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豆科根瘤菌共生质粒编码的一种根际蛋白的鉴定

Identification of a rhizosphere protein encoded by the symbiotic plasmid of Rhizobium leguminosarum.

作者信息

Dibb N J, Downie J A, Brewin N J

出版信息

J Bacteriol. 1984 May;158(2):621-7. doi: 10.1128/jb.158.2.621-627.1984.

Abstract

A protein was identified which was made by wild-type strains of Rhizobium leguminosarum but not by nodulation-deficient derivatives which had deletions of their symbiotic plasmids. The protein, which had a subunit molecular weight of ca. 24,000 ( 24K ), was found to be present in large amounts within bacteria that had been reisolated from the surface of inoculated pea roots but was not detected in bacteroids isolated from nodules. The protein could also be induced during growth of R. leguminosarum on nutrient medium and was purified from the cytoplasmic fraction of broken cells. Antiserum raised against the purified protein was used to screen transposon-induced mutants of R. leguminosarum, and four independent mutants were isolated which lacked the protein. The sites of the Tn5 insertions were found to map between the nitrogenase and nodulation genes on symbiotic plasmid pRL1JI , ca. 5 kilobases from the nitrogenase genes and 13 kilobases from the nodulation genes. Genetic determinants for the 24K protein were found to be closely linked to plasmid-borne nodulation genes for all strains of R. leguminosarum tested. However, the mutants which lacked the 24K protein still formed normal nitrogen-fixing nodules on peas, and the function of the protein is unknown.

摘要

一种蛋白质被鉴定出来,它由豌豆根瘤菌的野生型菌株产生,但共生质粒缺失的结瘤缺陷衍生物则不产生。该蛋白质的亚基分子量约为24,000(24K),在从接种的豌豆根表面重新分离的细菌中大量存在,但在从根瘤中分离的类菌体中未检测到。该蛋白质在豌豆根瘤菌在营养培养基上生长期间也可被诱导,并从破碎细胞的细胞质部分中纯化出来。用针对纯化蛋白质产生的抗血清筛选豌豆根瘤菌的转座子诱导突变体,分离出四个独立的缺乏该蛋白质的突变体。发现Tn5插入位点位于共生质粒pRL1JI上的固氮酶基因和结瘤基因之间,距固氮酶基因约5千碱基,距结瘤基因13千碱基。在所测试的所有豌豆根瘤菌菌株中,发现24K蛋白质的遗传决定因素与质粒携带的结瘤基因紧密相连。然而,缺乏24K蛋白质的突变体在豌豆上仍能形成正常的固氮根瘤,该蛋白质的功能尚不清楚。

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