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球形红杆菌glnB和glnA基因的核苷酸序列及特征分析

Nucleotide sequence and characterization of the Rhodobacter sphaeroides glnB and glnA genes.

作者信息

Zinchenko V, Churin Y, Shestopalov V, Shestakov S

机构信息

Department of Genetics, Moscow State University, Russia.

出版信息

Microbiology (Reading). 1994 Aug;140 ( Pt 8):2143-51. doi: 10.1099/13500872-140-8-2143.

Abstract

The glnA gene of Rhodobacter sphaeroides encoding glutamine synthetase (GS) has been cloned and sequenced. Molecular analysis revealed that there is a glnB gene upstream of glnA, in a single glnBA operon. A putative glnAp1-type promoter sequence, a consensus ntrC gene product binding site and a consensus upstream activator sequence were detected upstream of the glnB gene. The deduced amino acid sequences of the GS and GlnB proteins of R. sphaeroides showed strong homology with the same proteins from other Gram-negative bacteria. The sequence of the glnA gene isolated from glutamine auxotroph Gln83 was also determined. The glnA83 mutation was shown to result in premature termination of GS synthesis and formation of a 17 kDa C-truncated GS which could be complemented by a 5'-truncated glnA gene which encodes a 30 kDa N-truncated GS. This phenomenon is characteristic for interallelic complementation.

摘要

已克隆并测序了球形红细菌编码谷氨酰胺合成酶(GS)的glnA基因。分子分析表明,在单个glnBA操纵子中,glnA上游存在一个glnB基因。在glnB基因上游检测到一个推定的glnAp1型启动子序列、一个共有ntrC基因产物结合位点和一个共有上游激活序列。球形红细菌GS和GlnB蛋白的推导氨基酸序列与其他革兰氏阴性菌的相同蛋白具有高度同源性。还确定了从谷氨酰胺营养缺陷型Gln83分离的glnA基因的序列。结果表明,glnA83突变导致GS合成过早终止,并形成一个17 kDa的C端截短的GS,该GS可被一个编码30 kDa N端截短的GS的5'端截短的glnA基因互补。这种现象是等位基因间互补的特征。

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