Scherrer R, Moyed H S
Department of Microbiology and Molecular Genetics, California College of Medicine, University of California, Irvine 92717.
J Bacteriol. 1988 Aug;170(8):3321-6. doi: 10.1128/jb.170.8.3321-3326.1988.
Mutations in hipA, a gene of Escherichia coli K-12, greatly reduce the lethality of selective inhibition of peptidoglycan synthesis. These mutations have also been found to reduce the lethality that accompanies either selective inhibition of DNA synthesis or heat shock of strains defective in htpR. In addition, the mutant alleles of hipA are responsible for a reversible cold-sensitive block in cell division and synthesis of macromolecules, particularly peptidoglycan. Recombination between the chromosome of hipA mutants and plasmids containing noncomplementing fragments of hipA+ revealed that the mutations responsible for both cold sensitivity and reduced lethality were probably identical and, in any case, lay within the first 360 base pairs of the coding region of hipA, probably within the first 50 base pairs. We suggest that the pleiotropic effects of mutations in hipA reflect the involvement of this gene in cell division.
大肠杆菌K-12的hipA基因发生突变,可极大降低肽聚糖合成选择性抑制的致死率。这些突变还被发现可降低因DNA合成选择性抑制或htpR缺陷菌株热休克所伴随的致死率。此外,hipA的突变等位基因导致细胞分裂和大分子合成(尤其是肽聚糖)出现可逆的冷敏感阻滞。hipA突变体的染色体与含有hipA+非互补片段的质粒之间发生重组,结果表明,导致冷敏感性和致死率降低的突变可能相同,无论如何,这些突变位于hipA编码区的前360个碱基对之内,可能在前50个碱基对之内。我们认为,hipA突变的多效性效应反映了该基因参与细胞分裂。