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从弗氏柠檬酸杆菌中克隆、共表达甘油脱水酶和 1,3-丙二醇脱氢酶,并对其进行表征。

Molecular cloning, co-expression, and characterization of glycerol dehydratase and 1,3-propanediol dehydrogenase from Citrobacter freundii.

机构信息

School of Food and Biological Engineering, Jiangsu University, Zhenjiang, China.

出版信息

Mol Biotechnol. 2013 Jun;54(2):469-74. doi: 10.1007/s12033-012-9585-9.

Abstract

1,3-Propanediol (1,3-PD), an important material for chemical industry, is biologically synthesized by glycerol dehydratase (GDHt) and 1,3-propanediol dehydrogenase (PDOR). In present study, the dhaBCE and dhaT genes encoding glycerol dehydratase and 1,3-propanediol dehydrogenase respectively were cloned from Citrobacter freundii and co-expressed in E. coli. Sequence analysis revealed that the cloned genes were 85 and 77 % identical to corresponding gene of C. freundii DSM 30040 (GenBank No. U09771), respectively. The over-expressed recombinant enzymes were purified by nickel-chelate chromatography combined with gel filtration, and recombinant GDHt and PDOR were characterized by activity assay, kinetic analysis, pH, and temperature optimization. This research may form a basis for the future work on biological synthesis of 1,3-PD.

摘要

1,3-丙二醇(1,3-PD)是一种重要的化工原料,可通过甘油脱水酶(GDHt)和 1,3-丙二醇脱氢酶(PDOR)生物合成。本研究从弗氏柠檬酸杆菌中克隆了分别编码甘油脱水酶和 1,3-丙二醇脱氢酶的 dhaBCE 和 dhaT 基因,并在大肠杆菌中进行了共表达。序列分析表明,克隆的基因与弗氏柠檬酸杆菌 DSM 30040 相应基因(GenBank No. U09771)的同源性分别为 85%和 77%。通过镍螯合层析结合凝胶过滤对过表达的重组酶进行了纯化,并通过活性测定、动力学分析、pH 值和温度优化对重组 GDHt 和 PDOR 进行了表征。这项研究可能为未来的 1,3-PD 生物合成工作奠定基础。

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