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Overexpression in Escherichia coli of the AT-rich trpA and trpB genes from the hyperthermophilic archaeon Pyrococcus furiosus

机译:嗜热古菌激烈热球菌中富含AT的trpA和trpB基因在大肠杆菌中的过表达

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摘要

Expression of AT-rich genes from microorganisms such as archaea is often inefficient in Escherichia coli. The trpA and trpB genes encoding the tryptophan synthase subunits were cloned from the hyperthermophilic archaeon Pyrococcus furiosus. No apparent difference in codon bias was found between the genes. However, using a conventional cloning vector having the lac promoter, the trpB gene was expressed poorly in E. coli, whereas the trpA gene was overexpressed. The expression of the trpB gene was remarkably enhanced (> 12-fold) by the introduction of an overlapping leader open reading frame. The expression of the triA gene was also improved (similar to 1.5-fold). This approach may be useful for overexpressing various kinds of AT-rich genes. (C) 2002 Federation of European Microbiological Societies. Published by Elsevier Science B.V. All rights reserved. [References: 19]
机译:来自微生物如古细菌的富含AT的基因的表达在大肠杆菌中通常是无效的。从嗜热古菌激烈热球菌中克隆了编码色氨酸合酶亚基的trpA和trpB基因。基因之间没有发现密码子偏倚的明显差异。然而,使用具有lac启动子的常规克隆载体,trpB基因在大肠杆菌中表达差,而trpA基因过表达。通过引入重叠的前导开放阅读框,trpB基因的表达显着增强(> 12倍)。 triA基因的表达也得到了改善(类似于1.5倍)。此方法可能对于过表达各种富含AT的基因有用。 (C)2002年欧洲微生物学会联合会。由Elsevier Science B.V.保留所有权利。 [参考:19]

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