4.7 Article

Identification of Specific Glycosyltransferases Involved in Flavonol Glucoside Biosynthesis in Ginseng Using Integrative Metabolite Profiles, DIA Proteomics, and Phylogenetic Analysis

期刊

JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY
卷 69, 期 5, 页码 1714-1726

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.jafc.0c06989

关键词

flavonol; glycoside; proteomics; glucosyltransferase; galacosyltransferase; Panax ginseng

资金

  1. National Key R&D Program of China [2019YFC1711100]
  2. Fundamental Research Funds for the Central public welfare research institutes [ZZ13-YQ-097]
  3. China Postdoctoral Science Foundation [2018 M631705]
  4. National Science and Technology Major Project Creation of Major New Drugs [2019ZX09201005-006-004, 2019ZX09731-002]

向作者/读者索取更多资源

The study identified panasenoside and kaempferol 3-O-glucoside as commonly accumulated flavonol glycosides in ginseng leaves with cultivation years. A total of 50 UDP-glycosyltransferases (UGTs) were screened out to explore flavonol glycosylation in ginseng, with specific UGTs identified for the formation and modification of kaempferol 3-O-glucoside. The study highlights the significance of integrated metabolite profiles, proteomics, and phylogenetic analysis in understanding flavonol glycosylation pathways in ginseng.
Ginseng contains a variety of flavonol glycosides that possess diverse biological activities; however, scant information of flavonoid glycosylation was reported in ginseng. We found that panasenoside and kaempferol 3-O-glucoside were commonly accumulated along with cultivation years in leaves. In order to explore the procedure of flavonol glycosylation in ginseng, 50 UDP-glycosyltransferases (UGTs) were screened out using differentiated data-independent acquisition (DIA) proteomics and phylogenetic analysis. UGT92A10 and UGT94Q4 were found contributing to the formation of kaempferol 3-O-glucoside. UGT73A18, UGT74T4, and UGT75W1 could catalyze galactosylation of kaempferol 3-O-glucoside. Ser278, Trp335, Gln338, and Val339 were found forming hydrogen bonds with UDP-galactose in UGT75W1 by docking. MeJA induced transcripts of UGT73A18 and UGT74T4 by over fourfold, consistent with the decrease of kaempferol 3-O-glucoside, which indicated that these genes may be related to resisting adversity stress in ginseng. These results highlight the significance of integrative metabolite profiles, proteomics, and phylogenetic analysis for exploring flavonol glycosylation in ginseng.

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