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本文引用的文献

1
Heterologous expression of D-xylulokinase from Pichia stipitis enables high levels of xylitol production by engineered Escherichia coli growing on xylose.树干毕赤酵母D-木酮糖激酶的异源表达使工程化大肠杆菌在木糖上生长时能够高水平生产木糖醇。
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Analysis of NADPH supply during xylitol production by engineered Escherichia coli.工程化大肠杆菌生产木糖醇过程中NADPH供应的分析。
Biotechnol Bioeng. 2009 Jan 1;102(1):209-20. doi: 10.1002/bit.22060.
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Metabolic capacity estimation of Escherichia coli as a platform for redox biocatalysis: constraint-based modeling and experimental verification.将大肠杆菌作为氧化还原生物催化平台的代谢能力评估:基于约束的建模与实验验证。
Biotechnol Bioeng. 2008 Aug 15;100(6):1050-65. doi: 10.1002/bit.21837.
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Dihydrolipoamide dehydrogenase mutation alters the NADH sensitivity of pyruvate dehydrogenase complex of Escherichia coli K-12.二氢硫辛酰胺脱氢酶突变改变了大肠杆菌K-12丙酮酸脱氢酶复合体对NADH的敏感性。
J Bacteriol. 2008 Jun;190(11):3851-8. doi: 10.1128/JB.00104-08. Epub 2008 Mar 28.
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NADH availability limits asymmetric biocatalytic epoxidation in a growing recombinant Escherichia coli strain.烟酰胺腺嘌呤二核苷酸(NADH)的可用性限制了一株生长中的重组大肠杆菌菌株中的不对称生物催化环氧化反应。
Appl Environ Microbiol. 2008 Mar;74(5):1436-46. doi: 10.1128/AEM.02234-07. Epub 2008 Jan 11.
6
Construction of an Escherichia coli K-12 mutant for homoethanologenic fermentation of glucose or xylose without foreign genes.构建用于葡萄糖或木糖同型乙醇发酵且不含外源基因的大肠杆菌K-12突变体。
Appl Environ Microbiol. 2007 Mar;73(6):1766-71. doi: 10.1128/AEM.02456-06. Epub 2007 Jan 26.
7
Engineering Escherichia coli for xylitol production from glucose-xylose mixtures.工程改造大肠杆菌以利用葡萄糖-木糖混合物生产木糖醇。
Biotechnol Bioeng. 2006 Dec 20;95(6):1167-76. doi: 10.1002/bit.21082.
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Construction of Escherichia coli K-12 in-frame, single-gene knockout mutants: the Keio collection.大肠杆菌K-12框内单基因敲除突变体的构建:Keio文库。
Mol Syst Biol. 2006;2:2006.0008. doi: 10.1038/msb4100050. Epub 2006 Feb 21.
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Effect of overexpression of a soluble pyridine nucleotide transhydrogenase (UdhA) on the production of poly(3-hydroxybutyrate) in Escherichia coli.可溶性吡啶核苷酸转氢酶(UdhA)过表达对大肠杆菌中聚(3-羟基丁酸酯)产量的影响。
Biotechnol Prog. 2006 Mar-Apr;22(2):420-5. doi: 10.1021/bp050375u.
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Understanding and improving NADPH-dependent reactions by nongrowing Escherichia coli cells.通过非生长型大肠杆菌细胞理解和改善依赖烟酰胺腺嘌呤二核苷酸磷酸(NADPH)的反应。
Biotechnol Prog. 2004 Mar-Apr;20(2):403-11. doi: 10.1021/bp030044m.

大肠杆菌中不存在天然发酵途径时的厌氧必需木糖醇生产。

Anaerobic obligatory xylitol production in Escherichia coli strains devoid of native fermentation pathways.

机构信息

Department of Chemical Engineering, Pennsylvania State University, University Park, PA 16802, USA.

出版信息

Appl Environ Microbiol. 2011 Jan;77(2):706-9. doi: 10.1128/AEM.01890-10. Epub 2010 Nov 19.

DOI:10.1128/AEM.01890-10
PMID:21097593
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3020535/
Abstract

Anaerobic glucose oxidation was coupled to xylose reduction in a nonfermentative Escherichia coli strain expressing NADPH-dependent xylose reductase. Xylitol production serves as the primary means of NAD(P)(+) regeneration, as glucose is converted primarily to acetate and CO(2). The membrane-bound transhydrogenase PntAB is required to achieve the maximum theoretical yield of four moles of xylitol per mole of glucose consumed.

摘要

在表达 NADPH 依赖型木糖还原酶的非发酵型大肠杆菌菌株中,无氧葡萄糖氧化与木糖还原偶联。木糖醇的生产是 NAD(P)(+) 再生的主要手段,因为葡萄糖主要转化为乙酸盐和 CO(2)。需要膜结合的转氢酶 PntAB 才能实现每消耗 1 摩尔葡萄糖产生 4 摩尔木糖醇的最大理论产率。