Biosynthesis of the orthosomycin antibiotic avilamycin A:: deductions from the molecular analysis of the avi biosynthetic gene cluster of Streptomyces viridochromogenes Tu57 and production of new antibiotics

被引:112
作者
Weitnauer, G
Mühlenweg, A
Trefzer, A
Hoffmeister, D
Sussmuth, RD
Jung, G
Welzel, K
Vente, A
Girreser, U
Bechthold, A
机构
[1] Univ Freiburg, Inst Pharmazeut Biol, D-79104 Freiburg, Germany
[2] Combinat Biopharm AG, D-13125 Berlin, Germany
[3] Univ Tubingen, D-72076 Tubingen, Germany
[4] Scripps Res Inst, La Jolla, CA 92037 USA
[5] Univ Kiel, D-24118 Kiel, Germany
来源
CHEMISTRY & BIOLOGY | 2001年 / 8卷 / 06期
关键词
avilamycin; gavibamycin; orthosomycin; methyltransferase; halogenase;
D O I
10.1016/S1074-5521(01)00040-0
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
Background: Streptomyces viridochromogenes Tu57 is the producer of avilamycin A. The antibiotic consists of a heptasaccharide side chain and apolyketide-derived dichloroisoeverninic acid as aglycone. Molecular cloning and characterization of the genes governing the avilamycin A biosynthesis is of major interest as this information might set the direction for the development of new antimicrobial agents. Results: A 60-kb section of the S. viridochromogenes Tu57 chromosome containing genes involved in avilamycin biosynthesis was sequenced. Analysis of the DNA sequence revealed 54 open reading frames. Based on the putative function of the gene products a model for avilamycin biosynthesis is proposed. Inactivation of aviG4 and aviH, encoding a methyltransferase and a halogenase, respectively, prevented the mutant strains from producing the complete dichloroisoeverninic acid moiety resulting in the accumulation of new antibiotics named gavibamycins. Conclusions: The avilamycin A biosynthetic gene cluster represents an interesting system to study the formation and attachment of unusual deoxysugars. Several enzymes putatively responsible for specific steps of this pathway could be assigned. Two genes encoding enzymes involved in post-PKS tailoring reactions were deleted allowing the production of new analogues of avilamycin A. (C) 2001 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:569 / 581
页数:13
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