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细菌细胞壁合成的机制。膜中酶和类异戊二烯磷酸酯的组织。

The mechanism of wall synthesis in bacteria. The organization of enzymes and isoprenoid phosphates in the membrane.

作者信息

Anderson R G, Hussey H, Baddiley J

出版信息

Biochem J. 1972 Mar;127(1):11-25. doi: 10.1042/bj1270011.

Abstract
  1. The synthesis of peptidoglycan and teichoic acids by cell-free preparations from Bacillus licheniformis A.T.C.C. 9945 and Bacillus subtilis N.C.T.C. 3610 has been studied under a variety of conditions. 2. It was shown that poly(glycerol phosphate) is synthesized through a lipid intermediate, and it is concluded from this and other work that all major bacterial wall polymers are formed in a similar manner through such intermediates. 3. Close interrelation between the synthesis of peptidoglycan and teichoic acids was demonstrated, and inhibition studies confirm that the polyprenol phosphate molecules participating in the synthesis of peptidoglycan are shared with the systems that synthesize teichoic acids. 4. Nucleotides for the synthesis of one polymer are inhibitory towards synthesis of the other, and these effects can be enhanced or diminished by preincubation of the enzyme system with appropriate nucleotide precursors. 5. It is concluded that the return of undecaprenol phosphate to a common pool occurs only after the completion of polymer chains, and not after each cycle in the attachment of individual repeating units. This and other observations support a model for bacterial wall synthesis in which the multi-enzyme systems for each polymer are closely aligned in the membrane, with a molecule of undecaprenol phosphate located between them in a manner that enables it to be shared. The general mechanisms of wall synthesis and its control are discussed.
摘要
  1. 已在多种条件下研究了地衣芽孢杆菌A.T.C.C. 9945和枯草芽孢杆菌N.C.T.C. 3610的无细胞制剂合成肽聚糖和磷壁酸的情况。2. 结果表明,聚(甘油磷酸)是通过脂质中间体合成的,并且基于此及其他研究得出结论,所有主要的细菌细胞壁聚合物都是以类似方式通过此类中间体形成的。3. 已证明肽聚糖和磷壁酸的合成之间存在密切的相互关系,抑制研究证实,参与肽聚糖合成的聚戊烯醇磷酸分子与合成磷壁酸的系统共用。4. 用于一种聚合物合成的核苷酸对另一种聚合物的合成具有抑制作用,并且通过用适当的核苷酸前体对酶系统进行预孵育,这些作用可以增强或减弱。5. 得出的结论是,十一异戊烯醇磷酸只有在聚合物链完成后才返回共同的库中,而不是在单个重复单元连接的每个循环之后。这一观察结果及其他观察结果支持了一种细菌细胞壁合成模型,即每种聚合物的多酶系统在膜中紧密排列,其间有一个十一异戊烯醇磷酸分子,其位置使其能够被共用。文中还讨论了细胞壁合成及其控制的一般机制。

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