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

被引:28
作者
Zhang, Wei [1 ,2 ,3 ,4 ]
Zhang, Xuan [1 ,2 ,3 ]
Feng, Dandan [1 ,2 ,3 ]
Liang, Yajing [1 ,2 ,3 ]
Wu, Zhenying [1 ,2 ,3 ]
Du, Siyu [1 ,2 ,3 ]
Zhou, Yu [1 ,2 ,3 ]
Geng, Ce [1 ,2 ,3 ]
Men, Ping [1 ,2 ,3 ]
Fu, Chunxiang [1 ,2 ,3 ,4 ]
Huang, Xuenian [1 ,2 ,3 ,4 ]
Lu, Xuefeng [1 ,2 ,3 ,4 ,5 ]
机构
[1] Chinese Acad Sci, Qingdao Inst Bioenergy & Bioproc Technol, Shandong Prov Key Lab Synthet Biol, Qingdao 266101, Shandong, Peoples R China
[2] Shandong Energy Inst, Qingdao 266101, Shandong, Peoples R China
[3] Qingdao New Energy Shandong Lab, Qingdao 266101, Shandong, Peoples R China
[4] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[5] Qingdao Natl Lab Marine Sci & Technol, Marine Biol & Biotechnol Lab, Qingdao 266101, Shandong, Peoples R China
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
Biosynthesis; Filamentous Fungi; Flavonoids; NRPS-PKS Hybrids; Synthetic Biology; CHALCONE ISOMERASE; CHLORFLAVONIN;
D O I
10.1002/anie.202215529
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Flavonoids 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.
引用
收藏
页数:9
相关论文
共 35 条
[1]  
[Anonymous], 2010, PYMOL MOL GRAPHICS S
[2]  
[Anonymous], 2014, ANGEW CHEM, V126, P1463
[3]   The chalcone synthase superfamily of type III polyketide synthases [J].
Austin, MB ;
Noel, JP .
NATURAL PRODUCT REPORTS, 2003, 20 (01) :79-110
[4]   Aspcandine: A Pyrrolobenzazepine Alkaloid Synthesized by a Fungal Nonribosomal Peptide Synthetase-Polyketide Synthase Hybrid [J].
Chen, Lin ;
Tang, Jian-Wei ;
Liu, Yan Yee ;
Matsuda, Yudai .
ORGANIC LETTERS, 2022, :4816-4819
[5]   The Identification of Maize and Arabidopsis Type I FLAVONE SYNTHASEs Links Flavones with Hormones and Biotic Interactions [J].
Falcone Ferreyra, Maria Lorena ;
Emiliani, Julia ;
Jose Rodriguez, Eduardo ;
Alina Campos-Bermudez, Valeria ;
Grotewold, Erich ;
Casati, Paula .
PLANT PHYSIOLOGY, 2015, 169 (02) :1090-1107
[6]   Enzymatic Conversion of Flavonoids using Bacterial Chalcone Isomerase and Enoate Reductase [J].
Gall, Mechthild ;
Thomsen, Maren ;
Peters, Christin ;
Pavlidis, Ioannis V. ;
Jonczyk, Patrick ;
Gruenert, Philipp P. ;
Beutel, Sascha ;
Scheper, Thomas ;
Gross, Egon ;
Backes, Michael ;
Geissler, Torsten ;
Ley, Jakob P. ;
Hilmer, Jens-Michael ;
Krammer, Gerhard ;
Palm, Gottfried J. ;
Hinrichs, Winfried ;
Bornscheuer, Uwe T. .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2014, 53 (05) :1439-1442
[7]   Efficient Biosynthesis of (2S)-Naringenin from p-Coumaric Acid in Saccharomyces cerevisiae [J].
Gao, Song ;
Lyu, Yunbin ;
Zeng, Weizhu ;
Du, Guocheng ;
Zhou, Jingwen ;
Chen, Jian .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2020, 68 (04) :1015-1021
[8]   First bacterial chalcone isomerase isolated from Eubacterium ramulus [J].
Herles, C ;
Braune, A ;
Blaut, M .
ARCHIVES OF MICROBIOLOGY, 2004, 181 (06) :428-434
[9]   Structure and mechanism of the evolutionarily unique plant enzyme chalcone isomerase [J].
Jez J.M. ;
Bowman M.E. ;
Dixon R.A. ;
Noel J.P. .
Nature Structural Biology, 2000, 7 (9) :786-791
[10]   Flavones: From Biosynthesis to Health Benefits [J].
Jiang, Nan ;
Doseff, Andrea I. ;
Grotewold, Erich .
PLANTS-BASEL, 2016, 5 (02)