Komeda Y, Silverman M, Simon M
J Bacteriol. 1978 Jan;133(1):364-71. doi: 10.1128/jb.133.1.364-371.1978.
Previous studies showed that the structural gene for the flagellar hook subunit protein (molecular weight 42,000) was one of a group of flagellar genes located on the Escherichia coli genome near pyrC. Several lines of evidence indicate that the flaK gene is the structural gene for the hook subunit protein. Fla+ strains that were insensitive to chi infection could be isolated as revertants of an FlaK- amber mutant strain but from no other Fla- strain. The hook subunit proteins isolated from such chi-sensitive revertants of the FlaK- strain were shown to be antigenically and electrophoretically different from the hook protein isolated from the wild-type strain. Thus, reversion of a mutation in the flaK gene resulted in alteration of the structure of the hook protein. Furthermore, in programming experiments with hybrid lambda containing flagellar genes, lambdafla with flaK genetic activity programmed the synthesis of a 42,000-molecular weight protein, whereas lambdafla without flaK genetic activity did not.
先前的研究表明,鞭毛钩亚基蛋白(分子量42,000)的结构基因是位于大肠杆菌基因组中靠近pyrC的一组鞭毛基因之一。几条证据表明,flaK基因是钩亚基蛋白的结构基因。对chi感染不敏感的Fla +菌株可以作为FlaK-琥珀突变菌株的回复体分离出来,但不能从其他Fla-菌株中分离出来。从FlaK-菌株的这种对chi敏感的回复体中分离出的钩亚基蛋白在抗原性和电泳上与从野生型菌株中分离出的钩蛋白不同。因此,flaK基因中的突变回复导致钩蛋白结构的改变。此外,在用含有鞭毛基因的杂交λ进行的编程实验中,具有flaK遗传活性的λfla编程合成了分子量为42,000的蛋白质,而没有flaK遗传活性的λfla则没有。