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编码大肠杆菌K12的GMP还原酶的基因的核苷酸序列。

Nucleotide sequence of the gene encoding the GMP reductase of Escherichia coli K12.

作者信息

Andrews S C, Guest J R

机构信息

Department of Microbiology, University of Sheffield, U.K.

出版信息

Biochem J. 1988 Oct 1;255(1):35-43. doi: 10.1042/bj2550035.

Abstract

(1) The nucleotide sequence of a 1991 bp segment of DNA that expresses the GMP reductase (guaC) gene of Escherichia coli K12 was determined. (2) This gene comprises 1038 bp, 346 codons (including the initiation codon but excluding the termination codon), and it encodes a polypeptide of Mr 37,437 which is in good agreement with previous maxicell studies. (3) The sequence contains a putative promoter 102 bp upstream of the translational start codon, and this is immediately followed by a (G + C)-rich discriminator sequence suggesting that guaC expression may be under stringent control (4) The GMP reductase exhibits a high degree of sequence identity (34%) with IMP dehydrogenase (the guaB gene product) indicative of a close evolutionary relationship between the salvage pathway and the biosynthetic enzymes, GMP reductase and IMP dehydrogenase, respectively. (5) A single conserved cysteine residue, possibly involved in IMP binding to IMP dehydrogenase, was located within a region that possesses some of the features of a nucleotide binding site. (6) The IMP dehydrogenase polypeptide contains an internal segment of 123 amino acid residues that has no counterpart in GMP reductase and may represent an independent folding domain flanked by (alanine + glycine)-rich interdomain linkers.

摘要

(1) 测定了表达大肠杆菌K12的GMP还原酶(guaC)基因的1991 bp DNA片段的核苷酸序列。(2) 该基因由1038 bp组成,有346个密码子(包括起始密码子但不包括终止密码子),编码一个Mr为37,437的多肽,这与之前的大细胞研究结果高度一致。(3) 该序列在翻译起始密码子上游102 bp处含有一个假定的启动子,紧接着是一个富含(G + C)的鉴别序列,这表明guaC的表达可能受到严格调控。(4) GMP还原酶与IMP脱氢酶(guaB基因产物)表现出高度的序列同一性(34%),这分别表明补救途径与生物合成酶GMP还原酶和IMP脱氢酶之间存在密切的进化关系。(5) 一个可能参与IMP与IMP脱氢酶结合的单一保守半胱氨酸残基位于一个具有核苷酸结合位点某些特征的区域内。(6) IMP脱氢酶多肽包含一个123个氨基酸残基的内部片段,该片段在GMP还原酶中没有对应物,可能代表一个独立的折叠结构域,两侧是富含(丙氨酸 + 甘氨酸)的结构域间连接子。

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