Abstract

Phthoxazolin A, an oxazole-containing polyketide, has a broad spectrum of anti-oomycete activity and herbicidal activity. We recently identified phthoxazolin A as a cryptic metabolite of Streptomyces avermitilis that produces the important anthelmintic agent avermectin. Even though genome data of S. avermitilis is publicly available, no plausible biosynthetic gene cluster for phthoxazolin A is apparent in the sequence data. Here, we identified and characterized the phthoxazolin A (ptx) biosynthetic gene cluster through genome sequencing, comparative genomic analysis, and gene disruption. Sequence analysis uncovered that the putative ptx biosynthetic genes are laid on an extra genomic region that is not found in the public database, and 8 open reading frames in the extra genomic region could be assigned roles in the biosynthesis of the oxazole ring, triene polyketide and carbamoyl moieties. Disruption of the ptxA gene encoding a discrete acyltransferase resulted in a complete loss of phthoxazolin A production, confirming that the trans-AT type I PKS system is responsible for the phthoxazolin A biosynthesis. Based on the predicted functional domains in the ptx assembly line, we propose the biosynthetic pathway of phthoxazolin A.

Highlights

  • Polyketides and non-ribosomal peptides are structurally diverse classes of natural products representing important therapeutic and agricultural chemicals [1,2]

  • The genome has no orthologue of OzmO, which is necessary for the biosynthesis of an oxazole ring moiety

  • We have shown that strain KA320 harbors an extra genomic region, which is absent in the publicly available genome of strain K139, and that a biosynthetic gene cluster for phthoxazolin A is laid on the extra region of strain KA-320

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Summary

Introduction

Polyketides and non-ribosomal peptides are structurally diverse classes of natural products representing important therapeutic and agricultural chemicals [1,2]. Polyketides are typically produced by polyketide synthase (PKS) assembly lines that are composed of functional modules. Each module is responsible for one step of chain extension of the growing products and consists of a set of domains which dictate the chemical functionality of the incorporated building block [3,4]. The minimal domains of a PKS module are an acyltransferase (AT), ketosynthase (KS) and acyl carrier protein (ACP) domain, where the AT domain loads a coenzyme A-activated dicarboxylic acid extender unit onto the ACP domain and the KS domain of the preceding domain catalyzes condensation of the nascent polyketide with the extender unit.

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