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海洋芽孢杆菌大环内酯糖基转移酶BmmGT1底物广谱性探究
引用本文:刘权权,刘增智,刘扬,秦文,任鹏飞,李花月,李文利.海洋芽孢杆菌大环内酯糖基转移酶BmmGT1底物广谱性探究[J].中国海洋药物,2017,36(4):11-17.
作者姓名:刘权权  刘增智  刘扬  秦文  任鹏飞  李花月  李文利
作者单位:中国海洋大学教育部海洋药物重点实验室,中国海洋大学教育部海洋药物重点实验室,中国海洋大学教育部海洋药物重点实验室,中国海洋大学教育部海洋药物重点实验室,中国海洋大学教育部海洋药物重点实验室,中国海洋大学教育部海洋药物重点实验室,中国海洋大学教育部海洋药物重点实验室
基金项目:国家自然科学(31070072, 41506157)资助
摘    要:目的 对海洋芽孢杆菌B-9987中糖基转移酶BmmGT1糖基受体的广谱性进行探究。方法 以UDP-D-葡萄糖为糖基供体,与不同糖基受体进行体外酶促反应,通过高效液相色谱(HPLC)检测反应产物,并采用高分辨质谱(HRMS)手段对糖基化产物进行初步鉴定。结果 糖基转移酶BmmGT1能够以UDP-D-葡萄糖为糖基供体,识别两性霉素B以及氯霉素,分别生成两性霉素B双糖基化和单糖基化衍生物以及氯霉素单糖基化衍生物得到三个糖基化产物。结论 糖基转移酶BmmGT1具对糖基受体的选择具有灵活性,可作为潜在的工具酶用于化合物结构多样性研究。

关 键 词:海洋芽孢杆菌  糖基转移酶  体外糖基化反应  底物宽泛性
收稿时间:2017/3/4 0:00:00
修稿时间:2017/4/19 0:00:00

Substrate promiscuity of macrolide glycosyltransferase BmmG1 from marine Bacillus regarding sugar receptor
LIU Quan-quan,LIU Zeng-zhi,LIU Yang,QIN Wen,REN Peng-fei,LI Hua-yue and LI Wen-li.Substrate promiscuity of macrolide glycosyltransferase BmmG1 from marine Bacillus regarding sugar receptor[J].Chinese Journal of Marine Drugs,2017,36(4):11-17.
Authors:LIU Quan-quan  LIU Zeng-zhi  LIU Yang  QIN Wen  REN Peng-fei  LI Hua-yue and LI Wen-li
Institution:Key Laboratory of Marine Drugs,Ministry Education of China,School of Medicine and Pharmacy,Ocean University of China,Key Laboratory of Marine Drugs,Ministry Education of China,School of Medicine and Pharmacy,Ocean University of China,Key Laboratory of Marine Drugs,Ministry Education of China,School of Medicine and Pharmacy,Ocean University of China,Key Laboratory of Marine Drugs,Ministry Education of China,School of Medicine and Pharmacy,Ocean University of China,Key Laboratory of Marine Drugs,Ministry Education of China,School of Medicine and Pharmacy,Ocean University of China,Key Laboratory of Marine Drugs,Ministry Education of China,School of Medicine and Pharmacy,Ocean University of China,Key Laboratory of Marine Drugs,Ministry Education of China,School of Medicine and Pharmacy,Ocean University of China
Abstract:Objective To study the substrate promiscuity of macrolide glycosyltransferase BmmG1 from marine Bacillus regarding sugar receptor. Methods In vitro enzymatic reactions were set up using different antibiotics as sugar receptors and UDP-D-glucose as sugar donor, which were followed by HPLC and HRMS analysis. Results BmmGT1 is able to transfer glucosyl moiety onto Amphotericin B (Amph B) and Chloramphenicol (Chl), leading to formation of two glucosylated Amph B derivatives and one glucosylated Chl derivative, respectively. Conclusion BmmGT1 exhibits broad substrate specificity with regards to sugar receptor, which demonstrated its potential application as an effective tool enzyme in structure diversification of natural products.
Keywords:marine  Bacillus  glycosyltransferase  in  vitro glycosylation  reaction  substrate  promiscuity
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