Catalytic repertoire of bacterial bisindole formation

被引:13
作者
Du, Yi-Ling [1 ]
Ryan, Katherine S. [1 ]
机构
[1] Univ British Columbia, Dept Chem, 2036 Main Mall, Vancouver, BC V6T 1Z1, Canada
关键词
CHROMOPYRROLIC ACID SCAFFOLD; ANTICANCER AGENTS; BIOSYNTHETIC PATHWAYS; NATURAL-PRODUCTS; GENE-CLUSTER; INDOLOCARBAZOLE; REBECCAMYCIN; TRYPTOPHAN; STAUROSPORINE; ALKALOIDS;
D O I
10.1016/j.cbpa.2016.01.017
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Bacterial bisindole alkaloids that derive from the oxidative dimerization of L-tryptophan possess diversified biological activities and unique molecular structures. In recent years, the number of bisindoles and their gene clusters has greatly expanded, revealing a large genetic toolbox for the generation of unique structural modifications. In this review, we will discuss the enzymatic pathways leading to diverse bisindoles structures. We will focus on the discovery of molecules through metagenomic mining, the elucidation of new enzymatic mechanisms, and the identification of new biosynthetic protecting group strategies. We will also highlight the newest work in combinatorial engineering and synthetic biology.
引用
收藏
页码:74 / 81
页数:8
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