CELL-FREE SYNTHESIS OF POLYKETIDES BY RECOMBINANT ERYTHROMYCIN POLYKETIDE SYNTHASES

被引:94
作者
PIEPER, R
LUO, GL
CANE, DE
KHOSLA, C
机构
[1] STANFORD UNIV,DEPT CHEM ENGN,STANFORD,CA 94305
[2] BROWN UNIV,DEPT CHEM,PROVIDENCE,RI 02912
关键词
D O I
10.1038/378263a0
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Modular polyketide synthases (PKSs) are complex multi-enzyme proteins that catalyse the bacterial biosynthesis of many pharmaceutically useful polyketides. The PKSs are organized into a series of modules, each containing the active catalytic sites required for one step in the synthesis process(1,4). Here we report a method for cell-free enzymatic synthesis of 6-deoxyerythronolide B (6-dEB), the parent molecule of the antibiotic erythromycin A, using recombinant 6-deoxyerythronolide B synthase (DEBS), a modular PKS with at least 28 distinct active sites. We have also synthesized in vitro a triketide lactone by using a truncated mutant of DEBS. The availability of such cell-free synthetic routes will allow direct investigation of the structural and mechanistic basis for the unusual combination of high substrate specificity(5-10) and tolerance to genetic reprogramming(2,11-15) found in this enzyme family.
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页码:263 / 266
页数:4
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