Institute for Biological Interfaces (IBG1), Karlsruhe Institute of Technology (KIT), Hermann-von-Helmholtz-Platz 1, Karlsruhe, 76344, Germany.
Department of Genetics and Cytology, National Research Centre (NRC), 33 El Buhouth St., Cairo, 12622, Egypt.
Chemistry. 2022 Nov 25;28(66):e202202157. doi: 10.1002/chem.202202157. Epub 2022 Sep 29.
All-enzyme hydrogel (AEH) particles with a hydrodynamic diameter of up to 120 nm were produced intracellularly with an Escherichia coli-based in vivo system. The inCell-AEH nanoparticles were generated from polycistronic vectors enabling simultaneous expression of two interacting enzymes, the Lactobacillus brevis alcohol dehydrogenase (ADH) and the Bacillus subtilis glucose-1-dehydrogenase (GDH), fused with a SpyCatcher or SpyTag, respectively. Formation of inCell-AEH was analyzed by dynamic light scattering and atomic force microscopy. Using the stereoselective two-step reduction of a prochiral diketone substrate, we show that the inCell-AEH approach can be advantageously used in whole-cell flow biocatalysis, by which flow reactors could be operated for >4 days under constant substrate perfusion. More importantly, the inCell-AEH concept enables the recovery of efficient catalyst materials for stable flow bioreactors in a simple and economical one-step procedure from crude bacterial lysates. We believe that our method will contribute to further optimization of sustainable biocatalytic processes.
采用基于大肠杆菌的体内系统,在细胞内制备了直径高达 120nm 的全酶水凝胶 (AEH) 颗粒。InCell-AEH 纳米颗粒是由多顺反子载体产生的,能够同时表达两种相互作用的酶,即短乳杆菌醇脱氢酶 (ADH) 和枯草芽孢杆菌葡萄糖-1-脱氢酶 (GDH),分别与 SpyCatcher 或 SpyTag 融合。通过动态光散射和原子力显微镜分析了 InCell-AEH 的形成。使用前手性二酮底物的立体选择性两步还原,我们表明,InCell-AEH 方法可以在全细胞流动生物催化中有利地使用,通过该方法,在恒定底物灌注下,流动反应器可以持续运行超过 4 天。更重要的是,InCell-AEH 概念能够从粗菌裂解物中以简单经济的一步法从粗菌裂解物中回收高效的催化剂材料,用于稳定的流动生物反应器。我们相信,我们的方法将有助于进一步优化可持续的生物催化过程。