Literature DB >> 20630485

High cell-density processes in batch mode of a genetically engineered Escherichia coli strain with minimized overflow metabolism using a pressurized bioreactor.

Ingo Knabben1, Lars Regestein, Frank Marquering, Sven Steinbusch, Alvaro R Lara, Jochen Büchs.   

Abstract

A common method to minimize overflow metabolism and to enable high cell-density is to operate microbial processes in fed-batch mode under carbon-limiting conditions. This requires sophisticated process control schemes with expensive hardware equipment and software and well-characterized processes parameters. To generate high-cell density, a more simplified strategy would be beneficial. Therefore, a genetically engineered Escherichia coli strain with a modified glucose uptake system was cultivated in batch mode. In the applied strain, the usual phosphotransferase system of a K12-derived strain was inactivated, while the galactose permease system was amplified. Upon cultivating this E. coli strain in pure minimal media, the acetate concentration did not exceed values of 0.35 g L(-1), even when the batch fermentation was started with a glucose concentration of 130 g L(-1). Finally, maximum biomass concentrations of 48 g L(-1) dry cell weight and maximum space-time yields of 2.10 g L(-1) h(-1) were reached. To provide an unlimited growth under fully aerobic conditions (DOT>30%) at comparatively low values for specific power input (3-4 kW m(-3)), a pressurized bioreactor was used. Consequentially, to our knowledge, this study using a bioreactor with elevated headspace pressure generate the highest oxygen transfer rate (451 mmol L(-1) h(-1)) ever reached in batch cultivations.
Copyright © 2010 Elsevier B.V. All rights reserved.

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Year:  2010        PMID: 20630485     DOI: 10.1016/j.jbiotec.2010.07.006

Source DB:  PubMed          Journal:  J Biotechnol        ISSN: 0168-1656            Impact factor:   3.307


  5 in total

1.  Engineering Escherichia coli to increase plasmid DNA production in high cell-density cultivations in batch mode.

Authors:  Gheorghe M Borja; Eugenio Meza Mora; Blanca Barrón; Guillermo Gosset; Octavio T Ramírez; Alvaro R Lara
Journal:  Microb Cell Fact       Date:  2012-09-19       Impact factor: 5.328

2.  A novel cytosolic NADH:quinone oxidoreductase from Methanothermobacter marburgensis.

Authors:  Eva Ullmann; Tien Chye Tan; Thomas Gundinger; Christoph Herwig; Christina Divne; Oliver Spadiut
Journal:  Biosci Rep       Date:  2014-12-23       Impact factor: 3.840

3.  Application of Plasmid Engineering to Enhance Yield and Quality of Plasmid for Vaccine and Gene Therapy.

Authors:  Olusegun Folarin; Darren Nesbeth; John M Ward; Eli Keshavarz-Moore
Journal:  Bioengineering (Basel)       Date:  2019-06-19

4.  Glucose transport engineering allows mimicking fed-batch performance in batch mode and selection of superior producer strains.

Authors:  Daniela Velazquez; Juan-Carlos Sigala; Luz María Martínez; Paul Gaytán; Guillermo Gosset; Alvaro R Lara
Journal:  Microb Cell Fact       Date:  2022-09-07       Impact factor: 6.352

5.  New insights on the reorganization of gene transcription in Pseudomonas putida KT2440 at elevated pressure.

Authors:  Stéphanie Follonier; Isabel F Escapa; Pilar M Fonseca; Bernhard Henes; Sven Panke; Manfred Zinn; María Auxiliadora Prieto
Journal:  Microb Cell Fact       Date:  2013-03-28       Impact factor: 5.328

  5 in total

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