Institute for Chemical and Bioengineering, Department of Chemistry & Applied Biosciences, ETH Zürich, Vladimir Prelog Weg 1, 8093, Zürich, Switzerland.
Chemistry of Biogenic Resources, Technical University of Munich, Campus Straubing for Biotechnology and Sustainability, Schulgasse 16, 94315, Straubing, Germany.
Angew Chem Int Ed Engl. 2024 Dec 2;63(49):e202409610. doi: 10.1002/anie.202409610. Epub 2024 Nov 6.
Recent decades have seen a dramatic increase in the commercial use of biocatalysts, transitioning from energy-intensive traditional chemistries to more sustainable methods. Current enzyme engineering techniques, such as directed evolution, require the generation and testing of large mutant libraries to identify optimized variants. Unfortunately, conventional screening methods are unable to screen such large libraries in a robust and timely manner. Droplet-based microfluidic systems have emerged as a powerful high-throughput tool for library screening at kilohertz rates. Unfortunately, almost all reported systems are based on fluorescence detection, restricting their use to a limited number of enzyme types that naturally convert fluorogenic substrates or require the use of surrogate substrates. To expand the range of enzymes amenable to evolution using droplet-based microfluidic systems, we present an absorbance-activated droplet sorter that allows droplet sorting at kilohertz rates without the need for optical monitoring of the microfluidic system. To demonstrate the utility of the sorter, we rapidly screen a 10-member aldehyde dehydrogenase library towards D-glyceraldehyde using a NADH mediated coupled assay that generates WST-1 formazan as the colorimetric product. We successfully identify a variant with a 51 % improvement in catalytic efficiency and a significant increase in overall activity across a broad substrate spectrum.
近几十年来,生物催化剂的商业用途显著增加,已经从能源密集型的传统化学方法转变为更加可持续的方法。目前的酶工程技术,如定向进化,需要生成和测试大量的突变文库,以确定优化的变体。不幸的是,传统的筛选方法无法快速有效地筛选如此庞大的文库。基于液滴的微流控系统已成为高通量文库筛选的强大工具,其筛选速度可达千赫兹。然而,几乎所有报道的系统都基于荧光检测,这限制了它们在酶的使用范围,仅适用于那些天然转化为荧光底物或需要使用替代底物的有限数量的酶类。为了扩展适用于基于液滴的微流控系统的进化的酶的范围,我们提出了一种基于吸光度的液滴分拣器,该分拣器允许在不依赖于微流控系统的光学监测的情况下,以千赫兹的速率进行液滴分拣。为了证明该分拣器的实用性,我们使用 NADH 介导的偶联测定法,对 10 个成员的醛脱氢酶文库进行了 D-甘油醛的快速筛选,该测定法生成 WST-1 甲臜作为比色产物。我们成功地鉴定出一种变体,其催化效率提高了 51%,在广泛的底物谱中整体活性显著提高。