首页> 美国卫生研究院文献>Journal of Bacteriology >Genetics of xanthan production in Xanthomonas campestris: the xanA and xanB genes are involved in UDP-glucose and GDP-mannose biosynthesis.
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Genetics of xanthan production in Xanthomonas campestris: the xanA and xanB genes are involved in UDP-glucose and GDP-mannose biosynthesis.

机译:桔小黄单胞菌生产黄原胶的遗传学:xanA和xanB基因参与UDP-葡萄糖和GDP-甘露糖的生物合成。

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摘要

The nucleotide sequence of a 3.4-kb EcoRI-PstI DNA fragment of Xanthomonas campestris pv. campestris revealed two open reading frames, which were designated xanA and xanB. The genes xanA and xanB encode proteins of 448 amino acids (molecular weight of 48,919) and 466 amino acids (molecular weight of 50,873), respectively. These genes were identified by analyzing insertion mutants which were known to be involved in xanthan production. Specific tests for the activities of enzymes involved in the biosynthesis of UDP-glucose and GDP-mannose indicated that the xanA gene product was involved in the biosynthesis of both glucose 1-phosphate and mannose 1-phosphate. The deduced amino acid sequence of xanB showed a significant degree of homology (59%) to the phosphomannose isomerase of Pseudomonas aeruginosa, a key enzyme in the biosynthesis of alginate. Moreover, biochemical analysis and complementation experiments with the Escherichia coli manA fragment revealed that xanB encoded a bifunctional enzyme, phosphomannose isomerase-GDP-mannose pyrophosphorylase.
机译:Xanthomonas campestris pv的3.4-kb EcoRI-PstI DNA片段的核苷酸序列。 Campestris揭示了两个开放阅读框,分别称为xanA和xanB。 xanA和xanB基因分别编码448个氨基酸(分子量为48,919)和466个氨基酸(分子量为50,873)的蛋白质。通过分析已知与黄原胶生产有关的插入突变体来鉴定这些基因。对UDP-葡萄糖和GDP-甘露糖的生物合成中涉及的酶活性的具体测试表明,xanA基因产物参与了1-磷酸葡萄糖和1-磷酸甘露糖的生物合成。推导的xanB氨基酸序列显示出与铜绿假单胞菌(Pseudomonas aeruginosa)的磷酸甘露糖异构酶的高度同源性(59%),铜绿假单胞菌是藻酸盐生物合成中的关键酶。此外,大肠杆菌manA片段的生化分析和互补实验表明,xanB编码一种双功能酶,磷酸甘露糖异构酶-GDP-甘露糖焦磷酸化酶。

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