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Minimal Functions and Physiological Conditions Required for Growth of Salmonella enterica on Ethanolamine in the Absence of the Metabolosome

机译:没有代谢球体时沙门氏菌在乙醇胺上生长沙门氏菌所需的最低功能和生理条件

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摘要

During growth on ethanolamine, Salmonella enterica synthesizes a multimolecular structure that mimics the carboxysome used by some photosynthetic bacteria to fix CO2. In S. enterica, this carboxysome-like structure (hereafter referred to as the ethanolamine metabolosome) is thought to contain the enzymatic machinery needed to metabolize ethanolamine into acetyl coenzyme A (acetyl-CoA). Analysis of the growth behavior of mutant strains of S. enterica lacking specific functions encoded by the 17-gene ethanolamine utilization (eut) operon established the minimal biochemical functions needed by this bacterium to use ethanolamine as a source of carbon and energy. The data obtained support the conclusion that the ethanolamine ammnonia-lyase (EAL) enzyme (encoded by the eutBC genes) and coenzyme B12 are necessary and sufficient to grow on ethanolamine. We propose that the EutD phosphotransacetylase and EutG alcohol dehydrogenase are important to maintain metabolic balance. Glutathione (GSH) had a strong positive effect that compensated for the lack of the EAL reactivase EutA protein under aerobic growth on ethanolamine. Neither GSH nor EutA was needed during growth on ethanolamine under reduced-oxygen conditions. GSH also stimulated growth of a strain lacking the acetaldehyde dehydrogenase (EutE) enzyme. The role of GSH in ethanolamine catabolism is complex and requires further investigation. Our data show that the ethanolamine metabolosome is not involved in the biochemistry of ethanolamine catabolism. We propose the metabolosome is needed to concentrate low levels of ethanolamine catabolic enzymes, to keep the level of toxic acetaldehyde low, to generate enough acetyl-CoA to support cell growth, and to maintain a pool of free CoA.
机译:在乙醇胺上生长期间,小肠沙门氏菌会合成多分子结构,该结构模仿某些光合细菌用来固定CO2的羧基体。在肠炎沙门氏菌中,该羧基体样结构(以下称为乙醇胺代谢球体)被认为含有将乙醇胺代谢为乙酰辅酶A(乙酰辅酶A)所需的酶促机制。分析缺乏由17基因乙醇胺利用(eut)操纵子编码的特定功能的肠道链球菌突变株的生长行为,确定了该细菌使用乙醇胺作为碳和能量来源所需的最低生化功能。获得的数据支持以下结论:乙醇胺氨分解酶(EAL)酶(由eutBC基因编码)和辅酶B12在乙醇胺上生长是必需和充分的。我们建议EutD磷酸转乙酰酶和EutG醇脱氢酶对于维持代谢平衡很重要。谷胱甘肽(GSH)具有很强的积极作用,可以补偿有氧乙醇乙醇生长下EAL活化酶EutA蛋白的缺乏。在低氧条件下在乙醇胺上生长期间,既不需要GSH也不需要EutA。 GSH还刺激了缺乏乙醛脱氢酶(EutE)酶的菌株的生长。 GSH在乙醇胺分解代谢中的作用很复杂,需要进一步研究。我们的数据显示乙醇胺代谢空间不参与乙醇胺分解代谢的生物化学。我们提出需要代谢球体来浓缩低水平的乙醇胺分解代谢酶,以保持低毒性乙醛水平,产生足够的乙酰辅酶A以支持细胞生长,并维持大量游离辅酶A。

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