Molecular characterization of ltp3 and ltp4, essential for C24-branched chain sterol-side-chain degradation in Rhodococcus rhodochrous DSM 43269
In: Microbiology, Jg. 158 (2012-12-01), S. 3054-3062
Online
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Zugriff:
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.
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Molecular characterization of ltp3 and ltp4, essential for C24-branched chain sterol-side-chain degradation in Rhodococcus rhodochrous DSM 43269
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Autor/in / Beteiligte Person: | Dijkhuizen, Lubbert ; Robert van der Geize ; Maarten Hotse Wilbrink ; Interactions, Host-Microbe ; Groningen Biomolecular Sciences and Biotechnology |
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Zeitschrift: | Microbiology, Jg. 158 (2012-12-01), S. 3054-3062 |
Veröffentlichung: | Microbiology Society, 2012 |
Medientyp: | unknown |
ISSN: | 1465-2080 (print) ; 1350-0872 (print) |
DOI: | 10.1099/mic.0.059501-0 |
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