A High-Throughput Droplet-based Method to Facilitate Microbial Conjugation.

Droplet microfluidic platforms have been broadly used to facilitate DNA transfer in mammalian and bacterial hosts via methods such as transformation, transfection, and conjugation, as introduced in our previous work. Herein, we recapitulate our method for conjugal DNA transfer between strains in a droplet for increased conjugation efficiency and throughput of an otherwise laborious protocol. By co-incubating the donor and recipient strains in droplets, our method confines cells into close proximity allowing for increased cell-to-cell interactions. This methodology is advantageous in its potential to automate and accelerate the genetic modification of undomesticated organisms that may be difficult to cultivate. This device is also designed for modularity and can be integrated into a variety of experimental workflows in which fine-tuning of donor-to-recipient cell ratios, growth rates, and media substrate concentrations may be necessary. Key features • Builds on previous -conjugation methods introduced by Brophy et al. [1] increasing the throughput by flowing the donors and recipients into a droplet microfluidic chip. • Experiments performed on this chip increase conjugation efficiency as compared to conjugation performed traditionally by co-incubating the cells in free culture. • This platform enables fine-tuning of experimental parameters, e.g., donor-to-recipient cell ratios, induction concentration, and incubation times, all critical factors in engineering undomesticated organisms. • Adaptable for upstream automation of bacterial cultivation and downstream analysis of transconjugants encapsulated in droplets.