O'Connell C, Pattee P A, Foster T J
Microbiology Department, Moyne Institute, Trinity College, Dublin, Ireland.
J Gen Microbiol. 1993 Jul;139(7):1449-60. doi: 10.1099/00221287-139-7-1449.
The aroA gene of Staphylococcus aureus 8325-4 was cloned. Sequence analysis and the phenotype of directed plasmid insertions 5' to aroA suggest that aroA is located in an operon and that it maps 3' to the aroC and aroB genes. A revised consensus sequence for the aroA gene product EPSP synthase binding site for its substrate (phosphoenolpyruvate) and an inhibitor (glyphosate) is proposed. An aroA insertion mutant isolated by allelic replacement was employed in genetic mapping experiments which demonstrated the gene order thy aroA tyrB in SmaI fragment A of the S. aureus 8325-4 chromosome. The aroA::Tcr mutant required aromatic amino acids but remained independent of p-aminobenzoic acid (PAB). This could be due to the insertion being located close to the 5' end of the gene, allowing expression of a truncated protein. The PAB independence may explain the finding that the mutant was not attenuated in mouse infection experiments. It was not possible to isolate a null mutant in aroA.
克隆了金黄色葡萄球菌8325 - 4的aroA基因。序列分析以及aroA上游定向质粒插入的表型表明,aroA位于一个操纵子中,并且它位于aroC和aroB基因的下游。提出了aroA基因产物5-烯醇丙酮酰莽草酸-3-磷酸合酶(EPSP合酶)与其底物(磷酸烯醇丙酮酸)和抑制剂(草甘膦)结合位点的修订共有序列。通过等位基因替换分离得到的aroA插入突变体用于遗传作图实验,该实验证明了在金黄色葡萄球菌8325 - 4染色体的SmaI片段A中基因顺序为thy aroA tyrB。aroA::Tcr突变体需要芳香族氨基酸,但仍然不依赖对氨基苯甲酸(PAB)。这可能是由于插入位于基因的5'端附近,使得截短蛋白得以表达。PAB不依赖性可能解释了该突变体在小鼠感染实验中未减毒的这一发现。不可能分离到aroA的无效突变体。