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橙色粘球菌主要σ因子编码基因的克隆与特性分析

Cloning and characterization of the gene encoding the major sigma factor of Stigmatella aurantiaca.

作者信息

Skladny H, Heidelbach M, Schairer H U

机构信息

Zentrum für Molekulare Biologie, Universität Heidelberg, Germany.

出版信息

Gene. 1994 May 27;143(1):123-7. doi: 10.1016/0378-1119(94)90616-5.

Abstract

The gene (sigA) encoding the major sigma factor of the myxobacterium, Stigmatella aurantiaca, was cloned and sequenced. The deduced polypeptide contains 706 amino acids (aa) and has a deduced M(r) of 79,910. It exhibits four different aa sequence motifs which correlate with the conserved domains of the major sigma factors of Myxococcus xanthus (sigma 80), Escherichia coli (sigma 70) and Bacillus subtilis (sigma 43). The sigma factor (sigma A) was detected in crude lysates of vegetative cells and in cells of different developmental stages from S. aurantiaca with an antiserum to M. xanthus sigma 80 by Western blot analysis. The SigA polypeptide copurified with RNA polymerase from vegetative S. aurantiaca cells. The aa sequence of its N terminus matches a sequence located 25 codons downstream from the proposed start codon. The sigA gene was expressed in E. coli and the corresponding gene product cross-reacted with the SigA antiserum as a polypeptide of 100 kDa, which is identical in size to the sigma A detected in vegetative cells of S. aurantiaca.

摘要

编码粘细菌橙色标桩菌主要σ因子的基因(sigA)被克隆并测序。推导的多肽含有706个氨基酸(aa),推导的分子量(M(r))为79,910。它呈现出四种不同的氨基酸序列基序,这些基序与黄色粘球菌(σ80)、大肠杆菌(σ70)和枯草芽孢杆菌(σ43)主要σ因子的保守结构域相关。通过蛋白质免疫印迹分析,用抗黄色粘球菌σ80的抗血清在橙色标桩菌营养细胞的粗裂解物以及不同发育阶段的细胞中检测到了σ因子(σA)。SigA多肽与橙色标桩菌营养细胞的RNA聚合酶共同纯化。其N端的氨基酸序列与位于推测起始密码子下游25个密码子处的序列匹配。sigA基因在大肠杆菌中表达,相应的基因产物与SigA抗血清发生交叉反应,作为一条100 kDa的多肽,其大小与在橙色标桩菌营养细胞中检测到的σA相同。

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