Abstract

The organization and function of the Bacillus subtilis YsiA regulon involved in fatty acid degradation were investigated. Northern and primer extension analyses indicated that this regulon comprises five operons, i.e. lcfA-ysiA-B-etfB-A, ykuF-G, yhfL, yusM-L-K-J, and ywjF-acdA-rpoE. YusJ and AcdA, YsiB and YusL, and YusK presumably encode acyl-CoA dehydrogenases, 3-hydroxyl-CoA dehydrogenase/enoyl-CoA hydratase complexes, and acetyl-CoA C-acyltransferase, respectively, which are directly involved in the fatty acid beta-oxidation cycle. In addition, LcfA and YhfL are likely to encode long chain acyl-CoA ligases. On gel retardation and footprinting analyses involving the purified YsiA protein, we identified cis-sequences for YsiA binding (YsiA boxes) in the promoter regions upstream of ysiA, ykuF, yusL, yhfL, and ywjF, the equilibrium dissociation constants (K(d)) for YsiA binding being 20, 21, 37, 43, and 65 nm, respectively. YsiA binding was specifically inhibited by long chain acyl-CoAs with 14-20 carbon atoms, acyl-CoAs with 18 carbon atoms being more effective; out of long chain acyl-CoAs tested, monounsaturated oleoyl-CoA, and branched chain 12-metyltetradecanoyl-CoA were most effective. These in vitro findings were supported by the in vivo observation that the knock-out of acyl-CoA dehydrogenation through yusJ, etfA, or etfB disruption resulted in YsiA inactivation, probably because of the accumulation of long chain acyl-CoAs in the cells. Furthermore, the disruption of yusL, yusK, yusJ, etfA, etfB, or ykuG affected the utilization of palmitic acid, a representative long chain fatty acid. Based on this work, ysiA, ysiB, ykuF, ykuG, yhfL, yusM, yusL, yusK, yusJ, and ywjF can be renamed fadR, fadB, fadH, fadG, lcfB, fadM, fadN, fadA, fadE, and fadF.

Highlights

  • Reference or source168 FU788 LCFAd BFS2426 BFS2427 ETFAd ETFBd YKUFd BFS1835 YHFLd BFS1341 BFS1347 BFS1346 BFS1345 BFS1246 ACDAd typC2 ysiA::cat trpC2 lcfA::pMUTIN trpC2 ysiA::pMUTIN trpC2 ysiB::pMUTIN trpC2 etfA::pMUTIN trpC2 etfB::pMUTIN trpC2 ykuF::pMUTIN trpC2 ykuG::pMUTIN trpC2 yhfL::pMUTIN trpC2 yusM::pMUTIN trpC2 yusL::pMUTIN trpC2 yusK::pMUTIN trpC2 yusJ::pMUTIN trpC2 ywjF::pMUTIN trpC2 acdA::pMUTIN trpC2

  • Model prokaryote, Escherichia coli [1]

  • Bacillus subtilis mainly produces branched chain fatty acids and possesses two FabH isoenzymes that differ from the E. coli enzyme in that they are selective for branched chain acyl-CoAs [4]

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Summary

Reference or source

168 FU788 LCFAd BFS2426 BFS2427 ETFAd ETFBd YKUFd BFS1835 YHFLd BFS1341 BFS1347 BFS1346 BFS1345 BFS1246 ACDAd typC2 ysiA::cat trpC2 lcfA::pMUTIN trpC2 ysiA::pMUTIN trpC2 ysiB::pMUTIN trpC2 etfA::pMUTIN trpC2 etfB::pMUTIN trpC2 ykuF::pMUTIN trpC2 ykuG::pMUTIN trpC2 yhfL::pMUTIN trpC2 yusM::pMUTIN trpC2 yusL::pMUTIN trpC2 yusK::pMUTIN trpC2 yusJ::pMUTIN trpC2 ywjF::pMUTIN trpC2 acdA::pMUTIN trpC2. DNA microarray analysis involving the wild type strain and a disruptant as to ysiA, encoding one of the helix-turn-helix transcription regulatory proteins, indicated that the YsiA protein negatively regulates more than 10 genes, the majority of which most likely participate in fatty acid ␤-oxidation, which presumably plays a central regulatory role in fatty acid degradation. In this communication, we describe the organization and function of the YsiA regulon comprising the lcfA-ysiA-B-etfB-A, ykuF-G, yhfL, yusM-L-K-J, and ywjF-acdA-rpoE operons. The in vivo as well as in vitro experiments suggested that long chain acylCoAs are most likely inducers (or ligands) that antagonize YsiA as to its binding to YsiA boxes

EXPERIMENTAL PROCEDURES
Primers used in this study
GGAAGGAACGATGACATATGAAGCAAA GCAAGCTTTCAACCGCAAGTGAAATTGC
RESULTS
Full Text
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