparison of chromosome structures among genome sequences of pseudomonad PGPR. Pair-wise alignments between genome sequences of P. fluorescens Pf-5, P. chlororaphis GP72, and P. aeruginosa M18 were performed using WebACT [41]. Red bars indicate collinear regions of similarity; blue bars represent regions of similarity that have been inverted in one of the two genomes. Only matches larger than 1 kb are shown.

thumbnailFigure 3. BLAST atlas diagram showing homology among pseudomonad PGPR. Comparisons between P. chlororaphis GP72 and three other pseudomonad PGPR. Colors indicate strains, as follows (starting from the outermost line): red, P. fluorescens Pf-5 (line 1); green, P. aeruginosa M18 (line 2); blue, P. stutzeri A1501 (line 3). Lack of color indicates that genes at that position in GP72 were absent from genome of strain in that line. Predicted CDSs of reference genome (GP72) on plus and minus strand are shown as blue and red blocks; rRNA genes are shown in green, tRNA genes are shown in turquoise. GC skew (line 6) and percent AT (line 7) are also shown.

We established a phylogenetic tree of completely sequenced pseudomonads based on two housekeeping genes (gyrB and rpoD) (Figure 4). The tree showed that GP72 was most closely related to P. fluorescens, and was more closely related to P. aeruginosa M18 than to other opportunistic pathogenic strains of P. aeruginosa. This was probably because the rhizosphere-originated M18 strain has evolved strain-specific genomic features, which benefit its environmental adaptability and competitiveness under certain conditions in the rhizosphere niche.

thumbnailFigure 4. Phylogenetic relationships among completely sequenced Pseudomonas species. Phylogenetic tree for members of the genus Pseudomonas was constructed based on aligned concatenated sequences of gyrB and rpoD using the neighbor-joining method with 1000 bootstrap replicates. Analysis was carried out using Phylip 3.67 software and the tree was plotted using iTOL software. Colors on the phylogenetic tree indicate membership in Pseudomonas phylogenetic groups according to NCBI taxonomy. Completely sequenced species in the genus Pseudomonas include P. aeruginosa (yellow), P. brassicacearum (olive), P. entomophila (purple), P. fluorescens (green), P. fulva (blue), P. mendocina (pink), P. putida (navy), P. stutzeri (magenta), and P. syringae (cyan). In this research, the tree branch of P. chlororaphis, whose draft genome sequence was reported recently, is shown in red. Bar chart associated with nodes indicates numbers of genes conserved between GP72 and the corresponding organism. Conserved genes were determined using mGenomeSubtractor.

An in silico subtractive hybridization analysis using the mGenomeSubtractor web server identified specific and conserved proteins. In this analysis, proteins with homology (H) values of less than 0.42 or more than 0.81 are defined arbitrarily as specific or conserved, respectively [43]. The BLASTP-based homology value distribution of 6091 predicted CDSs from P. chlororaphis GP72 was individually compared with those of the other three subject genomes (Figure 5A) to determine the degree of protein conservation between GP72 and each of the other genomes. Among the genes encoded in the GP72 genome, 3,544 had counterparts in the genome sequence of Pf-5. There were 999 genes conserved among the genomes of GP72, Pf-5, and M18. Comparison among GP72 and all of the other three strains (Pf-5, M18, and A1501) revealed 602 homologous genes and 994 CDSs that were strain-specific to GP72 (Figure 5B). The number of homologs in each genome is shown in Figure 4. In addition, GP72 contained 463 CDSs that were identified as strain-specific (E-value <10-5) when its genome was compared with those of 27 other completely sequenced Pseudomonas strains. Further analyses of these strain-specific CDS may provide clues to the phenotype and the specific environmental adaptations of each strain.

thumbnailFigure 5. Homology analysis between P. chlororaphis GP72 genome and three subject genomes. The mGenomeSubtractor arbitrarily defines CDSs with homology (H) values less than 0.42 as strain-specific, and those with H values greater than 0.81 as conserved [43]. (A) Histogram of BLASTP-based homology value distribution of 6091 predicted CDSs from P. chlororaphis GP72 compared individually with those of three other genomes: P. fluorescens Pf-5, P. aeruginosa M18, and P. stutzeri A1501. (B) Numbers of conserved and specific genes in GP72 compared with three other PGPR strains. Total numbers of conserved and specific genes are shown above columns.

Environmental adaptability

Catabolism

PGPR can use a wide range of nutrients to colonize the rhizosphere successfully. The central metabolic pathways in GP72, such as the Entner–Doudoroff pathway, the pentose phosphate pathway, and the tricarboxylic acid cycle, are consistent with those reported for other Pseudomonas species [44]. Like other Pseudomonas strains, GP72 lacks 6-phosphofructokinase; therefore, it may not have a functional Embden–Meyerhof pathway. The genomes of GP72, Pf-5, M18, and A1501 contained genes encoding a fructose-specific IIA component, I-phosphofructokinase. This enzyme is involved in the fructose dissimilation pathway, catalyzing the conversion of fructose to fructose-1,6-diphosphate [45].

PGPR have a variety of genes related to catabolism and transport of plant-derived compounds, such as amino acids, fatty acids, nucleotides, organic acids, carbohydrates, and other exudates [46,47]. Amino acids are one of the major components of root exudates. Accordingly, there were at least 500 genes involved in amino acid transport and metabolism in the genomes of GP72, Pf-5, and M18, and more than 300 in the genome of A1501.

The ability to catabolize aromatic compounds in exudates is one strategy that could confer a selective advantage in the rhizosphere environment. Oxygenases play key roles in the chemical transformation of recalcitrant organic compounds [48,49]. P. putida modifies diverse aromatics to common intermediates, which feed into central pathways [50]. For example, P. putida KT2440 is able to use aromatic compounds including benzoate, phenylacetate, tyrosine, and vanillate, as the sole carbon and energy source [51]. There were 21 genes encoding dioxygenases (DOs) in the genome of GP72, 22 in M18, 21 in Pf-5, and 9 in A1501. The DOs in GP72, including benzoate 1,2-dioxygenase, anthranilate 1,2-dioxygenase, protocatechuate 3,4-dioxygenase, and catechol 1,2-dioxygenase, were related to degradation of aromatic compounds. We compared the degradation pathways of aromatic compounds, including the three main pathways (Table 2) and several peripheral pathways, among the four species (Additional file 1).

Additional file 1. Comparison of putative genes related to peripheral pathways for aromatic catabolism among pseudomonad PGPR.

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Table 2. Comparison of putative genes related to main pathways for central aromatic catabolism among pseudomonad PGPR

Genes encoding components of the 3-oxoadipate pathway, which is common in soil and plant-associated microorganisms [52], were present in the genomes of all four PGPR analyzed in this study. The pathway has two branches: one converting catechol and the other converting protocatechuate. Both branches produce two tricarboxylic acid cycle intermediates. Based on the comparative genomic analysis, the former branch may derive from the degradation of tryptophan [53], benzoate [54], salicylate [55], phenol [56,57], and so on, while the protocatechuate branch is generated from 4-hydroxybenzoate [58], and numerous lignin monomers such as vanillate [59] and quinate [60]. Analyses of aromatic compound catabolism not only reveal the broad metabolic activities of PGPR, but also provide insights into mediating the production of useful secondary metabolites such as phenazine [61], pyocyanin (PYO) [62], and C-1027 [63].

Some bacteria and fungi degrade tyrosine (Tyr) via the central intermediate homogentisate (2,5-dihydroxyphenylacetate). The reaction proceeds with conversion of Tyr into 4-hydroxyphenylpyruvate (HPP) (by tyrosine aminotransferase), and then formation of homogentisate (by HPP dioxygenase), which is degraded via the homogentisate central pathway [64]. The central pathway involves three enzymes: homogentisate 1,2-dioxygenase (HmgA), fumarylacetoacetate hydrolase (HmgB), and maleylacetoacetate isomerase (HmgC), and yields fumarate and acetoacetate [65]. The comparative genomic analysis indicated that GP72, Pf-5, and M18 could degrade Tyr via the homogentisate pathway. Some Gram-positive bacteria can convert Tyr into homoprotocatechuate (3,4-dihydroxyphenylacetate), rather than homogentisate, producing pyruvate and succinate [66,67]. A variety of microorganisms contain 3,4-dihydroxyphenylacetate 2,3-dioxygenases (HPCD) [68,69], such as Fe(II) (HPCD) and Mn(II) (MndD). These enzymes contain different active sites resulting in different structures and HPCD activities [70,71]. The annotated amino acid sequence of the HPCD from GP72 exhibited 63–64% identities with those of the corresponding enzymes from Escherichia coli[68] and Klebsiella pneumonia[69]. Further research is required to characterize the activities of HPCD in different Pseudomonas species.

In a few organisms, phenylethylamine, an intermediate of phenylalanine degradation, can be converted into phenylacetaldehyde by quinohemoprotein amine dehydrogenase, and then transformed into phenylacetate by phenylacetaldehyde dehydrogenase [72-74]. The corresponding genes were predicted in the genomes of GP72 and Pf-5, but they were not located in a single operon.

Phenylacetyl-CoA is derived from various substrates such as phenylalanine, lignin-related aromatic compounds, and environmental contaminants, and can be degraded to succinyl-CoA and acetyl-CoA [75,76]. Based on the genomic comparison at the 60% identity threshold, we found that the phenylacetate degradation pathway was present in GP72 and Pf-5. However, this pathway was not detected in M18 or A1501 at the same identity level, indicating potentially different evolutionary directions in specific niches.

Five putative phenylpropionate dioxygenases and related ring-hydroxylating dioxygenases of unknown specificity can also participate in aromatic compound catabolism [77].

Plant-derived substances not only serve as important carbon and energy sources for rhizosphere bacteria, but also influence bacterial behaviors [78,79]. For example, the ratio of rhizospheric carbon:nitrogen (C:N) can alter the nutritional status of Rhizoctonia solani, making the fungus a pathogen [80]. Tomato root exudates promote germination of spores of the tomato root pathogen F. oxysporum f. sp. radicis-lycopersici, whereas the biocontrol agent P. fluorescens WCS365 delays this process [81]. Microarray analyses showed that root exudates affected the transcriptome of P. aeruginosa PAO1 by influencing genes encoding enzymes related to alginate biosynthesis and twitching motility [82]. Therefore, the production of plant-derived exudates could alter the composition of rhizospheric microorganism communities. Further research is required to investigate the molecular mechanisms underlying changes in community structure.

Transport

Consistent with the abundance of genes related to metabolism of plant-derived substances, the four PGPR contained many putative transport genes related to substrate uptake and excretion (Table 3). GP72 and Pf-5 contained similar numbers of transport genes. In bacteria, secretion systems play an important role in transport or translocation of effectors for adaptation to their natural surroundings. The genomes of these four PGPR contained type I, type II, type IV, type V, and type VI secretion systems, as well as the chaperone-usher secretion system and the twin-arginine translocation system. M18 also contained the Type III (flagellar/pathogenesis) secretion system, a key virulence factor in pathogenic Pseudomonas[83].

Table 3. Numbers of putative genes encoding transporters in genomes of four pseudomonad PGPR

Defense pathways

Previous studies showed that GP72 resists streptomycin up to a concentration of 100 μg ml-1, and tolerates salt (5% NaCl solution). Both of these resistances are stronger than those of P. chlororaphis strain 30–84 [7]. Antibiotic resistance assays showed that GP72 displays resistance to penicillin, spectinomycin, streptomycin, and tetracycline. Here, our genomic analyses confirmed different kinds of defenses in the four PGPR, including resistance/tolerance to heavy metals, temperature stress, osmotic stress, oxidative stress, and multiple drugs.

Many essential trace elements contain metal ions that are important components of the active sites of many enzymes. As such, they play a vital role in many biological processes, including photosynthetic and respiratory pathways. However, most heavy metals are toxic at higher concentrations. For example, copper ions can damage the cytoplasmic membrane of E. coli by catalyzing harmful redox reactions [84]. In many regions, agricultural soils are heavily contaminated with various heavy metals originating from chemical fertilizers and industrial processes. Consequently, certain soil bacteria have developed resistance to toxic metals, either via active efflux mechanisms to pump the toxic metals out [85], or by enzymatic detoxification to convert a toxic ion into a harmless one [86,87]. Our genomic analysis revealed many genes related to heavy metal resistance (summarized in Table 4).

Table 4. Summary and comparison of putative genes related to metal resistance in four pseudomonad PGPR genomes

The four pseudomonad PGPR studied contained at least two different copper resistance systems, which resemble those identified in the plant growth-promoting endophytic bacterium P. putida W619 [15]. One system is periplasmic detoxification encoded by copABCDGcopRS, which is well-characterized in the plasmid pPT23D from P. syringae pv. tomato strain PT23.2 [88]. This system is also widely distributed in other Pseudomonas species [15,88,89]. Another copper resistance system is the cytoplasmic detoxification system cue, which maintains a strict quota of cellular copper in other organisms [90,91]. The Cu(I)-responsive transcriptional regulator CueR [91] activates expression of a copper-translocating P-type ATPase (CopA) [92], a periplasmic multicopper oxidase (CueO) [93], and a copper chaperone (CopZ) [90] under mild copper stress. CopA exports Cu(I) from the cytoplasm to the periplasm, and then Cu(I) is converted into the less toxic Cu(II) form by CueO. A third copper resistance strategy in the genome of GP72 consisted of cusFABBC (MOK_00020-00016) and copRS (MOK_00012-00013). The cus operon is related to periplasmic detoxification, and is exclusively found in Gram-negative bacteria [94,95]. Therefore, the mechanism for copper resistance in P. chlororaphis is very complex, and has not been completely characterized yet. Further research is required to clarify the details of this system.

Pseudomonas spp. have arsenic-resistance genes (arsRB, arsCH and arsC) that are dispersed throughout the genome. The chromosomal ars operon was characterized in P. aeruginosa. A homologous ars operon was detected in some, but not all, Pseudomonas species, indicating that some other mechanisms are involved in arsenic resistance in pseudomonads [96]. Our genomic analysis indicated that the GP72 genome lacked a homologous gene encoding an arsenite- and antimonite-stimulated ATPase (ArsA). However, a previous study showed that ArsB could export arsenite ions in the absence of ArsA in E. coli[97]. Since ArsB was predicted in the genome of GP72, we can assume that this strain also shows arsenic resistance. The czcABCRD operon encoding a cation-proton antiporter, which is responsible for cobalt, zinc, and cadmium resistances [98], was predicted in the genomes of GP72 and Pf-5. Other genes found in their genomes may also be related to heavy metal resistance, such as homologs of chrA and chrB genes involved in chromate resistance [99], and homologs of genes encoding siderophores that participate in metal homeostasis in P. aeruginosa[100].

In recent years, multidrug resistance has reached alarming levels, especially in the field of medicine [101]. Such resistance mechanisms have been fully described by Alekshun and Levy [102]. Some PGPR strains contain a broad spectrum of putative multidrug resistance genes, including genes related to well-developed efflux systems [103], penicillin-binding protein-mediated resistance [104], and enzymes that degrade antibiotics (Additional file 2). Efflux systems contribute significantly to resistance to multiple antimicrobial compounds. This is a very important mechanism to enhance biological fitness [105]. Like other Pseudomonas species, GP72 contained 37 putative ABC transporters, which potentially participate in the uptake or efflux of toxic metabolites and other drugs. Some secondary transport system genes were also present in GP72 (Table 3); there were 35 genes encoding RND family members, three genes for MATE family members, and four genes for SMR family members. All pseudomonad PGPR contained genes encoding the efflux pumps TtgABC and TtgDEF (toluene tolerance genes). These enzymes prevent the accumulation of toluene and other related aromatics, such as phenol [106]. Genes encoding an MexEF-OprN efflux pump, a member of the RND family, were also present in the genomes of GP72, Pf-5, M18, and A1501, but the order of the efflux pump genes in the genome differed among the four strains. The efflux pump operon is upregulated by MexT under nitrosative stress and chloramphenicol stress [107]. Overexpression of this system can decrease the production of several secondary metabolites such as PYO, elastase, and rhamnolipids [108]. AcrB (homologous to MOK_00261 in the GP72 genome), which also belongs to the RND family [109], plays a role in pumping out basic dyes (such as acriflavine), most antibiotics (except aminoglycosides), and detergents (such as bile salts, Triton X-100, and SDS) [110]. In conclusion, the genomic data indicated that these PGPR harbor genes that can confer resistance to multiple drugs, including penicillin, aminoglycosides, fluoroquinolones, trimethoprim-sulfamethoxazole, lipid A, and acriflavine.

Additional file 2. Putative genes involved in tolerance to antibiotics, osmotic-, and temperature-shock in the pseudomonad PGPR genomes.

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Bacteria that inhabit the rhizosphere of plants can use plant-derived compounds as nutrients; however, they must be able to tolerate damaging compounds produced by plants, such as reactive oxygen species (ROS). Several ROS are continuously produced during aerobic metabolism of plants. They participate in regulating plant cell expansion [111] and other biological processes. ROS show antimicrobial activities [112], as they can damage proteins, nucleic acids, and cell membranes. Rhizospheric bacteria produce several enzymes to resist oxidative stress [113]. Genes encoding these enzymes have already been identified in the genomes of Pf-5 and A1501 [17,18]. Putative ROS-detoxifying enzymes in GP72 included 11 peroxidases, five catalases, two superoxide dismutases, and 19 glutathione S-transferases. There was no significant difference in the numbers of these enzymes among the four PGPR (Figure 6). Genes encoding regulators of the oxidative stress response, including the two-component regulator GacS/GacA [114], SoxR, and OxyR [113,115] were present in the genomes of GP72, Pf-5, M18, and A1501. However, a homolog of SoxR in P. aeruginosa did not function as a key regulatory player in the bacterial oxidative stress response [116]. Exopolysaccharides such as alginate [117] and polyhydroxyalkanoates (PHAs) [118] are important for tolerance to oxidative stress under ambient pressure. For instance, PHA accumulation enhances the survival of pseudomonads under salinity stress, oxidative stress, and cold-shock [119,120]. Additionally, a pyrroloquinoline-quinine (PQQ) synthase expressed in E. coli improves its resistance to photodynamically produced ROS [121].

thumbnailFigure 6. Numbers of predicted enzymes with roles in oxidative stress response. Predicted proteins with roles in the oxidative stress response found in P. chlororaphis GP72, P. fluorescens Pf-5, P. aeruginosa M18, and P. stutzeri A1501. Four types of enzymes (glutathione S-transferase, peroxidase, catalase, and superoxide dismutase) were compared among the four species.

Rhizosphere bacteria usually survive in a changeable environment; therefore, they have evolved several traits related to adaptation [122]. The genomes of GP72, Pf-5, M18, and A1501 contained homologs of genes related to tolerating cold-shock, including cspACDG, which is constitutively expressed at 37°C [123]. In P. aeruginosa cells, a temperature increase from 30 to 45°C enhances production of 17 proteins, including the heat-shock proteins DnaK and GroEL [124]. A chaperone system formed by DnaK, DnaJ, and GrpE proteins modulates the heat-shock response in E. coli[125] (Additional file 2). As an opportunistic pathogen, P. aeruginosa has evolved to survive in diverse stressful environments. A microarray analysis showed that P. aeruginosa synthesizes osmoprotective compounds, such as hydrophilins and osmoprotectants, to cope with osmotic stress [126,127]. Glycine betaine (GB), a major osmoprotectant for many bacteria [128], can accumulate via de novo synthesis or via absorption from the environment [126]. Mutant analyses and 13C NMR studies confirmed GB catabolism in P. aeruginosa[129]. Previously, it was shown that GP72 shows strong osmotic stress tolerance [7]. The genomic analysis in this study showed that the genomes of GP72, Pf-5, and M18 contained at least one complete gene set required for conversion of GB to glycine; this gene set included gbcAB, dgcAB, and soxGADB. In contrast, A1501 contained only a homolog of the betAB operon, which encodes a system for oxidation of choline to GB under osmotic stress conditions [130]. Osmoregulated periplasmic glucans are highly branched oligosaccharides found in the periplasm of Gram-negative bacteria. They are probably produced in response to periplasmic osmolality, which is controlled by the products of mdoD and mdoG[131]. Enteric bacteria can modulate their cytoplasmic osmolality through mobilizing K+, glutamate, and other compatible solutes, such as trehalose, proline, and GB [132]. K+ first responds to osmotic upshifts via the transporters Trk and Kdp, possibly acting as a putative osmoregulatory second messenger [126,133]. The genes related to osmotic stress tolerance are listed in Additional file 2.

We found that resistance genes were present in the genomes of all four PGPR, although some genes showed low similarity to others. These results indicated that PGPR may undergo long-term evolution to adapt to specific ecological niches. To adapt to changeable environments, each pseudomonad PGPR strain has a complex array of regulatory networks, including sigma factors, transcriptional regulators, and a variety of two-component transcriptional regulators.

Rhizosphere colonization

A confocal laser scanning microscopy analysis showed that P. fluorescens WCS365 and P. chlororaphis PCL1391 are able to effectively colonize the tomato rhizosphere [134], and the major traits for niche competition were identified [135]. Development of new genetic approaches such as in vivo expression technology (IVET) together with “omic” technologies has provided opportunities to identify genes required for rhizosphere competence, and to elucidate the genetic mechanisms of plant–microbe interactions [14,136]. Pseudomonad PGPR show certain competitive colonization traits, such as motility and the ability to attach to the root surface.

First, motility is a major trait for the competitive tomato root-tip colonization of P. fluorescens, based on chemotaxis [137,138]. We found genes related to chemotaxis and motility in the genomes of the four PGPR; GP72 contained 14 genes responsible for various aspects of chemotaxis, including genes encoding a two-component system (CheA/CheY). The activity of the histidine kinase CheA can be regulated by methyl-accepting chemoreceptor proteins (MCPs) during chemotaxis [139]. Swimming behavior can be initiated when the phosphorylated CheY binds to the flagellar switch protein, Flim [140]. In the present study, we found 28 genes encoding MCPs and 40 genes associated with flagella biosynthesis, including the flg and fli operons.

The second trait of competitive colonization is attachment to the root surface. In this study, several genes involved in attachment were predicted in the PGPR genomes (Additional file 3). The functions of some genes have been confirmed experimentally in certain Pseudomonas species, including genes associated with type IV pili and twitching motility [141], genes for biosynthesis of alginate [142], hemolysin [135,143], filamentous hemagglutinin [144], and lipopolysaccharide O-antigen [145], and genes for other enzymes or factors involved in adhesion [135]. For instance, twitching motility, a type of flagella-independent surface motility mediated by type IV pili, is a mechanism of rapid bacterial colonization [141]. As well as the common type IV pilus assembly proteins, we identified a second set of genes in P. chlororaphis GP72 that were previously reported to play roles in the biogenesis of the Flp subfamily of type IVb

    t
ight
    ad
herence (Tad) pili [146]. However, tad genes were not found in the genomes of the other three PGPR at the 60% identity threshold, when compared with the genome of GP72. Tad pili are an essential and conserved host-colonization factor in Bifidobacterium species [147]. Therefore, we can speculate that the tad genes are probably derived from organisms outside of the genus Pseudomonas. In strain P. putida KT2440, a series of rap genes (root-activated promoters) were identified during maize root colonization by IVET [148]. Some of the promoters isolated by rap fusions responsible for adhesion were present in the genomes of GP72, Pf-5, and M18, such as secB (rap1-2 fusion) [135] and algD (rap2-45 fusion) [142]. The genetic locus aggA, which is involved in agglutination and adherence [149], was also predicted in the genomes of GP72 and Pf-5. Espinosa-Urgel et al. [143] characterized several mus (mutants unattached to seeds) loci in P. putida, and confirmed that mutants of these loci show impaired attachment to corn seeds. The genome of GP72 contained four mus loci: mus-13, mus-21, mus-24, and mus-27, with possible functions as a carbon starvation protein, transporter, calcium-binding protein, and hemolysin, respectively. Genes involved in competitive rhizosphere colonization have been well studied in P. fluorescens. These include xerC, which encodes a site-specific recombinase. xerC is a homolog of sss in P. chlororaphis PCL1391; sss plays a role in phase variation caused by DNA rearrangements [3,150]. The nuo operon encodes subunits of NADH: ubiquinone oxidoreductase, which is related to ATP-dependent rotation of flagella [145]. Some of the genes isolated by IVET and identified to play roles in plant–microbe interactions [14,151] were present in the genomes of GP72, Pf-5, M18, and A1501 when compared with the genome of P. fluorescens SBW25 (data not shown). However, it remains to be confirmed whether these genes specifically contribute to rhizosphere competence.

Additional file 3. Comparison of putative genes related to attachment to plant rhizosphere among pseudomonad PGPR.

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GP72, Pf-5, and A1501 lacked virulence factors found in plant pathogens, such as the type III secretion system, phytotoxins, and exoenzymes associated with cell wall degradation. Homologs of genes encoding phytotoxins produced by P. syringae (coronatine, syringomycin, syringopeptin, tabtoxin, and phaseolotoxin) [152] were also absent from the genomes of GP72, Pf-5, M18, and A1501. Their genomes did not contain genes related to the biosyntheses of cellulases, pectinases, or pectin lyases, which play roles in the degradation of cell wall components. Therefore, the lack of these genes can result in efficient rhizosphere colonization and improvement of plant growth.

Biocontrol activities

Biocontrol activities are important mechanisms by which PGPR suppress plant pathogens. The main biocontrol strategy is the production of a spectrum of antibiotics [2]. The antibiotics produced by the biocontrol agents GP72, Pf-5, and M18 are listed in Table 5. Phenazines are versatile secondary metabolites produced by P. fluorescens, P. chlororaphis, and Pseudomonas aureofaciens[153]. These compounds play critical roles in the biological control activities of Pseudomonas spp. [5]. Previous studies showed that GP72 can completely suppress various phytopathogens, mainly because of the production of PCA and 2-OH-PHZ. Clusters of phenazine-compound biosynthetic genes were present in the genomes of both GP72 and M18, but the genes differed between the two species. The GP72 genome contained phzO, encoding an aromatic monooxygenase [154] that converts PCA to 2-OH-PHZ, whereas M18 contained two phz gene clusters and one set of modified phzMS genes. phzM and phzS encode a putative S-adenosylmethionine-dependent N-methyltransferase and a putative flavin-dependent hydroxylase, respectively. They participate in the conversion of PCA to PYO in P. aeruginosa. PYO is a virulence factor to cystic fibrosis patients infected by pathogenic pseudomonads [155]. However, M18 does not produce detectable levels of PYO at 28°C, mainly because of the temperature-dependent expression of phzM and its regulatory genes lasI and ptsP. The biocontrol activity of M18 is, therefore, not attributed to PYO but to PCA [33], and it shows lower pathogenicity than other closely related strains. Previous studies showed that some plant pathogens are more strongly inhibited by 2-OH-PHZ than by PCA [154]. Another important antibiotic is Plt, which is produced by both Pf-5 and M18. Strains with the ability to produce the insect toxin ‘Fit’ (P.

    f
luorescens
    i
nsecticidal
    t
oxin) [156] show potent insecticidal activity [157]. The fitD gene encoding the cytotoxin in GP72 showed 84% identity to that in Pf-5. The amino acid sequence of Fit shared 77% amino acid identity with the insect toxin Mcf (
    m
akes
    c
aterpillars
    f
loppy) produced by the entomopathogen Photorhabdus luminescens[157].

Table 5. Secondary metabolites produced by pseudomonad biocontrol strains

Fluorescent pseudomonads can produce pyoverdin (Pvd), a fluorescent siderophore, and chelate Fe(III) efficiently under low-iron conditions to improve their biocontrol activity [158,159]. The fluorescent pseudomonads GP72, Pf-5, and M18 contained the complete Pvd biosynthetic gene cluster. In addition, Pf-5 and M18 contained genes encoding another siderophore, Pch, which has antifungal activity [160]. GP72 lacked these genes, but it contained putative genes for synthesis of achromobactin (Acr), a temperature-regulated secondary siderophore. The related biosynthetic gene clusters in GP72 included acsFDECBA, yhcA, and acrABCD, which are responsible for the biosynthesis of Acr, permease, and a specific outer membrane receptor, respectively [161,162]. Siderophores can bind metals other than iron [163] and, therefore, can play roles in sequestering toxic metals including aluminum, cobalt, copper, and lead [100]. GP72 contained a locus (MOK_02694) encoding a nickel-uptake substrate-specific transmembrane protein, adjacent to the acr operon. Acr in GP72 may be involved in metal transport, signaling pathways, or antimicrobial activities. The comparative genomic analysis indicated that there was no homology of the acr operon between Pf-5 and M18. As well as producing their own siderophores, Pseudomonas can also use siderophores produced by other microorganisms. For example, A1501 may obtain iron via heterologous siderophores, since it lacks pathways for siderophore biosynthesis [18]. Genes involved in the uptake of soluble Fe(III) complexes, that is, those encoding putative outer membrane receptors, were present in the genomes of the four pseudomonads: 31 genes in GP72, 45 in Pf-5, 36 in M18, and 24 in A1501. The variable iron acquisition systems among Pseudomonas reflect their large capacity for niche colonization, providing insights into how their biocontrol abilities can be improved. Therefore, the availability of complete genome sequences provides an excellent opportunity to explore the diversity and evolution of biosynthetic pathways in different species/strains [153,164].

Direct plant-growth promotion

Rhizobacteria can directly promote plant growth, and some strains have been developed as ‘biofertilizers’. The mechanisms underlying plant-growth promotion include nitrogen fixation, increased nutrient availability, production of phytohormones, and so on [165]. The biofertilizers Azotobacter[12] and P. stutzeri[18], both of which belong to the Pseudomonadaceae, are able to fix nitrogen. The genome of A1501 contains a cluster of 59 genes specific to nitrogen fixation, and the nif operon shows a high degree of similarity to that in the genome of Azotobacter vinelandii. Therefore, we compared A1501 with GP72, Pf-5, and M18 at a threshold of 30% identity to screen for putative genes related to nitrogen fixation. The analyses revealed 13, 13, and 14 homologous genes in GP72, Pf-5, and M18, respectively (Additional file 4); however, these three strains lacked the nitrogenase complex-encoding genes nifDK[166,167]. We conducted a similar screen for denitrification genes; of 45 genes in A1501, 7 homologs were found in the genome of Pf-5, and 21 in the genome of GP72. We can speculate that the low identities may be because of the relatively distant evolutionary relationship, as shown in the phylogenetic analysis (Figure 4). GP72 and M18 contained several genes involved in denitrification: narL and narX, which encode a two-component regulatory system; narGHJI, which encodes respiratory nitrate reductase [168]; and nor genes, which are involved in nitric oxide metabolism. Previous studies reported that P. fluorescens and P. chlororaphis produce N2O as the only detectable gaseous product of denitrification [169], while P. stutzeri emits only N2, and P. aeruginosa produces both N2 and N2O [170]. Thus, the denitrification process can accommodate large quantities of anthropogenic nutrients, converting nitrate into nitrogen. This could decrease nitrate accumulation and counteract eutrophication in the environment [171].

Additional file 4. Comparison of putative genes involved in nitrogen fixation and denitrification process among pseudomonad PGPR.

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Limited quantities of soluble phosphate can restrict plant growth. The genomes of GP72, Pf-5, M18, and A1501 contained several genes encoding nonspecific phosphatases, inositol phosphate phosphatases, and C-P lyases. These enzymes catalyze the conversion of insoluble phosphorus into plant-available forms, thereby facilitating plant growth [172]. In addition, many PGPR can produce phytohormones to stimulate plant growth. GP72 can synthesize IAA [7] via a tryptophan-dependent pathway [173], since it contained genes encoding tryptophan-2-monooxygenase (iaaM, MOK_03651/04103/05943) and indoleacetamide hydrolase (iaaH, MOK_00889/01660/02975). A1501 lacks the putative IAA synthesis pathway [18]. The genomes of GP72, Pf-5, M18, and A1501 contained putative 1-aminocyclopropane-1-carboxylate (ACC) deaminases. This enzyme can counteract the ethylene response in plants by degrading the ethylene precursor ACC. In other Pseudomonas strains, ACC deaminases promote root elongation and suppress plant diseases [174]. Biosynthetic genes for PQQ, a plant-growth promotion factor, are clustered in the conserved pqqABCDEF operon [175]. This operon was present in the genomes of Pf-5, M18, and A1501. GP72 lacked pqqA, but the enzyme encoded by pqqA is not required for biosynthesis of PQQ in Methylobacterium[176].

Conclusions

We analyzed plant growth-promoting traits by a comparative genomics analysis of four representative pseudomonad PGPR strains. The genes that were conserved among the different Pseudomonas species have provided clues to the common characteristics of pseudomonad PGPR, such as rhizosphere competence traits (nutrient catabolism and transport, resistance to various environmental stresses, and rhizosphere colonization). The strain-specific genes differentiated each strain on the basis of its lifestyle, specific ecological adaptations, and physiological role in the rhizosphere. The recently reported genome of P. chlororaphis, together with other sequenced strains of different species of pseudomonad PGPR, provides insights into the genetic basis of diversity and adaptation to specific environmental niches. Comparative genomic analyses, combined with certain IVET-based analyses, can reveal many genetic factors related to plant growth promotion. First, the strong adaptability of PGPR to their environment is related to putative genes involved in catabolism and transport of plant-derived compounds and resistance to various environmental stresses (heavy metals, ROS, cold-, heat-, or osmotic-shock, and multiple drugs). These genes were very common in the genomes of PGPR, especially those of P. chlororaphis and P. fluorescens, and provide the foundation for rhizosphere fitness. Second, we compared genes involved in rhizosphere colonization. Some related genes showed low similarity between P. chlororaphis GP72 and the other three strains, including biosynthetic genes for the O-antigen and type IV pilus assembly. Hence, GP72 may have stronger rhizosphere competence than the other three strains. Third, we analyzed genes related to biocontrol activities, namely those encoding production of antifungal metabolites such as PCA and Plt. The genomic information indicated that the secondary metabolites differ markedly among the four PGPR. For example, GP72 contained putative gene clusters for biosynthesis of the siderophore Acr, whereas the other strains contained gene clusters for biosynthesis of different siderophores. Some rhizobacteria cannot produce antifungal compounds, but promote plant growth in the absence of pathogens. One such strain was P. stutzeri A1501, which fixes nitrogen. Therefore, the metabolic pathways, transporters, and regulators related to cell metabolism provide directions to improve plant growth-promoting activities. Genetic modification may accelerate the commercialization of PGPR as biocontrol agents, which could further contribute to sustainable development of agriculture.

Methods

Medium and growth conditions for P. chlororaphis GP72

P. chlororaphis GP72 (deposited in China General Microbiological Culture Collection Center; collection number 1748), isolated from green pepper rhizosphere in eastern China, was incubated at 28°C in King’s medium B [177].

Genome sequencing and annotation

The genome of P. chlororaphis GP72 was sequenced using the Illumina GAIIx platform and assembled using VELVET 1.1.07. The genome of GP72 was automatically annotated using the RAST server [178], and proceeded with manual curation and comparative analysis using the IMG/ER system (https://img.jgi.doe.gov/cgi-bin/er/main.cgi webcite) [179]. The genome sequence is available at the IMG database [39]. Information of COGs [40], combined with that from the Conserved Domain Database, was also used in the comparisons. The metabolic pathways were examined using KAAS (KEGG Automatic Annotation Server) [180] and the MetaCyc database [181].

Nucleotide sequence accession number

This whole genome shotgun project has been deposited in DDBJ/EMBL/GenBank under the accession number AHAY00000000.

Genome comparisons

The genome sequence of GP72 was aligned against sequences of other Pseudomonas genomes from NCBI’s Entrez database and the IMG database. Pair-wise alignments were performed using WebACT (http://www.webact.org/WebACT/home webcite) [41]. BLAST atlases [42] were generated using the CBS DTU online tool, GeneWiz browser 0.94 server (http://www.cbs.dtu.dk/services/gwBrowser/ webcite). Strain-specific and conserved genes were identified using the mGenomeSubtractor web server (http://bioinfo-mml.sjtu.edu.cn/mGS/ webcite) [43]. The conserved CDSs were identified using a homology (H) value cut-off of 0.42 at E-value <10-5. Comparative genomic analyses of GP72, Pf-5, M18, and A1501 were conducted using the tool set available at the IMG website; genes homologous to those in GP72 were computed with an E-value < 10-2 and at 60% identity; BLAST comparisons between PGPR and P. stutzeri A1501 were screened at the 30% identity threshold.

Phylogenetic analysis

The phylogenetic relationships among completely sequenced Pseudomonas were determined by a multilocus sequence analysis using a concatenated data set of gyrB and rpoD genes. Multiple-sequence alignments were carried out with Clustal W (http://www.genome.jp/tools/clustalw/ webcite) [182]. Evolutionary distances were calculated using the neighbor-joining method [183] with 1000 bootstrap replicates, using Phylip 3.67 software (http://evolution.genetics.washington.edu/phylip.html webcite). The phylogenetic tree was generated using interactive tree of life (iTOL) software [184].

Abbreviations

PGPR: Plant growth-promoting rhizobacteria; COG: Clusters of Orthologous Groups; Plt: Pyoluteorin; Prn: Pyrrolnitrin; PCA: Phenazine-1-carboxylic acid; 2-OH-PHZ: 2-Hydroxyphenazine; HCN: Hydrogen cyanide; IAA: Indole-3-acetic acid; PYO: Pyocyanin; Pvd: Pyoverdin; Pch: Pyochelin; ACT: Artemis Comparison Tool; DO: Dioxygenase; Tyr: Tyrosine; HPP: 4-Hydroxyphenylpyruvate; HPC: Homoprotocatechuate (3,4-Dihydroxyphenylacetate); HPCD: 3,4-Dihydroxyphenylacetate 2,3-dioxygenases; ROS: Reactive oxygen species; PHA: Polyhydroxyalkanoate; PQQ: Pyrrolquinoline quinine; GB: Glycine betaine; IVET: in vivo expression technology; ABC transporter: ATP binding cassette transporter; MFS: Major facilitator superfamily; TRAP-T: Tripartite ATP-independent periplasmic transporter; PTS: Phosphotransferase system; GntT: Guconate transporter; LysE family: Lysine exporter family; RhtB family: Resistance to homoserine/threonine family; APC family: Amino acid-polyamine-organocation family; DMT family: Drug/metabolite transporter family; RND family: Resistance-nodulation-cell-division family; MATE family: Multidrug and toxic compound extrusion family; SMR family: Small multidrug resistance family; Fit: P. fluorescens insecticidal toxin; Mcf: Makes caterpillars floppy; Acr: Achromobactin; ACC: 1-Aminocyclopropane-1-carboxylate; iTOL: Interactive tree of life

Competing interests

The authors declare that they have no competing interests.

Authors’ contributions

XHZ, XMS, HBH, and HSP conceived, coordinated, and designed the study. WW, XHZ and XMS were responsible for sequencing, finishing, and annotating. XMS, XHZ, and HSP performed experiments and data analyses. XHZ, XMS, and HBH drafted the manuscript. All authors read and approved the final manuscript.

Acknowledgements

We are grateful to many people who have extended their support to us during this project. First, we thank Dr. Huajun Zheng and his colleagues for genome sequencing performed at the Chinese National Human Genome Center, Shanghai. We thank Dr. Hongyu Ou, Shanghai Jiao Tong University, for assistance with annotation. We thank Dr. Jia Xu for advice on the manuscript. We also thank Prof. Yuquan Xu for assistance with research on P. aeruginosa M18. This work was supported by the National Key Basic Research Program of China (No. 2009CB118906 and No. 2012CB721005), the National Natural Science Foundation of China (No. 31270084), and the National High Technology Research and Development Program of China (No. 2012AA022107).

References

  1. Clarke PH: The metabolic versatility of pseudomonads.

    Antonie Van Leeuwenhoek 1982, 48(2):105-130. PubMed Abstract | Publisher Full Text OpenURL

  2. Haas D, Defago G: Biological control of soil-borne pathogens by fluorescent pseudomonads.

    Nat Rev Microbiol 2005, 3(4):307-319. PubMed Abstract | Publisher Full Text OpenURL

  3. Chin AWTF, Bloemberg GV, Mulders IH, Dekkers LC, Lugtenberg BJ: Root colonization by phenazine-1-carboxamide-producing bacterium Pseudomonas chlororaphis PCL1391 is essential for biocontrol of tomato foot and root rot.

    Mol Plant Microbe Interact 2000, 13(12):1340-1345. PubMed Abstract | Publisher Full Text OpenURL

  4. Raaijmakers JM, Bonsall RF, Weller DM: Effect of population density of Pseudomonas fluorescens on production of 2,4-diacetylphloroglucinol in the rhizosphere of wheat.

    Phytopathology 1999, 89(6):470-475. PubMed Abstract | Publisher Full Text OpenURL

  5. Thomashow LS, Weller DM: Role of a phenazine antibiotic from Pseudomonas fluorescens in biological control of Gaeumannomyces graminis var. tritici.

    J Bacteriol 1988, 170(8):3499-3508. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  6. Huang X, Zhang X, Xu Y: PltR expression modulated by the global regulators GacA, RsmA, LasI and RhlI in Pseudomonas sp. M18.

    Res Microbiol 2008, 159(2):128-136. PubMed Abstract | Publisher Full Text OpenURL

  7. Liu H, He Y, Jiang H, Peng H, Huang X, Zhang X, Thomashow LS, Xu Y: Characterization of a phenazine-producing strain Pseudomonas chlororaphis GP72 with broad-spectrum antifungal activity from green pepper rhizosphere.

    Curr Microbiol 2007, 54(4):302-306. PubMed Abstract | Publisher Full Text OpenURL

  8. Howell CR, Stipanovic RD: Suppression of Pythium ultimum-induced damping-off of cotton seedlings by Pseudomonas fluorescens and its antibiotic, pyoluteorin.

    Phytopathology 1980, 70:712-715. Publisher Full Text OpenURL

  9. Nowak-Thompson B, Chaney N, Wing JS, Gould SJ, Loper JE: Characterization of the pyoluteorin biosynthetic gene cluster of Pseudomonas fluorescens Pf-5.

    J Bacteriol 1999, 181(7):2166-2174. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  10. Hammer PE, Hill DS, Lam ST, Van Pee KH, Ligon JM: Four genes from Pseudomonas fluorescens that encode the biosynthesis of pyrrolnitrin.

    Appl Environ Microbiol 1997, 63(6):2147-2154. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  11. Laville J, Blumer C, Von Schroetter C, Gaia V, Defago G, Keel C, Haas D: Characterization of the hcnABC gene cluster encoding hydrogen cyanide synthase and anaerobic regulation by ANR in the strictly aerobic biocontrol agent Pseudomonas fluorescens CHA0.

    J Bacteriol 1998, 180(12):3187-3196. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  12. Okon Y, Bloemberg GV, Lugtenberg BJJ: Biotechnology of biofertilization and phytostimulation. In In Agricultural Biotechnology . Edited by Altman A. New York: Marcel Dekker; 1998:327-349. OpenURL

  13. Rodríguez-Palenzuela P, Matas IM, Murillo J, López-Solanilla E, Bardaji L, Pérez-Martínez I, Rodríguez-Moskera ME, Penyalver R, López MM, Quesada JM, Biehl BS, Perna NT, Glasner JD, Cabot EL, Neeno-Eckwall E, Ramos C: Annotation and overview of the Pseudomonas savastanoi pv. savastanoi NCPPB 3335 draft genome reveals the virulence gene complement of a tumour-inducing pathogen of woody hosts.

    Environ Microbiol 2010, 12(6):1604-1620. PubMed Abstract | Publisher Full Text OpenURL

  14. Silby MW, Cerdeño-Tárraga AM, Vernikos GS, Giddens SR, Jackson RW, Preston GM, Zhang X, Moon CD, Gehrig SM, Godfrey SAC, Knight CG, Malone JG, Robinson Z, Spiers AJ, Harris S, Challis GL, Yaxley AM, Harris D, Seeger K, Murphy L, Rutter S, Squares R, Quail MA, Saunders E, Mavromatis K, Brettin TS, Bentley SD, Hothersall J, Stephens E, Thomas CM: Genomic and genetic analyses of diversity and plant interactions of Pseudomonas fluorescens.

    Genome Biol 2009, 10(5):R51. PubMed Abstract | BioMed Central Full Text | PubMed Central Full Text OpenURL

  15. Wu X, Monchy S, Taghavi S, Zhu W, Ramos J, van der Lelie D: Comparative genomics and functional analysis of niche-specific adaptation in Pseudomonas putida.

    FEMS Microbiol Rev 2011, 35(2):299-323. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  16. Collins FS, Green ED, Guttmacher AE, Guyer MS: A vision for the future of genomics research.

    Nature 2003, 422(6934):835-847. PubMed Abstract | Publisher Full Text OpenURL

  17. Paulsen IT, Press CM, Ravel J, Kobayashi DY, Myers GSA, Mavrodi DV, DeBoy RT, Seshadri R, Ren Q, Madupu R, Dodson RJ, Durkin AS, Brinkac LM, Daugherty SC, Sullivan SA, Rosovitz MJ, Gwinn ML, Zhou L, Schneider DJ, Cartinhour SW, Nelson WC, Weidman J, Watkins K, Tran K, Khouri H, Pierson EA, Pierson LS 3rd, Thomashow LS, Loper JE: Complete genome sequence of the plant commensal Pseudomonas fluorescens Pf-5.

    Nat Biotechnol 2005, 23(7):873-878. PubMed Abstract | Publisher Full Text OpenURL

  18. Yan Y, Yang J, Dou Y, Chen M, Ping S, Peng J, Lu W, Zhang W, Yao Z, Li H, Liu W, He S, Geng L, Zhang X, Yang F, Yu H, Zhan Y, Li D, Lin Z, Wang Y, Elmerich C, Lin M, Jin Q: Nitrogen fixation island and rhizosphere competence traits in the genome of root-associated Pseudomonas stutzeri A1501.

    Proc Natl Acad Sci U S A 2008, 105(21):7564-7569. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  19. Nelson KE, Weinel C, Paulsen IT, Dodson RJ, Hilbert H, Martins dos Santos VAP, Fouts DE, Gill SR, Pop M, Holmes M, Brinkac L, Beanan M, DeBoy RT, Daugherty S, Kolonay J, Madupu R, Nelson W, White O, Peterson J, Khouri H, Hance I, Chris Lee P, Holtzapple E, Scanlan D, Tran K, Moazzez A, Utterback T, Rizzo M, Lee K, Kosack D: Complete genome sequence and comparative analysis of the metabolically versatile Pseudomonas putida KT2440.

    Environ Microbiol 2002, 4(12):799-808. PubMed Abstract | Publisher Full Text OpenURL

  20. Yu H, Tang H, Wang L, Yao Y, Wu G, Xu P: Complete genome sequence of the nicotine-degrading Pseudomonas putida strain S16.

    J Bacteriol 2011, 193(19):5541-5542. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  21. Stover CK, Pham XQ, Erwin AL, Mizoguchi SD, Warrener P, Hickey MJ, Brinkman FS, Hufnagle WO, Kowalik DJ, Lagrou M, Garber RL, Goltry L, Tolentino E, Westbrock-Wadman S, Yuan Y, Brody LL, Coulter SN, Folger KR, Kas A, Larbig K, Lim R, Smith K, Spencer D, Wong GK, Wu Z, Paulsen IT, Reizer J, Saier MH, Hancock RE, Lory S: Complete genome sequence of Pseudomonas aeruginosa PAO1, an opportunistic pathogen.

    Nature 2000, 406(6799):959-964. PubMed Abstract | Publisher Full Text OpenURL

  22. Wu D, Ye J, Ou H, Wei X, Huang X, He Y, Xu Y: Genomic analysis and temperature-dependent transcriptome profiles of the rhizosphere originating strain Pseudomonas aeruginosa M18.

    BMC Genomics 2011, 12(1):438. PubMed Abstract | BioMed Central Full Text | PubMed Central Full Text OpenURL

  23. Buell CR, Joardar V, Lindeberg M, Selengut J, Paulsen IT, Gwinn ML, Dodson RJ, Deboy RT, Durkin AS, Kolonay JF, Madupu R, Daugherty S, Brinkac L, Beanan MJ, Haft DH, Nelson WC, Davidsen T, Zafar N, Zhou L, Liu J, Yuan Q, Khouri H, Fedorova N, Tran B, Russell D, Berry K, Utterback T, Van Aken SE, Feldblyum TV, D'Ascenzo M: The complete genome sequence of the Arabidopsis and tomato pathogen Pseudomonas syringae pv. tomato DC3000.

    Proc Natl Acad Sci U S A 2003, 100(18):10181-10186. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  24. Vodovar N, Vallenet D, Cruveiller S, Rouy Z, Barbe V, Acosta C, Cattolico L, Jubin C, Lajus A, Segurens B, Vacherie B, Wincker P, Weissenbach J, Lemaitre B, Medigue C, Boccard F: Complete genome sequence of the entomopathogenic and metabolically versatile soil bacterium Pseudomonas entomophila.

    Nat Biotechnol 2006, 24(6):673-679. PubMed Abstract | Publisher Full Text OpenURL

  25. Liu H, Yan A, Zhang X, Xu Y: Phenazine-1-carboxylic acid biosynthesis in Pseudomonas chlororaphis GP72 is positively regulated by the sigma factor RpoN.

    World J Microbiol Biotechnol 2008, 24(9):1961-1966. Publisher Full Text OpenURL

  26. Maddula VSRK, Pierson EA, Pierson LS 3rd: Altering the ratio of phenazines in Pseudomonas chlororaphis (aureofaciens) strain 30–84: effects on biofilm formation and pathogen inhibition.

    J Bacteriol 2008, 190(8):2759-2766. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  27. Spencer M, Ryu CM, Yang KY, Kim YC, Kloepper JW, Anderson AJ: Induced defence in tobacco by Pseudomonas chlororaphis strain O6 involves at least the ethylene pathway.

    Physiol Molec Plant Pathol 2003, 63(1):27-34. Publisher Full Text OpenURL

  28. Shen X, Chen M, Hu H, Wang W, Peng H, Xu P, Zhang X: Genome sequence of Pseudomonas chlororaphis GP72, a root-colonizing biocontrol strain.

    J Bacteriol 2012, 194(5):1269-1270. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  29. Liu H, Dong D, Peng H, Zhang X, Xu Y: Genetic diversity of phenazine- and pyoluteorin-producing pseudomonads isolated from green pepper rhizosphere.

    Arch Microbiol 2006, 185(2):91-98. PubMed Abstract | Publisher Full Text OpenURL

  30. Huang L, Chen M, Wang W, Hu H, Peng H, Xu Y, Zhang X: Enhanced production of 2-hydroxyphenazine in Pseudomonas chlororaphis GP72.

    Eur J Appl Microbiol Biotech 2010, 89(1):169-177. OpenURL

  31. Howell C, Stipanovic R: Control of Rhizoctonia solani on cotton seedlings with Pseudomonas fluorescens and with an antibiotic produced by the bacterium.

    Phytopathology 1979, 69(5):480-482. Publisher Full Text OpenURL

  32. Ge Y, Huang X, Wang S, Zhang X, Xu Y: Phenazine-1-carboxylic acid is negatively regulated and pyoluteorin positively regulated by gacA in Pseudomonas sp. M18.

    FEMS Microbiol Lett 2004, 237(1):41-47. PubMed Abstract | Publisher Full Text OpenURL

  33. Huang J, Xu Y, Zhang H, Li Y, Huang X, Ren B, Zhang X: Temperature-dependent expression of phzM and its regulatory genes lasI and ptsP in rhizosphere isolate Pseudomonas sp. strain M18.

    Appl Environ Microbiol 2009, 75(20):6568-6580. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  34. Mavrodi DV, Bonsall RF, Delaney SM, Soule MJ, Phillips G, Thomashow LS: Functional analysis of genes for biosynthesis of pyocyanin and phenazine-1-carboxamide from Pseudomonas aeruginosa PAO1.

    J Bacteriol 2001, 183(21):6454-6465. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  35. Gibson J, Sood A, Hogan DA: Pseudomonas aeruginosa-Candida albicans interactions: localization and fungal toxicity of a phenazine derivative.

    Appl Environ Microbiol 2009, 75(2):504-513. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  36. Qiu Y, Mo X, You C, Wang D: Investigation of dinitrogen fixation bacteria isolated from rice rhizosphere.

    Chinese Sc bull (kexuetongbao) 1981, 26(26):383-384. OpenURL

  37. Vermeiren H, Willems A, Schoofs G, de Mot R, Keijers V, Hai W, Vanderleyden J: The rice inoculant strain Alcaligenes faecalis A15 is a nitrogen-fixing Pseudomonas stutzeri.

    Syst Appl Microbiol 1999, 22(2):215-224. PubMed Abstract | Publisher Full Text OpenURL

  38. Li D, Yan Y, Ping S, Chen M, Zhang W, Li L, Lin W, Geng L, Liu W, Lu W, Lin M: Genome-wide investigation and functional characterization of the beta-ketoadipate pathway in the nitrogen-fixing and root-associated bacterium Pseudomonas stutzeri A1501.

    BMC Microbiol 2010, 10(1):36. PubMed Abstract | BioMed Central Full Text | PubMed Central Full Text OpenURL

  39. Markowitz VM, Korzeniewski F, Palaniappan K, Szeto E, Werner G, Padki A, Zhao X, Dubchak I, Hugenholtz P, Anderson I, Lykidis A, Mavromatis K, Ivanova N, Kyrpides NC: The integrated microbial genomes (IMG) system.

    Nucleic Acids Res 2006, 34(Database issue):344-348. OpenURL

  40. Tatusov RL, Natale DA, Garkavtsev IV, Tatusova TA, Shankavaram UT, Rao BS, Kiryutin B, Galperin MY, Fedorova ND, Koonin EV: The COG database: new developments in phylogenetic classification of proteins from complete genomes.

    Nucleic Acids Res 2001, 29(1):22-28. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  41. Carver TJ, Rutherford KM, Berriman M, Rajandream MA, Barrell BG, Parkhill J: ACT: the Artemis Comparison Tool.

    Bioinformatics 2005, 21(16):3422-3423. PubMed Abstract | Publisher Full Text OpenURL

  42. Hallin PF, Binnewies TT, Ussery DW: The genome BLASTatlas – a GeneWiz extension for visualization of whole-genome homology.

    Mol Biosyst 2008, 4(5):363-371. PubMed Abstract | Publisher Full Text OpenURL

  43. Shao Y, He X, Harrison EM, Tai C, Ou HY, Rajakumar K, Deng Z: mGenomeSubtractor: a web-based tool for parallel in silico subtractive hybridization analysis of multiple bacterial genomes.

    Nucleic Acids Res 2010, 38(Web Server issue):194-200. OpenURL

  44. Lessie TG, Phibbs PV Jr: Alternative pathways of carbohydrate utilization in pseudomonads.

    Annu Rev Microbiol 1984, 38:359-388. PubMed Abstract | Publisher Full Text OpenURL

  45. Jones-Mortimer MC, Kornberg HL: Genetical analysis of fructose utilization by Escherichia coli.

    Proc R Soc Lond B Biol Sci 1974, 187(1087):121-131. PubMed Abstract | Publisher Full Text OpenURL

  46. Rovira AD: Plant root exudates.

    Bot Rev 1969, 35:35-57. Publisher Full Text OpenURL

  47. Bais HP, Weir TL, Perry LG, Gilroy S, Vivanco JM: The role of root exudates in rhizosphere interactions with plants and other organisms.

    Annu Rev Plant Biol 2006, 57:233-266. PubMed Abstract | Publisher Full Text OpenURL

  48. Gibson DT, Parales RE: Aromatic hydrocarbon dioxygenases in environmental biotechnology.

    Curr Opin Biotechnol 2000, 11(3):236-243. PubMed Abstract | Publisher Full Text OpenURL

  49. Gao J, Ellis LB, Wackett LP: The University of Minnesota biocatalysis/biodegradation database: improving public access.

    Nucleic Acids Res 2010, 38(Database issue):488-491. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  50. Dagley S: Catabolism of aromatic compounds by micro-organisms.

    Adv Microb Physiol 1971, 6:1-46. PubMed Abstract OpenURL

  51. Jimenez JI, Minambres B, Garcia JL, Diaz E: Genomic analysis of the aromatic catabolic pathways from Pseudomonas putida KT2440.

    Environ Microbiol 2002, 4(12):824-841. PubMed Abstract | Publisher Full Text OpenURL

  52. Harwood CS, Parales RE: The beta-ketoadipate pathway and the biology of self-identity.

    Annu Rev Microbiol 1996, 50:553-590. PubMed Abstract | Publisher Full Text OpenURL

  53. Kurnasov O, Jablonski L, Polanuyer B, Dorrestein P, Begley T, Osterman A: Aerobic tryptophan degradation pathway in bacteria: novel kynurenine formamidase.

    FEMS Microbiol Lett 2003, 227(2):219-227. PubMed Abstract | Publisher Full Text OpenURL

  54. Neidle E, Hartnett C, Ornston L, Bairoch A, Rekik M, Harayama S: Nucleotide sequences of the Acinetobacter calcoaceticus benABC genes for benzoate 1, 2-dioxygenase reveal evolutionary relationships among multicomponent oxygenases.

    J Bacteriol 1991, 173(17):5385-5395. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  55. Balashova NV, Stolz A, Knackmuss HJ, Kosheleva IA, Naumov AV, Boronin AM: Purification and characterization of a salicylate hydroxylase involved in 1-hydroxy-2-naphthoic acid hydroxylation from the naphthalene and phenanthrene-degrading bacterial strain Pseudomonas putida BS202-P1.

    Biodegradation 2001, 12(3):179-188. PubMed Abstract | Publisher Full Text OpenURL

  56. Powlowski J, Sahlman L, Shingler V: Purification and properties of the physically associated meta-cleavage pathway enzymes 4-hydroxy-2-ketovalerate aldolase and aldehyde dehydrogenase (acylating) from Pseudomonas sp. strain CF600.

    J Bacteriol 1993, 175(2):377-385. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  57. Lee SJ, Ko JH, Kang HY, Lee Y: Coupled expression of MhpE aldolase and MhpF dehydrogenase in Escherichia coli.

    Biochem Biophys Res Commun 2006, 346(3):1009-1015. PubMed Abstract | Publisher Full Text OpenURL

  58. Harwood CS, Nichols NN, Kim MK, Ditty JL, Parales RE: Identification of the pcaRKF gene cluster from Pseudomonas putida: involvement in chemotaxis, biodegradation, and transport of 4-hydroxybenzoate.

    J Bacteriol 1994, 176(21):6479-6488. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  59. Priefert H, Rabenhorst J, Steinbuchel A: Molecular characterization of genes of Pseudomonas sp. strain HR199 involved in bioconversion of vanillin to protocatechuate.

    J Bacteriol 1997, 179(8):2595-2607. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  60. Adachi O, Tanasupawat S, Yoshihara N, Toyama H, Matsushita K: 3-Dehydroquinate production by oxidative fermentation and further conversion of 3-dehydroquinate to the intermediates in the shikimate pathway.

    Biosci Biotechnol Biochem 2003, 67(10):2124-2131. PubMed Abstract | Publisher Full Text OpenURL

  61. Herrmann KM, Weaver LM: The shikimate pathway.

    Annu Rev Plant Physiol Plant Mol Biol 1999, 50:473-503. PubMed Abstract | Publisher Full Text OpenURL

  62. Essar DW, Eberly L, Hadero A, Crawford IP: Identification and characterization of genes for a second anthranilate synthase in Pseudomonas aeruginosa: interchangeability of the two anthranilate synthases and evolutionary implications.

    J Bacteriol 1990, 172(2):884-900. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  63. Liu W, Christenson SD, Standage S, Shen B: Biosynthesis of the enediyne antitumor antibiotic C-1027.

    Science 2002, 297(5584):1170-1173. PubMed Abstract | Publisher Full Text OpenURL

  64. Serre L, Sailland A, Sy D, Boudec P, Rolland A, Pebay-Peyroula E, Cohen-Addad C: Crystal structure of Pseudomonas fluorescens 4-hydroxyphenylpyruvate dioxygenase: an enzyme involved in the tyrosine degradation pathway.

    Structure 1999, 7(8):977-988. PubMed Abstract | Publisher Full Text OpenURL

  65. Arias-Barrau E, Olivera ER, Luengo JM, Fernández C, Galán B, García JL, Díaz E, Miñambres B: The homogentisate pathway: a central catabolic pathway involved in the degradation of L-phenylalanine, L-tyrosine, and 3-hydroxyphenylacetate in Pseudomonas putida.

    J Bacteriol 2004, 186(15):5062-5077. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  66. Sparnins VL, Chapman PJ: Catabolism of L-tyrosine by the homoprotocatechuate pathway in Gram-positive bacteria.

    J Bacteriol 1976, 127(1):362-366. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  67. Barbour MG, Bayly RC: Control of meta-cleavage degradation of 4-hydroxyphenylacetate in Pseudomonas putida.

    J Bacteriol 1981, 147(3):844-850. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  68. Roper DI, Cooper RA: Subcloning and nucleotide sequence of the 3,4-dihydroxyphenylacetate (homoprotocatechuate) 2,3-dioxygenase gene from Escherichia coli C.

    FEBS Lett 1990, 275(1–2):53-57. PubMed Abstract | Publisher Full Text OpenURL

  69. Gibello A, Ferrer E, Martin M, Garrido-Pertierra A: 3, 4-Dihydroxyphenylacetate 2, 3-dioxygenase from Klebsiella pneumoniae, a Mg (2+)-containing dioxygenase involved in aromatic catabolism.

    Biochem J 1994, 301(Pt 1):145. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  70. Vetting MW, Wackett LP, Que L Jr, Lipscomb JD, Ohlendorf DH: Crystallographic comparison of manganese- and iron-dependent homoprotocatechuate 2,3-dioxygenases.

    J Bacteriol 2004, 186(7):1945-1958. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  71. Lipscomb JD: Mechanism of extradiol aromatic ring-cleaving dioxygenases.

    Curr Opin Struct Biol 2008, 18(6):644-649. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  72. Hanlon SP, Hill TK, Flavell MA, Stringfellow JM, Cooper RA: 2-Phenylethylamine catabolism by Escherichia coli K-12: gene organization and expression.

    Microbiology 1997, 143:513-518. PubMed Abstract | Publisher Full Text OpenURL

  73. Sun D, Ono K, Okajima T, Tanizawa K, Uchida M, Yamamoto Y, Mathews FS, Davidson VL: Chemical and kinetic reaction mechanisms of quinohemoprotein amine dehydrogenase from Paracoccus denitrificans.

    Biochemistry 2003, 42(37):10896-10903. PubMed Abstract | Publisher Full Text OpenURL

  74. Arias S, Olivera ER, Arcos M, Naharro G, Luengo JM: Genetic analyses and molecular characterization of the pathways involved in the conversion of 2-phenylethylamine and 2-phenylethanol into phenylacetic acid in Pseudomonas putida U.

    Environ Microbiol 2008, 10(2):413-432. PubMed Abstract | Publisher Full Text OpenURL

  75. Olivera ER, Minambres B, Garcia B, Muniz C, Moreno MA, Ferrandez A, Diaz E, Garcia JL, Luengo JM: Molecular characterization of the phenylacetic acid catabolic pathway in Pseudomonas putida U: the phenylacetyl-CoA catabolon.

    Proc Natl Acad Sci U S A 1998, 95(11):6419-6424. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  76. Luengo JM, Garcia JL, Olivera ER: The phenylacetyl-CoA catabolon: a complex catabolic unit with broad biotechnological applications.

    Mol Microbiol 2001, 39(6):1434-1442. PubMed Abstract | Publisher Full Text OpenURL

  77. Parales RE, Resnick SM: Aromatic ring hydroxylating dioxygenases.

    Pseudomonas 2006, 287:287-340. OpenURL

  78. Bertin C, Yang X, Weston LA: The role of root exudates and allelochemicals in the rhizosphere.

    Plant Soil 2003, 256(1):67-83. OpenURL

  79. Lugtenberg B, Kamilova F: Plant-growth-promoting rhizobacteria.

    Annu Rev Microbioz 2009, 63(1):541-556. Publisher Full Text OpenURL

  80. Van Gundy SD, Kirkpatrick JD, Golden J: The nature and role of metabolic leakage from root-knot nematode galls and infection by Rhizoctonia solani.

    J Nematol 1977, 9(2):113-121. PubMed Abstract | PubMed Central Full Text OpenURL

  81. Kamilova F, Lamers G, Lugtenberg B: Biocontrol strain Pseudomonas fluorescens WCS365 inhibits germination of Fusarium oxysporum spores in tomato root exudate as well as subsequent formation of new spores.

    Environ Microbiol 2008, 10(9):2455-2461. PubMed Abstract | Publisher Full Text OpenURL

  82. Mark GL, Dow JM, Kiely PD, Higgins H, Haynes J, Baysse C, Abbas A, Foley T, Franks A, Morrissey J, O'Gara F: Transcriptome profiling of bacterial responses to root exudates identifies genes involved in microbe-plant interactions.

    Proc Natl Acad Sci U S A 2005, 102(48):17454-17459. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  83. Roy-Burman A, Savel RH, Racine S, Swanson BL, Revadigar NS, Fujimoto J, Sawa T, Frank DW, Wiener-Kronish JP: Type III protein secretion is associated with death in lower respiratory and systemic Pseudomonas aeruginosa infections.

    J Infect Dis 2001, 183(12):1767-1774. PubMed Abstract | Publisher Full Text OpenURL

  84. Hoshino N, Kimura T, Yamaji A, Ando T: Damage to the cytoplasmic membrane of Escherichia coli by catechin-copper (II) complexes.

    Free Radic Biol Med 1999, 27(11–12):1245-1250. PubMed Abstract | Publisher Full Text OpenURL

  85. Nies DH: Efflux-mediated heavy metal resistance in prokaryotes.

    FEMS Microbiol Rev 2003, 27(2–3):313-339. PubMed Abstract OpenURL

  86. Mejare M, Bulow L: Metal-binding proteins and peptides in bioremediation and phytoremediation of heavy metals.

    Trends Biotechnol 2001, 19(2):67-73. PubMed Abstract | Publisher Full Text OpenURL

  87. Vuilleumier S, Pagni M: The elusive roles of bacterial glutathione S-transferases: new lessons from genomes.

    Appl Microbiol Biotechnol 2002, 58(2):138-146. PubMed Abstract | Publisher Full Text OpenURL

  88. Cha JS, Cooksey DA: Copper resistance in Pseudomonas syringae mediated by periplasmic and outer membrane proteins.

    Proc Natl Acad Sci U S A 1991, 88(20):8915-8919. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  89. Zhang X, Rainey PB: Regulation of copper homeostasis in Pseudomonas fluorescens SBW25.

    Environ Microbiol 2008, 10(12):3284-3294. PubMed Abstract | Publisher Full Text OpenURL

  90. Rae TD, Schmidt PJ, Pufahl RA, Culotta VC, O'Halloran TV: Undetectable intracellular free copper: the requirement of a copper chaperone for superoxide dismutase.

    Science 1999, 284(5415):805-808. PubMed Abstract | Publisher Full Text OpenURL

  91. Changela A, Chen K, Xue Y, Holschen J, Outten CE, O'Halloran TV, Mondragon A: Molecular basis of metal-ion selectivity and zeptomolar sensitivity by CueR.

    Science 2003, 301(5638):1383-1387. PubMed Abstract | Publisher Full Text OpenURL

  92. Rensing C, Fan B, Sharma R, Mitra B, Rosen BP: CopA: an Escherichia coli Cu(I)-translocating P-type ATPase.

    Proc Natl Acad Sci U S A 2000, 97(2):652-656. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  93. Roberts SA, Weichsel A, Grass G, Thakali K, Hazzard JT, Tollin G, Rensing C, Montfort WR: Crystal structure and electron transfer kinetics of CueO, a multicopper oxidase required for copper homeostasis in Escherichia coli.

    Proc Natl Acad Sci U S A 2002, 99(5):2766-2771. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  94. Franke S, Grass G, Rensing C, Nies DH: Molecular analysis of the copper-transporting efflux system CusCFBA of Escherichia coli.

    J Bacteriol 2003, 185(13):3804-3812. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  95. Pontel LB, Soncini FC: Alternative periplasmic copper-resistance mechanisms in Gram-negative bacteria.

    Mol Microbiol 2009, 73(2):212-225. PubMed Abstract | Publisher Full Text OpenURL

  96. Cai J, Salmon K, DuBow MS: A chromosomal ars operon homologue of Pseudomonas aeruginosa confers increased resistance to arsenic and antimony in Escherichia coli.

    Microbiology 1998, 144(Pt 10):2705-2713. PubMed Abstract | Publisher Full Text OpenURL

  97. Dey S, Rosen BP: Dual mode of energy coupling by the oxyanion-translocating ArsB protein.

    J Bacteriol 1995, 177(2):385-389. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  98. Nies DH: The cobalt, zinc, and cadmium efflux system CzcABC from Alcaligenes eutrophus functions as a cation-proton antiporter in Escherichia coli.

    J Bacteriol 1995, 177(10):2707-2712. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  99. Pimentel BE, Moreno-Sanchez R, Cervantes C: Efflux of chromate by Pseudomonas aeruginosa cells expressing the ChrA protein.

    FEMS Microbiol Lett 2002, 212(2):249-254. PubMed Abstract | Publisher Full Text OpenURL

  100. Schalk IJ, Hannauer M, Braud A: New roles for bacterial siderophores in metal transport and tolerance.

    Environ Microbiol 2011, 13(11):2844-2854. PubMed Abstract | Publisher Full Text OpenURL

  101. Xavier D, Picão R, Girardello R, Fehlberg L, Gales A: Efflux pumps expression and its association with porin down-regulation and β-lactamase production among Pseudomonas aeruginosa causing bloodstream infections in Brazil.

    BMC Microbiol 2010, 10(1):217. PubMed Abstract | BioMed Central Full Text | PubMed Central Full Text OpenURL

  102. Alekshun MN, Levy SB: Molecular mechanisms of antibacterial multidrug resistance.

    Cell 2007, 128(6):1037-1050. PubMed Abstract | Publisher Full Text OpenURL

  103. Poole K: Efflux-mediated multiresistance in Gram-negative bacteria.

    Clin Microbiol Infect 2004, 10(1):12-26. PubMed Abstract | Publisher Full Text OpenURL

  104. Georgopapadakou NH: Penicillin-binding proteins and bacterial resistance to beta-lactams.

    Antimicrob Agents Chemother 1993, 37(10):2045-2053. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  105. Saier MH Jr, Paulsen IT: Phylogeny of multidrug transporters.

    Semin Cell Dev Biol 2001, 12(3):205-213. PubMed Abstract | Publisher Full Text OpenURL

  106. Mosqueda G, Ramos JL: A set of genes encoding a second toluene efflux system in Pseudomonas putida DOT-T1E is linked to the tod genes for toluene metabolism.

    J Bacteriol 2000, 182(4):937-943. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  107. Fetar H, Gilmour C, Klinoski R, Daigle DM, Dean CR, Poole K: mexEF-oprN multidrug efflux operon of Pseudomonas aeruginosa: regulation by the MexT activator in response to nitrosative stress and chloramphenicol.

    Antimicrob Agents Chemother 2011, 55(2):508-514. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  108. Kohler T, van Delden C, Curty LK, Hamzehpour MM, Pechere JC: Overexpression of the MexEF-OprN multidrug efflux system affects cell-to-cell signaling in Pseudomonas aeruginosa.

    J Bacteriol 2001, 183(18):5213-5222. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  109. Takatsuka Y, Chen C, Nikaido H: Mechanism of recognition of compounds of diverse structures by the multidrug efflux pump AcrB of Escherichia coli.

    Proc Natl Acad Sci U S A 2010, 107(15):6559-6565. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  110. Ma D, Alberti M, Lynch C, Nikaido H, Hearst JE: The local repressor AcrR plays a modulating role in the regulation of acrAB genes of Escherichia coli by global stress signals.

    Mol Microbiol 1996, 19(1):101-112. PubMed Abstract | Publisher Full Text OpenURL

  111. Foreman J, Demidchik V, Bothwell JHF, Mylona P, Miedema H, Torres MA, Linstead P, Costa S, Brownlee C, Jones JDG, Davies JM, Dolan L: Reactive oxygen species produced by NADPH oxidase regulate plant cell growth.

    Nature 2003, 422(6930):442-446. PubMed Abstract | Publisher Full Text OpenURL

  112. Bolwell G, Wojtaszek P: Mechanisms for the generation of reactive oxygen species in plant defence – a broad perspective.

    Physiol Molec Plant Pathol 1997, 51(6):347-366. Publisher Full Text OpenURL

  113. Storz G, Imlay JA: Oxidative stress.

    Curr Opin Microbiol 1999, 2(2):188-194. PubMed Abstract | Publisher Full Text OpenURL

  114. Whistler CA, Corbell NA, Sarniguet A, Ream W, Loper JE: The two-component regulators GacS and GacA influence accumulation of the stationary-phase sigma factor σS and the stress response in Pseudomonas fluorescens Pf-5.

    J Bacteriol 1998, 180(24):6635-6641. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  115. Ochsner UA, Vasil ML, Alsabbagh E, Parvatiyar K, Hassett DJ: Role of the Pseudomonas aeruginosa oxyR-recG operon in oxidative stress defense and DNA repair: OxyR-dependent regulation of katB-ankB, ahpB, and ahpC-ahpF.

    J Bacteriol 2000, 182(16):4533-4544. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  116. Palma M, Zurita J, Ferreras JA, Worgall S, Larone DH, Shi L, Campagne F, Quadri LE: Pseudomonas aeruginosa SoxR does not conform to the archetypal paradigm for SoxR-dependent regulation of the bacterial oxidative stress adaptive response.

    Infect Immun 2005, 73(5):2958-2966. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  117. Chang WS, Li X, Halverson LJ: Influence of water limitation on endogenous oxidative stress and cell death within unsaturated Pseudomonas putida biofilms.

    Environ Microbiol 2009, 11(6):1482-1492. PubMed Abstract | Publisher Full Text OpenURL

  118. Fones H, Preston GM: Reactive oxygen and oxidative stress tolerance in plant pathogenic Pseudomonas.

    FEMS Microbiol Lett 2012, 327(1):1-8. PubMed Abstract | Publisher Full Text OpenURL

  119. Ayub ND, Tribelli PM, Lopez NI: Polyhydroxyalkanoates are essential for maintenance of redox state in the Antarctic bacterium Pseudomonas sp. 14–3 during low temperature adaptation.

    Extremophiles 2009, 13(1):59-66. PubMed Abstract | Publisher Full Text OpenURL

  120. Castro-Sowinski S, Burdman S, Matan O, Okon Y: Natural functions of bacterial polyhydroxyalkanoates. In In Plastics from Bacteria . Edited by Chen GGQ. Berlin/Heidelberg: Springer; 2010:39-61. OpenURL

  121. Khairnar NP, Misra HS, Apte SK: Pyrroloquinoline-quinone synthesized in Escherichia coli by pyrroloquinoline-quinone synthase of Deinococcus radiodurans plays a role beyond mineral phosphate solubilization.

    Biochem Biophys Res Commun 2003, 312(2):303-308. PubMed Abstract | Publisher Full Text OpenURL

  122. Ramos JL, Gallegos MT, Marques S, Ramos-Gonzalez MI, Espinosa-Urgel M, Segura A: Responses of Gram-negative bacteria to certain environmental stressors.

    Curr Opin Microbiol 2001, 4(2):166-171. PubMed Abstract | Publisher Full Text OpenURL

  123. Ermolenko DN, Makhatadze GI: Bacterial cold-shock proteins.

    Cell Mol Life Sci 2002, 59(11):1902-1913. PubMed Abstract | Publisher Full Text OpenURL

  124. Allan B, Linseman M, MacDonald LA, Lam JS, Kropinski AM: Heat shock response of Pseudomonas aeruginosa.

    J Bacteriol 1988, 170(8):3668-3674. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  125. Gamer J, Multhaup G, Tomoyasu T, McCarty JS, Rudiger S, Schonfeld HJ, Schirra C, Bujard H, Bukau B: A cycle of binding and release of the DnaK, DnaJ and GrpE chaperones regulates activity of the Escherichia coli heat shock transcription factor sigma32.

    EMBO J 1996, 15(3):607-617. PubMed Abstract | PubMed Central Full Text OpenURL

  126. Csonka LN: Physiological and genetic responses of bacteria to osmotic stress.

    Microbiol Rev 1989, 53(1):121-147. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  127. Aspedon A, Palmer K, Whiteley M: Microarray analysis of the osmotic stress response in Pseudomonas aeruginosa.

    J Bacteriol 2006, 188(7):2721-2725. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  128. Brown AD: Microbial water stress.

    Bacteriol Rev 1976, 40(4):803-846. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  129. Wargo MJ, Szwergold BS, Hogan DA: Identification of two gene clusters and a transcriptional regulator required for Pseudomonas aeruginosa glycine betaine catabolism.

    J Bacteriol 2008, 190(8):2690-2699. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  130. Styrvold OB, Falkenberg P, Landfald B, Eshoo MW, Bjornsen T, Strom AR: Selection, mapping, and characterization of osmoregulatory mutants of Escherichia coli blocked in the choline-glycine betaine pathway.

    J Bacteriol 1986, 165(3):856-863. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  131. Lequette Y, Odberg-Ferragut C, Bohin JP, Lacroix JM: Identification of mdoD, an mdoG paralog which encodes a twin-arginine-dependent periplasmic protein that controls osmoregulated periplasmic glucan backbone structures.

    J Bacteriol 2004, 186(12):3695-3702. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  132. Miller KJ, Wood JM: Osmoadaptation by rhizosphere bacteria.

    Annu Rev Microbiol 1996, 50:101-136. PubMed Abstract | Publisher Full Text OpenURL

  133. Booth IR, Higgins CF: Enteric bacteria and osmotic stress: intracellular potassium glutamate as a secondary signal of osmotic stress?

    FEMS Microbiol Rev 1990, 6(2–3):239-246. PubMed Abstract OpenURL

  134. Bolwerk A, Lagopodi AL, Wijfjes AH, Lamers GE, Chin AWTF, Lugtenberg BJ, Bloemberg GV: Interactions in the tomato rhizosphere of two Pseudomonas biocontrol strains with the phytopathogenic fungus Fusarium oxysporum f. sp. radicis-lycopersici.

    Mol Plant Microbe Interact 2003, 16(11):983-993. PubMed Abstract | Publisher Full Text OpenURL

  135. Lugtenberg BJ, Dekkers L, Bloemberg GV: Molecular determinants of rhizosphere colonization by Pseudomonas.

    Annu Rev Phytopathol 2001, 39:461-490. PubMed Abstract | Publisher Full Text OpenURL

  136. Kiely PD, Haynes JM, Higgins CH, Franks A, Mark GL, Morrissey JP, O'Gara F: Exploiting new systems-based strategies to elucidate plant-bacterial interactions in the rhizosphere.

    Microb Ecol 2006, 51(3):257-266. PubMed Abstract | Publisher Full Text OpenURL

  137. Boyd A, Simon M: Bacterial chemotaxis.

    Annu Rev Physiol 1982, 44(1):501-517. PubMed Abstract | Publisher Full Text OpenURL

  138. de Weert S, Vermeiren H, Mulders IH, Kuiper I, Hendrickx N, Bloemberg GV, Vanderleyden J, De Mot R, Lugtenberg BJ: Flagella-driven chemotaxis towards exudate components is an important trait for tomato root colonization by Pseudomonas fluorescens.

    Mol Plant Microbe Interact 2002, 15(11):1173-1180. PubMed Abstract | Publisher Full Text OpenURL

  139. Wadhams GH, Armitage JP: Making sense of it all: bacterial chemotaxis.

    Nat Rev Mol Cell Biol 2004, 5(12):1024-1037. PubMed Abstract | Publisher Full Text OpenURL

  140. Barak R, Eisenbach M: Correlation between phosphorylation of the chemotaxis protein CheY and its activity at the flagellar motor.

    Biochemistry 1992, 31(6):1821-1826. PubMed Abstract | Publisher Full Text OpenURL

  141. Wall D, Kaiser D: Type IV pili and cell motility.

    Mol Microbiol 1999, 32(1):1-10. PubMed Abstract | Publisher Full Text OpenURL

  142. Bianciotto V, Andreotti S, Balestrini R, Bonfante P, Perotto S: Mucoid mutants of the biocontrol strain Pseudomonas fluorescens CHA0 show increased ability in biofilm formation on mycorrhizal and nonmycorrhizal carrot roots.

    Mol Plant Microbe Interact 2001, 14(2):255-260. PubMed Abstract | Publisher Full Text OpenURL

  143. Espinosa-Urgel M, Salido A, Ramos JL: Genetic analysis of functions involved in adhesion of Pseudomonas putida to seeds.

    J Bacteriol 2000, 182(9):2363-2369. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  144. Rojas CM, Ham JH, Deng WL, Doyle JJ, Collmer A: HecA, a member of a class of adhesins produced by diverse pathogenic bacteria, contributes to the attachment, aggregation, epidermal cell killing, and virulence phenotypes of Erwinia chrysanthemi EC16 on Nicotiana clevelandii seedlings.

    Proc Natl Acad Sci U S A 2002, 99(20):13142-13147. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  145. Dekkers LC, van der Bij AJ, Mulders IH, Phoelich CC, Wentwoord RA, Glandorf DC, Wijffelman CA, Lugtenberg BJ: Role of the O-antigen of lipopolysaccharide, and possible roles of growth rate and of NADH:ubiquinone oxidoreductase (nuo) in competitive tomato root-tip colonization by Pseudomonas fluorescens WCS365.

    Mol Plant Microbe Interact 1998, 11(8):763-771. PubMed Abstract | Publisher Full Text OpenURL

  146. Tomich M, Planet PJ, Figurski DH: The tad locus: postcards from the widespread colonization island.

    Nat Rev Microbiol 2007, 5(5):363-375. PubMed Abstract | Publisher Full Text OpenURL

  147. O'Connell Motherway M, Zomer A, Leahy SC, Reunanen J, Bottacini F, Claesson MJ, O'Brien F, Flynn K, Casey PG, Munoz JA, Kearney B, Houston AM, O'Mahony C, Higgins DG, Shanahan F, Palva A, de Vos WM, Fitzgerald GF, Ventura M, O'Toole PW, van Sinderen D: Functional genome analysis of Bifidobacterium breve UCC2003 reveals type IVb tight adherence (Tad) pili as an essential and conserved host-colonization factor.

    Proc Natl Acad Sci U S A 2011, 108(27):11217-11222. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  148. Ramos-Gonzalez MI, Campos MJ, Ramos JL: Analysis of Pseudomonas putida KT2440 gene expression in the maize rhizosphere: in vivo expression technology capture and identification of root-activated promoters.

    J Bacteriol 2005, 187(12):4033-4041. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  149. Buell CR, Anderson AJ: Genetic analysis of the aggA locus involved in agglutination and adherence of Pseudomonas putida, a beneficial fluorescent pseudomonad.

    Mol Plant Microbe Interact 1992, 5(2):154-162. PubMed Abstract | Publisher Full Text OpenURL

  150. Dekkers LC, Phoelich CC, van der Fits L, Lugtenberg BJ: A site-specific recombinase is required for competitive root colonization by Pseudomonas fluorescens WCS365.

    Proc Natl Acad Sci U S A 1998, 95(12):7051-7056. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  151. Gal M, Preston GM, Massey RC, Spiers AJ, Rainey PB: Genes encoding a cellulosic polymer contribute toward the ecological success of Pseudomonas fluorescens SBW25 on plant surfaces.

    Mol Ecol 2003, 12(11):3109-3121. PubMed Abstract | Publisher Full Text OpenURL

  152. Bender CL, Alarcon-Chaidez F, Gross DC: Pseudomonas syringae phytotoxins: mode of action, regulation, and biosynthesis by peptide and polyketide synthetases.

    Microbiol Mol Biol Rev 1999, 63(2):266-292. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  153. Mavrodi DV, Peever TL, Mavrodi OV, Parejko JA, Raaijmakers JM, Lemanceau P, Mazurier S, Heide L, Blankenfeldt W, Weller DM, Thomashow LS: Diversity and evolution of the phenazine biosynthesis pathway.

    Appl Environ Microbiol 2010, 76(3):866-879. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  154. Delaney SM, Mavrodi DV, Bonsall RF, Thomashow LS: phzO, a gene for biosynthesis of 2-hydroxylated phenazine compounds in Pseudomonas aureofaciens 30–84.

    J Bacteriol 2001, 183(1):318-327. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  155. Parsons JF, Greenhagen BT, Shi K, Calabrese K, Robinson H, Ladner JE: Structural and functional analysis of the pyocyanin biosynthetic protein PhzM from Pseudomonas aeruginosa.

    Biochemistry 2007, 46(7):1821-1828. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  156. Pechy-Tarr M, Bruck DJ, Maurhofer M, Fischer E, Vogne C, Henkels MD, Donahue KM, Grunder J, Loper JE, Keel C: Molecular analysis of a novel gene cluster encoding an insect toxin in plant-associated strains of Pseudomonas fluorescens.

    Environ Microbiol 2008, 10(9):2368-2386. PubMed Abstract | Publisher Full Text OpenURL

  157. Daborn PJ, Waterfield N, Silva CP, Au CP, Sharma S, Ffrench-Constant RH: A single Photorhabdus gene, makes caterpillars floppy (mcf), allows Escherichia coli to persist within and kill insects.

    Proc Natl Acad Sci U S A 2002, 99(16):10742-10747. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  158. Meyer JM: Pyoverdines: pigments, siderophores and potential taxonomic markers of fluorescent Pseudomonas species.

    Arch Microbiol 2000, 174(3):135-142. PubMed Abstract | Publisher Full Text OpenURL

  159. Kloepper JW, Leong J, Teintze M, Schroth MN: Enhanced plant growth by siderophores produced by plant growth-promoting rhizobacteria.

    Nature 1980, 286(5776):885-886. Publisher Full Text OpenURL

  160. Phoebe CH Jr, Combie J, Albert FG, Van Tran K, Cabrera J, Correira HJ, Guo Y, Lindermuth J, Rauert N, Galbraith W, Selitrennikoff CP: Extremophilic orgainisms as an unexplored source of antifungal compounds.

    J Antibiot 2001, 54(1):56-65. PubMed Abstract | Publisher Full Text OpenURL

  161. Franza T, Mahe B, Expert D: Erwinia chrysanthemi requires a second iron transport route dependent of the siderophore achromobactin for extracellular growth and plant infection.

    Mol Microbiol 2005, 55(1):261-275. PubMed Abstract | Publisher Full Text OpenURL

  162. Owen JG, Ackerley DF: Characterization of pyoverdine and achromobactin in Pseudomonas syringae pv. phaseolicola1448a.

    BMC Microbiol 2011, 11:218. PubMed Abstract | BioMed Central Full Text | PubMed Central Full Text OpenURL

  163. Cornelis P: Iron uptake and metabolism in pseudomonads.

    Appl Microbiol Biotechnol 2010, 86(6):1637-1645. PubMed Abstract | Publisher Full Text OpenURL

  164. Mithani A, Hein J, Preston GM: Comparative analysis of metabolic networks provides insight into the evolution of plant pathogenic and nonpathogenic lifestyles in Pseudomonas.

    Mol Biol Evol 2010, 28(1):483-499. PubMed Abstract | Publisher Full Text OpenURL

  165. Vessey KJ: Plant growth promoting rhizobacteria as biofertilizers.

    Plant Soil 2003, 255:571-586. Publisher Full Text OpenURL

  166. Roberts GP, MacNeil T, MacNeil D, Brill WJ: Regulation and characterization of protein products coded by the nif (nitrogen fixation) genes of Klebsiella pneumoniae.

    J Bacteriol 1978, 136(1):267-279. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  167. Yan Y, Ping S, Peng J, Han Y, Li L, Yang J, Dou Y, Li Y, Fan H, Fan Y, Li D, Zhan Y, Chen M, Lu W, Zhang W, Cheng Q, Jin Q, Lin M: Global transcriptional analysis of nitrogen fixation and ammonium repression in root-associated Pseudomonas stutzeri A1501.

    BMC Genomics 2010, 11:11. PubMed Abstract | BioMed Central Full Text | PubMed Central Full Text OpenURL

  168. Stewart V, Parales J Jr: Identification and expression of genes narL and narX of the nar (nitrate reductase) locus in Escherichia coli K-12.

    J Bacteriol 1988, 170(4):1589-1597. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  169. Greenberg EP, Becker GE: Nitrous oxide as end product of denitrification by strains of fluorescent pseudomonads.

    Can J Microbiol 1977, 23(7):903-907. PubMed Abstract | Publisher Full Text OpenURL

  170. Carlson CA, Ingraham JL: Comparison of denitrification by Pseudomonas stutzeri, Pseudomonas aeruginosa, and Paracoccus denitrificans.

    Appl Environ Microbiol 1983, 45(4):1247-1253. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  171. Seitzinger SP: Denitrification in freshwater and coastal marine ecosystems: ecological and geochemical significance.

    Limnol Oceanogr 1988, 702-724. OpenURL

  172. Rodriguez H, Fraga R: Phosphate solubilizing bacteria and their role in plant growth promotion.

    Biotechnol Adv 1999, 17(4–5):319-339. PubMed Abstract | Publisher Full Text OpenURL

  173. Palm CJ, Gaffney T, Kosuge T: Cotranscription of genes encoding indoleacetic acid production in Pseudomonas syringae subsp. savastanoi.

    J Bacteriol 1989, 171(2):1002-1009. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  174. Wang C, Knill E, Glick BR, Defago G: Effect of transferring 1-aminocyclopropane-1-carboxylic acid (ACC) deaminase genes into Pseudomonas fluorescens strain CHA0 and its gacA derivative CHA96 on their growth-promoting and disease-suppressive capacities.

    Can J Microbiol 2000, 46(10):898-907. PubMed Abstract OpenURL

  175. Choi O, Kim J, Kim JG, Jeong Y, Moon JS, Park CS, Hwang I: Pyrroloquinoline quinone is a plant growth promotion factor produced by Pseudomonas fluorescens B16.

    Plant Physiol 2008, 146(2):657-668. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  176. Toyama H, Lidstrom ME: pqqA is not required for biosynthesis of pyrroloquinoline quinone in Methylobacterium extorquens AM1.

    Microbiology 1998, 144(Pt 1):183-191. PubMed Abstract | Publisher Full Text OpenURL

  177. King EO, Ward MK, Raney DE: Two simple media for the demonstration of pyocyanin and fluorescin.

    J lab clin Med 1954, 44(2):301-307. PubMed Abstract OpenURL

  178. Aziz RK, Bartels D, Best AA, DeJongh M, Disz T, Edwards RA, Formsma K, Gerdes S, Glass EM, Kubal M, Meyer F, Olsen GJ, Olson R, Osterman AL, Overbeek RA, McNeil LK, Paarmann D, Paczian T, Parrello B, Pusch GD, Reich C, Stevens R, Vassieva O, Vonstein V, Wilke A, Zagnitko O: The RAST server: rapid annotations using subsystems technology.

    BMC Genomics 2008, 9:75. PubMed Abstract | BioMed Central Full Text | PubMed Central Full Text OpenURL

  179. Markowitz VM, Mavromatis K, Ivanova NN, Chen IM, Chu K, Kyrpides NC: IMG ER: a system for microbial genome annotation expert review and curation.

    Bioinformatics 2009, 25(17):2271-2278. PubMed Abstract | Publisher Full Text OpenURL

  180. Kanehisa M, Araki M, Goto S, Hattori M, Hirakawa M, Itoh M, Katayama T, Kawashima S, Okuda S, Tokimatsu T, Yamanishi Y: KEGG for linking genomes to life and the environment.

    Nucleic Acids Res 2008, 36(Database issue):480-484. OpenURL

  181. Caspi R, Altman T, Dreher K, Fulcher CA, Subhraveti P, Keseler IM, Kothari A, Krummenacker M, Latendresse M, Mueller LA, Ong Q, Paley S, Pujar A, Shearer AG, Travers M, Weerasinghe D, Zhang P, Karp PD: The MetaCyc database of metabolic pathways and enzymes and the BioCyc collection of pathway/genome databases.

    Nucleic Acids Res 2012, 40(Database issue):742-753. OpenURL

  182. Thompson JD, Higgins DG, Gibson TJ: CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice.

    Nucleic Acids Res 1994, 22(22):4673-4680. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  183. Saitou N, Nei M: The neighbor-joining method: a new method for reconstructing phylogenetic trees.

    Mol Biol Evol 1987, 4(4):406-425. PubMed Abstract | Publisher Full Text OpenURL

  184. Letunic I, Bork P: Interactive tree of life (iTOL): an online tool for phylogenetic tree display and annotation.

    Bioinformatics 2007, 23(1):127-128. PubMed Abstract | Publisher Full Text OpenURL