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编码大肠杆菌三磷酸腺苷酶复合体膜部(F0)亚基的三个基因。

Three genes coding for subunits of the membrane sector (F0) of the Escherichia coli adenosine triphosphatase complex.

作者信息

Downie J A, Cox G B, Langman L, Ash G, Becker M, Gibson F

出版信息

J Bacteriol. 1981 Jan;145(1):200-10. doi: 10.1128/jb.145.1.200-210.1981.

DOI:10.1128/jb.145.1.200-210.1981
PMID:6450744
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC217262/
Abstract

Two mutant unc alleles, unc-469 and unc-476, have been characterized as affecting a previously undescribed gene, designated uncF. The uncF gene is part of the unc operon (with the gene order being uncBFEAGDC), although some uncertainty remains as to the relative order of the uncF and uncE genes. Mutant strains carrying the uncF469 or uncF476 allele lack the 18,000-molecular-weight component of the F0 sector of the adenosine triphosphatase in the cell membrane but retain the dicyclohexylcarbodiimide-binding protein (molecular weight, 8,400). Conversely, strains carrying mutations in the uncE gene lack the dicyclohexylcarbodiimide-binding protein but retain the 18,000-molecular-weight protein in the cell membrane. Strains carrying mutations in the uncB gene have both the 18,000-molecular-weight protein and the dicyclohexylcarbodiimide-binding protein present in the cell membranes. The three proteins of the F0 portion of the adenosine triphosphatase, viz., 24,000, 18,000, and 8,400 molecular weights, became membrane associated after in vitro transcription-translation with plasmid pAN51 as template. Plasmids carrying deletions which affected the UncBFE region were isolated from plasmid pAN51 and characterized genetically. A comparison of the genes that were absent from the various deletion plasmids with the membrane-associated products formed after in vitro transcription-translation indicated that the uncB gene coded for the 24,000-molecular-weight protein and that the gene order was probably uncBFE. A correlation between length of deoxyribonucleic acid, genes present, and their products is presented in relation to plasmid pAN51.

摘要

两个突变的unc等位基因unc-469和unc-476,已被鉴定为影响一个先前未描述的基因,命名为uncF。uncF基因是unc操纵子的一部分(基因顺序为uncBFEAGDC),尽管uncF和uncE基因的相对顺序仍存在一些不确定性。携带uncF469或uncF476等位基因的突变菌株缺乏细胞膜中三磷酸腺苷酶F0区段的18,000分子量组分,但保留二环己基碳二亚胺结合蛋白(分子量8,400)。相反,携带uncE基因突变的菌株缺乏二环己基碳二亚胺结合蛋白,但在细胞膜中保留18,000分子量的蛋白质。携带uncB基因突变的菌株在细胞膜中同时存在18,000分子量的蛋白质和二环己基碳二亚胺结合蛋白。以质粒pAN51为模板进行体外转录-翻译后,三磷酸腺苷酶F0部分的三种蛋白质,即分子量为24,000、18,000和8,400的蛋白质,与膜结合。从质粒pAN51中分离出影响UncBFE区域的缺失质粒,并进行遗传特征分析。将各种缺失质粒中缺失的基因与体外转录-翻译后形成的膜相关产物进行比较,表明uncB基因编码24,000分子量的蛋白质,基因顺序可能是uncBFE。本文还给出了与质粒pAN51相关的脱氧核糖核酸长度、存在的基因及其产物之间的相关性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5669/217262/0bc6002caaa4/jbacter00272-0228-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5669/217262/4dcef117e0d2/jbacter00272-0224-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5669/217262/2c5ac0ef31ea/jbacter00272-0225-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5669/217262/1068f89c160c/jbacter00272-0226-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5669/217262/72d09e64eddc/jbacter00272-0228-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5669/217262/0bc6002caaa4/jbacter00272-0228-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5669/217262/4dcef117e0d2/jbacter00272-0224-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5669/217262/2c5ac0ef31ea/jbacter00272-0225-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5669/217262/1068f89c160c/jbacter00272-0226-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5669/217262/72d09e64eddc/jbacter00272-0228-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5669/217262/0bc6002caaa4/jbacter00272-0228-b.jpg

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