Department of Molecular Biology, Institute of Biochemistry, Faculty of Biology, University of Warsaw, Miecznikowa 1, Warsaw 02-096, Poland.
Institute of Physical Chemistry of Polish Academy of Sciences, Kasprzaka 44/52, Warsaw 01-224, Poland.
Anal Chem. 2024 Oct 8;96(40):15931-15940. doi: 10.1021/acs.analchem.4c02979. Epub 2024 Sep 25.
Traditional bacterial isolation methods are often costly, have limited throughput, and may not accurately reflect the true microbial community composition. Consequently, identifying rare or slow-growing taxa becomes challenging. Over the past decade, a new approach has been proposed to replace traditional flasks or multiwell plates with ultrahigh-throughput droplet microfluidic screening assays. In this study, we present a novel passive droplet-based method designed for isolating proteolytic microorganisms, which are crucial in various biotechnology industries. Following the encapsulation of single cells in gelatin microgel compartments and their subsequent clonal cultivation, microcultures are passively sorted at high throughput based on the deformability of droplets. Our novel chip design offers a 50-fold improvement in throughput compared to a previously developed deformability-based droplet sorter. This method expands an array of droplet-based microbial enrichment assays and significantly reduces the time and resources required to isolate proteolytic bacteria strains.
传统的细菌分离方法通常成本高昂、通量有限,并且可能无法准确反映真实的微生物群落组成。因此,鉴定稀有或生长缓慢的分类群变得具有挑战性。在过去的十年中,已经提出了一种新的方法,即用超高通量液滴微流控筛选测定法代替传统的烧瓶或多孔板。在这项研究中,我们提出了一种新的基于被动液滴的方法,用于分离在各种生物技术产业中至关重要的蛋白酶微生物。在将单细胞包封在明胶微凝胶隔室中并随后进行克隆培养之后,基于液滴的变形性以高通量进行微培养的被动分选。与之前开发的基于变形性的液滴分选器相比,我们的新型芯片设计将通量提高了 50 倍。该方法扩展了一系列基于液滴的微生物富集测定法,并大大减少了分离蛋白酶细菌株所需的时间和资源。