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cis-fumagillin, a new methionine aminopeptidase (type 2) inhibitor produced by Penicillium sp. F2757.
- Source :
-
The Journal of antibiotics [J Antibiot (Tokyo)] 2000 Aug; Vol. 53 (8), pp. 799-806. - Publication Year :
- 2000
-
Abstract
- Selective inhibition against the yeast MetAP2 (methionine aminopeptidase type 2) was detected in the fermentation broth of a fungus F2757 that was later identified as Penicillium janczewskii. A new compound cis-fumagillin methyl ester (1) was isolated from the diazomethane treated fermentation extracts together with the known compound fumagillin methyl ester (2). The cis-fumagillin methyl ester, a stereoisomer of fumagillin methyl ester at the C2'-C3' position of the aliphatic side chain, selectively inhibited growth of the map1 mutant yeast strain (MetAP1 deletion strain) at a concentration as low as 1 ng. However, the wild type yeast w303 and the mutant map2 (MetAP2 deleted) strains were resistant up to 10 microg of the compound. In enzyme experiments, compound 1 inhibited the MetAP2 with an IC50 value of 6.3 nM, but it did not inhibit the MetAP1 (IC50 >200 microM). Compound 2 also inhibited the MetAP2 with an IC50 value of 9.2 nM and 105 microM against MetAP1.
- Subjects :
- Epoxy Compounds metabolism
Fatty Acids, Unsaturated metabolism
Fermentation
Inhibitory Concentration 50
Molecular Structure
Penicillium classification
Aminopeptidases antagonists & inhibitors
Epoxy Compounds isolation & purification
Epoxy Compounds pharmacology
Fatty Acids, Unsaturated isolation & purification
Fatty Acids, Unsaturated pharmacology
Metalloendopeptidases antagonists & inhibitors
Penicillium metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 0021-8820
- Volume :
- 53
- Issue :
- 8
- Database :
- MEDLINE
- Journal :
- The Journal of antibiotics
- Publication Type :
- Academic Journal
- Accession number :
- 11079802
- Full Text :
- https://doi.org/10.7164/antibiotics.53.799