Please use this identifier to cite or link to this item: https://doi.org/10.1002/(SICI)1097-0290(20000520)68:43.0.CO;2-G
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dc.titleGrowth kinetics of Pseudomonas putida in cometabolism of phenol end 4- chlorophenol in the presence of a conventional carbon source
dc.contributor.authorWang, S.-J.
dc.contributor.authorLoh, K.-C.
dc.date.accessioned2014-10-09T09:54:27Z
dc.date.available2014-10-09T09:54:27Z
dc.date.issued2000-05-20
dc.identifier.citationWang, S.-J.,Loh, K.-C. (2000-05-20). Growth kinetics of Pseudomonas putida in cometabolism of phenol end 4- chlorophenol in the presence of a conventional carbon source. Biotechnology and Bioengineering 68 (4) : 437-447. ScholarBank@NUS Repository. <a href="https://doi.org/10.1002/(SICI)1097-0290(20000520)68:43.0.CO;2-G" target="_blank">https://doi.org/10.1002/(SICI)1097-0290(20000520)68:43.0.CO;2-G</a>
dc.identifier.issn00063592
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/92023
dc.description.abstractGrowth kinetics of Pseudomonas putida (ATCC 49451) in cometabolism of phenol and 4-chlorophenol (4-cp) in the presence of sodium glutamate (SG) were studied. In the ternary substrate mixture, phenol and SG are growth substrates while 4-cp is a nongrowth substrate. Cell growth on phenol was found to follow Andrews kinetics and cells displayed substrate inhibition pattern on sodium glutamate in the range of 0-4 g L-1 as well. A cell growth model for the ternary substrate system was established based on a simplified cell growth mechanism and subsequently modified by experimental results. Model analysis over a wide range of substrate concentrations shows that the inhibition of SG is much larger than phenol at low phenol concentrations (≤200 mg L-1) while phenol exerts dominant inhibition on cell growth at higher phenol concentrations (≥600 mg L-1). The nongrowth substrate, 4-cp, inhibits cell growth mainly through inactivation of cells (cell decay) and competitive inhibition to cell growth on phenol. In the absence of SG, 4-cp retards cell growth severely and cells cannot grow at 250 mg L-1 4-cp. Addition of sodium glutamate, however, greatly attenuates the toxicity of 4-cp and supports cell growth at 4-cp concentration higher than 250 mg L-1. By using the proposed cell growth model, we were able to optimize the amount of SG needed to enhance cell growth rate and validate model predictions against experimental data. (C) 2000 John Wiley and Sons, Inc.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1002/(SICI)1097-0290(20000520)68:43.0.CO;2-G
dc.sourceScopus
dc.subjectCell decay
dc.subjectCell growth kinetics
dc.subjectCometabolism
dc.subjectInhibition
dc.subjectModeling
dc.subjectTernary substrate system
dc.typeArticle
dc.contributor.departmentCHEMICAL & ENVIRONMENTAL ENGINEERING
dc.description.doi10.1002/(SICI)1097-0290(20000520)68:43.0.CO;2-G
dc.description.sourcetitleBiotechnology and Bioengineering
dc.description.volume68
dc.description.issue4
dc.description.page437-447
dc.description.codenBIBIA
dc.identifier.isiutNOT_IN_WOS
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