Chair for Bioprocess Engineering, Department of Biochemical and Chemical Engineering, TU Dortmund University, D-44227 Dortmund, Germany.
Institute of Pharmaceutical Sciences, University of Freiburg, D-79104 Freiburg, Germany.
Biomolecules. 2021 Apr 16;11(4):590. doi: 10.3390/biom11040590.
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 ADK, PPK2, and PPK2 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.
多酶级联反应在最近几十年中在复杂产物的合成方面变得越来越重要。与单一生物转化相比,它们具有以下优势:可以在不纯化反应中间体的情况下合成复杂分子,更容易处理不稳定的中间体,并通过偶联平衡处理不利的热力学。在这项研究中,成功开发了一种由 ADK、PPK2 和 PPK2 组成的四酶级联反应,用于从腺苷中合成 ATP,与环状 GMP-AMP 合酶(cGAS)偶联,催化环状 GMP-AMP(2'3'-cGAMP)的形成。2'3'-cGAMP 的合成速率与单步反应中达到的最大反应速率相当。对底物、辅因子和酶浓度进行迭代优化,导致每摩尔腺苷产生 0.08 摩尔 2'3'-cGAMP 的总产率,这与化学合成相当。所建立的酶级联反应能够从 GTP 和廉价的腺苷以及多磷酸盐在生物催化一锅反应中合成 2'3'-cGAMP,展示了多酶级联反应在合成具有药学相关性的产品方面的性能。