Microfluidic cell culture chambers with nanoporous walls for chemical communication

Thesis: S.M., Massachusetts Institute of Technology, Department of Mechanical Engineering, 2013. === Cataloged from PDF version of thesis. === Includes bibliographical references (pages 63-68). === Reconstruction of phylogenetic trees based on 16S rRNA gene sequencing reveals that so far only a tiny...

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Main Author: Ge, Zhifei, Ph. D. Massachusetts Institute of Technology
Other Authors: Cullen R. Buie.
Format: Others
Language:English
Published: Massachusetts Institute of Technology 2014
Subjects:
Online Access:http://hdl.handle.net/1721.1/85502
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spelling ndltd-MIT-oai-dspace.mit.edu-1721.1-855022019-05-02T16:01:21Z Microfluidic cell culture chambers with nanoporous walls for chemical communication Ge, Zhifei, Ph. D. Massachusetts Institute of Technology Cullen R. Buie. Massachusetts Institute of Technology. Department of Mechanical Engineering. Massachusetts Institute of Technology. Department of Mechanical Engineering. Mechanical Engineering. Thesis: S.M., Massachusetts Institute of Technology, Department of Mechanical Engineering, 2013. Cataloged from PDF version of thesis. Includes bibliographical references (pages 63-68). Reconstruction of phylogenetic trees based on 16S rRNA gene sequencing reveals that so far only a tiny fraction of microbial diversity has been cultured in the laboratory. One major reason behind this "unculturability" is that many microbes function in symbiosis, frequently exchanging metabolites to sustain their own metabolism, while key exchanged metabolites have hardly been identified. To advance the culturability of diverse microbes we propose a method to engineer a microfluidic co-culture platform, the Microfluidic Cell Culture Chambers, which mimics natural conditions for bacterial growth. The key innovation is to physically isolate bacteria while allowing chemical communication through metabolite diffusion. In this work, the device enables both high-throughput screening and real-time observation of bacterial growth. In our method, we use a porous material, poly(2-hydroxyethyl methacrylateco-ethylene dimethacrylate) (HEMA-EDMA), to fabricate a microwell array with 105 individual culture chambers. Pore size of HEMA-EDMA was confirmed by ESEM imaging to be less than 200 nm, adequate for isolating all identified bacteria. We have video-recorded fluorescence labeled Escherichia coli swimming in confined HEMA-EDMA wells and observed that E. coli is unable to travel between culture chambers. Single-strain E. coli is cultured with the device to test biocompatibility of the device. Syntrophic pairs of E. coli were constructed to test the devices' ability to culture inter-dependent species with physical isolation. In future work, culture of quorum sensing strains is suggested to look into inter-species chemical communication in the Microfluidic Cell Culture Chambers. The future device may be applied to recover uncultured microbial species from natural habitat. by Zhifei Ge. S.M. 2014-03-06T15:46:39Z 2014-03-06T15:46:39Z 2013 2013 Thesis http://hdl.handle.net/1721.1/85502 871003444 eng M.I.T. theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. See provided URL for inquiries about permission. http://dspace.mit.edu/handle/1721.1/7582 68 pages application/pdf Massachusetts Institute of Technology
collection NDLTD
language English
format Others
sources NDLTD
topic Mechanical Engineering.
spellingShingle Mechanical Engineering.
Ge, Zhifei, Ph. D. Massachusetts Institute of Technology
Microfluidic cell culture chambers with nanoporous walls for chemical communication
description Thesis: S.M., Massachusetts Institute of Technology, Department of Mechanical Engineering, 2013. === Cataloged from PDF version of thesis. === Includes bibliographical references (pages 63-68). === Reconstruction of phylogenetic trees based on 16S rRNA gene sequencing reveals that so far only a tiny fraction of microbial diversity has been cultured in the laboratory. One major reason behind this "unculturability" is that many microbes function in symbiosis, frequently exchanging metabolites to sustain their own metabolism, while key exchanged metabolites have hardly been identified. To advance the culturability of diverse microbes we propose a method to engineer a microfluidic co-culture platform, the Microfluidic Cell Culture Chambers, which mimics natural conditions for bacterial growth. The key innovation is to physically isolate bacteria while allowing chemical communication through metabolite diffusion. In this work, the device enables both high-throughput screening and real-time observation of bacterial growth. In our method, we use a porous material, poly(2-hydroxyethyl methacrylateco-ethylene dimethacrylate) (HEMA-EDMA), to fabricate a microwell array with 105 individual culture chambers. Pore size of HEMA-EDMA was confirmed by ESEM imaging to be less than 200 nm, adequate for isolating all identified bacteria. We have video-recorded fluorescence labeled Escherichia coli swimming in confined HEMA-EDMA wells and observed that E. coli is unable to travel between culture chambers. Single-strain E. coli is cultured with the device to test biocompatibility of the device. Syntrophic pairs of E. coli were constructed to test the devices' ability to culture inter-dependent species with physical isolation. In future work, culture of quorum sensing strains is suggested to look into inter-species chemical communication in the Microfluidic Cell Culture Chambers. The future device may be applied to recover uncultured microbial species from natural habitat. === by Zhifei Ge. === S.M.
author2 Cullen R. Buie.
author_facet Cullen R. Buie.
Ge, Zhifei, Ph. D. Massachusetts Institute of Technology
author Ge, Zhifei, Ph. D. Massachusetts Institute of Technology
author_sort Ge, Zhifei, Ph. D. Massachusetts Institute of Technology
title Microfluidic cell culture chambers with nanoporous walls for chemical communication
title_short Microfluidic cell culture chambers with nanoporous walls for chemical communication
title_full Microfluidic cell culture chambers with nanoporous walls for chemical communication
title_fullStr Microfluidic cell culture chambers with nanoporous walls for chemical communication
title_full_unstemmed Microfluidic cell culture chambers with nanoporous walls for chemical communication
title_sort microfluidic cell culture chambers with nanoporous walls for chemical communication
publisher Massachusetts Institute of Technology
publishDate 2014
url http://hdl.handle.net/1721.1/85502
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