Torres-Cabassa A S, Gottesman S
J Bacteriol. 1987 Mar;169(3):981-9. doi: 10.1128/jb.169.3.981-989.1987.
lon mutants of Escherichia coli K-12 are defective in an ATP-dependent protease, are UV sensitive, and overproduce the capsular polysaccharide colanic acid. Six structural genes needed for capsular polysaccharide synthesis (cps) are transcriptionally regulated by lon as well as by three other regulatory genes, rcsA, -B, and -C (S. Gottesman, P. Trisler, and A. S. Torres-Cabassa, J. Bacteriol. 162:1111-1119, 1985). We have cloned rcsA, the gene for a positive regulator of capsule synthesis, onto multicopy plasmids and defined the gene by both insertions and deletions. The product of rcsA has been identified as an unstable protein of 27 kilodaltons. RcsA has a half-life of 5 min in lon+ cells and one of 20 min in lon cells. The availability of RcsA is the limiting factor for capsule synthesis; doubling the gene dosage of rcsA+ significantly increases expression of cps genes. Our results are consistent with a model in which the presence of a lon mutation increases the synthesis of capsular polysaccharide via stabilization of RcsA.
大肠杆菌K - 12的lon突变体在一种ATP依赖性蛋白酶方面存在缺陷,对紫外线敏感,并且过量产生荚膜多糖柯氏酸。荚膜多糖合成(cps)所需的六个结构基因受到lon以及其他三个调控基因rcsA、-B和-C的转录调控(S. 戈特斯曼、P. 特里斯勒和A. S. 托雷斯 - 卡巴萨,《细菌学杂志》162:1111 - 1119,1985年)。我们已将rcsA(荚膜合成的正调控基因)克隆到多拷贝质粒上,并通过插入和缺失对该基因进行了定义。rcsA的产物已被鉴定为一种27千道尔顿的不稳定蛋白质。RcsA在lon +细胞中的半衰期为5分钟,在lon细胞中的半衰期为20分钟。RcsA的可利用性是荚膜合成的限制因素;将rcsA +的基因剂量加倍会显著增加cps基因的表达。我们的结果与一个模型一致,即lon突变的存在通过RcsA的稳定化增加荚膜多糖的合成。