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首页> 外文期刊>Journal of bacteriology >Transcription initiation at multiple promoters of the pfl gene by E sigma 70-dependent transcription in vitro and heterologous expression in Pseudomonas putida in vivo.
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Transcription initiation at multiple promoters of the pfl gene by E sigma 70-dependent transcription in vitro and heterologous expression in Pseudomonas putida in vivo.

机译:在体外通过E sigma 70依赖性转录在pfl基因的多个启动子处启动转录,在体内通过恶臭假单胞菌进行异源表达。

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摘要

In vitro transcription experiments were used to provide further evidence that the gene encoding pyruvate formate-lyase (EC 2.3.1.54) from Escherichia coli is transcribed from seven promoters which cover a region of 1.2 kilobase pairs of DNA (G. Sawers and A. B?ck, J. Bacteriol., 171:2485-2498, 1989). The results demonstrated that all promoters were recognized by the major RNA polymerase holoenzyme species E sigma 70 in vitro. Further corroboration for multiple functional promoters came from heterologous expression of the pfl operon in the obligate aerobe Pseudomonas putida. An immunological analysis indicated that the pyruvate formate-lyase protein was synthesized from a multicopy plasmid in P. putida, and S1 nuclease protection of RNA transcripts confirmed that all the pfl promoters on the plasmid were recognized by the host RNA polymerase. Transcription initiated at the same sites in P. putida and in E. coli for all the transcripts that were analyzed.
机译:体外转录实验用于提供进一步的证据,表明来自大肠杆菌的编码丙酮酸甲酸酯裂解酶(EC 2.3.1.54)的基因是从覆盖1.2 kb碱基对DNA的七个启动子转录而来的(G. Sawers和A. B)。 ,J.Bacteriol。,171:2485-2498,1989)。结果表明,所有启动子在体外均被主要的RNA聚合酶全酶E sigma 70识别。多功能功能启动子的进一步确证来自于专一的拟氧假单胞菌假单胞菌中pfl操纵子的异源表达。免疫学分析表明丙酮酸甲酸酯裂解酶蛋白是由恶臭假单胞菌中的多拷贝质粒合成的,RNA转录本的S1核酸酶保护证实了质粒上的所有pfl启动子均被宿主RNA聚合酶识别。转录在恶臭假单胞菌和大肠杆菌中的相同位点开始,用于分析的所有转录本。

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