首页> 美国卫生研究院文献>Journal of Bacteriology >Novel rkp Gene Clusters of Sinorhizobium meliloti Involved in Capsular Polysaccharide Production and Invasion of the Symbiotic Nodule: the rkpK Gene Encodes a UDP-Glucose Dehydrogenase
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Novel rkp Gene Clusters of Sinorhizobium meliloti Involved in Capsular Polysaccharide Production and Invasion of the Symbiotic Nodule: the rkpK Gene Encodes a UDP-Glucose Dehydrogenase

机译:苜蓿中华根瘤菌的新型rkp基因簇参与荚膜多糖的生产和共生根瘤的入侵:rkpK基因编码UDP葡萄糖脱氢酶。

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摘要

The production of exopolysaccharide (EPS) was shown to be required for the infection process by rhizobia that induce the formation of indeterminate nodules on the roots of leguminous host plants. In Sinorhizobium meliloti (also known as Rhizobium meliloti) Rm41, a capsular polysaccharide (KPS) analogous to the group II K antigens of Escherichia coli can replace EPS during symbiotic nodule development and serve as an attachment site for the strain-specific bacteriophage φ16-3. The rkpA to -J genes in the chromosomal rkp-1 region code for proteins that are involved in the synthesis, modification, and transfer of an as-yet-unknown lipophilic molecule which might function as a specific lipid carrier during KPS biosynthesis. Here we report that with a phage φ16-3-resistant population obtained after random Tn5 mutagenesis, we have identified novel mutants impaired in KPS production by genetic complementation and biochemical studies. The mutations represent two novel loci, designated the rkp-2 and rkp-3 regions, which are required for the synthesis of rhizobial KPS. The rkp-2 region harbors two open reading frames (ORFs) organized in monocistronic transcription units. Although both genes are required for normal lipopolysaccharide production, only the second one, designated rkpK, is involved in the synthesis of KPS. We have demonstrated that RkpK possesses UDP-glucose dehydrogenase activity, while the protein product of ORF1 might function as a UDP-glucuronic acid epimerase.
机译:根瘤菌的感染过程表明胞外多糖(EPS)的产生是必需的,这种根瘤菌诱导了豆科宿主植物根部上不确定的根瘤的形成。在苜蓿中华根瘤菌(Rhi41)中,类似于大肠杆菌IIK抗原的荚膜多糖(KPS)可以在共生结节形成过程中替代EPS,并作为菌株特异性噬菌体φ16-3的附着位点。染色体rkp-1区中的rkpA至-J基因编码参与迄今未知的亲脂分子的合成,修饰和转移的蛋白质,该分子在KPS生物合成过程中可能起特定的脂质载体的作用。在这里我们报告说,通过随机Tn5诱变后获得的噬菌体φ16-3-抗性种群,我们已经通过遗传互补和生化研究确定了在KPS生产中受损的新型突变体。突变代表两个新的基因座,称为rkp-2和rkp-3区,这是合成根瘤菌KPS所必需的。 rkp-2区域包含以单顺反子转录单位组织的两个开放阅读框(ORF)。尽管两个基因都是正常脂多糖生产所必需的,但只有第二个基因(称为rkpK)参与了KPS的合成。我们已经证明RkpK具有UDP-葡萄糖脱氢酶活性,而ORF1的蛋白质产物可能起UDP-葡萄糖醛酸差向异构酶的作用。

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