Organization of the biosynthetic gene cluster for the polyketide anthelmintic macrolide avermectin in Streptomyces avermitilis

被引:278
作者
Ikeda, H
Nonomiya, T
Usami, M
Ohta, T
Ömura, S
机构
[1] Kitasato Univ, Sch Pharmaceut Sci, Tokyo 1088641, Japan
[2] Kitasato Inst, Biol Funct Res Ctr, Tokyo 1088642, Japan
关键词
D O I
10.1073/pnas.96.17.9509
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Analysis of the gene cluster from Streptomyces avermitilis that governs the biosynthesis of the polyketide anthelmintic avermectin revealed that it contains four large ORFs encoding giant multifunctional polypeptides of the avermectin polyketide synthase (AVES 1, AVES 2, AVES 3, and AVES 4), These clustered polyketide synthase genes responsible for avermectin biosynthesis together encode 12 homologous sets of enzyme activities (modules), each catalyzing a specific round of polyketide chain elongation. The clustered genes encoding polyketide synthase are organized as two sets of six modular repeats, aveA1-aveA2 and aveA3-aveA4, which are convergently transcribed. The total of 55 constituent active sites makes this the most complex multifunctional enzyme system identified to date. The sequenced DNA region contains 14 additional ORFs, some of which encode polypeptides governing other key steps in avermectin biosynthesis. Between the two sets of polyketide synthase genes lie two genes involved in postpolyketide modification, one of which encodes cynthochrome P450 hydroxylase that probably catalyzes furan ring formation at C6 to C8a, Immediately right of the large polyketide synthase genes is a set of genes involved in oleandrose biosynthesis and its transglycosylation to polyketide-derived aglycons, This cluster includes nine genes, but one is not functional in the biosynthesis of avermectin. On the left side of polyketide synthase genes, two ORFs encoding methyltransferase and nonpolyketide synthase ketoreductase involved in postpolyketide modification are located to the left of the polyketide synthase genes, and an adjacent gene encodes a regulatory function that may be involved in activation of the transcription of avermectin biosynthetic genes.
引用
收藏
页码:9509 / 9514
页数:6
相关论文
共 31 条
[1]   BASIC LOCAL ALIGNMENT SEARCH TOOL [J].
ALTSCHUL, SF ;
GISH, W ;
MILLER, W ;
MYERS, EW ;
LIPMAN, DJ .
JOURNAL OF MOLECULAR BIOLOGY, 1990, 215 (03) :403-410
[2]  
[Anonymous], METHOD ENZYMOL
[3]   Biosynthesis of the ansamycin antibiotic rifamycin: deductions from the molecular analysis of the rif biosynthetic gene cluster of Amycolatopsis mediterranei S699 [J].
August, PR ;
Tang, L ;
Yoon, YJ ;
Ning, S ;
Muller, R ;
Yu, TW ;
Taylor, M ;
Hoffmann, D ;
Kim, CG ;
Zhang, XH ;
Hutchinson, CR ;
Floss, HG .
CHEMISTRY & BIOLOGY, 1998, 5 (02) :69-79
[4]  
AZIZ MA, 1982, LANCET, V2, P171
[5]   6-DEOXYERYTHRONOLIDE-B SYNTHASE-2 FROM SACCHAROPOLYSPORA-ERYTHRAEA - CLONING OF THE STRUCTURAL GENE, SEQUENCE-ANALYSIS AND INFERRED DOMAIN-STRUCTURE OF THE MULTIFUNCTIONAL ENZYME [J].
BEVITT, DJ ;
CORTES, J ;
HAYDOCK, SF ;
LEADLAY, PF .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1992, 204 (01) :39-49
[6]   AVERMECTINS, NEW FAMILY OF POTENT ANTHELMINTIC AGENTS - PRODUCING ORGANISM AND FERMENTATION [J].
BURG, RW ;
MILLER, BM ;
BAKER, EE ;
BIRNBAUM, J ;
CURRIE, SA ;
HARTMAN, R ;
KONG, YL ;
MONAGHAN, RL ;
OLSON, G ;
PUTTER, I ;
TUNAC, JB ;
WALLICK, H ;
STAPLEY, EO ;
OIWA, R ;
OMURA, S .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1979, 15 (03) :361-367
[7]   BIOSYNTHETIC ORIGIN OF THE CARBON SKELETON AND OXYGEN-ATOMS OF THE AVERMECTINS [J].
CANE, DE ;
LIANG, TC ;
KAPLAN, L ;
NALLIN, MK ;
SCHULMAN, MD ;
HENSENS, OD ;
DOUGLAS, AW ;
ALBERSSCHONBERG, G .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1983, 105 (12) :4110-4112
[8]   AN UNUSUALLY LARGE MULTIFUNCTIONAL POLYPEPTIDE IN THE ERYTHROMYCIN-PRODUCING POLYKETIDE SYNTHASE OF SACCHAROPOLYSPORA-ERYTHRAEA [J].
CORTES, J ;
HAYDOCK, SF ;
ROBERTS, GA ;
BEVITT, DJ ;
LEADLAY, PF .
NATURE, 1990, 348 (6297) :176-178
[9]   MODULAR ORGANIZATION OF GENES REQUIRED FOR COMPLEX POLYKETIDE BIOSYNTHESIS [J].
DONADIO, S ;
STAVER, MJ ;
MCALPINE, JB ;
SWANSON, SJ ;
KATZ, L .
SCIENCE, 1991, 252 (5006) :675-679
[10]   NOVEL AVERMECTINS PRODUCED BY MUTATIONAL BIOSYNTHESIS [J].
DUTTON, CJ ;
GIBSON, SP ;
GOUDIE, AC ;
HOLDOM, KS ;
PACEY, MS ;
RUDDOCK, JC ;
BULOCK, JD ;
RICHARDS, MK .
JOURNAL OF ANTIBIOTICS, 1991, 44 (03) :357-365