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Continuous cultivation of fission yeast: Analysis of single‐cell protein synthesis kinetics
Author(s) -
Agar D. W.,
Bailey J. E.
Publication year - 1981
Publication title -
biotechnology and bioengineering
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.136
H-Index - 189
eISSN - 1097-0290
pISSN - 0006-3592
DOI - 10.1002/bit.260231014
Subject(s) - schizosaccharomyces pombe , population , biological system , cell division , population balance equation , kinetics , yeast , fission , function (biology) , biophysics , chemistry , biology , cell , saccharomyces cerevisiae , biochemistry , microbiology and biotechnology , physics , demography , quantum mechanics , sociology , neutron
A fundamental problem in microbial reactor analysis is identification of the relationship between environment and individual cell metabolic activity. Population balance equations provide a link between experimental measurements of composition frequency functions in microbial populations on the one hand and macromolecular synthesis kinetics and cell division control parameters for single cells on the other. Flow microfluorometry measurements of frequency functions for single‐cell protein content in Schizosaccharomyces pombe in balanced exponential growth have been analyzed by two different methods. One approach utilizes the integrated form of the population balance equation known as the Collins‐Richmond equation, and the other method involves optimization of parameters in assumed kinetic and cell division functional forms in order to best fit measured frequency functions with corresponding model solutions. Both data interpretation techniques indicate that rates of protein synthesis increase most in small protein content cells as the population specific growth rate increases, leading to parabolic single‐cell protein synthesis kinetics at large specific growth rates. Utilization of frequency function data for an asynchronous population is shown in this case to be a far more sensitive method for determination of single‐cell kinetics than is monitoring the metabolic dynamics of a single cell or, equivalently, synchronous culture analyses.