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二酮哌嗪类化合物生物合成研究进展
引用本文:李文利,夏娟.二酮哌嗪类化合物生物合成研究进展[J].微生物学通报,2014,41(1):111-121.
作者姓名:李文利  夏娟
作者单位:中国海洋大学 医药学院 教育部海洋药物重点实验室 山东 青岛 266003;中国海洋大学 医药学院 教育部海洋药物重点实验室 山东 青岛 266003
基金项目:国家自然科学基金项目(No. 31171201,31070072);教育部新世纪优秀人才支持计划项目(No. NCET-09-0717)
摘    要:二酮哌嗪类化合物(Diketopiperazines,DKPs)的特征结构是由两个氨基酸通过肽键缩合而成的环二肽(Cyclic dipeptides),稳定的六元环骨架结构使DKPs在药物化学中成为一个重要的药效团,表现出多种生物活性与药理活性,日益引起人们的极大关注。随着现代生物技术和高通量测序技术的飞速发展,人们对DKPs生物合成的分子机制与酶学机理的认识不断深入,DKPs中氨基酸缩合的分子机制主要有两种:非核糖体肽合成酶(Non-ribosomal peptide synthases,NRPSs)途径和环二肽合成酶(Cycliodipeptide synthases,CDPSs)途径。本文就近年来DKPs的生物合成相关研究进展进行了综述。

关 键 词:二酮哌嗪类化合物,非核糖体肽合成酶,环二肽合成酶

Recent advances in diketopiperazines biosynthesis
LI Wen-Li and XIA Juan.Recent advances in diketopiperazines biosynthesis[J].Microbiology,2014,41(1):111-121.
Authors:LI Wen-Li and XIA Juan
Institution:Key Laboratory of Marine Drugs, Chinese Ministry of Education, School of Medicine and Pharmacy, Ocean University of China, Qingdao, Shandong 266003, China;Key Laboratory of Marine Drugs, Chinese Ministry of Education, School of Medicine and Pharmacy, Ocean University of China, Qingdao, Shandong 266003, China
Abstract:Diketopiperazines (DKPs) are derivatives of cyclodipeptides resulted from the condensation of two amino acids. The conformationally constrained six-membered ring makes DKP an attractive pharmacophore in medicinal chemistry. Recently, there has been increasing interest in the natural DKPs due to their diverse bioactivities and pharmacological activities. Advances in modern biotechnologies and high throughput sequencing technologies have promoted our understanding of DKPs biosynthesis both on enzymatic and genetic levels. Biosynthesis of DKPs can be achieved either by non-ribosomal peptide synthases (NRPSs) or cycliodipeptide synthases (CDPSs). This paper provides a brief overview of recent progresses on DKPs biosynthesis.
Keywords:Diketopiperazines  Non-ribosomal peptide synthases  Cycliodipeptide synthases
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