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Quantitative Biology

ISSN 2095-4689

ISSN 2095-4697(Online)

CN 10-1028/TM

邮发代号 80-971

Quantitative Biology  2018, Vol. 6 Issue (2): 129-141   https://doi.org/10.1007/s40484-018-0143-8
  本期目录
Developing a low-cost milliliter-scale chemostat array for precise control of cellular growth
David Skelding1(), Samuel F M Hart1, Thejas Vidyasagar2, Alexander E Pozhitkov1, Wenying Shou1()
1. Division of Basic Sciences, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA
2. University of Washington, Seattle, WA 98195-3770, USA
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Abstract

Background: Multiplexed milliliter-scale chemostats are useful for measuring cell physiology under various degrees of nutrient limitation and for carrying out evolution experiments. In each chemostat, fresh medium containing a growth rate-limiting metabolite is pumped into the culturing chamber at a constant rate, while culture effluent exits at an equal rate. Although such devices have been developed by various labs, key parameters — the accuracy, precision, and operational range of flow rate — are not explicitly characterized.

Methods: Here we re-purpose a published multiplexed culturing device to develop a multiplexed milliliter-scale chemostat. Flow rates for eight chambers can be independently controlled to a wide range, corresponding to population doubling times of 3~13 h, without the use of expensive feedback systems.

Results: Flow rates are precise, with the maximal coefficient of variation among eight chambers being less than 3%. Flow rates are accurate, with average flow rates being only slightly below targets, i.e., 3%–6% for 13-h and 0.6%–1.0% for 3-h doubling times. This deficit is largely due to evaporation and should be correctable. We experimentally demonstrate that our device allows accurate and precise quantification of population phenotypes.

Conclusions: We achieve precise control of cellular growth in a low-cost milliliter-scale chemostat array, and show that the achieved precision reduces the error when measuring biological processes.

Key wordschemostats    microbes    evolution    physiology    multiplex
收稿日期: 2017-11-24      出版日期: 2018-06-11
Corresponding Author(s): David Skelding,Wenying Shou   
 引用本文:   
. [J]. Quantitative Biology, 2018, 6(2): 129-141.
David Skelding, Samuel F M Hart, Thejas Vidyasagar, Alexander E Pozhitkov, Wenying Shou. Developing a low-cost milliliter-scale chemostat array for precise control of cellular growth. Quant. Biol., 2018, 6(2): 129-141.
 链接本文:  
https://academic.hep.com.cn/qb/CN/10.1007/s40484-018-0143-8
https://academic.hep.com.cn/qb/CN/Y2018/V6/I2/129
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1 Watson, T. G. (1972) The present status and future prospects of the turbidostat. J. Appl. Chem. Biotechnol., 22, 229–243
https://doi.org/10.1002/jctb.5020220206
2 Takahashi, C. N., Miller, A. W., Ekness, F., Dunham, M. J. and Klavins, E. (2015) A low cost, customizable turbidostat for use in synthetic circuit characterization. ACS Synth. Biol., 4, 32–38
https://doi.org/10.1021/sb500165g pmid: 25036317
3 Novick, A. and Szilard, L. (1950) Experiments with the chemostat on spontaneous mutations of bacteria. Proc. Natl. Acad. Sci. USA, 36, 708–719
https://doi.org/10.1073/pnas.36.12.708 pmid: 14808160
4 Miller, A.W., Befort, C., Kerr, E.O., and Dunham, M. J. (2013) Design and use of multiplexed chemostat arrays. JoVEJ. Vis. Exp., 72, e50262
pmid: 23462663
5 Matteau, D., Baby, V., Pelletier, S. and Rodrigue, S. (2015) A small-volume, low-cost, and versatile continuous culture device. PLoS One, 10, e0133384
https://doi.org/10.1371/journal.pone.0133384 pmid: 26197065
6 Callens, C., Coelho, N. C., Miller, A. W., Sananes, M. R. D., Dunham, M. J., Denoual, M. and Coudreuse, D. (2017) A multiplex culture system for the long-term growth of fission yeast cells. Yeast, 34, 343–355
https://doi.org/10.1002/yea.3237 pmid: 28426144
7 MATERIALS DATA _2003_ version 3.doc- materials.pdf.. Available from:
8 Microsoft Word- Teflon- teflon.pdf. Available from:
9 Varma, A. and Palsson, B.O. (1994) Stoichiometric flux balance models quantitatively predict growth and metabolic by-product secretion in wild-type Escherichia coli W3110. Appl. Environ. Microbiol., 60, 3724–3731
10 Shou, W., Ram, S. and Vilar, J. M. (2007) Synthetic cooperation in engineered yeast populations. Proc. Natl. Acad. Sci. USA, 104, 1877–1882
https://doi.org/10.1073/pnas.0610575104 pmid: 17267602
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