Gray J E, Wallen J W, Calhoun D H
J Bacteriol. 1982 Jul;151(1):127-34. doi: 10.1128/jb.151.1.127-134.1982.
The effect of the ilvG671, ilvG468, and ilvG603 mutations (phenotype, IlvG+ Valr; formerly ilvO) upon proteins synthesized was determined by infection of irradiated Escherichia coli K-12 cells, using specifically constructed derivatives of lambda dilv phage. These ilvG alleles are similar to the previously studied ilvG2096(Valr) allele in that they activate the latent ilvG gene which is present in the wild-type strain, leading to the synthesis of a 62,000-dalton protein. In addition, all of these ilvG (Valr) alleles increase the synthesis of a 15,000-dalton protein. To localize the gene coding for the 15,000-dalton protein, the proteins produced in maxicells containing plasmids with specific deletions of ilv and rrnX DNA segments were analyzed. The gene coding for the 15,000-dalton protein was located within a region about 1,000 base pairs long between ilv and trpT. The function of the 15,000-dalton protein is not known.
利用专门构建的λdilv噬菌体衍生物感染经辐照的大肠杆菌K - 12细胞,确定ilvG671、ilvG468和ilvG603突变(表型为IlvG + Valr;以前为ilvO)对合成蛋白质的影响。这些ilvG等位基因与先前研究的ilvG2096(Valr)等位基因相似,因为它们激活野生型菌株中存在的潜在ilvG基因,导致合成一种62,000道尔顿的蛋白质。此外,所有这些ilvG(Valr)等位基因都会增加一种15,000道尔顿蛋白质的合成。为了定位编码15,000道尔顿蛋白质的基因,分析了在含有ilv和rrnX DNA片段特定缺失质粒的最大细胞中产生的蛋白质。编码15,000道尔顿蛋白质的基因位于ilv和trpT之间约1000个碱基对长的区域内。15,000道尔顿蛋白质的功能尚不清楚。