Plant-Microbe Interaction Group, Research School of Biological Sciences, Australian National University, GPO Box 475, Canberra City ACT 2601, Australia.
Appl Environ Microbiol. 1993 Apr;59(4):1058-64. doi: 10.1128/aem.59.4.1058-1064.1993.
The acid-tolerant Rhizobium leguminosarum biovar trifolii strain ANU1173 exhibited several new phenotypes when cured of its symbiotic (Sym) plasmid and the second largest megaplasmid. Strain P22, which has lost these two plasmids, had reduced exopolysaccharide production and cell mobility on TY medium. The parent strain ANU1173 was able to grow easily in laboratory media at pH 4.5, whereas the derivative strain P22 was unable to grow in media at a pH of <4.7. The intracellular pH of strain ANU1173 was 6.8 when the external pH was 4.5. In contrast, strain P22 had an acidic intracellular pH of <6.4 when the external pH was <5.5. Strain P22 had a dramatically increased membrane permeability to protons and decreased proton extrusion activity. Analysis with sodium dodecyl sulfate-polyacrylamide gels showed that strain P22 lacked a slow-migrating lipopolysaccharide (LPS) banding group which was present in the parent strain. Mobilization of the second largest megaplasmid of strain ANU1173 back into strain P22 restored the altered LPS structure and physiological characteristics of strain P22. Mobilization of the Sym plasmid of strain ANU1173 into strain P22 showed that the second largest megaplasmid of strain ANU1173 was required for the establishment of nitrogen-fixing nodules on Trifolium repens and Trifolium subterraneum. Furthermore, an examination of a large number of specific exopolysaccharide- or LPS-deficient Rhizobium mutants did not show a positive correlation between exopolysaccharide or LPS synthesis and acid tolerance.
耐酸根瘤菌属菌株 ANU1173 在消除共生(Sym)质粒和第二大亚质粒后表现出多种新的表型。失去这两个质粒的 P22 菌株在 TY 培养基上的多糖产量和细胞迁移能力降低。亲本菌株 ANU1173 能够在 pH4.5 的实验室培养基中轻松生长,而衍生菌株 P22 则无法在 pH<4.7 的培养基中生长。当外部 pH 为 4.5 时,菌株 ANU1173 的细胞内 pH 为 6.8。相比之下,当外部 pH<5.5 时,菌株 P22 的细胞内 pH 酸性低于 6.4。菌株 P22 的质子跨膜通透性显著增加,质子外排活性降低。十二烷基硫酸钠-聚丙烯酰胺凝胶分析表明,菌株 P22 缺乏存在于亲本菌株中的缓慢迁移脂多糖(LPS)带群。将第二大亚质粒从菌株 P22 中重新转移到菌株 ANU1173 中,恢复了 P22 菌株改变的 LPS 结构和生理特征。将菌株 ANU1173 的 Sym 质粒转移到菌株 P22 中表明,第二大亚质粒是菌株 ANU1173 在三叶草和地下三叶草上建立固氮结瘤所必需的。此外,对大量特定的多糖或 LPS 缺陷型根瘤菌突变体的检查表明,多糖或 LPS 合成与耐酸之间没有正相关关系。