MODULAR ORGANIZATION OF GENES REQUIRED FOR COMPLEX POLYKETIDE BIOSYNTHESIS

被引:758
作者
DONADIO, S [1 ]
STAVER, MJ [1 ]
MCALPINE, JB [1 ]
SWANSON, SJ [1 ]
KATZ, L [1 ]
机构
[1] ABBOTT LABS,BIOACT MICROBIAL METABOLITE PROJECT,N CHICAGO,IL 60064
关键词
D O I
10.1126/science.2024119
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
In Saccharopolyspora erythraea, the genes that govern synthesis of the polyketide portion of the macrolide antibiotic erythromycin are organized in six repeated units that encode fatty acid synthase (FAS)-like activities. Each repeated unit is designated a module, and two modules are contained in a single open reading frame. A model for the synthesis of this complex polyketide is proposed, where each module encodes a functional synthase unit and each synthase unit participates specifically in one of the six FAS-like elongation steps required for formation of the polyketide. In addition, genetic organization and biochemical order of events appear to be colinear. Evidence for the model is provided by construction of a selected mutant and by isolation of a polyketide of predicted structure.
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页码:675 / 679
页数:5
相关论文
共 39 条
[1]  
BALTZ RH, 1988, ANNU REV MICROBIOL, V42, P547
[2]   THE MULTIFUNCTIONAL 6-METHYLSALICYLIC ACID SYNTHASE GENE OF PENICILLIUM-PATULUM - ITS GENE STRUCTURE RELATIVE TO THAT OF OTHER POLYKETIDE SYNTHASES [J].
BECK, J ;
RIPKA, S ;
SIEGNER, A ;
SCHILTZ, E ;
SCHWEIZER, E .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1990, 192 (02) :487-498
[3]   ANALYSIS OF THE NUCLEOTIDE-SEQUENCE OF THE STREPTOMYCES-GLAUCESCENS TCML GENES PROVIDES KEY INFORMATION ABOUT THE ENZYMOLOGY OF POLYKETIDE ANTIBIOTIC BIOSYNTHESIS [J].
BIBB, MJ ;
BIRO, S ;
MOTAMEDI, H ;
COLLINS, JF ;
HUTCHINSON, CR .
EMBO JOURNAL, 1989, 8 (09) :2727-2736
[4]   CLONING AND ANALYSIS OF THE PROMOTER REGION OF THE ERYTHROMYCIN RESISTANCE GENE (ERME) OF STREPTOMYCES-ERYTHRAEUS [J].
BIBB, MJ ;
JANSSEN, GR ;
WARD, JM .
GENE, 1985, 38 (1-3) :215-226
[5]   STUDIES IN RELATION TO BIOSYNTHESIS .1. SOME POSSIBLE ROUTES TO DERIVATIVES OF ORCINOL AND PHLOROGLUCINOL [J].
BIRCH, AJ ;
DONOVAN, FW .
AUSTRALIAN JOURNAL OF CHEMISTRY, 1953, 6 (04) :360-368
[6]   MACROLIDE BIOSYNTHESIS .4. INTACT INCORPORATION OF A CHAIN-ELONGATION INTERMEDIATE INTO ERYTHROMYCIN [J].
CANE, DE ;
YANG, CC .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1987, 109 (04) :1255-1257
[7]  
CHIRALA SS, 1989, J BIOL CHEM, V264, P3750
[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]   A COMPREHENSIVE SET OF SEQUENCE-ANALYSIS PROGRAMS FOR THE VAX [J].
DEVEREUX, J ;
HAEBERLI, P ;
SMITHIES, O .
NUCLEIC ACIDS RESEARCH, 1984, 12 (01) :387-395
[10]   EVIDENCE FOR A SEX FACTOR IN STREPTOMYCES-ERYTHREUS [J].
DEWITT, JP .
JOURNAL OF BACTERIOLOGY, 1985, 164 (02) :969-971