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大肠杆菌中一种产生NADH的葡萄糖-6-磷酸脱氢酶的代谢影响。

Metabolic impact of an NADH-producing glucose-6-phosphate dehydrogenase in Escherichia coli.

作者信息

Olavarria K, De Ingeniis J, Zielinski D C, Fuentealba M, Muñoz R, McCloskey D, Feist A M, Cabrera R

机构信息

Facultad de Ciencias, Universidad de Chile, Santiago, Chile.

Sanford-Burnham Medical Research Institute, La Jolla, CA, USA.

出版信息

Microbiology (Reading). 2014 Dec;160(Pt 12):2780-2793. doi: 10.1099/mic.0.082180-0. Epub 2014 Sep 22.

Abstract

In Escherichia coli, the oxidative branch of the pentose phosphate pathway (oxPPP) is one of the major sources of NADPH when glucose is the sole carbon nutrient. However, unbalanced NADPH production causes growth impairment as observed in a strain lacking phosphoglucoisomerase (Δpgi). In this work, we studied the metabolic response of this bacterium to the replacement of its glucose-6-phosphate dehydrogenase (G6PDH) by an NADH-producing variant. The homologous enzyme from Leuconostoc mesenteroides was studied by molecular dynamics and site-directed mutagenesis to obtain the NAD-preferring LmG6PDH(R46E,Q47E). Through homologous recombination, the zwf loci (encoding G6PDH) in the chromosomes of WT and Δpgi E. coli strains were replaced by DNA encoding LmG6PDH(R46E,Q47E). Contrary to some predictions performed with flux balance analysis, the replacements caused a substantial effect on the growth rates, increasing 59 % in the Δpgi strain, while falling 44 % in the WT. Quantitative PCR (qPCR) analysis of the zwf locus showed that the expression level of the mutant enzyme was similar to the native enzyme and the expression of genes encoding key enzymes of the central pathways also showed moderate changes among the studied strains. The phenotypic and qPCR data were integrated into in silico modelling, showing an operative G6PDH flux contributing to the NADH pool. Our results indicated that, in vivo, the generation of NADH by G6PDH is beneficial or disadvantageous for growth depending on the operation of the upper Embden-Meyerhof pathway. Interestingly, a genomic database search suggested that in bacteria lacking phosphofructokinase, the G6PDHs tend to have similar preferences for NAD and NADP. The importance of the generation of NADPH in a pathway such as the oxPPP is discussed.

摘要

在大肠杆菌中,当葡萄糖是唯一碳源营养时,磷酸戊糖途径的氧化分支(oxPPP)是NADPH的主要来源之一。然而,如在缺乏磷酸葡萄糖异构酶的菌株(Δpgi)中观察到的那样,NADPH产生不平衡会导致生长受损。在这项工作中,我们研究了这种细菌对用产生NADH的变体替代其葡萄糖-6-磷酸脱氢酶(G6PDH)的代谢反应。通过分子动力学和定点诱变研究了来自肠系膜明串珠菌的同源酶,以获得偏好NAD的LmG6PDH(R46E,Q47E)。通过同源重组,野生型和Δpgi大肠杆菌菌株染色体中的zwf基因座(编码G6PDH)被编码LmG6PDH(R46E,Q47E)的DNA所取代。与通量平衡分析所做的一些预测相反,这种替代对生长速率产生了实质性影响,在Δpgi菌株中增加了59%,而在野生型中下降了44%。对zwf基因座的定量PCR(qPCR)分析表明,突变酶的表达水平与天然酶相似,并且研究菌株中编码中心途径关键酶的基因表达也显示出适度变化。表型和qPCR数据被整合到计算机模拟中,显示出有助于NADH库的有效G6PDH通量。我们的结果表明,在体内,G6PDH产生NADH对生长是有益还是有害取决于上Embden-Meyerhof途径的运行情况。有趣的是,基因组数据库搜索表明,在缺乏磷酸果糖激酶的细菌中,G6PDH对NAD和NADP往往具有相似的偏好。本文讨论了在oxPPP等途径中产生NADPH的重要性。

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