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来自豌豆根瘤菌蚕豆生物型和三叶草生物型的ropA同源基因的分离与鉴定。

Isolation and characterization of ropA homologous genes from Rhizobium leguminosarum biovars viciae and trifolii.

作者信息

Roest H P, Bloemendaal C J, Wijffelman C A, Lugtenberg B J

机构信息

Institute of Molecular Plant Sciences, Leiden University, The Netherlands.

出版信息

J Bacteriol. 1995 Sep;177(17):4985-91. doi: 10.1128/jb.177.17.4985-4991.1995.

Abstract

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.

摘要

ropA编码豌豆根瘤菌蚕豆生物型248菌株的一种36 kDa外膜蛋白,该蛋白构成抗原组III的低分子量部分(R.A. 德马格德、I.H.M. 马尔德斯、H.C.J. 坎特·克雷默斯、B.J.J. 卢滕贝格,《细菌学杂志》174:214 - 221,1992年)。我们观察到与ropA同源的基因存在于248菌株以及其他豌豆根瘤菌菌株中,并且我们描述了其中两个基因的克隆和特性分析。对来自豌豆根瘤菌蚕豆生物型248菌株的一个与ropA杂交的2.2 kb Bg/II片段进行测序,发现一个1074 bp的大开放阅读框,编码一个38.096 kDa的成熟蛋白。该基因与ropA在DNA水平上的同源性为91.8%。由于移码,氨基酸水平上的同源性仅为69.9%。基于同源性和免疫化学特性,我们得出结论,该基因编码共生期间被抑制的外膜蛋白抗原组III的高分子量部分。我们将这个基因命名为ropA2。我们克隆的第二个基因是豌豆根瘤菌三叶草生物型LPR5020菌株的ropA同源基因。除了第43位氨基酸外,相应蛋白N端部分似乎与248菌株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,并将启动子区域与248菌株ropA的启动子区域进行了比较。未推断出明确的共有序列。讨论了豌豆根瘤菌蚕豆生物型248菌株的ropA和ropA2与流产布鲁氏菌的两个相似基因之间的关系。

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