METHOD OF SEARCH FOR MICROBIAL INHIBITORS OF MEVALONATE BIOSYNTHESIS USING ANIMAL-CELLS

被引:19
作者
KUMAGAI, H
TOMODA, H
OMURA, S
机构
[1] KITASATO INST,TOKYO 108,JAPAN
[2] KITASATO UNIV,SCH PHARMACEUT SCI,MINATO KU,TOKYO 108,JAPAN
关键词
D O I
10.7164/antibiotics.43.397
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
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-MEMsupplemented 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 1 1,000 soil isolates. The ²-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-CoAreductase, were also detected and identified. © 1990, JAPAN ANTIBIOTICS RESEARCH ASSOCIATION. All rights reserved.
引用
收藏
页码:397 / 402
页数:6
相关论文
共 21 条
[1]   MEVINOLIN - A HIGHLY POTENT COMPETITIVE INHIBITOR OF HYDROXYMETHYLGLUTARYL-COENZYME-A REDUCTASE AND A CHOLESTEROL-LOWERING AGENT [J].
ALBERTS, AW ;
CHEN, J ;
KURON, G ;
HUNT, V ;
HUFF, J ;
HOFFMAN, C ;
ROTHROCK, J ;
LOPEZ, M ;
JOSHUA, H ;
HARRIS, E ;
PATCHETT, A ;
MONAGHAN, R ;
CURRIE, S ;
STAPLEY, E ;
ALBERSSCHONBERG, G ;
HENSENS, O ;
HIRSHFIELD, J ;
HOOGSTEEN, K ;
LIESCH, J ;
SPRINGER, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1980, 77 (07) :3957-3961
[2]   ANTIBIOTIC-1233A - A FUNGAL BETA-LACTONE [J].
ALDRIDGE, DC ;
GILES, D ;
TURNER, WB .
JOURNAL OF THE CHEMICAL SOCIETY D-CHEMICAL COMMUNICATIONS, 1970, (11) :639-&
[3]   SEMI-MICRO, DYE-BINDING ASSAY FOR RABBIT INTERFERON [J].
ARMSTRONG, JA .
APPLIED MICROBIOLOGY, 1971, 21 (04) :723-+
[4]   CRYSTAL AND MOLECULAR-STRUCTURE OF COMPACTIN, A NEW ANTIFUNGAL METABOLITE FROM PENICILLIUM-BREVICOMPACTUM [J].
BROWN, AG ;
SMALE, TC ;
KING, TJ ;
HASENKAMP, R ;
THOMPSON, RH .
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 1976, (11) :1165-1173
[5]  
BROWN MS, 1984, SCI AM, V251, P52
[6]  
CHANG YC, 1988, J ORG CHEM, V53, P4599
[7]   MONACOLIN-J AND MONACOLIN-L NEW INHIBITORS OF CHOLESTEROL-BIOSYNTHESIS PRODUCED BY MONASCUS-RUBER [J].
ENDO, A ;
HASUMI, K ;
NEGISHI, S .
JOURNAL OF ANTIBIOTICS, 1985, 38 (03) :420-422
[8]   MONACOLIN-K, A NEW HYPOCHOLESTEROLEMIC AGENT PRODUCED BY A MONASCUS SPECIES [J].
ENDO, A .
JOURNAL OF ANTIBIOTICS, 1979, 32 (08) :852-854
[9]   ML-236A, ML-236B, AND ML-236C, NEW INHIBITORS OF CHOLESTEROGENESIS PRODUCED BY PENICILLIUM CITRINUM [J].
ENDO, A ;
KURODA, M ;
TSUJITA, Y .
JOURNAL OF ANTIBIOTICS, 1976, 29 (12) :1346-1348
[10]  
GREENSPAN MD, 1988, FASEB J, V2, pA1037