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首页> 外文期刊>Journal of bacteriology >Biosynthesis of linkage units for teichoic acids in gram-positive bacteria: distribution of related enzymes and their specificities for UDP-sugars and lipid-linked intermediates.
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Biosynthesis of linkage units for teichoic acids in gram-positive bacteria: distribution of related enzymes and their specificities for UDP-sugars and lipid-linked intermediates.

机译:革兰氏阳性细菌中磷壁酸的连接单元的生物合成:相关酶的分布及其对UDP糖和脂质连接的中间体的特异性。

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摘要

The distribution and substrate specificities of enzymes involved in the formation of linkage units which contain N-acetylglucosamine (GlcNAc) and N-acetylmannosamine (ManNAc) or glucose and join teichoic acid chains to peptidoglycan were studied among membrane systems obtained from the following two groups of gram-positive bacteria: group A, including Bacillus subtilis, Bacillus licheniformis, Bacillus pumilus, Staphylococcus aureus, and Lactobacillus plantarum; group B, Bacillus coagulans. All the membrane preparations tested catalyzed the synthesis of N-acetylglucosaminyl pyrophosphorylpolyprenol (GlcNAc-PP-polyprenol). The enzymes transferring glycosyl residues to GlcNAc-PP-polyprenol were specific to either UDP-ManNAc (group A strains) or UDP-glucose (group B strains). In the synthesis of the disaccharide-bound lipids, GlcNAc-PP-dolichol could substitute for GlcNAc-PP-undecaprenol. ManNAc-GlcNAc-PP-undecaprenol, ManNAc-GlcNAc-PP-dolichol, Glc-GlcNAc-PP-undecaprenol, Glc-GlcNAc-PP-dolichol, and GlcNAc-GlcNAc-PP-undecaprenol were more or less efficiently converted to glycerol phosphate-containing lipid intermediates and polymers in the membrane systems of B. subtilis W23 and B. coagulans AHU 1366. However, GlcNAc-GlcNAc-PP-dolichol could not serve as an intermediate in either of these membrane systems. Further studies on the exchangeability of ManNAc-GlcNAc-PP-undecaprenol and Glc-GlcNAc-PP-undecaprenol revealed that in the membrane systems of S. aureus strains and other B. coagulans strains both disaccharide-inked lipids served almost equally as intermediates in the synthesis of polymers. In the membrane systems of other B. subtilis strains as well as B. licheniformis and B. pumilus strains, however, the replacement of ManNAc-GlcNAc-PP-undecaprenol by Glc-GlcNAc-PP-undecaprenol led to a great accumulation of (glycerol phosphate)-Glc-GlcNAc-PP-undecaprenol accompanied by a decrease in the formation of polymers.
机译:研究了从以下两组中获得的膜系统中涉及形成连接单元的酶的分布和底物特异性,该连接单元包含N-乙酰氨基葡萄糖(GlcNAc)和N-乙酰甘露糖胺(ManNAc)或葡萄糖,并结合了条酸酸链与肽聚糖。革兰氏阳性菌:A组,包括枯草芽孢杆菌,地衣芽孢杆菌,短小芽孢杆菌,金黄色葡萄球菌和植物乳杆菌; B组,凝结芽孢杆菌。所有测试的膜制剂均催化了N-乙酰氨基葡萄糖氨基焦磷酸基聚戊二烯(GlcNAc-PP-聚丙烯)的合成。将糖基残基转移至GlcNAc-PP-聚戊烯醇的酶对UDP-ManNAc(A组菌株)或UDP-葡萄糖(B组菌株)具有特异性。在与二糖结合的脂质的合成中,GlcNAc-PP-去氢胆甾醇可以替代GlcNAc-PP-十一碳烯醇。 ManNAc-GlcNAc-PP-十一碳烯醇,ManNAc-GlcNAc-PP-二十二烯醇,Glc-GlcNAc-PP-十一碳烯醇,Glc-GlcNAc-PP-十一碳烯醇和GlcNAc-GlcNAc-PP-十一碳烯醇或多或少地被转化为甘油磷酸-甘油枯草芽孢杆菌W23和凝结芽孢杆菌AHU 1366的膜系统中含有脂质中间体和聚合物。但是,GlcNAc-GlcNAc-PP-二氢乙醇不能在这两种膜系统中用作中间体。对ManNAc-GlcNAc-PP-十一碳烯醇和Glc-GlcNAc-PP-十一碳烯醇的交换性的进一步研究表明,在金黄色葡萄球菌菌株和其他凝结芽孢杆菌的膜系统中,双糖墨水都几乎等同地充当了脂质中间产物。聚合物的合成。然而,在其他枯草芽孢杆菌菌株以及地衣芽孢杆菌和短小芽孢杆菌菌株的膜系统中,用Glc-GlcNAc-PP-undecaprenol替代ManNAc-GlcNAc-PP-undecaprenol导致大量的(甘油磷酸)-Glc-GlcNAc-PP-十一碳烯醇伴随着聚合物形成的减少。

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