Department of Biochemistry, Molecular Biology & Biophysics, University of Minnesota, 140 Gortner Laboratory, 1479 Gortner Avenue, Saint Paul, MN 55108, USA.
Heterogeneous biocatalysis laboratory, Instituto de Síntesis Química y Catálisis Homogénea (ISQCH-CSIC), University of Zaragoza, C/ Pedro Cerbuna 12, 50009, Zaragoza, Spain; ARAID, Aragon I+D foundation, Zaragoza, Spain.
Curr Opin Chem Biol. 2019 Apr;49:97-104. doi: 10.1016/j.cbpa.2018.11.021. Epub 2018 Dec 11.
During the past decades, biocatalysis has made important contributions to chemical manufacturing by using both whole-cell and cell-free biotransformation reactions. More recently, multi-enzyme systems that can run step-wise reactions in one-pot with high selectivity are increasingly being developed. The use of multiple isolated enzymes to perform a series of reactions offers operational and process advantages over the use of living or resting cells, but such cell free processes need to be optimized to meet industrial productivity and titer requirements. Major advances have been made in enzyme discovery and engineering in order to access new activities and increase catalytic efficiency and stability. Yet, the efficient operation of multiple enzymatic reactions simultaneously requires new approaches for optimization. Inspired by the spatial organization of metabolic networks in cells, researchers have recently begun to exploit these mechanisms to increase the efficiency of multi-enzyme systems. This review highlights recent examples that adopt cellular enzyme co-localization mechanisms for multi-enzyme biocatalysis, which include enzyme attachment to preformed surfaces, enzyme clustering and enzyme encapsulation. Co-immobilization of multiple enzymes is achieved by merging tools from protein engineering and synthetic biology with approaches from material sciences.
在过去几十年中,生物催化通过使用全细胞和无细胞生物转化反应为化学制造做出了重要贡献。最近,能够以高选择性一步一步进行多步反应的多酶系统越来越多地被开发出来。与使用活细胞或休眠细胞相比,使用多个分离酶来进行一系列反应具有操作和过程上的优势,但此类无细胞过程需要进行优化以满足工业生产力和滴度要求。为了获得新的活性并提高催化效率和稳定性,在酶的发现和工程方面已经取得了重大进展。然而,要有效地同时进行多个酶反应,需要新的优化方法。受细胞内代谢网络空间组织的启发,研究人员最近开始利用这些机制来提高多酶系统的效率。这篇综述重点介绍了最近采用细胞内酶共定位机制进行多酶生物催化的例子,其中包括酶附着在预先形成的表面上、酶聚类和酶包封。通过将蛋白质工程和合成生物学的工具与材料科学的方法相结合,可以实现多种酶的共固定化。