Harayama S, Hazelbauer G L
J Bacteriol. 1982 Sep;151(3):1391-6. doi: 10.1128/jb.151.3.1391-1396.1982.
Hybrid plasmids carrying trg, the genetic locus in closest proximity to terC, coded for several polypeptides in addition to the Trg protein. Polypeptides of 59,000 and 61,000 apparent molecular weight were the most prominent products synthesized in minicells containing the hybrid plasmids. Analysis of the effects of deletions generated by a restriction endonuclease identified a region of DNA immediately adjacent to trg as the putative gene coding for the two polypeptides. Studies with whole cells and minicells showed that the 59,000-dalton polypeptide is a periplasmic protein. Analysis by limited proteolysis indicated that the two polypeptides are related, and a number of observations support the notion that the 61,000-dalton protein is a precursor form of the 59,000-dalton mature exported protein. The identification and characterization of a protein, in addition to Trg, which is produced by a gene in close proximity to terC emphasizes the fact that the region does contain intact and active genes.
携带trg(与terC最接近的遗传位点)的杂种质粒,除了Trg蛋白外,还编码几种多肽。在含杂种质粒的微小细胞中合成的最主要产物是表观分子量为59,000和61,000的多肽。用限制性内切酶产生的缺失片段进行效应分析,确定紧邻trg的一段DNA区域是编码这两种多肽的推定基因。对全细胞和微小细胞的研究表明,59,000道尔顿的多肽是一种周质蛋白。有限蛋白酶解分析表明这两种多肽有关联,并且大量观察结果支持61,000道尔顿的蛋白是59,000道尔顿成熟输出蛋白的前体形式这一观点。除Trg外,由紧邻terC的一个基因产生的一种蛋白质的鉴定和特性分析强调了该区域确实含有完整且有活性的基因这一事实。