Article(id=1304406835482620727, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1304406818550206926, articleNumber=null, orderNo=null, doi=10.7501/j.issn.0253-2670.2026.01.024, pmid=null, cstr=null, oa=null, hot=0, price=null, onlineType=0, articleFormat=0, articleType=null, articleTypeStr=null, receivedDate=1759334400000, receivedDateStr=2025-10-02, revisedDate=null, revisedDateStr=null, acceptedDate=null, acceptedDateStr=null, onlineDate=1788924424286, onlineDateStr=2026-09-09, pubDate=null, pubDateStr=null, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1788924424286, onlineIssueDateStr=2026-09-09, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1788924424286, creator=13701087609, updateTime=1788924424286, updator=13701087609, issue=Issue{id=1304406818550206926, tenantId=1146029695717560320, journalId=1302319053441957962, year='2026', volume='57', issue='1', pageStart='1', pageEnd='389', issueExtLink='null', onlineDate='null', pubDate='1768147200000', pubDateStr='2026-01-12', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=-1, specialIssue=null, createTime=1788924420249, creator='13701087609', updateTime=1788924674802, updator='13701087609', preIssue=null, nextIssue=null, articleTotal=null, ext={EN=IssueExt(id=1304407886289986387, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1304406818550206926, language=EN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=), CN=IssueExt(id=1304407886289986388, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1304406818550206926, language=CN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=)}, issueFiles=null, downloadFileDto=null}, startPage=270, endPage=281, ext={EN=ArticleExt(id=1304406835839136569, articleId=1304406835482620727, tenantId=1146029695717560320, journalId=1302319053441957962, language=EN, title=Cloning and functional validation of flavonoid glycosyltransferase gene PgUGT72B21 from Platycodon grandiflorus, columnId=null, journalTitle=Chinese Traditional and Herbal Drugs, columnName=null, runingTitle=null, highlight=null, articleAbstract=Objective Taking the glycosyltransferase in Platycodon grandiflorus as the research object, the bioinformatics analysis, gene cloning and recombinant plasmid construction, protein expression and purification, catalytic function validation, enzymatic properties, and substrate promiscuity of the glycosyltransferase gene PgUGT72B21 were investigated. Methods The key glycosyltransferase PgUGT72B21 was screened from the transcriptome data of P. grandiflorus and subsequently cloned. A prokaryotic expression vector, pET-28a-PgUGT72B21, was constructed using gene recombination technology and transformed into Escherichia coli BL21(DE3) competent cells. Protein purification was performed according to the instructions of the His-tagged protein purification kit, and protein expression was detected by SDS-PAGE electrophoresis. The enzymatic reaction products were analyzed using HPLC and LCMS systems. Results P. grandiflorus glycosyltransferase gene Pg UGT72B21 obtained through cloning had an open reading frame(ORF) of 1 407 bp, encoding 468 amino acid residues with a relative molecular mass of approximately 51 000. A highly conserved plant secondary product glycosyltransferase(PSPG) motif was identified at the C-terminus. Phylogenetic analysis indicated that this glycosyltransferase belongs to the UGT72 family. In vitro enzymatic assays demonstrated that PgUGT72B21 could catalyze the glycosylation of the C3 hydroxyl group of quercetin to produce isoquercitrin. After heterologous expression and purification, the recombinant protein was obtained, and its enzymatic properties were analyzed. The optimal pH and temperature for the catalytic reaction were determined to be 6.0 and 60 ℃, respectively, with the highest substrate conversion rate achieved after 2 h of reaction. The kinetic parameters for quercetin catalysis were Km = 390.10 μmol/L and kcat = 11.10/min. Further substrate promiscuity studies revealed that PgUGT72B21 could not only catalyze flavonols such as quercetin but also flavonoids such as apigenin. Conclusion The newly discovered glycosyltransferase PgUGT72B21 holds significant importance for enriching the glycosylation tool enzyme library and provides a foundation for further elucidating the glycosylation process of flavonoid glycosides in P. grandiflorus., authors=LI Tao, HAO Zhipeng, REN Xingrong, ZHAO Yuying, WANG Caixia, XUE Qiang, authorsList=LI Tao, HAO Zhipeng, REN Xingrong, ZHAO Yuying, WANG Caixia, XUE Qiang, authorCompany=null, correspAuthors=null, authorNote=null, correspAuthorsNote=null, copyrightStatement=null, copyrightOwner=null, extLink=null, articleAbsUrl=null, sourceXml=null, magXml=null, pdfUrl=null, pdf=null, pdfFileSize=null, pdfExtLink=null, richHtmlUrl=null, mobilePdfUrl=null, reviewReport=null, pdfFirstPage=null, abstractGraph=null, abstractGraphContent=null, abstractVideo=null, citation=null, cebUrl=null, magXmlContent=null, mapNumber=null, fund=null), CN=ArticleExt(id=1304406835759444792, articleId=1304406835482620727, tenantId=1146029695717560320, journalId=1302319053441957962, language=CN, title=桔梗中黄酮类糖基转移酶基因PgUGT72B21的克隆与功能验证, columnId=1304140203967410414, journalTitle=中草药, columnName=药材与资源, runingTitle=null, highlight=null, articleAbstract=目的 以桔梗Platycodon grandiflorus中糖基转移酶为研究对象,进行糖基转移酶PgUGT72B21基因的生物信息学分析、基因克隆与重组质粒构建、蛋白表达与纯化、催化功能验证、酶学性质研究、底物宽泛性考察。方法 基于桔梗转录组数据筛选得到桔梗中关键糖基转移酶PgUGT72B21,进行基因克隆;利用基因重组技术构建了原核表达载体pET-28a-PgUGT72B21,转化至大肠杆菌BL21(DE3)感受态;根据His标签蛋白纯化试剂盒说明进行蛋白纯化,应用SDS-PAGE凝胶电泳检测蛋白的表达情况;通过HPLC和LC-MS系统检测酶促反应产物。结果 通过克隆得到的桔梗糖基转移酶基因PgUGT72B21开放阅读框(open reading frame,ORF)长度1 407 bp,编码468个氨基酸残基,相对分子质量约为51 000,C末端存在高度保守的植物次生产物糖基转移酶(plant secondary product glycosyltransferase,PSPG)基序。系统进化分析表明,该糖基转移酶属于UGT72家族。体外酶促结果显示,PgUGT72B21可催化槲皮素C3位羟基糖基化生成异槲皮苷。通过异源表达与纯化得到重组蛋白后对其酶学性质进行了分析,表明PgUGT72B21催化反应的最适pH为6.0,最适温度为60℃,反应2 h后的底物转化率达到最高。其催化槲皮素的酶动力学参数米氏常数(Km)为390.10μmol/L,转化数(kcat)为11.10/min。进一步的底物宽泛性研究显示PgUGT72B21不仅能够催化槲皮素等黄酮醇类化合物,还能够催化芹菜素等黄酮类化合物。结论 发现的新糖基转移酶PgUGT72B21对于丰富糖基化工具酶库具有重要意义,且能为进一步解析桔梗中黄酮糖苷的糖基化过程奠定基础。, authors=李涛1, 郝志鹏1,2, 任星榕1, 赵钰萤3, 王彩霞2, 薛强2, authorsList=李涛, 郝志鹏, 任星榕, 赵钰萤, 王彩霞, 薛强, authorCompany=1 山西农业大学林学院, 山西 晋中 030801;
2 中国中医科学院中药研究所 道地药材品质保障与资源持续利用全国重点实验室, 北京 100700;
3 山西卫生健康职业学院 基础部, 山西 晋中 030600, correspAuthors=薛强, authorNote=李涛: 李涛,副教授,研究方向为植物分子生理学。E-mail:litao@sxau.edu.cn 郝志鹏: 郝志鹏,硕士研究生,研究方向为植物分子生药学。E-mail:haozhipeng5384@163.com, correspAuthorsNote=null, copyrightStatement=null, copyrightOwner=null, extLink=null, articleAbsUrl=null, sourceXml=null, magXml=null, pdfUrl=null, pdf=JdILS68lzuCUK5/Hqq67kg==, pdfFileSize=2559818, pdfExtLink=null, richHtmlUrl=null, mobilePdfUrl=null, reviewReport=null, pdfFirstPage=null, abstractGraph=null, abstractGraphContent=null, abstractVideo=null, citation=null, cebUrl=null, magXmlContent=null, mapNumber=null, fund=中国中医科学院科技创新工程项目 (CI2023E002); 中国中医科学院中药研究所自主创新课题 (ZXKT22048); 国家自然科学基金项目 (32200308); 山西省基础研究计划(自由探索类)面上项目 (202403021211036))}, authors=null, keywords=[Keyword(id=1304406835990131514, tenantId=1146029695717560320, journalId=1302319053441957962, articleId=1304406835482620727, language=CN, orderNo=1, keyword=桔梗), Keyword(id=1304406836057240379, tenantId=1146029695717560320, journalId=1302319053441957962, 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李超,张欢,汲晨锋.桔梗化学成分、药理作用及现代应用研究进展[J]. 中国药学杂志, 38(6):1-17.
刘一杰,薛永常.植物黄酮类化合物的研究进展[J]. 中国生物工程杂志, 2016, 36(9):81-86.
李晓波,刘雪,赵广荣.微生物合成黄酮糖苷类天然产物研究进展[J]. 中国生物工程杂志, 2016, 36(8):105-112.
王佳蕊.苦荞黄酮糖苷相关糖基转移酶基因的鉴定及功能验证[D]. 贵阳:贵州师范大学, 2023.
熊瑞琦.苦荞类黄酮糖基转移酶基因FtUFGT4的克隆及功能鉴定[D]. 贵阳:贵州大学, 2024.
Liu N, Zou Y P, Jiang Z Q, et al. Multiomics driven identification of glycosyltransferases in flavonoid glycoside biosynthesis in safflower[J]. Hortic Plant J,2024, 10(3):245-258.
Li S Y, Wang G Q, Long L, et al. Functional and structural dissection of glycosyltransferases underlying the glycodiversity of wolfberry-derived bioactive ingredients lycibarbarspermidines[J]. Nat Commun, 2024, 15(1):4588.
Wang Z L, Du X Q, Ye G, et al. Functional characterization, structural basis, and protein engineering of a rare flavonoid 2’-O-glycosyltransferase from Scutellaria baicalensis[J]. Acta Pharm Sin B, 2024, 14(8):3746-3759.
Chen J, Qiu X J, Sun Z M, et al. Genome-wide analysis of UDP-glycosyltransferase family in Citrus sinensis and characterization of a UGT gene encoding flavonoid 1-2rhamnosyltransferase[J]. Int J Biol Macromol, 2024,280(Pt 2):135752.
Bao Y O, Zhang M, Li H R, et al. Functional characterization and protein engineering of a glycosyltransferase GcCGT to produce flavone 6, 8-di-C-and 6-C-4'-O-glycosides[J]. ACS Catal, 2024, 14(2):1075-1082.
Benavente-García O, Castillo J. Update on uses and properties of Citrus flavonoids:New findings in anticancer, cardiovascular, and anti-inflammatory activity[J]. J Agric Food Chem, 2008, 56(15):6185-6205.
Huong N T, Son N T. Icaritin:A phytomolecule with enormous pharmacological values[J]. Phytochemistry,2023, 213:113772.
Sajid M, Channakesavula C N, Stone S R, et al. Synthetic biology towards improved flavonoid pharmacokinetics[J]. Biomolecules, 2021, 11(5):754.
Li H B, Lyv Y, Zhou S H, et al. Microbial cell factories for the production of flavonoids-barriers and opportunities[J]. Bioresour Technol, 2022, 360:127538.
Lv Y K, Marsafari M, Koffas M, et al. Optimizing oleaginous yeast cell factories for flavonoids and hydroxylated flavonoids biosynthesis[J]. ACS Synth Biol,2019, 8(11):2514-2523.
Tohge T, de Souza L P, Fernie A R. Current understanding of the pathways of flavonoid biosynthesis in model and crop plants[J]. J Exp Bot, 2017, 68(15):4013-4028.
Abdulai I L, Kwofie S K, Gbewonyo W S, et al.Multitargeted effects of vitexin and isovitexin on diabetes mellitus and its complications[J]. Sci World J, 2021, 2021:6641128.
Peng Y, Gan R Y, Li H B, et al. Absorption, metabolism,and bioactivity of vitexin:Recent advances in understanding the efficacy of an important nutraceutical[J]. Crit Rev Food Sci Nutr, 2021, 61(6):1049-1064.
Singh S, Phillips G N Jr, Thorson J S. The structural biology of enzymes involved in natural product glycosylation[J]. Nat Prod Rep, 2012, 29(10):1201-1237.
Li J, Shi M, Ma B L, et al. Antitumor activity and safety evaluation of nanaparticle-based delivery of quercetin through intravenous administration in mice[J]. Mater Sci Eng C Mater Biol Appl, 2017, 77:803-810.
Saija A, Tomaino A, Trombetta D, et al.‘In vitro’antioxidant and photoprotective properties and interaction with model membranes of three new quercetin esters[J]. Eur J Pharm Biopharm, 2003, 56(2):167-174.
Park S H, Kim H J, Yim S H, et al. Delineation of the role of glycosylation in the cytotoxic properties of quercetin using novel assays in living vertebrates[J]. J Nat Prod,2014, 77(11):2389-2396.
Liang D M, Liu J H, Wu H, et al. Glycosyltransferases:Mechanisms and applications in natural product development[J]. Chem Soc Rev, 2015, 44(22):8350-8374.
Nam Y H, Kim E B, Kang J E, et al. Ameliorative effects of flavonoids from Platycodon grandiflorus aerial parts on alloxan-induced pancreatic islet damage in zebrafish[J]. Nutrients, 2023, 15(7):1798.
Jang D S, Lee Y M, Jeong I H, et al. Constituents of the flowers of Platycodon grandiflorum with inhibitory activity on advanced glycation end products and rat lens aldose reductase in vitro[J]. Arch Pharm Res, 2010, 33(6):875-880.)
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桔梗中黄酮类糖基转移酶基因PgUGT72B21的克隆与功能验证
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中草药 | 药材与资源 2026,57(1): 270-281
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中草药 |药材与资源 2026 , 57 (1) : 270 -281
桔梗中黄酮类糖基转移酶基因PgUGT72B21的克隆与功能验证
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李涛1, 郝志鹏1,2, 任星榕1, 赵钰萤3, 王彩霞2, 薛强2
作者信息
    1 山西农业大学林学院, 山西 晋中 030801;
    2 中国中医科学院中药研究所 道地药材品质保障与资源持续利用全国重点实验室, 北京 100700;
    3 山西卫生健康职业学院 基础部, 山西 晋中 030600
通讯作者:
薛强
作者简介:
李涛: 李涛,副教授,研究方向为植物分子生理学。E-mail:litao@sxau.edu.cn 郝志鹏: 郝志鹏,硕士研究生,研究方向为植物分子生药学。E-mail:haozhipeng5384@163.com
Cloning and functional validation of flavonoid glycosyltransferase gene PgUGT72B21 from Platycodon grandiflorus
  • LI Tao, HAO Zhipeng, REN Xingrong, ZHAO Yuying, WANG Caixia, XUE Qiang
  • Affiliations
    doi: 10.7501/j.issn.0253-2670.2026.01.024
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    目的 以桔梗Platycodon grandiflorus中糖基转移酶为研究对象,进行糖基转移酶PgUGT72B21基因的生物信息学分析、基因克隆与重组质粒构建、蛋白表达与纯化、催化功能验证、酶学性质研究、底物宽泛性考察。方法 基于桔梗转录组数据筛选得到桔梗中关键糖基转移酶PgUGT72B21,进行基因克隆;利用基因重组技术构建了原核表达载体pET-28a-PgUGT72B21,转化至大肠杆菌BL21(DE3)感受态;根据His标签蛋白纯化试剂盒说明进行蛋白纯化,应用SDS-PAGE凝胶电泳检测蛋白的表达情况;通过HPLC和LC-MS系统检测酶促反应产物。结果 通过克隆得到的桔梗糖基转移酶基因PgUGT72B21开放阅读框(open reading frame,ORF)长度1 407 bp,编码468个氨基酸残基,相对分子质量约为51 000,C末端存在高度保守的植物次生产物糖基转移酶(plant secondary product glycosyltransferase,PSPG)基序。系统进化分析表明,该糖基转移酶属于UGT72家族。体外酶促结果显示,PgUGT72B21可催化槲皮素C3位羟基糖基化生成异槲皮苷。通过异源表达与纯化得到重组蛋白后对其酶学性质进行了分析,表明PgUGT72B21催化反应的最适pH为6.0,最适温度为60℃,反应2 h后的底物转化率达到最高。其催化槲皮素的酶动力学参数米氏常数(Km)为390.10μmol/L,转化数(kcat)为11.10/min。进一步的底物宽泛性研究显示PgUGT72B21不仅能够催化槲皮素等黄酮醇类化合物,还能够催化芹菜素等黄酮类化合物。结论 发现的新糖基转移酶PgUGT72B21对于丰富糖基化工具酶库具有重要意义,且能为进一步解析桔梗中黄酮糖苷的糖基化过程奠定基础。
    桔梗  /  糖基转移酶  /  UDP-葡萄糖  /  槲皮素  /  功能验证  /  酶动力学
    Objective Taking the glycosyltransferase in Platycodon grandiflorus as the research object, the bioinformatics analysis, gene cloning and recombinant plasmid construction, protein expression and purification, catalytic function validation, enzymatic properties, and substrate promiscuity of the glycosyltransferase gene PgUGT72B21 were investigated. Methods The key glycosyltransferase PgUGT72B21 was screened from the transcriptome data of P. grandiflorus and subsequently cloned. A prokaryotic expression vector, pET-28a-PgUGT72B21, was constructed using gene recombination technology and transformed into Escherichia coli BL21(DE3) competent cells. Protein purification was performed according to the instructions of the His-tagged protein purification kit, and protein expression was detected by SDS-PAGE electrophoresis. The enzymatic reaction products were analyzed using HPLC and LCMS systems. Results P. grandiflorus glycosyltransferase gene Pg UGT72B21 obtained through cloning had an open reading frame(ORF) of 1 407 bp, encoding 468 amino acid residues with a relative molecular mass of approximately 51 000. A highly conserved plant secondary product glycosyltransferase(PSPG) motif was identified at the C-terminus. Phylogenetic analysis indicated that this glycosyltransferase belongs to the UGT72 family. In vitro enzymatic assays demonstrated that PgUGT72B21 could catalyze the glycosylation of the C3 hydroxyl group of quercetin to produce isoquercitrin. After heterologous expression and purification, the recombinant protein was obtained, and its enzymatic properties were analyzed. The optimal pH and temperature for the catalytic reaction were determined to be 6.0 and 60 ℃, respectively, with the highest substrate conversion rate achieved after 2 h of reaction. The kinetic parameters for quercetin catalysis were Km = 390.10 μmol/L and kcat = 11.10/min. Further substrate promiscuity studies revealed that PgUGT72B21 could not only catalyze flavonols such as quercetin but also flavonoids such as apigenin. Conclusion The newly discovered glycosyltransferase PgUGT72B21 holds significant importance for enriching the glycosylation tool enzyme library and provides a foundation for further elucidating the glycosylation process of flavonoid glycosides in P. grandiflorus.
    Platycodon grandifloras L.  /  glycosyltransferase  /  UDP-glucose  /  quercetin  /  functional verification  /  enzyme kinetics
    李涛, 郝志鹏, 任星榕, 赵钰萤, 王彩霞, 薛强. 桔梗中黄酮类糖基转移酶基因PgUGT72B21的克隆与功能验证. 中草药, 2026 , 57 (1) : 270 -281 . DOI: 10.7501/j.issn.0253-2670.2026.01.024
    LI Tao, HAO Zhipeng, REN Xingrong, ZHAO Yuying, WANG Caixia, XUE Qiang. Cloning and functional validation of flavonoid glycosyltransferase gene PgUGT72B21 from Platycodon grandiflorus[J]. Chinese Traditional and Herbal Drugs, 2026 , 57 (1) : 270 -281 . DOI: 10.7501/j.issn.0253-2670.2026.01.024

      中国中医科学院科技创新工程项目 (CI2023E002); 中国中医科学院中药研究所自主创新课题 (ZXKT22048); 国家自然科学基金项目 (32200308); 山西省基础研究计划(自由探索类)面上项目 (202403021211036)

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    刘一杰,薛永常.植物黄酮类化合物的研究进展[J]. 中国生物工程杂志, 2016, 36(9):81-86.
    李晓波,刘雪,赵广荣.微生物合成黄酮糖苷类天然产物研究进展[J]. 中国生物工程杂志, 2016, 36(8):105-112.
    王佳蕊.苦荞黄酮糖苷相关糖基转移酶基因的鉴定及功能验证[D]. 贵阳:贵州师范大学, 2023.
    熊瑞琦.苦荞类黄酮糖基转移酶基因FtUFGT4的克隆及功能鉴定[D]. 贵阳:贵州大学, 2024.
    Liu N, Zou Y P, Jiang Z Q, et al. Multiomics driven identification of glycosyltransferases in flavonoid glycoside biosynthesis in safflower[J]. Hortic Plant J,2024, 10(3):245-258.
    Li S Y, Wang G Q, Long L, et al. Functional and structural dissection of glycosyltransferases underlying the glycodiversity of wolfberry-derived bioactive ingredients lycibarbarspermidines[J]. Nat Commun, 2024, 15(1):4588.
    Wang Z L, Du X Q, Ye G, et al. Functional characterization, structural basis, and protein engineering of a rare flavonoid 2’-O-glycosyltransferase from Scutellaria baicalensis[J]. Acta Pharm Sin B, 2024, 14(8):3746-3759.
    Chen J, Qiu X J, Sun Z M, et al. Genome-wide analysis of UDP-glycosyltransferase family in Citrus sinensis and characterization of a UGT gene encoding flavonoid 1-2rhamnosyltransferase[J]. Int J Biol Macromol, 2024,280(Pt 2):135752.
    Bao Y O, Zhang M, Li H R, et al. Functional characterization and protein engineering of a glycosyltransferase GcCGT to produce flavone 6, 8-di-C-and 6-C-4'-O-glycosides[J]. ACS Catal, 2024, 14(2):1075-1082.
    Benavente-García O, Castillo J. Update on uses and properties of Citrus flavonoids:New findings in anticancer, cardiovascular, and anti-inflammatory activity[J]. J Agric Food Chem, 2008, 56(15):6185-6205.
    Huong N T, Son N T. Icaritin:A phytomolecule with enormous pharmacological values[J]. Phytochemistry,2023, 213:113772.
    Sajid M, Channakesavula C N, Stone S R, et al. Synthetic biology towards improved flavonoid pharmacokinetics[J]. Biomolecules, 2021, 11(5):754.
    Li H B, Lyv Y, Zhou S H, et al. Microbial cell factories for the production of flavonoids-barriers and opportunities[J]. Bioresour Technol, 2022, 360:127538.
    Lv Y K, Marsafari M, Koffas M, et al. Optimizing oleaginous yeast cell factories for flavonoids and hydroxylated flavonoids biosynthesis[J]. ACS Synth Biol,2019, 8(11):2514-2523.
    Tohge T, de Souza L P, Fernie A R. Current understanding of the pathways of flavonoid biosynthesis in model and crop plants[J]. J Exp Bot, 2017, 68(15):4013-4028.
    Abdulai I L, Kwofie S K, Gbewonyo W S, et al.Multitargeted effects of vitexin and isovitexin on diabetes mellitus and its complications[J]. Sci World J, 2021, 2021:6641128.
    Peng Y, Gan R Y, Li H B, et al. Absorption, metabolism,and bioactivity of vitexin:Recent advances in understanding the efficacy of an important nutraceutical[J]. Crit Rev Food Sci Nutr, 2021, 61(6):1049-1064.
    Singh S, Phillips G N Jr, Thorson J S. The structural biology of enzymes involved in natural product glycosylation[J]. Nat Prod Rep, 2012, 29(10):1201-1237.
    Li J, Shi M, Ma B L, et al. Antitumor activity and safety evaluation of nanaparticle-based delivery of quercetin through intravenous administration in mice[J]. Mater Sci Eng C Mater Biol Appl, 2017, 77:803-810.
    Saija A, Tomaino A, Trombetta D, et al.‘In vitro’antioxidant and photoprotective properties and interaction with model membranes of three new quercetin esters[J]. Eur J Pharm Biopharm, 2003, 56(2):167-174.
    Park S H, Kim H J, Yim S H, et al. Delineation of the role of glycosylation in the cytotoxic properties of quercetin using novel assays in living vertebrates[J]. J Nat Prod,2014, 77(11):2389-2396.
    Liang D M, Liu J H, Wu H, et al. Glycosyltransferases:Mechanisms and applications in natural product development[J]. Chem Soc Rev, 2015, 44(22):8350-8374.
    Nam Y H, Kim E B, Kang J E, et al. Ameliorative effects of flavonoids from Platycodon grandiflorus aerial parts on alloxan-induced pancreatic islet damage in zebrafish[J]. Nutrients, 2023, 15(7):1798.
    Jang D S, Lee Y M, Jeong I H, et al. Constituents of the flowers of Platycodon grandiflorum with inhibitory activity on advanced glycation end products and rat lens aldose reductase in vitro[J]. Arch Pharm Res, 2010, 33(6):875-880.
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    doi: 10.7501/j.issn.0253-2670.2026.01.024
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    鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
    小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
    多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
    红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
    小菇属 Mycena 11 5.26
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