Watson Sean P, Antonio Martin, Foster Simon J
Department of Molecular Biology and Biotechnology, University of Sheffield,Firth Court, Western Bank, Sheffield 510 2TN,UK.
Microbiology (Reading). 1998 Nov;144 ( Pt 11):3159-3169. doi: 10.1099/00221287-144-11-3159.
Ten Staphylococcus aureus mutants, defective in the starvation-induced stationary phase of growth were isolated from two independent Tn917-LTV1 transposon insertion libraries and were designated suv as they had apparent survival defects. Seven of these mutants were defective under amino-acid-limiting conditions alone. Two mutants (suv-3 and suv-20) demonstrated lower plating efficiency when starved for glucose, phosphate or amino acids and one mutant (suv-11) had reduced plating efficiency after amino acid or glucose starvation. All of the mutants tested were as resistant to hydrogen peroxide assault as the parent, but six were more sensitive to low pH conditions. All the mutants were physically mapped on the S. aureus chromosome using PFGE. Chromosomal DNA flanking the Tn917-LTV1 insertion sites was rescued by cloning into Escherichia coli. DNA sequence analysis resulted in the identification of a number of transposon-disrupted ORFs encoding putative components such as superoxide dismutase (suv-1), haem A synthase (suv-3), a component of the SOS response (suv-9) and hypoxanthine-guanine phosphoribosyltransferase (suv-20). The Tn917-LTV1 insertion created lacZ transcriptional fusions for some of the stationary-phase loci. Expression analysis indicated that suv-4 was induced at mid-exponential phase, whereas suv-3 and suv-11 were induced at the onset of stationary phase. The possible roles of these suv components in stationary-phase survival or recovery is discussed.
从两个独立的Tn917-LTV1转座子插入文库中分离出10株在饥饿诱导的生长静止期存在缺陷的金黄色葡萄球菌突变体,因其具有明显的存活缺陷而被命名为suv。其中7个突变体仅在氨基酸限制条件下存在缺陷。两个突变体(suv-3和suv-20)在葡萄糖、磷酸盐或氨基酸饥饿时表现出较低的平板接种效率,一个突变体(suv-11)在氨基酸或葡萄糖饥饿后平板接种效率降低。所有测试的突变体对过氧化氢攻击的抗性与亲本相同,但有6个对低pH条件更敏感。使用脉冲场凝胶电泳(PFGE)将所有突变体定位在金黄色葡萄球菌染色体上。通过克隆到大肠杆菌中拯救了Tn917-LTV1插入位点两侧的染色体DNA。DNA序列分析鉴定出一些转座子破坏的开放阅读框,这些开放阅读框编码推定的成分,如超氧化物歧化酶(suv-1)、血红素A合酶(suv-3)、SOS反应的一个成分(suv-9)和次黄嘌呤-鸟嘌呤磷酸核糖基转移酶(suv-20)。Tn917-LTV1插入为一些静止期基因座创建了lacZ转录融合。表达分析表明,suv-4在指数中期被诱导,而suv-3和suv-11在静止期开始时被诱导。讨论了这些suv成分在静止期存活或恢复中的可能作用。