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利用动物细胞寻找甲羟戊酸生物合成微生物抑制剂的方法。

Method of search for microbial inhibitors of mevalonate biosynthesis using animal cells.

作者信息

Kumagai H, Tomoda H, Omura S

机构信息

Kitasato Institute and School of Pharmaceutical Sciences, Kitasato University, Tokyo, Japan.

出版信息

J Antibiot (Tokyo). 1990 Apr;43(4):397-402. doi: 10.7164/antibiotics.43.397.

Abstract

A new screening method for specific inhibitors of mevalonate biosynthesis was established using Vero cells, an animal cell line. The cultures selected were those which inhibited the growth of Vero cells in the EAGLE's minimum essential medium supplemented with 2% calf serum (2% CS-MEM) but lacked inhibitory activity against the growth of cells in 2% CS-MEM supplemented with 1 mM mevalonate. By this screening method, inhibitors of the two enzymes involved in mevalonate biosynthesis, 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) synthase and HMG-CoA reductase, were selected from about 11,000 soil isolates. The beta-lactone 1233A, a fungal metabolite, was found to be the first naturally occurring compound which inhibits HMG-CoA synthase specifically and strongly. Monacolins K and J, inhibitors of HMG-CoA reductase, were also detected and identified.

摘要

利用动物细胞系Vero细胞建立了一种新的甲羟戊酸生物合成特异性抑制剂筛选方法。所选择的培养物是那些在补充有2%小牛血清的伊格尔氏最低必需培养基(2%CS-MEM)中抑制Vero细胞生长,但对补充有1mM甲羟戊酸的2%CS-MEM中的细胞生长缺乏抑制活性的培养物。通过这种筛选方法,从约11000株土壤分离物中筛选出了参与甲羟戊酸生物合成的两种酶,即3-羟基-3-甲基戊二酰辅酶A(HMG-CoA)合酶和HMG-CoA还原酶的抑制剂。真菌代谢产物β-内酯1233A被发现是第一种特异性且强烈抑制HMG-CoA合酶的天然存在化合物。还检测并鉴定出了HMG-CoA还原酶抑制剂莫纳可林K和J。

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