Structure and mechanism of the 6-deoxyerythronolide B synthase

被引:218
作者
Khosla, Chaitan [1 ]
Tang, Yinyan
Chen, Alice Y.
Schnarr, Nathan A.
Cane, David E.
机构
[1] Stanford Univ, Dept Chem Engn, Stanford, CA 94305 USA
[2] Stanford Univ, Dept Chem, Stanford, CA 94305 USA
[3] Brown Univ, Dept Chem, Providence, RI 02912 USA
关键词
acyl carrier protein; acyl transferase; erythromycin; ketosynthase; polyketide synthase;
D O I
10.1146/annurev.biochem.76.053105.093515
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
6-Deoxyerythronolide B, the macrocyclic aglycone of the antibiotic erythromycin, is synthesized by a polyketide synthase (PKS) that has emerged as the prototypical modular megasynthase. A variety of molecular biological, protein chemical, and biosynthetic experiments over the past two decades have yielded insights into its mechanistic features. More recently, high-resolution structural images of portions of the 6-deoxyerythronolide B svnthase have provided a platform for interpreting this wealth of biochemical data, while at the same time presenting a fundamentally new basis for the design of more detailed investigations into this remarkable enzyme. For example, the critical roles of domain-domain interactions and non-conserved linkers, as well as large interdomain movements in the structure and function of modular PKSs, have been highlighted. In turn, these insights point the way for-ward for more sophisticated and efficient biosynthetic engineering of complex polyketide natural products.
引用
收藏
页码:195 / 221
页数:27
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