The single-cell chemostat: an agarose-based, microfluidic device for high-throughput, single-cell studies of bacteria and bacterial communities (original) (raw)
* Corresponding authors
a Center for Systems Biology, Harvard University, Cambridge, MA, USA
b School of Engineering and Applied Sciences, Harvard University, Cambridge, MA, USA
c Department of Molecular and Cellular Biology, Harvard University, Cambridge, MA, USA
E-mail: cluzel@mcb.harvard.edu
Tel: +617-495-8745
Abstract
Optical microscopy of single bacteria growing on solid agarose support is a powerful method for studying the natural heterogeneity in growth and gene expression. While the material properties of agarose make it an excellent substrate for such studies, the sheer number of exponentially growing cells eventually overwhelms the agarose pad, which fundamentally limits the duration and the throughput of measurements. Here we overcome the limitations of exponential growth by patterning agarose pads on the sub-micron-scale. Linear tracks constrain the growth of bacteria into a high density array of linear micro-colonies. Buffer flow through microfluidic lines washes away excess cells and delivers fresh nutrient buffer. Densely patterned tracks allow us to cultivate and image hundreds of thousands of cells on a single agarose pad over 30–40 generations, which drastically increases single-cell measurement throughput. In addition, we show that patterned agarose can facilitate single-cell measurements within bacterial communities. As a proof-of-principle, we study a community of E. coli auxotrophs that can complement the amino acid deficiencies of one another. We find that the growth rate of colonies of one strain decreases sharply with the distance to colonies of the complementary strain over distances of only a few cell lengths. Because patterned agarose pads maintain cells in a chemostatic environment in which every cell can be imaged, we term our device the single-cell chemostat. High-throughput measurements of single cells growing chemostatically should greatly facilitate the study of a variety of microbial behaviours.
You have access to this article
Please wait while we load your content... Something went wrong. Try again?
Supplementary files
- Supplementary movie AVI (3796K)
- Supplementary information PDF (1807K)
- Supplementary movie AVI (904K)
- Supplementary movie AVI (575K)
- Supplementary movie AVI (2144K)
- Supplementary movie AVI (1589K)
- Supplementary movie AVI (407K)
Article information
DOI
https://doi.org/10.1039/C2LC00009A
Article type
Paper
Submitted
03 Jan 2012
Accepted
20 Feb 2012
First published
22 Feb 2012
Download Citation
Lab Chip, 2012,12, 1487-1494
Permissions
The single-cell chemostat: an agarose-based, microfluidic device for high-throughput, single-cell studies of bacteria and bacterial communities
J. R. Moffitt, J. B. Lee and P. Cluzel,Lab Chip, 2012, 12, 1487DOI: 10.1039/C2LC00009A
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.