To improve the production of geldanamycin in Streptomyces hygroscopicus 17997, gene disruption was done to delete the naphthalenic AHBA genes (shnSOP), encoding the products that share the common biosynthetic substrates with geldanamycin. The resulting mutant strain (DSOP) was cultivated on a solid medium and the amount of spores collected from the plates was calculated from 5 to 14 days and the yield of geldanamycin was measured by HPLC. The geldanamycin production of the DSOP strain increased by 185% comparing with that of the parent strain. On solid medium, the DSOP strain underwent 2 cycles of sporulation and the growth of the second sporulation had the highest geldanamycin production.
赫卫清,周红霞,王红远,高群杰,王以光. 格尔德霉素基因工程高产菌株的构建和培养[J]. Chinese Journal of Biotechnology, 2008, 24(1): 15-20
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