Biosynthesis of aromatic polyketides in microorganisms using type II polyketide synthases

被引:63
作者
Wang, Jia [1 ]
Zhang, Ruihua [2 ]
Chen, Xin [1 ]
Sun, Xinxiao [1 ]
Yan, Yajun [2 ]
Shen, Xiaolin [1 ]
Yuan, Qipeng [1 ]
机构
[1] Beijing Univ Chem Technol, State Key Lab Chem Resource Engn, 15 Beisanhuan East Rd, Beijing 100029, Peoples R China
[2] Univ Georgia, Coll Engn, Sch Chem Mat & Biomed Engn, Athens, GA 30602 USA
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
Aromatic polyketides; Type II polyketide synthases; Starter units; Chain length; Tailoring reactions; STREPTOMYCES-PEUCETIUS; GENE-CLUSTER; DAUNORUBICIN BIOSYNTHESIS; ANTIBIOTIC BIOSYNTHESIS; HETEROLOGOUS EXPRESSION; ENGINEERED BIOSYNTHESIS; TAILORING ENZYMES; CRYSTAL-STRUCTURE; TETRACENOMYCIN-C; STARTER UNIT;
D O I
10.1186/s12934-020-01367-4
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Aromatic polyketides have attractive biological activities and pharmacological properties. Different from other polyketides, aromatic polyketides are characterized by their polycyclic aromatic structure. The biosynthesis of aromatic polyketides is usually accomplished by the type II polyketide synthases (PKSs), which produce highly diverse polyketide chains by sequential condensation of the starter units with extender units, followed by reduction, cyclization, aromatization and tailoring reactions. Recently, significant progress has been made in characterization and engineering of type II PKSs to produce novel products and improve product titers. In this review, we briefly summarize the architectural organizations and genetic contributions of PKS genes to provide insight into the biosynthetic process. We then review the most recent progress in engineered biosynthesis of aromatic polyketides, with emphasis on generating novel molecular structures. We also discuss the current challenges and future perspectives in the rational engineering of type II PKSs for large scale production of aromatic polyketides.
引用
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页数:11
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