|
Features of the bacteria considered in this paper |
||||||
| Strain |
RefSeq acession no. |
Source |
Topt |
Photolyase |
Popt |
Orthologs |
|
|
||||||
| Photobacterium profundum SS9 |
NC_006370 |
Sulu Sea |
15°C |
A |
28 MPa |
Vs |
| Vibrio fischeri ES114 |
NC_006840 |
Squid symbiont |
30°C |
P |
ND |
3028 |
| Vibrio parahaemolyticus RIMD |
NC_004603 |
Osaka |
20–43°C |
P |
0.1 MPa |
3469 |
| Vibrio vulnificus YJ016 |
NC_005139 |
Taiwan |
30–40°C |
P |
ND |
3362 |
|
|
||||||
| Shewanella benthica KT99 |
- |
Tonga-Kermadec Trench |
4–15°C |
A |
50 MPa |
Vs |
| Shewanella baltica OS155 |
NC_009052 |
Baltic Sea |
4°C |
P |
10 MPa |
3167 |
| Shewanella oneidensis MR-1 |
NC_004347 |
Oneida lake |
30°C |
P |
0.1 MPa |
2651 |
| Shewanella frigidimarina NCIMB 400 |
NC_008345 |
North Sea |
20–22°C |
P |
0.1 MPa |
2909 |
|
Columns report respectively: strain, NCBI accession number, isolation site, optimum growth temperature (Topt), presence (P) or absence (A) of the deoxyribodipyrimidine photo-lyase gene, optimum growth pressure (ND = Not Determined) and number of orthologous genes identified for each comparison. The omission of the ORFs encoding light-activated photolyase genes from the SS9 and KT99 genomes is due to the absence of sunlight in the deep sea. | ||||||
Campanaro et al. BMC Evolutionary Biology 2008 8:313 doi:10.1186/1471-2148-8-313 |
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