Goss T J, O'Hara G W, Dilworth M J, Glenn A R
Nitrogen Fixation Research Group, School of Biological and Environmental Sciences, Murdoch University, Western Australia.
J Bacteriol. 1990 Sep;172(9):5173-9. doi: 10.1128/jb.172.9.5173-5179.1990.
Four Tn5-induced mutants of Rhizobium meliloti WSM419 were unable to grow or maintain intracellular pH at an external pH of 5.6. Restriction analysis of DNA fragments carrying Tn5 and flanking sequences cloned from these mutants indicated that all four cloned mutations are unique and that the two strains (TG1-6 and TG1-11) carry Tn5 insertions which are within 4.4 kilobases of each other on a single EcoRI fragment. Southern analysis of total mutant DNA indicated a single copy of Tn5 in each mutant. A limited cosmid gene bank of wild-type WSM419 DNA was probed for homology to mutant DNA cloned from the acid-sensitive mutants. Dot hybridization experiments identified one cosmid element within this bank carrying wild-type DNA sequences corresponding to DNA implicated in acid tolerance. This cosmid was able to complement defects in growth and intracellular pH maintenance in TG1-11 but not TG1-6.
苜蓿中华根瘤菌WSM419的四个Tn5诱导突变体在外部pH值为5.6时无法生长或维持细胞内pH值。对从这些突变体中克隆的携带Tn5和侧翼序列的DNA片段进行限制性分析表明,所有四个克隆突变都是独特的,并且两个菌株(TG1-6和TG1-11)携带的Tn5插入位于单个EcoRI片段上彼此相距4.4千碱基以内。对总突变体DNA的Southern分析表明每个突变体中Tn5有一个拷贝。用野生型WSM419 DNA的有限黏粒基因文库探测与从酸敏感突变体克隆的突变体DNA的同源性。斑点杂交实验在该文库中鉴定出一个黏粒元件,其携带与耐酸性相关的DNA对应的野生型DNA序列。该黏粒能够弥补TG1-11中生长和细胞内pH维持的缺陷,但不能弥补TG1-6的缺陷。