Abstract

The biological active compound rishirilide B is produced by Streptomyces bottropensis. The cosmid cos4 contains the complete rishirilide B biosynthesis gene cluster. Its heterologous expression in the host Streptomyces albus J1074 led to the production of rishirilide B as a major compound and to small amounts of rishirilide A, rishirilide D and lupinacidin A. In order to gain more insights into the biosynthesis, gene inactivation experiments and gene expression experiments were carried out. This study lays the focus on the functional elucidation of the genes involved in the early biosynthetic pathway. A total of eight genes were deleted and six gene cassettes were generated. Rishirilide production was not strongly affected by mutations in rslO2, rslO6 and rslH. The deletion of rslK4 and rslO3 led to the formation of polyketides with novel structures. These results indicated that RslK4 and RslO3 are involved in the generation or selection of the starter unit for rishirilide biosynthesis. In the rslO10 mutant strain, two novel compounds were detected, which were also produced by a strain containing solely the genes rslK1, rslK2, rslK3, rslK4, and rslA. rslO1 and rslO4 mutants predominately produce galvaquinones. Therefore, the ketoreductase RslO10 is involved in an early step of rishirilide biosynthesis and the oxygenases RslO1 and RslO4 are most probably acting on an anthracene moiety. This study led to the functional elucidation of several genes of the rishirilide pathway, including rslK4, which is involved in selecting the unusual starter unit for polyketide synthesis.

Highlights

  • Polyketides are biosynthesized by polyketide synthases (PKS), which share striking similarities with fatty acid synthases

  • Rishirilide biosynthesis is controlled by four regulatory genes that belong to the family of SARP-regulatory genes, the family of LAL regulatory genes and the family of MarR transcriptional regulatory genes, respectively [4]

  • We observed that S. albus J1074 containing cos4 and pUWL-H-rslR1 + rslR2 + rslR3 produced more rishirilide B than S. albus J1074 containing only cos4

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Summary

Introduction

Polyketides are biosynthesized by polyketide synthases (PKS), which share striking similarities with fatty acid synthases. Streptomyces rishiriensis OFR-1056 in the course of screening for new α2-macroglobulin inhibitors [2] This compound was described as a product of S. olivaceus SCSIO T05, which produced rishirilide C, lupinacidin A and galvaquinone A and B [3] (Figure 1). A rishirilide biosynthetic gene cluster was cloned on a cosmid (cos4) (Figure S1) from S. bottropensis Gene deletion experiments and in vitro enzyme studies were employed in S. bottropensis to identify key biosynthetic intermediates and expose intricate redox tailoring steps for the formation of rishirilides A, B, D and lupinacidin A. We have heterologously expressed genes from the rishirilid gene cluster in S. albus J1074 J1074 (rslK1, rslK2, rslK3, rslK4, rslA, (minPKS genes), as well as two genes, involved in the selection of the starter unit. A HPLC/ESI-MS analysis revealed that the emerging compounds were similar to the compounds of the gene deletion experiments, which provides us important information about rishirilide B biosynthesis

Results
Galvaquinone A Is Produced by Mutants Lacking RslO1
Galvaquinone A and B Are Produced by Mutants Lacking rslO4
Discussion
General
Generation of Gene Deletion Mutants
Generation of Strains Containing Different Gene Cassettes
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