Inactivation of putative PKS genes can double geldanamycin yield in Streptomyces hygroscopicus 17997

被引:2
作者
Li, Y. H. [1 ,2 ]
Li, M. [1 ]
He, W. Q. [2 ]
Wang, Y. G. [2 ]
Shao, R. G. [2 ]
机构
[1] Xinxiang Med Univ, Henan Cultivating Key Lab Hereditary Dis Targeted, Sch Life Sci & Technol, Xinxiang, Peoples R China
[2] Chinese Acad Med Sci, Peking Union Med Coll, Inst Med Biotechnol, Beijing 100730, Peoples R China
关键词
Geldanamycin; Inactivation; PKS; Hsp90; inhibitor; BIOSYNTHESIS; IDENTIFICATION; STREPTOMYCES-HYGROSCOPICUS-17997;
D O I
10.4238/2013.June.21.3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The putative polyketide biosynthesis (PKS) genes cos10 and pg10 were inactivated by insertion of a kanamycin-resistance gene into the genome of the geldanamycin-producing strain, Streptomyces hygroscopicus 17997. The resultant inactivation were confirmed by PCR analysis. The abilities of the PKS gene inactivation strains to produce geldanamycin were compared with the natural geldanamycin-producing strain, S. hygroscopicus 17997. The cos10-inactivated strain exhibited an unchanged ability to produce geldanamycin, but the pg10-inactivated strain can produce twice the yield of the natural strain when grown under the same conditions. We propose that there is a sub-PKS pathway in the geldanamycin-producing strain, S. hygroscopicus 17997.
引用
收藏
页码:2076 / 2085
页数:10
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