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Sökning: (WFRF:(Hu Jinfu)) > (2022) > Catalytic promiscui...

Catalytic promiscuity of O-methyltransferases from Corydalis yanhusuo leading to the structural diversity of benzylisoquinoline alkaloids

Bu, Junling (författare)
China Academy of Chinese Medical Sciences
Zhang, Xiuhua (författare)
China Academy of Chinese Medical Sciences
Li, Qishuang (författare)
China Academy of Chinese Medical Sciences
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Ma, Ying (författare)
China Academy of Chinese Medical Sciences
Hu, Zhimin (författare)
China Academy of Chinese Medical Sciences
Yang, Jian (författare)
China Academy of Chinese Medical Sciences
Liu, Xiuyu (författare)
Henan University of Chinese Medicine
Wang, Ruishan (författare)
China Academy of Chinese Medical Sciences
Jiao, Xiang, 1990 (författare)
Chalmers tekniska högskola,Chalmers University of Technology
Chen, Tong (författare)
China Academy of Chinese Medical Sciences
Lai, Changjiangsheng (författare)
China Academy of Chinese Medical Sciences
Cui, Guanghong (författare)
China Academy of Chinese Medical Sciences
Tang, Jinfu (författare)
China Academy of Chinese Medical Sciences
Kong, Yu (författare)
Yang, Lei (författare)
Lin, Sheng (författare)
Chen, Yun, 1978 (författare)
Chalmers tekniska högskola,Chalmers University of Technology
Guo, Juan (författare)
China Academy of Chinese Medical Sciences
Huang, Luqi (författare)
China Academy of Chinese Medical Sciences
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 (creator_code:org_t)
2022-07-06
2022
Engelska.
Ingår i: Horticulture Research. - : Oxford University Press (OUP). - 2662-6810 .- 2052-7276. ; 9
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • O-methyltransferases play essential roles in producing structural diversity and improving the biological properties of benzylisoquinoline alkaloids (BIAs) in plants. In this study, Corydalis yanhusuo, a plant used in traditional Chinese medicine due to the analgesic effects of its BIA-active compounds, was employed to analyze the catalytic characteristics of O-methyltransferases in the formation of BIA diversity. Seven genes encoding O-methyltransferases were cloned, and functionally characterized using seven potential BIA substrates. Specifically, an O-methyltransferase (CyOMT2) with highly efficient catalytic activity of both 4′- and 6-O-methylations of 1-BIAs was found. CyOMT6 was found to perform two sequential methylations at both 9- and 2-positions of the essential intermediate of tetrahydroprotoberberines, (S)-scoulerine. Two O-methyltransferases (CyOMT5 and CyOMT7) with wide substrate promiscuity were found, with the 2-position of tetrahydroprotoberberines as the preferential catalytic site for CyOMT5 (named scoulerine 2-O-methyltransferase) and the 6-position of 1-BIAs as the preferential site for CyOMT7. In addition, results of integrated phylogenetic molecular docking analysis and site-directed mutation suggested that residues at sites 172, 306, 313, and 314 in CyOMT5 are important for enzyme promiscuity related to O-methylations at the 6- and 7-positions of isoquinoline. Cys at site 253 in CyOMT2 was proved to promote the methylation activity of the 6-position and to expand substrate scopes. This work provides insight into O-methyltransferases in producing BIA diversity in C. yanhusuo and genetic elements for producing BIAs by metabolic engineering and synthetic biology.

Ämnesord

NATURVETENSKAP  -- Biologi -- Biokemi och molekylärbiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Biochemistry and Molecular Biology (hsv//eng)
TEKNIK OCH TEKNOLOGIER  -- Industriell bioteknik -- Biokatalys och enzymteknik (hsv//swe)
ENGINEERING AND TECHNOLOGY  -- Industrial Biotechnology -- Biocatalysis and Enzyme Technology (hsv//eng)
NATURVETENSKAP  -- Kemi -- Organisk kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences -- Organic Chemistry (hsv//eng)

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