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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 words:
chemostats
microbes
evolution
physiology
multiplex
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收稿日期: 2017-11-24
出版日期: 2018-06-11
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Corresponding Author(s):
David Skelding,Wenying Shou
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