Identification and Heterologous Production of a Benzoyl-Primed Tricarboxylic Acid Polyketide Intermediate from the Zaragozic Acid A Biosynthetic Pathway

被引:69
作者
Liu, Nicholas [1 ]
Hung, Yiu-Sun [1 ]
Gao, Shu-Shan [1 ]
Hang, Leibniz [2 ]
Zou, Yi [1 ]
Chooi, Yit-Heng [3 ]
Tang, Yi [1 ,2 ]
机构
[1] Univ Calif Los Angeles, Dept Chem & Biomol Engn, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Dept Chem & Biochem, Los Angeles, CA 90095 USA
[3] Univ Western Australia, Sch Mol Sci, Perth, WA 6009, Australia
基金
澳大利亚研究理事会;
关键词
SQUALENE SYNTHASE; STREPTOMYCES-MARITIMUS; NATURAL-PRODUCT; RELAY COMPOUND; GENE-CLUSTER; INHIBITORS; SQUALESTATINS; DISCOVERY; REVEALS; CLONING;
D O I
10.1021/acs.orglett.7b01534
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Zaragozic acid A (1) is a potent cholesterol lowering, polyketide natural product made by various filamentous fungi. The reconstitution of enzymes responsible for the initial steps of the biosynthetic pathway of 1 is accomplished using an engineered fungal heterologous host. These initial steps feature the priming of a benzoic acid starter unit onto a highly reducing polyketide synthase (HRPKS), followed by oxaloacetate extension and product release to generate a tricarboxylic acid containing product 2. The reconstitution studies demonstrated that only three enzymes, HRPKS, citrate synthase, and hydrolase, are needed in A. nidulans to produce the structurally complex product.
引用
收藏
页码:3560 / 3563
页数:4
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