Ultra-high throughput droplet microfluidics for cultivation and functional screening of environmental microbial strains and consortia.

Abstract

Screening of microbial diversity is critical for discovering novel strains with enhanced biocatalytic capabilities. Traditional cultivation techniques often miss rare or slow-growing microorganisms, limiting our understanding of environmental microbiomes and its practical applications. Droplet-based microfluidics has emerged as a powerful platform for ultra-high-throughput screening of single cells or microbial consortia, encapsulated within microscale droplets that act as precisely controlled bioreactors. This tutorial review focuses on the application of droplet microfluidics for microbial cultivation and isolation, emphasizing advantages such as high throughput and the ability to perform functional assays on colonies originated from individual cells. Unlike previous reviews that broadly address microfluidic technologies or target specific applications like antibiotic resistance or enzyme discovery, we concentrate on protocols specifically designed for the clonal and parallel cultivation of microorganisms from environmental samples. Droplet microfluidics has already shown significant potential in environmental biotechnology, bioremediation, and microbial ecology. Reducing assay volumes and costs while increasing screening efficiency, positions droplet microfluidics as a key technology for the future of environmental microbiology research.

Transparent peer review

To support increased transparency, we offer authors the option to publish the peer review history alongside their article.

View this article’s peer review history

Article information

Article type
Tutorial Review
Submitted
03 Dec 2025
Accepted
07 Apr 2026
First published
15 Apr 2026

Lab Chip, 2026, Accepted Manuscript

Ultra-high throughput droplet microfluidics for cultivation and functional screening of environmental microbial strains and consortia.

L. Potenza, J. Krzak, M. S. Andrzejewski, A. Pyzik and T. Kaminski, Lab Chip, 2026, Accepted Manuscript , DOI: 10.1039/D5LC01115A

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements