非核糖体肽
聚酮
生物
计算生物学
生物化学
聚酮合酶
生物合成
大肠杆菌
异源的
酶
基因
作者
Meredith A. Skiba,Finn P. Maloney,Qingyun Dan,Amy E. Fraley,Courtney C. Aldrich,Janet L. Smith,William Clay Brown
出处
期刊:Methods in Enzymology
日期:2018-01-01
卷期号:: 45-88
被引量:16
标识
DOI:10.1016/bs.mie.2018.01.035
摘要
The structural diversity and complexity of marine natural products have made them a rich and productive source of new bioactive molecules for drug development. The identification of these new compounds has led to extensive study of the protein constituents of the biosynthetic pathways from the producing microbes. Essential processes in the dissection of biosynthesis have been the elucidation of catalytic functions and the determination of 3D structures for enzymes of the polyketide synthases and nonribosomal peptide synthetases that carry out individual reactions. The size and complexity of these proteins present numerous difficulties in the process of going from gene to structure. Here, we review the problems that may be encountered at the various steps of this process and discuss some of the solutions devised in our and other labs for the cloning, production, purification, and structure solution of complex proteins using Escherichia coli as a heterologous host.
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