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海洋放线菌Kocuria sp.次级代谢产物的研究
引用本文:姚 蓉,马 明,付 晖,单伟光,林文翰. 海洋放线菌Kocuria sp.次级代谢产物的研究[J]. 中国海洋药物, 2017, 36(3): 11-17
作者姓名:姚 蓉  马 明  付 晖  单伟光  林文翰
作者单位:浙江工业大学药学院,北京大学天然药物及仿生药物国家重点实验室,浙江工业大学药学院,浙江工业大学药学院,北京大学天然药物及仿生药物国家重点实验室
基金项目:国家自然科学基金项目(41376127)
摘    要:目的 研究海洋放线菌Kocuria sp.的次级代谢产物。方法 菌株摇瓶发酵,采用现代色谱学方法(硅胶柱色谱、Sephadex LH-20凝胶柱色谱、半制备HPLC),对发酵产物进行分离,利用现代波谱学技术对化合物进行结构鉴定。结果 从海洋放线菌Kocuria sp.发酵液的乙酸乙酯萃取部分分离得到16个单体化合物:环(L-苯丙氨酸-L-脯氨酸)2 (1)、环(L-色氨酸-L-脯氨酸) (2)、环(L-色氨酸-D-脯氨酸) (3)、环(L-苯丙氨酸-D-脯氨酸) (4)、环(L-羟脯氨酸-L-苯丙氨酸) (5)、环(D-羟脯氨酸-L-苯丙氨酸) (6)、环(L-羟脯氨酸-L-酪氨酸) (7)、环(L-异亮氨酸-D-脯氨酸) (8)、环(L-亮氨酸-D-脯氨酸) (9)、环(L-亮氨酸-L-脯氨酸) (10)、环(L-苯丙氨酸-L-酪氨酸) (11)、环(L-亮氨酸-D-酪氨酸) (12)、环(L-亮氨酸-L-苯丙氨酸) (13)、环(D-缬氨酸-L-苯丙氨酸) (14)、环(D-亮氨酸-甘氨酸) (15)、环(D-异亮氨酸-甘氨酸) (16)。结论 海洋放线菌Kocuria sp.可产生结构丰富多样的环肽类化合物,所有化合物均首次从Kocuria属放线菌中分离得到。

关 键 词:海洋放线菌  Kocuria属  次级代谢产物  环肽
收稿时间:2017-01-07
修稿时间:2017-03-19

Studies on the secondary metabolites of marine actinomycete Kocuria sp.
YAO Rong,MA Ming,FU Hui,SHAN Wei-guang and LIN Wen-han. Studies on the secondary metabolites of marine actinomycete Kocuria sp.[J]. Chinese Journal of Marine Drugs, 2017, 36(3): 11-17
Authors:YAO Rong  MA Ming  FU Hui  SHAN Wei-guang  LIN Wen-han
Affiliation:College of Pharmaceutical Science,Zhejiang University of Technology,Hangzhou,State Key Laboratory of Natural and Biomimetic Drugs,Peking University,College of Pharmaceutical Science,Zhejiang University of Technology,Hangzhou,College of Pharmaceutical Science,Zhejiang University of Technology,Hangzhou,State Key Laboratory of Natural and Biomimetic Drugs,Peking University
Abstract:Objective To study the secondary metabolites of marine actinomycete Kocuria sp. Methods The strain was cultured in flasks. The fermentation products were separated by column chromatography (silica gel and Sephadex LH-20), and semi-preparative HPLC. The structures of the purified compounds were elucidated by spectroscopic analyses. Results Sixteen compounds were obtained from the ethyl acetate extracts and were identified as: cyclo(L-Phe-L-Pro)2 (1), cyclo(L-Trp-L-Pro) (2), cyclo(L-Trp-D-Pro) (3), cyclo(L-Phe-D-Pro) (4), cyclo(L-4-hydroxyl-Pro-L-Phe) (5), cyclo(D-4-hydroxyl-Pro-L-Phe) (6), cyclo(L-4-hydroxyl-Pro-L-Tyr) (7), cyclo(L-Ile-D-Pro) (8), cyclo(L-Leu-D-Pro) (9), cyclo(L-Leu-L-Pro) (10), cyclo(L-Phe-L-Tyr) (11), cyclo(L-Leu-D-Tyr) (12), cyclo(L-Leu-L-Phe) (13), cyclo(D-Val-L-Phe) (14), cyclo(D-Leu-Gly) (15), and cyclo(D-Ile-Gly) (16). Conclusion The marine actinomycete Kocuria sp. could produce cyclopeptides with diverse structures, and all the compounds were isolated from the genus Kocuria for the first time.
Keywords:marine actinomycete   Kocuria   secondary metabolites   cyclopeptide
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