Terminal Alkyne Biosynthesis in Marine Microbes

被引:3
|
作者
Zhu, Xuejun [1 ]
Zhang, Wenjun [1 ,2 ]
机构
[1] Univ Calif Berkeley, Berkeley, CA 94720 USA
[2] Chan Zuckerberg Biohub, San Francisco, CA 94158 USA
关键词
NONRIBOSOMAL PEPTIDE SYNTHETASES; POLYKETIDE SYNTHASE; ALKANE HYDROXYLASE; DIRECTED EVOLUTION; MEMBRANE-PROTEINS; ESCHERICHIA-COLI; CLICK CHEMISTRY; GENE-CLUSTER; FATTY-ACIDS; DESATURASE;
D O I
10.1016/bs.mie.2018.01.040
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The terminal alkyne is a readily derivatized functionality valued for its diverse applications in material synthesis, pharmaceutical science, and chemical biology. The synthetic biology routes to terminal alkynes are highly desired and yet underexplored. Some marine natural products contain a terminal alkyne functionality, and the discovery of the biosynthetic gene clusters for jamaicamide B and carmabin A marked the beginning of a new era in the understanding and engineering of terminal alkyne biosynthesis. In this chapter, we will overview recent advances in understanding the biosynthetic machinery for terminal alkyne synthesis. We will first describe how to elucidate terminal alkyne biosynthetic mechanism through heterologous expression, purification, and in vitro biochemical assays of individual pathway proteins. This will be followed by the description of an in vivo reporting system for the characterization of a membrane-bound bifunctional desaturase/acetylenase involved in terminal alkyne formation. The chapter will also cover the strategies for discovering additional protein homologs for terminal alkyne synthesis from microbes as well as the applications of click chemistry to identify and quantify terminal alkyne-bearing metabolites from microbial cultures. We will conclude this chapter with current challenges and future directions in this field.
引用
收藏
页码:89 / 112
页数:24
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