Nieuwlandt D T, Pattee P A
Department of Microbiology, Iowa State University, Ames 50011.
J Bacteriol. 1989 Sep;171(9):4906-13. doi: 10.1128/jb.171.9.4906-4913.1989.
A simple and reliable method for polyethylene glycol-induced plasmid transformation of a temperature-sensitive peptidoglycan-deficient mutant of Staphylococcus aureus is described. The procedure uses strains carrying the tofA372 mutation grown under conditions that yield osmotically fragile cells capable of efficient wall regeneration. The peptidoglycan-deficient cells were transformed with plasmids pE194 and pI258 at frequencies comparable with those obtained with protoplasts prepared with lysostaphin treatment. A readily portable tofA372 mutation was constructed by isolating an insertion of the erythromycin resistance transposon Tn551 adjacent to tofA372. tofA372 was shown by protoplast fusion and transformation analyses to be in the gene order hly-421-omega [Chr::Tn551]1059-tofA372-uraB232-omega [Chr::Tn916]1101-thrB106 on the chromosome of S. aureus NCTC 8325.
本文描述了一种简单可靠的方法,用于通过聚乙二醇诱导对温度敏感的金黄色葡萄球菌肽聚糖缺陷型突变体进行质粒转化。该程序使用携带tofA372突变的菌株,在能产生具有高效细胞壁再生能力的渗透脆弱细胞的条件下培养。用质粒pE194和pI258对肽聚糖缺陷型细胞进行转化的频率,与用溶葡萄球菌素处理制备的原生质体所获得的频率相当。通过分离与tofA372相邻的红霉素抗性转座子Tn551的插入片段,构建了一个易于携带的tofA372突变体。通过原生质体融合和转化分析表明,在金黄色葡萄球菌NCTC 8325的染色体上,tofA372的基因顺序为hly-421-omega [Chr::Tn551]1059-tofA372-uraB232-omega [Chr::Tn916]1101-thrB106。