Exploiting Cell-Free Systems: Implementation and Debugging of a System of Biotransformations

被引:74
作者
Bujara, Matthias [1 ]
Schuemperli, Michael [1 ]
Billerbeek, Sonja [1 ]
Heinemann, Matthias [2 ]
Panke, Sven [1 ]
机构
[1] Swiss Fed Inst Technol, Dept Biosyst Sci & Engn, Bioproc Lab, CH-4058 Basel, Switzerland
[2] Swiss Fed Inst Technol, Inst Mol Syst Biol, Zurich, Switzerland
关键词
cell-free synthesis; carbohydrate synthesis; multi-enzyme catalysis; dihydroxyacetone phosphate; aldolase; FREE PROTEIN-SYNTHESIS; ESCHERICHIA-COLI K-12; DIHYDROXYACETONE PHOSPHATE; SYNTHETIC BIOLOGY; ORGANIC-SYNTHESIS; ENZYMATIC ROUTES; AMP NUCLEOSIDASE; FREE EXPRESSION; IN-VITRO; ENZYMES;
D O I
10.1002/bit.22666
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
The orchestration of a multitude of enzyme. catalysts allows cells to carry out complex and thermodynamically unfavorable chemical conversions. In an effort to, recruit these advantages for in vitro biotransformations, we have assembled a 10-step catalytic system-a system of biotransformations (SBT)-for the synthesis of unnatural inonosaccharides based on the versatile building block dihydroxyacetone phosphate (DHAP). To facilitate the assembly of such a network, we have insulated a production;. pathway from Escherichia coli's central carbon metabolism. This pathway consists of the endogenous glycolysis without triose-phosphate isomerase to enable accumulation of DHAP and was completed with lactate dehydrogenase to regenerate NAD(+). It could be readily extended for the synthesis of unnatural sugar molecules, such as the unnatural monosaccharide phosphate 5,6,7-trideoxy-D-threo-heptulose-1-phosphate from DHAP and butanal. Insulation required in particular inactivation of the amn gene encoding the AMP nucleosidase, which otherwise led to glucose-independent DHAP production from adenosine phosphates. The work demonstrates that a sufficiently insulated in vitro multi-step enzymatic system can be readily assembled from central carbon metabolism pathways. Biotechnol. Bioeng. 2010;106: 376-389. (C) 2010 Wiley Periodicals, Inc.
引用
收藏
页码:376 / 389
页数:14
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