Loss of Single‐Domain Function in a Modular Assembly Line Alters the Size and Shape of a Complex Polyketide

The structural wealth of complex polyketide metabolites produced by bacteria results from intricate, highly evolved biosynthetic programs of modular assembly lines, in which the number of modules defines the size of the backbone, and the domain composition controls the degree of functionalization. W...

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Bibliographic Details
Published inAngewandte Chemie Vol. 131; no. 50; pp. 18420 - 18424
Main Authors Peng, Huiyun, Ishida, Keishi, Hertweck, Christian
Format Journal Article
LanguageEnglish
Published Weinheim Wiley Subscription Services, Inc 09.12.2019
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Summary:The structural wealth of complex polyketide metabolites produced by bacteria results from intricate, highly evolved biosynthetic programs of modular assembly lines, in which the number of modules defines the size of the backbone, and the domain composition controls the degree of functionalization. We report a remarkable case where polyketide chain length and scaffold depend on the function of a single β‐keto processing domain: A ketoreductase domain represents a switch between diverging biosynthetic pathways leading either to the antifungal aureothin or to the nematicidal luteoreticulin. By a combination of heterologous expression, mutagenesis, metabolite analyses, and in vitro biotransformation we elucidate the factors governing non‐colinear polyketide assembly involving module skipping and demonstrate that a simple point mutation in type I polyketide synthase (PKS) can have a dramatic effect on the metabolic profile. This finding sheds new light on possible evolutionary scenarios and may inspire future synthetic biology approaches. Biosynthetischer Schalter: Genetische und chemische Analysen zeigten einen bemerkenswerten Fall, in dem die Länge der Polyketidkette und das Gerüst von der Funktion einer einzelnen β‐Keto‐Prozessierungsdomäne einer multimodularen Polyketidsynthase abhängen. Eine Ketoreduktasedomäne wirkt als molekularer Schalter zwischen divergierenden Routen, die entweder zum antimykotischen Aureothin oder zum nematiziden Luteoreticulin führen.
ISSN:0044-8249
1521-3757
DOI:10.1002/ange.201911315