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Aerobic glycerol dissimilation via the Enterococcus faecalis DhaK pathway depends on NADH oxidase and a phosphotransfer reaction from PEP to DhaK via EIIADha.好氧甘油异化通过粪肠球菌 DhaK 途径,依赖于 NADH 氧化酶和通过 EIIADha 将 PEP 磷酸转移反应至 DhaK。
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丙酮酸盐-甲酸裂解酶对于粪肠球菌 W11 菌株中依赖延胡索酸盐的无氧甘油利用是必需的。

Pyruvate formate-lyase is essential for fumarate-independent anaerobic glycerol utilization in the Enterococcus faecalis strain W11.

机构信息

Department of Applied Chemistry and Biotechnology, Faculty of Engineering, Okayama University of Science, Okayama, Okayama, Japan

Department of Applied Chemistry and Biotechnology, Faculty of Engineering, Okayama University of Science, Okayama, Okayama, Japan.

出版信息

J Bacteriol. 2014 Jul;196(13):2472-80. doi: 10.1128/JB.01512-14. Epub 2014 Apr 25.

DOI:10.1128/JB.01512-14
PMID:24769696
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4054171/
Abstract

Although anaerobic glycerol metabolism in Enterococcus faecalis requires exogenous fumarate for NADH oxidation, E. faecalis strain W11 can metabolize glycerol in the absence of oxygen without exogenous fumarate. In this study, metabolic end product analyses and reporter assays probing the expression of enzymes involved in pyruvate metabolism were performed to investigate this fumarate-independent anaerobic metabolism of glycerol in W11. Under aerobic conditions, the metabolic end products of W11 cultured with glycerol were similar to those of W11 cultured with glucose. However, when W11 was cultured anaerobically, most of the glucose was converted to l-lactate, but glycerol was converted to ethanol and formate. During anaerobic culture with glycerol, the expression of the l-lactate dehydrogenase and pyruvate dehydrogenase E1αβ genes in W11 was downregulated, whereas the expression of the pyruvate formate-lyase (Pfl) and aldehyde/alcohol dehydrogenase genes was upregulated. These changes in the expression levels caused the change in the composition of end products. A pflB gene disruptant (Δpfl mutant) of W11 could barely utilize glycerol under anaerobic conditions, but the growth of the Δpfl mutant cultured with either glucose or dihydroxyacetone (DHA) under anaerobic conditions was the same as that of W11. Glucose metabolism and DHA generates one NADH molecule per pyruvate molecule, whereas glycerol metabolism in the dehydrogenation pathway generates two NADH molecules per pyruvate molecule. These findings demonstrate that NADH generated from anaerobic glycerol metabolism in the absence of fumarate is oxidized through the Pfl-ethanol fermentation pathway. Thus, Pfl is essential to avoid the accumulation of excess NADH during fumarate-independent anaerobic glycerol metabolism.

摘要

尽管粪肠球菌(Enterococcus faecalis)的无氧甘油代谢需要外源富马酸盐来氧化 NADH,但 W11 菌株可以在无氧条件下无需外源富马酸盐代谢甘油。在这项研究中,通过代谢终产物分析和探测参与丙酮酸代谢的酶表达的报告基因实验,研究了 W11 中这种无氧甘油代谢的富马酸盐独立性。在有氧条件下,用甘油培养的 W11 的代谢终产物与用葡萄糖培养的 W11 的代谢终产物相似。然而,当 W11 进行无氧培养时,大部分葡萄糖被转化为 l-乳酸,但甘油被转化为乙醇和甲酸盐。在无氧培养过程中,W11 中的 l-乳酸脱氢酶和丙酮酸脱氢酶 E1αβ 基因的表达下调,而丙酮酸甲酸裂解酶(Pfl)和醛/醇脱氢酶基因的表达上调。这些表达水平的变化导致了终产物组成的变化。W11 的 pflB 基因敲除(Δpfl 突变体)在无氧条件下几乎不能利用甘油,但在无氧条件下用葡萄糖或二羟丙酮(DHA)培养的Δpfl 突变体的生长与 W11 相同。葡萄糖代谢和 DHA 每丙酮酸分子生成一个 NADH 分子,而甘油代谢脱氢途径每丙酮酸分子生成两个 NADH 分子。这些发现表明,无氧条件下富马酸盐独立的甘油代谢产生的 NADH 通过 Pfl-乙醇发酵途径被氧化。因此,Pfl 对于避免在富马酸盐独立的无氧甘油代谢过程中过量 NADH 的积累是必不可少的。