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Kinetics of the cellular intake of a gene expression inducer at high concentrations

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Details

Original languageEnglish
Pages (from-to)2579-2587
Number of pages9
JournalMolecular Biosystems
Volume11
Issue number9
DOIs
Publication statusPublished - 20 Jul 2015
Publication typeA1 Journal article-refereed

Abstract

From in vivo single-event measurements of the transient and steady-state transcription activity of a single-copy lac-ara-1 promoter in Escherichia coli, we characterize the intake kinetics of its inducer (IPTG) from the media. We show that the empirical data are well-fit by a model of intake assuming a bilayer membrane, with the passage through the second layer being rate-limiting, coupled to a stochastic, sub-Poissonian, multi-step transcription process. Using this model, we show that for a wide range of extracellular inducer levels (up to 1.25 mM) the intake process is diffusive-like, suggesting unsaturated membrane permeability. Inducer molecules travel from the periplasm to the cytoplasm in, on average, 31.7 minutes, strongly affecting cells' response time. The novel methodology followed here should aid the study of cellular intake mechanisms at the single-event level.

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Field of science, Statistics Finland