薄皮甜瓜UDP-糖基转移酶CmUGT6的生物信息学及原核表达分析OA
Bioinformatic and Prokaryotic Expression Analysis of UDP-Glycosyltransferase CmUGT6 in Oriental Melon(Cucumis melo)
甜瓜(Cucumis melo)中的葫芦素B类化合物具有抗癌、抗炎等重要功效,其化学合成及提取成本较高,因此其生物合成途径关键基因的挖掘及功能解析备受瞩目.截止目前,甜瓜中催化葫芦素B生成葫芦素B-O-β-D-葡萄糖苷的关键基因尚未明确.本研究以西瓜(Citrullus lanatus)中催化葫芦素E糖基化的糖基转移酶(UDP-glycosyltransferase 74F2,UGT74F2)氨基酸序列为探针,在甜瓜基因组中找到与其相似度较高的UDP-糖基转移酶CmUGT6基因.以薄皮甜瓜'玉美人'为材料,克隆到了1 401 bp的CmUGT6基因片段,共编码467个氨基酸.通过生物信息学分析发现,CmUGT6包含糖基转移酶家族的特异性结构域,蛋白带有负电荷,存在46个磷酸化位点、3个N-糖基化位点及4个O-糖基化位点,不存在跨膜结构域,启动子区域存在如激素反应、光反应、厌氧诱导、代谢调节等多个顺式作用元件.CmUGT6基因在薄皮甜瓜的根部和果实中均有表达,且在根中表达量最高.对CmUGT6基因进行原核表达与纯化,获得了100 kD左右的融合蛋白条带.CmUGT6与葫芦素B的分子模拟对接显示,二者结合能为-8.9 kcal/mol.本研究为探讨CmUGT6基因的功能及甜瓜中葫芦素B糖基化修饰机制提供了参考.
Cucurbitacin B-type compounds in melon(Cucumis melo)possess important pharmacological effects such as anticancer and anti-inflammatory activities.Due to the high costs associated with their chemical synthesis and extraction,the mining and functional characterization of key genes involved in their biosynthetic pathways have attracted significant attention.To date,the key gene responsible for catalyzing the conversion of cucurbitacin B to cucurbitacin B-O-β-D-glucoside in melon remains unidentified.In this study,using the amino acid sequence of glycosyltransferases UDP-glycosyltransferase 74F2(UGT74F2),which catalyzed the glycosylation of cucurbitacin E in watermelon(Citrullus lanatus),as a probe,the glycosyltransferases CmUGT6 gene in the melon genome with relatively high similarity was identified.Using the oriental melon variety'Yumeiren'as experimental material,a 1 401 bp fragment of the CmUGT6 gene was cloned,encoding 467 amino acids.Bioinformatics analysis revealed that CmUGT6 contained a specific domain of the glycosyltransferase family,carried a negative charge,and possessed 46 phosphorylation sites,3 N-glycosylation sites,and 4 O-glycosylation sites,with no transmembrane domain.The promoter region contained several cis-acting elements such as hormone responses,light responses,anaerobic induction,and metabolic regulation.Meanwhile,the CmUGT6 gene expressed in both the roots and fruits of the thin-skinned melon,with the highest expression level observed in the roots.Additionally,prokaryotic expression and purification of the CmUGT6 gene yielded a fusion protein band of approximately 100 kD.Molecular docking simulations between CmUGT6 and cucurbitacin B showed a binding energy of-8.9 kcal/mol.This study provides a reference for the subsequent in-depth exploration of the function of the CmUGT6 gene and the mechanism of glycosylation modification of cucurbitacin B in melon.
李晓雪;姚雪洋;任洁;张鸿雁;张娜;刘宁;白继新;纪海鹏;陈存坤
天津市农业科学院农产品保鲜与加工技术研究所(国家农产品保鲜工程技术研究中心(天津))/蔬菜生物育种国家重点实验室/农业农村部农产品贮藏保鲜重点实验室/天津市农产品采后生理与贮藏保鲜重点实验室,天津 300384南开大学生命科学学院,天津 300071天津农学院食品科学与生物工程学院,天津 300392天津农学院食品科学与生物工程学院,天津 300392天津市农业科学院农产品保鲜与加工技术研究所(国家农产品保鲜工程技术研究中心(天津))/蔬菜生物育种国家重点实验室/农业农村部农产品贮藏保鲜重点实验室/天津市农产品采后生理与贮藏保鲜重点实验室,天津 300384辽宁东盛塑业有限公司,营口 115002云南淏丰农业科技开发有限公司,大理 671604天津市农业科学院农产品保鲜与加工技术研究所(国家农产品保鲜工程技术研究中心(天津))/蔬菜生物育种国家重点实验室/农业农村部农产品贮藏保鲜重点实验室/天津市农产品采后生理与贮藏保鲜重点实验室,天津 300384天津市农业科学院农产品保鲜与加工技术研究所(国家农产品保鲜工程技术研究中心(天津))/蔬菜生物育种国家重点实验室/农业农村部农产品贮藏保鲜重点实验室/天津市农产品采后生理与贮藏保鲜重点实验室,天津 300384||云南淏丰农业科技开发有限公司,大理 671604
农业科技
薄皮甜瓜糖基转移酶生物信息学分析基因表达特性原核表达
Oriental MelonGlycosyltransferaseBioinformatics analysisGene expression characteristicsProkaryotic expression
《农业生物技术学报》 2026 (4)
733-742,10
国家自然科学基金面上项目(32472805)天津市自然科学基金(23JCYBJC0084024JCQNJC01120)天津市农业科学院青年创新基金(TJNKY012508)
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