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首页> 外文期刊>Archives of microbiology >Mutation in the cobO gene generates auxotrophy for cobalamin and methionine and impairs the symbiotic properties of Sinorhizobium fredii HH103 with soybean and other legumes.
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Mutation in the cobO gene generates auxotrophy for cobalamin and methionine and impairs the symbiotic properties of Sinorhizobium fredii HH103 with soybean and other legumes.

机译:cobO基因的突变产生钴胺素和蛋氨酸的营养缺陷,并损害了Sinorhizobium fredii HH103与大豆和其他豆类的共生特性。

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We report here the isolation of a methionine and cobalamin mutant strain (SVQ336) of Sinorhizobium fredii HH103 obtained by Tn5-lacZ mutagenesis. Sequence analysis showed that the transposon was inserted into a gene homologous to cobO. This gene codes for a cobalamin adenosyltransferase which is involved in the biosynthesis of vitamin B12. Another HH103 cobO mutant (strain SVQ524), was constructed by the insertion of Omega interposon. Both cobO mutants required the addition of methionine because cobalamin acts as a cofactor of the enzyme MetH, which catalyses the last step of the methionine biosynthesis. Mutant SVQ524 failed to nodulate on Vigna radiate but was able to nodulate on Glycine max cvs. Williams and Peking and Cajanus cajan, although the total number of nodules formed was highly reduced in comparison with that of plants inoculated with the wild-type strain HH103. The roots of these plants did not seem to secrete enough cobalamin and/or methionine to support growth of cobalamin/methionine auxotrophs in the rhizosphere. In all cases, the phenotype of SVQ524 was nearly overcome by the addition of methionine or cobalamin to the plant growth media or by the presence of a copy of the cobO gene in cosmid pMUS756.
机译:我们在这里报告了通过Tn5-lacZ诱变获得的弗氏中华根瘤菌HH103的蛋氨酸和钴胺素突变株(SVQ336)的分离。序列分析表明转座子被插入到与cobO同源的基因中。该基因编码参与维生素B12生物合成的钴胺素腺苷转移酶。通过插入欧米茄插入子构建了另一个HH103 cobO突变体(菌株SVQ524)。这两个cobO突变体都需要添加蛋氨酸,因为钴胺素充当了MetH酶的辅助因子,该酶催化蛋氨酸生物合成的最后一步。 SVQ524突变体未能在Vigna辐射上结瘤,但能够在Glycine max cvs上结瘤。 Williams和Peking和Cajanus cajan,尽管与接种野生型HH103的植物相比,结节的总数大大减少。这些植物的根似乎没有分泌足够的钴胺素和/或蛋氨酸来支持根际中钴胺素/蛋氨酸营养缺陷型的生长。在所有情况下,通过向植物生长培养基中添加甲硫氨酸或钴胺素或粘粒pMUS756中存在cobO基因的拷贝,几乎可以克服SVQ524的表型。

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