Research article

Insights on the evolution of trehalose biosynthesis

Nelson Avonce^1,2 , Alfredo Mendoza-Vargas¹ , Enrique Morett¹ and Gabriel Iturriaga²

¹  Centro de Investigación en Biotecnología-UAEM, Av. Universidad 1001, Col. Chamilpa, Cuernavaca 62210, Mexico

²  Instituto de Biotecnología-UNAM, Av. Universidad 2001, Col. Chamilpa, Cuernavaca 62210, Mexico

author email corresponding author email

BMC Evolutionary Biology 2006, 6:109doi:10.1186/1471-2148-6-109

Published:	19 December 2006

Abstract

Background

The compatible solute trehalose is a non-reducing disaccharide, which accumulates upon heat, cold or osmotic stress. It was commonly accepted that trehalose is only present in extremophiles or cryptobiotic organisms. However, in recent years it has been shown that although higher plants do not accumulate trehalose at significant levels they have actively transcribed genes encoding the corresponding biosynthetic enzymes.

Results

In this study we show that trehalose biosynthesis ability is present in eubacteria, archaea, plants, fungi and animals. In bacteria there are five different biosynthetic routes, whereas in fungi, plants and animals there is only one. We present phylogenetic analyses of the trehalose-6-phosphate synthase (TPS) and trehalose-phosphatase (TPP) domains and show that there is a close evolutionary relationship between these domains in proteins from diverse organisms. In bacteria TPS and TPP genes are clustered, whereas in eukaryotes these domains are fused in a single protein.

Conclusion

We have demonstrated that trehalose biosynthesis pathways are widely distributed in nature. Interestingly, several eubacterial species have multiple pathways, while eukaryotes have only the TPS/TPP pathway. Vertebrates lack trehalose biosynthetic capacity but can catabolise it. TPS and TPP domains have evolved mainly in parallel and it is likely that they have experienced several instances of gene duplication and lateral gene transfer.