首页> 美国卫生研究院文献>Journal of Bacteriology >Isolation and characterization of ropA homologous genes from Rhizobium leguminosarum biovars viciae and trifolii.
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Isolation and characterization of ropA homologous genes from Rhizobium leguminosarum biovars viciae and trifolii.

机译:豆根瘤菌和紫花苜蓿根瘤菌ropA同源基因的分离和鉴定。

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摘要

ropA encodes a 36-kDa outer membrane protein of Rhizobium leguminosarum bv. viciae strain 248 which constitutes the low-M(r) part of antigen group III (R.A. de Maagd, I.H.M. Mulders, H.C.J. Canter Cremers, B.J.J. Lugtenberg, J. Bacteriol. 174:214-221, 1992). We observed that genes homologous to ropA are present in strain 248 as well as in other R. leguminosarum strains, and we describe the cloning and characterization of two of these genes. Sequencing of a 2.2-kb Bg/II fragment from R. leguminosarum bv. viciae strain 248 that hybridizes with ropA revealed one large open reading frame of 1,074 bp encoding a mature protein of 38.096 kDa. Homology between this gene and ropA is 91.8% on the DNA level. Homology on the amino acid level is only 69.9% as a result of a frameshift. On the basis of homology and immunochemical characteristics, we conclude that this gene encodes the high-M(r) part of the outer membrane protein antigen group III that is repressed during symbiosis. We named this gene ropA2. The second gene that we cloned was the ropA homologous gene of R. leguminosarum bv. trifolii strain LPR5020. Except for amino acid 43, the N-terminal part of the corresponding protein appeared to be identical to the first 51 amino acids of RopA of strain 248. The transcription start sites of both genes were determined, and the promoter regions were compared with that of ropA of strain 248. No clear consensus sequence could be deduced. The relationship of ropA and ropA2 of R. leguminosarum bv. viciae strain 248 with two similar genes from Brucella abortus is discussed.
机译:ropA编码豆科根瘤菌bv的36 kDa外膜蛋白。构成抗原组III的低M(r)部分的蚕豆菌株248(R.A.de Maagd,I.H.M.Mulders,H.C.J.Canter Cremers,B.J.J.Lugtenberg,J.Bacteriol.174:214-221,1992)。我们观察到与ropA同源的基因存在于248株以及其他豆科植物豆科菌株中,并且我们描述了其中两个基因的克隆和鉴定。豆科植物双歧杆菌2.2-kb Bg / II片段的测序与ropA杂交的蚕豆248菌株显示了一个1,074 bp的大开放阅读框,编码38.096 kDa的成熟蛋白。该基因与ropA之间的同源性在DNA水平上为91.8%。由于移码,氨基酸水平的同源性仅为69.9%。根据同源性和免疫化学特性,我们得出结论,该基因编码在共生过程中受阻的外膜蛋白抗原组III的高M(r)部分。我们将该基因命名为ropA2。我们克隆的第二个基因是豆科植物根瘤菌的ropA同源基因。三叶菌株LPR5020。除了氨基酸43外,相应蛋白质的N端部分似乎与248株RopA的前51个氨基酸相同。确定了这两个基因的转录起始位点,并将其启动子区与菌株248的ropA。无法推断出清晰的共有序列。豆科根瘤菌ropA和ropA2的关系讨论了具有来自流产布鲁氏菌的两个相似基因的蚕豆菌株248。

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