Comparative and functional genomics of Rhodococcus opacus PD630 for biofuels development.

TitleComparative and functional genomics of Rhodococcus opacus PD630 for biofuels development.
Publication TypeJournal Article
Year of Publication2011
AuthorsHolder, JW, Ulrich, JC, DeBono, AC, Godfrey, PA, Desjardins, CA, Zucker, J, Zeng, Q, Leach, ALB, Ghiviriga, I, Dancel, C, Abeel, T, Gevers, D, Kodira, CD, Desany, B, Affourtit, JP, Birren, BW, Sinskey, AJ
JournalPLoS Genet
Date Published2011 Sep
KeywordsBiofuels, Fatty Acids, Genome, Bacterial, Genomics, Lipids, Metabolic Networks and Pathways, Phylogeny, Rhodococcus, Triglycerides

The Actinomycetales bacteria Rhodococcus opacus PD630 and Rhodococcus jostii RHA1 bioconvert a diverse range of organic substrates through lipid biosynthesis into large quantities of energy-rich triacylglycerols (TAGs). To describe the genetic basis of the Rhodococcus oleaginous metabolism, we sequenced and performed comparative analysis of the 9.27 Mb R. opacus PD630 genome. Metabolic-reconstruction assigned 2017 enzymatic reactions to the 8632 R. opacus PD630 genes we identified. Of these, 261 genes were implicated in the R. opacus PD630 TAGs cycle by metabolic reconstruction and gene family analysis. Rhodococcus synthesizes uncommon straight-chain odd-carbon fatty acids in high abundance and stores them as TAGs. We have identified these to be pentadecanoic, heptadecanoic, and cis-heptadecenoic acids. To identify bioconversion pathways, we screened R. opacus PD630, R. jostii RHA1, Ralstonia eutropha H16, and C. glutamicum 13032 for growth on 190 compounds. The results of the catabolic screen, phylogenetic analysis of the TAGs cycle enzymes, and metabolic product characterizations were integrated into a working model of prokaryotic oleaginy.

Alternate JournalPLoS Genet
Citation Key255
PubMed ID21931557
PubMed Central IDPMC3169528
Grant ListHHSN272200900006C / AI / NIAID NIH HHS / United States