Characterization of an echinocandin B-producing strain blocked for sterigmatocystin biosynthesis reveals a translocation in the stcW gene of the aflatoxin biosynthetic pathway

被引:17
作者
Hodges, RL [1 ]
Kelkar, HS
Xuei, X
Skatrud, PL
Keller, NP
Adams, TH
Kaiser, RE
Vinci, VA
McGilvray, D
机构
[1] Eli Lilly & Co, Nat Prod Res & Dev, Lilly Res Labs, Indianapolis, IN 46285 USA
[2] Univ Georgia, Dept Genet, Athens, GA 30602 USA
[3] Abbott Labs, Dept 4PN, Abbott Pk, IL 60064 USA
[4] Eli Lilly & Co, Lilly Res Labs, Infect Dis Res, Indianapolis, IN 46285 USA
[5] Texas A&M Univ, Dept Plant Pathol & Microbiol, College Stn, TX 77843 USA
[6] Myst Res Ctr, Mystic, CT 06355 USA
[7] Eli Lilly & Co, Lilly Res Labs, Bioproc Analyt Dev, Indianapolis, IN 46285 USA
关键词
Aspergillus nidulans; aflatoxin; sterigmatocystin; mutagenesis; translocation; echinocandin B;
D O I
10.1038/sj.jim.7000076
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
Echinocandin B (ECB), a lipopolypeptide used as a starting material for chemical manufacture of the anti-Candida agent LY303366, is produced by fermentation using a strain of Aspergillus nidulans. In addition to ECB, the wild-type strain also produces a significant level of sterigmatocystin (ST), a potent carcinogen structurally related to the aflatoxins. Characterization of a mutant designated A42355-OC-1 (OC-l), which is blocked in ST biosynthesis, was the result of a chromosomal translocation. The chromosomal regions containing the breakpoints of the translocation were isolated and DNA sequencing and PCR analysis of the chromosomal breakpoints demonstrated the translocation occurred within the stcW gene of the ST biosynthetic pathway, resulting in disruption of the open reading frame for this gene. Biochemical feeding studies indicate the involvement of this gene product in the conversion of averufin to 1-hydroxy versicolorone. This work demonstrates an effective synergy between classical strain improvement methods and molecular genetics.
引用
收藏
页码:333 / 341
页数:9
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