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枯草芽孢杆菌无核细胞(微小细胞)对细胞包膜成分的合成。

Synthesis of cell envelope components by anucleate cells (minicells) of Bacillus subtilis.

作者信息

Mertens G, Reeve J N

出版信息

J Bacteriol. 1977 Mar;129(3):1198-207. doi: 10.1128/jb.129.3.1198-1207.1977.

Abstract

Minicells produced by Bacillus subtilis CU403 (divIVB1) are capable of mucopeptide biosynthesis as shown by the incorporation of L-alanine, D-alanine, and N-acetylglucosamine into trichloroacetic acid-precipitable material, which can be degraded to trichloroacetic acid-soluble material by lysozyme digestion. Incorporation of the precursors is sensitive to vancomycin and D-cycloserine and insensitive to chloramphenicol. Penicillin inhibits the incorporation of D- and L-alanine N-acetylglucosamine at concentrations in excess of 10 mug of penicillin per ml; however, minicells are insensitive to penicillin-induced lysis. The material synthesized in minicells from N-acetylglucosamine is not subject to turnover during a subsequent 6-h incubation period. [2-3H]glycerol is converted to a cold trichloroacetic acid-precipitable form by minicells. This synthesis is not inhibited by vancomycin, penicillin, D-cycloserine, or chloramphenicol. Fractionation of the material synthesized from glycerol into hot trichloroacetic acid-soluble material and chloroform/methanol-extractable material indicates that minicells convert glycerol into teichoic acid and lipid.

摘要

枯草芽孢杆菌CU403(divIVB1)产生的微细胞能够进行粘肽生物合成,这可通过将L-丙氨酸、D-丙氨酸和N-乙酰葡糖胺掺入三氯乙酸沉淀物质中得以证明,该物质可通过溶菌酶消化降解为三氯乙酸可溶物质。前体的掺入对万古霉素和D-环丝氨酸敏感,而对氯霉素不敏感。青霉素在浓度超过每毫升10微克青霉素时会抑制D-和L-丙氨酸N-乙酰葡糖胺的掺入;然而,微细胞对青霉素诱导的裂解不敏感。在微细胞中由N-乙酰葡糖胺合成的物质在随后6小时的孵育期内不会发生周转。[2-³H]甘油被微细胞转化为冷三氯乙酸沉淀形式。这种合成不受万古霉素、青霉素、D-环丝氨酸或氯霉素的抑制。将由甘油合成的物质分离为热三氯乙酸可溶物质和氯仿/甲醇可提取物表明,微细胞将甘油转化为磷壁酸和脂质。

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