Literature DB >> 10397827

Use of multi-staining flow cytometry to characterise the physiological state of Escherichia coli W3110 in high cell density fed-batch cultures.

C J Hewitt1, G Nebe-Von Caron, A W Nienow, C M McFarlane.   

Abstract

High cell density fed-batch fermentations of Escherichia coli W3110 have been carried out at specific growth rates of less than 0.3 h-1, to investigate the effect of glucose limitation on the physiological state of individual cells. After an initial exponential batch phase, the feed rate was held constant and a final dry cell weight of approximately 50 g per litre was achieved. The fermentations were monitored by mass spectrometry whilst measurements of pH, DOC, CFU/mL, TCN, OD500nm and residual glucose concentrations were made. Satisfactory and reproducible results were obtained. Flow cytometric analysis of cells in broth samples, based on either of two multi-staining protocols, revealed a progressive change in cell physiological state throughout the course of the fermentations. From these measurements it was concluded that the loss in reproductive viability towards the end of the fed-batch process is due to cell death and not due to the formation of a "viable but nonculturable state" as had previously been reported. Since the presence of a high proportion of dead or dying cells at any time during a fermentation has a detrimental effect on the synthesis of any desired product it is proposed that an on-line flow cytometric analysis and control strategy could be used as a means of increasing overall process efficiency. Copyright 1999 John Wiley & Sons, Inc.

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Year:  1999        PMID: 10397827     DOI: 10.1002/(sici)1097-0290(19990620)63:6<705::aid-bit8>3.0.co;2-m

Source DB:  PubMed          Journal:  Biotechnol Bioeng        ISSN: 0006-3592            Impact factor:   4.530


  14 in total

1.  The application of multi-parameter flow cytometry to the study of recombinant Escherichia coli batch fermentation processes.

Authors:  Gareth Lewis; Ian W Taylor; Alvin W Nienow; Christopher J Hewitt
Journal:  J Ind Microbiol Biotechnol       Date:  2004-07-13       Impact factor: 3.346

2.  Combined use of fluorescent dyes and flow cytometry to quantify the physiological state of Pichia pastoris during the production of heterologous proteins in high-cell-density fed-batch cultures.

Authors:  Petr Hyka; Thomas Züllig; Claudia Ruth; Verena Looser; Christian Meier; Joachim Klein; Karel Melzoch; Hans-Peter Meyer; Anton Glieder; Karin Kovar
Journal:  Appl Environ Microbiol       Date:  2010-05-14       Impact factor: 4.792

3.  Electrooptical monitoring of cell polarizability and cell size in aerobic Escherichia coli batch cultivations.

Authors:  Stefan Junne; M Nicolas Cruz-Bournazou; Alexander Angersbach; Peter Götz
Journal:  J Ind Microbiol Biotechnol       Date:  2010-05-29       Impact factor: 3.346

4.  Mapping stress-induced changes in autoinducer AI-2 production in chemostat-cultivated Escherichia coli K-12.

Authors:  M P DeLisa; J J Valdes; W E Bentley
Journal:  J Bacteriol       Date:  2001-05       Impact factor: 3.490

5.  Assessment and interpretation of bacterial viability by using the LIVE/DEAD BacLight Kit in combination with flow cytometry.

Authors:  Michael Berney; Frederik Hammes; Franziska Bosshard; Hans-Ulrich Weilenmann; Thomas Egli
Journal:  Appl Environ Microbiol       Date:  2007-03-23       Impact factor: 4.792

6.  Use of ethidium monoazide and PCR in combination for quantification of viable and dead cells in complex samples.

Authors:  Knut Rudi; Birgitte Moen; Signe Marie Drømtorp; Askild L Holck
Journal:  Appl Environ Microbiol       Date:  2005-02       Impact factor: 4.792

7.  Cytofluorometric detection of wine lactic acid bacteria: application of malolactic fermentation to the monitoring.

Authors:  Mohammad Salma; Sandrine Rousseaux; Anabelle Sequeira-Le Grand; Hervé Alexandre
Journal:  J Ind Microbiol Biotechnol       Date:  2012-10-19       Impact factor: 3.346

8.  Lycopene overproduction and in situ extraction in organic-aqueous culture systems using a metabolically engineered Escherichia coli.

Authors:  Julia Gallego-Jara; Teresa de Diego; Álvaro Del Real; Ana Écija-Conesa; Arturo Manjón; Manuel Cánovas
Journal:  AMB Express       Date:  2015-09-22       Impact factor: 3.298

9.  Evaluation of three industrial Escherichia coli strains in fed-batch cultivations during high-level SOD protein production.

Authors:  Karoline Marisch; Karl Bayer; Monika Cserjan-Puschmann; Markus Luchner; Gerald Striedner
Journal:  Microb Cell Fact       Date:  2013-06-11       Impact factor: 5.328

10.  Bioreactor mixing efficiency modulates the activity of a prpoS::GFP reporter gene in E. coli.

Authors:  Frank Delvigne; Mathieu Boxus; Sophie Ingels; Philippe Thonart
Journal:  Microb Cell Fact       Date:  2009-02-25       Impact factor: 5.328

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