Exploration of geosmin synthase from Streptomyces peucetius ATCC 27952 by deletion of doxorubicin biosynthetic gene cluster

被引:18
|
作者
Singh, Bijay [1 ]
Oh, Tae-Jin [1 ]
Sohng, Jae Kyung [1 ]
机构
[1] SunMoon Univ, Dept Pharmaceut Engn, iBR, Asan 336708, Chungnam, South Korea
关键词
Geosmin; Sesquiterpene synthase; Doxorubicin; Streptomyces peucetius; Overexpression; ESCHERICHIA-COLI; COENZYME-A; GERMACRADIENOL SYNTHASE; POLYKETIDE SYNTHASE; AVERMITILIS; CLONING; ELUCIDATION; COELICOLOR; EXPRESSION; PRODUCER;
D O I
10.1007/s10295-009-0605-0
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
Thorough investigation of Streptomyces peucetius ATCC 27952 genome revealed a sesquiterpene synthase, named spterp13, which encodes a putative protein of 732 amino acids with significant similarity to S. avermitilis MA-4680 (SAV2163, GeoA) and S. coelicolor A3(2) (SCO6073). The proteins encoded by SAV2163 and SCO6073 produce geosmin in the respective strains. However, the spterp13 gene seemed to be silent in S. peucetius. Deletion of the doxorubicin gene cluster from S. peucetius resulted in increased cell growth rate along with detectable production of geosmin. When we over expressed the spterp13 gene in S. peucetius DM07 under the control of an ermE* promoter, 2.4 +/- A 0.4-fold enhanced production of geosmin was observed.
引用
收藏
页码:1257 / 1265
页数:9
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