Brandt C, Karamata D
Institut de Génétique et de Biologie Microbiennes, Lausanne, Switzerland.
J Gen Microbiol. 1987 May;133(5):1159-70. doi: 10.1099/00221287-133-5-1159.
A collection of 655 thermosensitive mutants of Bacillus subtilis 168, obtained by indirect selection, was screened for those lysing at the non-permissive temperature. Thirty-three mutations thus identified were distributed by transformation into eight linkage groups designated lssA to lssH. The distribution was non-random. With the exception of group A, all groups were small, suggesting that mutations identified in each of them may map in one gene only. Linkage groups identified here were mapped in four different regions of the B. subtilis chromosome and their positions relative to reference markers were the following: (i) aroI-lssA-dal-purB; (ii) metC-lssB-lssC-furA-pyrE-cysC-lssD; (iii) lssF-gtaA-lssG-hisA-lssH-cysB; and (iv) cysA-lssE-dnaC-purA. Kinetics of N-acetyl-D-[1-14C]glucosamine incorporation revealed that groups A, B, C, D and F are deficient in peptidoglycan synthesis at the restrictive temperature. In group G, anomalies at the cell wall level were suggested by incorporation and growth curves. It appears that in almost all known cases, thermosensitive lysis mutations in B. subtilis either affect genes involved in peptidoglycan synthesis or lead, more or less directly, to induction of prophages.
通过间接选择获得了枯草芽孢杆菌168的655个热敏突变体集合,筛选其中在非允许温度下裂解的突变体。由此鉴定出的33个突变通过转化分布到八个连锁群中,命名为lssA至lssH。这种分布是非随机的。除了A组外,所有组都很小,这表明在每组中鉴定出的突变可能仅定位于一个基因。这里鉴定出的连锁群定位于枯草芽孢杆菌染色体的四个不同区域,它们相对于参考标记的位置如下:(i) aroI-lssA-dal-purB;(ii) metC-lssB-lssC-furA-pyrE-cysC-lssD;(iii) lssF-gtaA-lssG-hisA-lssH-cysB;以及(iv) cysA-lssE-dnaC-purA。N-乙酰-D-[1-14C]葡萄糖胺掺入的动力学表明,A、B、C、D和F组在限制温度下肽聚糖合成存在缺陷。在G组中,掺入和生长曲线表明细胞壁水平存在异常。似乎在几乎所有已知情况下,枯草芽孢杆菌中的热敏裂解突变要么影响参与肽聚糖合成的基因,要么或多或少直接导致原噬菌体的诱导。