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磷脂酰甘油作为双歧杆菌脂磷壁酸聚(甘油磷酸)主链的生物合成前体。

Phosphatidylglycerol as biosynthetic precursor for the poly(glycerol phosphate) backbone of bifidobacterial lipoteichoic acid.

作者信息

Op den Camp H J, Oosterhof A, Veerkamp J H

出版信息

Biochem J. 1985 Jun 15;228(3):683-8. doi: 10.1042/bj2280683.

Abstract

Phosphatidylglycerol functions as donor of the sn-glycerol 1-phosphate units in the synthesis in vitro of the 1,2-phosphodiester-linked glycerol phosphate backbone of the lipoteichoic acids of Bifidobacterium bifidum subsp. pennsylvanicum. The incorporation was catalysed by a membrane-bound enzyme system. After addition of chloroform/methanol the product formed coprecipitated with protein. The material was phenol-extractable and was co-eluted with purified lipoteichoic acid on Sepharose 6B. The reaction was stimulated by Triton X-100, UDP-glucose and UDP-galactose, but Mg2+ ions had no effect. The apparent values for Km and Vmax. of the phosphatidylglycerol incorporation were 1.4 mM and 3.1 nmol/h per mg of membrane protein, respectively. Labelled UDP-glucose and UDP-galactose were not incorporated into the lipoteichoic acid fraction by the particulate membrane preparation.

摘要

在体外合成宾夕法尼亚双歧杆菌亚种双歧杆菌脂磷壁酸的1,2 -磷酸二酯连接甘油磷酸主链时,磷脂酰甘油作为sn -甘油-1 -磷酸单元的供体。该掺入反应由膜结合酶系统催化。加入氯仿/甲醇后,形成的产物与蛋白质共沉淀。该物质可用苯酚提取,并与纯化的脂磷壁酸在琼脂糖6B上共洗脱。该反应受到Triton X - 100、UDP -葡萄糖和UDP -半乳糖的刺激,但Mg2 +离子无作用。磷脂酰甘油掺入的Km和Vmax表观值分别为1.4 mM和每毫克膜蛋白3.1 nmol/h。标记的UDP -葡萄糖和UDP -半乳糖未被颗粒膜制剂掺入脂磷壁酸部分。

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