Crank S F, Downie J A
John Innes Institute, Norwich, UK.
Mol Gen Genet. 1994 Apr;243(1):119-23. doi: 10.1007/BF00283884.
A population of Tn5 mutagenized Rhizobium leguminosarum cells was screened for mutants affected in protein secretion by introducing a plasmid carrying the Erwinia chrysanthemi prtB gene and screening for mutants defective in secretion of the protease PrtB. One such mutant (A301) also appeared to be defective in secretion of the R. leguminosarum nodulation protein NodO. Genetic analysis showed that the defect in A301 was caused by the Tn5 insertion. However the DNA sequence adjacent to the site of Tn5 insertion had significant homology to the Escherichia coli polA gene, which encodes DNA polymerase I. The mutant A301 showed increased sensitivity to ultraviolet light, a characteristic of polA mutants of E. coli. The apparent defect in secretion by A301 was due to a large decrease in the copy number of the IncQ group replicon on which prtB and nodO were cloned and this decreased the total amounts of PrtB or NodO protein synthesised and secreted by the polA mutant. The polA mutant had a lower growth rate than the parent strain on both rich and minimal media, but there was no obvious effect of the polA mutation on the symbiosis of R. leguminosarum bv. viciae with pea.
通过导入携带菊欧文氏菌prtB基因的质粒并筛选蛋白酶PrtB分泌缺陷型突变体,对Tn5诱变的豆科根瘤菌细胞群体进行筛选,以寻找蛋白质分泌受影响的突变体。其中一个这样的突变体(A301)似乎在豆科根瘤菌结瘤蛋白NodO的分泌方面也存在缺陷。遗传分析表明,A301中的缺陷是由Tn5插入引起的。然而,与Tn5插入位点相邻的DNA序列与编码DNA聚合酶I的大肠杆菌polA基因具有显著同源性。突变体A301对紫外线的敏感性增加,这是大肠杆菌polA突变体的一个特征。A301明显的分泌缺陷是由于克隆了prtB和nodO的IncQ组复制子的拷贝数大幅减少,这降低了polA突变体合成和分泌的PrtB或NodO蛋白的总量。在丰富培养基和基本培养基上,polA突变体的生长速率均低于亲本菌株,但polA突变对豌豆根瘤菌与豌豆的共生没有明显影响。