The biochemistry and genetics of the bacterial steroid catabolism have been extensively studied during the last years and their findings have been essential to the development of biotechnological applications. For instance, metabolic engineering of the steroid-eater strains has allowed to obtain intermediaries of industrial value. However, there are still some drawbacks that must be overcome, such as the redundancy of the steroid catabolism genes in the genome and a better knowledge of its genetic regulation. KshABs and KstDs are key enzymes involved in the aerobic breakage of the steroid nucleus. Chol-4 contains three genes, a single gene and three genes within its genome. In the present work, the growth of strains was evaluated on different steroids substrates; the promoter regions of these genes were analyzed; and their expression was followed by qRT-PCR in both wild type and mutants. Additionally, the transcription level of the genes was studied in the mutants. The results show that KshA2B and KshA1B are involved in AD metabolism, while KshA3B and KshA1B contribute to the cholesterol metabolism in . In the single mutants, expression of the remaining and genes is re-organized to survive on the steroid substrate. These data give insight into the fine regulation of steroid genes when several isoforms are present.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8228715 | PMC |
http://dx.doi.org/10.3390/microorganisms9061171 | DOI Listing |
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