Shand R F, Blum P H, Holzschu D L, Urdea M S, Artz S W
Department of Microbiology, University of California, Davis 95616.
J Bacteriol. 1989 Nov;171(11):6330-7. doi: 10.1128/jb.171.11.6330-6337.1989.
We isolated a collection of 67 independent, spontaneous Salmonella typhimurium his operon promoter mutants with decreased his expression. The mutants were isolated by selecting for resistance to the toxic lactose analog o-nitrophenyl-beta-D-thiogalactoside in a his-lac fusion strain. The collection included base pair substitutions. small insertions, a deletion, and one large insertion identified as IS30 (IS121), which is resident on the Mu d1 cts(Apr lac) phage used to construct the his-lac fusion. Of the 37 mutations that were sequenced, 14 were unique. Six of the 14 were isolated more than once, with the IS30 insertion occurring 16 times. The mutations were located throughout the his promoter region, with two in the conserved - 35 hexamer sequence, four in the conserved - 10 hexamer sequence (Pribnow box), seven in the spacer between the - 10 and -35 hexamer sequences, and the IS30 insertions just upstream of the -35 hexamer sequence. Four of the five substitution mutations changed a consensus base pair recognized by E sigma 70 RNA polymerase in the -10 or -35 hexamer. Decreased his expression caused by the 14 different his promoter mutations was measured in vivo. Relative to the wild-type promoter, the mutations resulted in as little as a 4-fold decrease to as much as a 357-fold decrease in his expression, with the largest decreases resulting from changes in the most highly conserved features of E sigma 70 promoters.
我们分离出了67个独立的、自发的鼠伤寒沙门氏菌组氨酸操纵子启动子突变体,这些突变体的组氨酸表达量降低。这些突变体是通过在一个组氨酸-乳糖融合菌株中筛选对有毒乳糖类似物邻硝基苯基-β-D-硫代半乳糖苷的抗性而分离得到的。该集合包括碱基对替换、小插入、一个缺失以及一个被鉴定为IS30(IS121)的大插入,IS30存在于用于构建组氨酸-乳糖融合的Mu d1 cts(Apr lac)噬菌体上。在测序的37个突变中,有14个是独特的。14个中的6个被多次分离出来,其中IS30插入出现了16次。这些突变位于组氨酸启动子区域的各处,其中两个在保守的-35六聚体序列中,四个在保守的-10六聚体序列(Pribnow框)中,七个在-10和-35六聚体序列之间的间隔区,而IS30插入位于-35六聚体序列的上游。五个替换突变中的四个改变了E sigma 70 RNA聚合酶在-10或-35六聚体中识别的共有碱基对。在体内测量了由14种不同的组氨酸启动子突变导致的组氨酸表达量降低情况。相对于野生型启动子,这些突变导致组氨酸表达量降低了4倍至357倍,其中最大的降低是由E sigma 70启动子最保守特征的变化引起的。