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大肠杆菌K12磷酸盐(无机)转运(pit)基因的分子克隆。pit +基因产物的鉴定及染色体pit - gor区域的物理图谱绘制。

Molecular cloning of the phosphate (inorganic) transport (pit) gene of Escherichia coli K12. Identification of the pit+ gene product and physical mapping of the pit-gor region of the chromosome.

作者信息

Elvin C M, Dixon N E, Rosenberg H

出版信息

Mol Gen Genet. 1986 Sep;204(3):477-84. doi: 10.1007/BF00331028.

Abstract

The pit+ gene, encoding the phosphate (inorganic) transport system of Escherichia coli, was isolated from a library of E. coli genes inserted in the cosmid vector pHC79. A 25.5-kb chromosomal DNA fragment was shown also to carry the gor locus encoding glutathione oxidoreductase. Physical mapping placed the two genes about 10 kb apart, confirming bacteriophage P1 mapping of the 77-min region. Subcloning and deletion analysis indicated that the entire pit+ gene was located within a 2.2-kb Sal1-Ava1 fragment. The pit+ gene product was identified by SDS-polyacrylamide gel electrophoresis as a 39-kdal inner membrane protein by two methods: 35S-methionine-labelling of minicells carrying pit+ plasmids or plasmids from which all or part of the pit+ gene was deleted. Overproduction of the Pit protein using a thermoinducible "runaway" replication plasmid. Complementation of the pit-1 mutant allele using a unit-copy-number pit+ plasmid indicated that the pit-1 mutation is recessive. Strains carrying a multicopy pit+ plasmid show a 10-fold increase in the initial rate of phosphate uptake; however there is no change in the steady-state level of 32Pi accumulation.

摘要

编码大肠杆菌磷酸盐(无机)转运系统的pit+基因,是从插入黏粒载体pHC79的大肠杆菌基因文库中分离得到的。一个25.5kb的染色体DNA片段还被证明携带编码谷胱甘肽氧化还原酶的gor基因座。物理图谱显示这两个基因相距约10kb,证实了噬菌体P1对77分钟区域的图谱绘制。亚克隆和缺失分析表明,整个pit+基因位于一个2.2kb的Sal1 - Ava1片段内。通过两种方法,利用十二烷基硫酸钠 - 聚丙烯酰胺凝胶电泳将pit+基因产物鉴定为一种39kdal的内膜蛋白:对携带pit+质粒或缺失全部或部分pit+基因的质粒的微小细胞进行35S - 甲硫氨酸标记。使用热诱导“失控”复制质粒过量表达Pit蛋白。使用单拷贝数pit+质粒对pit - 1突变等位基因进行互补,表明pit - 1突变是隐性的。携带多拷贝pit+质粒的菌株在磷酸盐摄取的初始速率上提高了10倍;然而,32Pi积累的稳态水平没有变化。

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