Bertram K C, Hancock I C, Baddiley J
J Bacteriol. 1981 Nov;148(2):406-12. doi: 10.1128/jb.148.2.406-412.1981.
Protoplasts of Bacillus subtilis W23 readily synthesized ribitol teichoic acid from nucleotide precursors in the surrounding medium. With cytidine diphosphate-ribitol they made poly(ribitol phosphate), presumably attached to lipoteichoic acid carrier; when cytidine diphosphate-glycerol and uridine diphosphate-N-acetylglucosamine were also present a 10-fold increase in the rate of polymer synthesis occurred, and the product contained both the main chain and the linkage unit. Synthesis was inhibited by trypsin or p-chloromercuribenzenesulfonate in the medium, and we concluded that it occurred at the outer surface of the membrane. During synthesis, which was also achieved readily by whole cells after a brief period of wall lysis, the cytidine phosphate portion of the nucleotide precursors did not pass through the membrane. No evidence could be obtained for a transphosphorylation mechanism for the translocation process. It is suggested that reaction with exogenous substrates was due to temporary exposure of a protein component of the enzyme complex at the outer surface of the membrane during the normal biosynthetic cycle.
枯草芽孢杆菌W23的原生质体能轻易地从周围培养基中的核苷酸前体合成核糖醇磷壁酸。利用胞苷二磷酸核糖醇,它们合成了聚(核糖醇磷酸),推测其附着在脂磷壁酸载体上;当同时存在胞苷二磷酸甘油和尿苷二磷酸-N-乙酰葡糖胺时,聚合物合成速率提高了10倍,且产物包含主链和连接单元。培养基中的胰蛋白酶或对氯汞苯磺酸盐会抑制合成,我们由此得出结论,合成发生在膜的外表面。在合成过程中,短暂细胞壁裂解后的完整细胞也能轻易实现合成,核苷酸前体的胞苷磷酸部分并未穿过膜。未获得转磷酸化机制参与转运过程的证据。有人提出,与外源底物的反应是由于在正常生物合成循环中,酶复合物的蛋白质成分暂时暴露于膜的外表面。