A Multi-Enzyme Cascade Reaction for the Production of 2′3′-cGAMP

被引:28
作者
Becker, Martin [1 ]
Nikel, Patrick [1 ]
Andexer, Jennifer N. [2 ]
Luetz, Stephan [1 ]
Rosenthal, Katrin [1 ]
机构
[1] TU Dortmund Univ, Dept Biochem & Chem Engn, Chair Bioproc Engn, D-44227 Dortmund, Germany
[2] Univ Freiburg, Inst Pharmaceut Sci, D-79104 Freiburg, Germany
关键词
enzyme cascade; polyphosphate kinase; multi-step reaction; ATP; 2; 3; '-cGAMP; cGAS; cyclic dinucleotide (CDN); in vitro biotransformation; biocatalysis;
D O I
10.3390/biom11040590
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
Multi-enzyme cascade reactions for the synthesis of complex products have gained importance in recent decades. Their advantages compared to single biotransformations include the possibility to synthesize complex molecules without purification of reaction intermediates, easier handling of unstable intermediates, and dealing with unfavorable thermodynamics by coupled equilibria. In this study, a four-enzyme cascade consisting of ScADK, AjPPK2, and SmPPK2 for ATP synthesis from adenosine coupled to the cyclic GMP-AMP synthase (cGAS) catalyzing cyclic GMP-AMP (2 ' 3 '-cGAMP) formation was successfully developed. The 2 ' 3 '-cGAMP synthesis rates were comparable to the maximal reaction rate achieved in single-step reactions. An iterative optimization of substrate, cofactor, and enzyme concentrations led to an overall yield of 0.08 mole 2 ' 3 '-cGAMP per mole adenosine, which is comparable to chemical synthesis. The established enzyme cascade enabled the synthesis of 2 ' 3 '-cGAMP from GTP and inexpensive adenosine as well as polyphosphate in a biocatalytic one-pot reaction, demonstrating the performance capabilities of multi-enzyme cascades for the synthesis of pharmaceutically relevant products.
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页数:13
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