Abstract

Cytochrome P450 monooxygenases (P450s) are considered nature’s most versatile catalysts and play a crucial role in regio- and stereoselective oxidation reactions on a broad range of organic molecules. The oxyfunctionalisation of unactivated carbon-hydrogen (C-H) bonds, in particular, represents a key step in the biosynthesis of many natural products as it provides substrates with increased reactivity for tailoring reactions. In this study, we investigated the function of the P450 enzyme TraB in the terrestric acid biosynthetic pathway. We firstly deleted the gene coding for the DNA repair subunit protein Ku70 by using split marker-based deletion plasmids for convenient recycling of the selection marker to improve gene targeting in Penicillium crustosum. Hereby, we reduced ectopic DNA integration and facilitated genetic manipulation in P. crustosum. Afterward, gene deletion in the Δku70 mutant of the native producer P. crustosum and heterologous expression in Aspergillus nidulans with precursor feeding proved the involvement of TraB in the formation of crustosic acid by catalysing the essential hydroxylation reaction of viridicatic acid.Key points•Deletion of Ku70 by using split marker approach for selection marker recycling.•Functional identification of the cytochrome P450 enzyme TraB.•Fulfilling the reaction steps in the terrestric acid biosynthesis.

Highlights

  • Natural products (NPs) isolated from microorganisms are well-known for their biological activities and are promising candidates for drug development (Katz and Baltz 2016)

  • To improve gene-targeting efficiency in Penicillium crustosum, we aimed to identify and delete the gene coding for the DNA repair protein subunit Ku70

  • An orthologue Pcr4870 was identified in the genome sequence of P. crustosum PRB-2 and differs from KAF7525404.1 at only two residues

Read more

Summary

Introduction

Natural products (NPs) isolated from microorganisms are well-known for their biological activities and are promising candidates for drug development (Katz and Baltz 2016). Recent advances in targeted gene manipulation, including gene disruption and heterologous expression, allowed the analysis of gene functions and Cytochrome P450 enzymes (P450s) are a ubiquitously occurring superfamily of heme-thiolate proteins and are distributed in all kingdoms of life, including humans, animals, plants, fungi, and bacteria (Harken and Li 2021; McIntosh et al 2014; Zhang et al 2021). They catalyse oxidation reactions in the biosynthesis of many natural products, such as alkaloids, terpenes, and polyketides. Biochemical investigation proved the function of the hybrid PKS-NRPS TraA and the enoyl reductase TraG for the formation of

Objectives
Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call