Discovery of a Unique Flavonoid Biosynthesis Mechanism in Fungi by Genome Mining

Author:

Zhang Wei1234,Zhang Xuan123,Feng Dandan123,Liang Yajing123,Wu Zhenying123,Du Siyu123,Zhou Yu123,Geng Ce123,Men Ping123,Fu Chunxiang1234,Huang Xuenian1234,Lu Xuefeng12345ORCID

Affiliation:

1. Shandong Provincial Key Laboratory of Synthetic Biology Qingdao Institute of Bioenergy and Bioprocess Technology Chinese Academy of Sciences Qingdao Shandong 266101 China

2. Shandong Energy Institute Qingdao Shandong 266101 China

3. Qingdao New Energy Shandong Laboratory Qingdao Shandong 266101 China

4. University of Chinese Academy of Sciences Beijing 100049 China

5. Marine Biology and Biotechnology Laboratory Qingdao National Laboratory for Marine Science and Technology Qingdao Shandong 266101 China

Abstract

AbstractFlavonoids are important plant natural products with variable structures and bioactivities. All known plant flavonoids are generated under the catalysis of a type III polyketide synthase (PKS) followed by a chalcone isomerase (CHI) and a flavone synthase (FNS). In this study, the biosynthetic gene cluster of chlorflavonin, a fungal flavonoid with acetolactate synthase inhibitory activity, was discovered using a self‐resistance‐gene‐directed strategy. A novel flavonoid biosynthetic pathway in fungi was revealed. A core nonribosomal peptide synthetase‐polyketide synthase (NRPS‐PKS) is responsible for the generation of the key precursor chalcone. Then, a new type of CHI catalyzes the conversion of a chalcone into a flavanone by a histidine‐mediated oxa‐Michael addition mechanism. Finally, the desaturation of flavanone to flavone is catalyzed by a new type of FNS, a flavin mononucleotide (FMN)‐dependent oxidoreductase.

Funder

National Key Research and Development Program of China

Young Scientists Fund

National Natural Science Foundation of China

Key Technology Research and Development Program of Shandong

Taishan Scholar Foundation of Shandong Province

Publisher

Wiley

Subject

General Chemistry,Catalysis

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