首页> 外文期刊>Molecular Microbiology >Identification of a conserved protein involved in anaerobic unsaturated fatty acid synthesis in Neiserria gonorrhoeae: implications for facultative and obligate anaerobes that lack FabA.
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Identification of a conserved protein involved in anaerobic unsaturated fatty acid synthesis in Neiserria gonorrhoeae: implications for facultative and obligate anaerobes that lack FabA.

机译:淋病奈瑟氏球菌厌氧不饱和脂肪酸合成中涉及的保守蛋白的鉴定:对缺乏FabA的兼性和专性厌氧菌的影响。

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Transcriptome analysis of the facultative anaerobe, Neisseria gonorrhoeae, revealed that many genes of unknown function were induced under anaerobic conditions. Mutation of one such gene, NGO1024, encoding a protein belonging to the 2-nitropropane dioxygenase-like superfamily of proteins, was found to result in an inability of gonococci to grow anaerobically. Anaerobic growth of an NG1024 mutant was restored upon supplementation with unsaturated fatty acids (UFA), but not with the saturated fatty acid palmitate. Gonococcal fatty acid profiles confirmed that NGO1024 was involved in UFA synthesis anaerobically, but not aerobically, demonstrating that gonococci contain two distinct pathways for the production of UFAs, with a yet unidentified aerobic mechanism, and an anaerobic mechanism involving NGO1024. Expression of genes involved in classical anaerobic UFA synthesis, fabA, fabM and fabB, was toxic in gonococci and unable to complement a NGO1024 mutation, suggesting that the chemistry involved in gonococcal anaerobic UFA synthesis is distinct from that of the classical pathway. NGO1024 homologues, which we suggest naming UfaA, form a distinct lineage within the 2-nitropropane dioxygenase-like superfamily, and are found in many facultative and obligate anaerobes that produce UFAs but lack fabA, suggesting that UfaA is part of a widespread pathway involved in UFA synthesis.
机译:兼性厌氧菌淋病奈瑟菌的转录组分析表明,许多功能未知的基因是在厌氧条件下诱导的。发现一种这样的基因,NGO1024的突变,其编码属于蛋白质的2-硝基丙烷双加氧酶样超家族的蛋白质,导致淋球菌无法厌氧生长。 NG1024突变体的厌氧生长通过添加不饱和脂肪酸(UFA)而不是饱和脂肪酸棕榈酸酯来恢复。淋球菌脂肪酸谱证实NGO1024厌氧但不需氧地参与UFA的合成,表明淋球菌包含两个不同的UFA产生途径,其尚不清楚的需氧机制和涉及NGO1024的厌氧机制。涉及经典厌氧UFA合成的基因fabA,fabM和fabB在淋球菌中有毒且不能补充NGO1024突变,这表明淋球菌厌氧UFA合成涉及的化学与经典途径不同。我们建议命名为UfaA的NGO1024同源物在2-硝基丙烷双加氧酶样超家族中形成独特的谱系,并且在许多产生UFA但缺乏fabA的兼性厌氧厌氧菌中发现,这表明UfaA是参与该过程的广泛途径的一部分UFA合成。

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