Diebold R, Noel K D
Department of Biology, Marquette University, Milwaukee, Wisconsin 53233.
J Bacteriol. 1989 Sep;171(9):4821-30. doi: 10.1128/jb.171.9.4821-4830.1989.
Ten independently generated mutants of Rhizobium leguminosarum biovar phaseoli CFN42 isolated after Tn5 mutagenesis formed nonmucoid colonies on all agar media tested and lacked detectable production of the normal acidic exopolysaccharide in liquid culture. The mutants were classified into three groups. Three mutants harbored Tn5 insertions on a 3.6-kilobase-pair EcoRI fragment and were complemented to have normal exopolysaccharide production by cosmids that shared an EcoRI fragment of this size from the CFN42 genome. The Tn5 inserts of five other mutants appeared to be located on a second, slightly smaller EcoRI fragment. Attempts to complement mutants of this second group with cloned DNA were unsuccessful. The mutations of the other two mutants were located in apparently adjacent EcoRI fragments carried on two cosmids that complemented those two mutants. The latter two mutants also lacked O-antigen-containing lipopolysaccharides and induced underdeveloped nodules that lacked nitrogenase activity on bean plants. The other eight mutants had normal lipopolysaccharides and wild-type symbiotic proficiencies on bean plants. Mutants in each of these groups were mated with R. leguminosarum strains that nodulated peas (R. leguminosarum biovar viciae) or clovers (R. leguminosarum biovar trifolii). Transfer of the Tn5 mutations resulted in exopolysaccharide-deficient R. leguminosarum biovar viciae or R. leguminosarum biovar trifolii transconjugants that were symbiotically deficient in all cases. These results support earlier suggestions that successful symbiosis with peas or clovers requires that rhizobia be capable of acidic exopolysaccharide production, whereas symbiosis with beans does not have this requirement.
在Tn5诱变后分离得到的10个独立产生的菜豆根瘤菌生物变种CFN42突变体,在所有测试的琼脂培养基上形成非黏液状菌落,并且在液体培养中检测不到正常酸性胞外多糖的产生。这些突变体被分为三组。三个突变体在一个3.6千碱基对的EcoRI片段上含有Tn5插入,并且通过含有来自CFN42基因组的这种大小的EcoRI片段的黏粒而互补,从而具有正常的胞外多糖产生。另外五个突变体的Tn5插入似乎位于第二个稍小的EcoRI片段上。用克隆DNA对第二组突变体进行互补的尝试未成功。另外两个突变体的突变位于两个黏粒上明显相邻的EcoRI片段中,这两个黏粒互补了那两个突变体。后两个突变体也缺乏含O抗原的脂多糖,并且在菜豆植株上诱导形成发育不良且缺乏固氮酶活性的根瘤。其他八个突变体具有正常的脂多糖,并且在菜豆植株上具有野生型共生能力。将这些组中的每个突变体与能使豌豆结瘤的菜豆根瘤菌菌株(豌豆根瘤菌生物变种)或能使三叶草结瘤的菜豆根瘤菌菌株(三叶草根瘤菌生物变种)进行杂交。Tn5突变的转移导致了胞外多糖缺陷的豌豆根瘤菌生物变种或三叶草根瘤菌生物变种转接合子,在所有情况下这些转接合子在共生方面都存在缺陷。这些结果支持了早期的观点,即与豌豆或三叶草成功共生要求根瘤菌能够产生酸性胞外多糖,而与菜豆共生则没有这个要求。