Journal
MICROBIOLOGY-SGM
Volume 158, Issue -, Pages 3054-3062Publisher
MICROBIOLOGY SOC
DOI: 10.1099/mic.0.059501-0
Keywords
-
Categories
Funding
- Integration of Biosynthesis and Organic Synthesis Program of Advanced Chemical Technologies for Sustainability
Ask authors/readers for more resources
A previously identified sterol catabolic gene cluster is widely dispersed among actinobacteria, enabling them to degrade and grow on naturally occurring sterols. We investigated the physiological roles of various genes by targeted inactivation in mutant RG32 of Rhodococcus rhodochrous, which selectively degrades sterol side-chains. The Itp3 and Itp4 deletion mutants were each completely blocked in side-chain degradation of beta-sitosterol and campesterol, but not of cholesterol. These results indicated a role for Itp3 and Itp4 in the removal of C24 branches specifically. Bioinformatic analysis of the encoded Ltp3 and Ltp4 proteins revealed relatively high similarity to thiolase enzymes, typically involved in beta-oxidation, but the catalytic residues characteristic for thiolase enzymes are not conserved in their amino acid sequences. Removal of the C24-branched side-chain carbons of beta-sitosterol was previously shown to proceed via aldolytic cleavage rather than by beta-oxidation. Our results therefore suggest that Itp3 and Itp4 probably encode aldol-lyases rather than thiolases. This is the first report, to our knowledge, on the molecular characterization of genes with specific and essential roles in carbon-carbon bond cleavage of C24-branched chain sterols in Rhodococcus strains, most likely acting as aldol-lyases. The results are a clear contribution to our understanding of sterol degradation in actinobacteria.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available