Yokoyama K, Mizuguchi H, Araki Y, Kaya S, Ito E
Department of Chemistry, Faculty of Science, Hokkaido University, Sapporo, Japan.
J Bacteriol. 1989 Feb;171(2):940-6. doi: 10.1128/jb.171.2.940-946.1989.
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.
在从以下两组革兰氏阳性细菌获得的膜系统中,研究了参与形成含有N - 乙酰葡糖胺(GlcNAc)和N - 乙酰甘露糖胺(ManNAc)或葡萄糖的连接单元并将磷壁酸链连接到肽聚糖的酶的分布和底物特异性: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。所有测试的膜制剂都催化了N - 乙酰葡糖胺基焦磷酸聚戊烯醇(GlcNAc - PP - 聚戊烯醇)的合成。将糖基残基转移到GlcNAc - PP - 聚戊烯醇上的酶对UDP - ManNAc(A组菌株)或UDP - 葡萄糖(B组菌株)具有特异性。在二糖结合脂质的合成中,GlcNAc - PP - 多萜醇可以替代GlcNAc - PP - 十一异戊烯醇。在枯草芽孢杆菌W23和凝结芽孢杆菌AHU 1366的膜系统中,ManNAc - GlcNAc - PP - 十一异戊烯醇、ManNAc - GlcNAc - PP - 多萜醇、Glc - GlcNAc - PP - 十一异戊烯醇、Glc - GlcNAc - PP - 多萜醇和GlcNAc - GlcNAc - PP - 十一异戊烯醇或多或少能有效地转化为含甘油磷酸的脂质中间体和聚合物。然而,GlcNAc - GlcNAc - PP - 多萜醇在这两种膜系统中都不能作为中间体。对ManNAc - GlcNAc - PP - 十一异戊烯醇和Glc - GlcNAc - PP - 十一异戊烯醇可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菌株的膜系统中,两种二糖连接脂质在聚合物合成中几乎同样作为中间体。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 - 十一异戊烯醇替代ManNAc - GlcNAc - PP - 十一异戊烯醇会导致(甘油磷酸) - Glc - GlcNAc - PP - 十一异戊烯醇大量积累,同时聚合物形成减少。