Geosmin biosynthesis in Streptomyces avermitilis.: Molecular cloning, expression, and mechanistic study of the germacradienol/geosmin synthase

被引:115
作者
Cane, David E.
He, Xiaofei
Kobayashi, Seiji
Omura, Satoshi
Ikeda, Haruo
机构
[1] Brown Univ, Dept Chem, Providence, RI 02912 USA
[2] Kitasato Inst, Minato Ku, Tokyo 1088642, Japan
[3] Kitasato Univ, Kitasato Inst Life Sci, Sagamihara, Kanagawa 2288555, Japan
关键词
sesquiterpene; biosynthesis; geosmin; Streptomyces avermitilis; Streptomyces coelicolor;
D O I
10.1038/ja.2006.66
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
Geosmin (1) is responsible for the characteristic odor of moist soil. The Gram-positive soil bacterium Streptomyces avermitilis produces geosmin (1) as well as its precursor germacradienol (3). The S. avermitilis gene SAV2163 (geoA) is extremely similar to the S. coelicolor A3(2) SCO6073 gene that encodes a germacradienol/geosmin synthase. S. avermitilis mutants with a deleted geoA were unable to produce either germacradienol (3) or geosmin (1). Biosynthesis of both compounds was restored by introducing an intact geoA gene into the mutants. Incubation of recombinant GeoA, encoded by the SAV2163 gene of S. avermitilis, with farnesyl diphosphate (2) in the presence of Mg(2=) gave a mixture of (4S,7R)-germacra-1(10)E,5E-diene-11-ol (3) (66%), (7S)-germacrene D (4) (24%), geosmin (1) (8%), and a hydrocarbon, tentatively assigned the structure of octalin 5 (2%). Incubation of this germacradienol/geosmin synthase with [1,1-(2)H(2)]FPP (2a) gave geosmin-d(1) (1a), as predicted. When recombinant GeoA from either S. avermitilis or S. coelicolor A3(2) was incubated with nerolidyl diphosphate (8), only the acyclic elimination products beta-farnesene (10), (Z)-alpha-farnesene (11), and (E)-alpha-farnesene (12) were formed, thereby ruling out nerolidyl diphosphate as an intermediate in the conversion of farnesyl diphosphate to geosmin, germacradienol, and germacrene D.
引用
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页码:471 / 479
页数:9
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