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research article

An automated microreactor for semi-continuous biosensor measurements

Buffi, Nina  
•
Beggah, Siham
•
Truffer, Frederic
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2016
Lab on a Chip

Living bacteria or yeast cells are frequently used as bioreporters for the detection of specific chemical analytes or conditions of sample toxicity. In particular, bacteria or yeast equipped with synthetic gene circuitry that allows the production of a reliable non-cognate signal (e.g., fluorescent protein or bioluminescence) in response to a defined target make robust and flexible analytical platforms. We report here how bacterial cells expressing a fluorescence reporter (“bactosensors”), which are mostly used for batch sample analysis, can be deployed for automated semi-continuous target analysis in a single concise biochip. Escherichia coli-based bactosensor cells were continuously grown in a 13 or 50 nanoliter-volume reactor on a two-layered polydimethylsiloxane-on-glass microfluidic chip. Physiologically active cells were directed from the nl-reactor to a dedicated sample exposure area, where they were concentrated and reacted in 40 minutes with the target chemical by localized emission of the fluorescent reporter signal. We demonstrate the functioning of the bactosensor-chip by the automated detection of 50 μgarsenite-As l−1 in water on consecutive days and after a one-week constant operation. Best induction of the bactosensors of 6–9-fold to 50 μg l−1 was found at an apparent dilution rate of 0.12 h−1 in the 50 nl microreactor. The bactosensor chip principle could be widely applicable to construct automated monitoring devices for a variety of targets in different environments.

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Type
research article
DOI
10.1039/C6LC00119J
Web of Science ID

WOS:000374224900011

Author(s)
Buffi, Nina  
Beggah, Siham
Truffer, Frederic
Geiser, Martial
Van Lintel, Harald  
Renaud, Philippe  
Van Der Meer, Jan Roelof
Date Issued

2016

Publisher

Royal Society of Chemistry

Published in
Lab on a Chip
Volume

16

Issue

8

Start page

1383

End page

1392

Editorial or Peer reviewed

REVIEWED

Written at

EPFL

EPFL units
LMIS4  
Available on Infoscience
April 18, 2016
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/125734
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