Hafner E W, Tabor C W, Tabor H
J Bacteriol. 1977 Dec;132(3):832-40. doi: 10.1128/jb.132.3.832-840.1977.
An Escherichia coli metK mutant, designated metK110, was isolated among spontaneous ethionine-resistant organisms selected at 42 degrees C. The S-adenosylmethionine synthetase activity of this mutant was present at lower levels than in the corresponding wild-type strain and was more labile than the wild-type enzyme when heated or dialyzed. A mixture of mutant and wild-type enzyme preparations had an activity equal to the sum of the component activities. These facts strongly suggest that the mutated gene in this strain is the structural gene for this enzyme. Genetic mapping experiments placed the metK110 mutation near or at the site of other known metK mutants (i.e., 63 min), confirming its designation as a metK mutant. A revised gene order has been established for this region, i.e., metC glc speC metK speB serA.
在42℃下筛选出的自发抗乙硫氨酸的微生物中,分离出了一株大肠杆菌metK突变体,命名为metK110。该突变体的S-腺苷甲硫氨酸合成酶活性水平低于相应的野生型菌株,并且在加热或透析时比野生型酶更不稳定。突变型和野生型酶制剂的混合物的活性等于各组分活性之和。这些事实强烈表明,该菌株中的突变基因是该酶的结构基因。遗传图谱实验将metK110突变定位在其他已知metK突变体的位点附近或该位点处(即63分钟),证实了其作为metK突变体的命名。已确定该区域的修订基因顺序,即metC glc speC metK speB serA。