Literature DB >> 9079287

Automated fed-batch fermentation with feed-back controls based on dissolved oxygen (DO) and pH for production of DNA vaccines.

W Chen1, C Graham, R B Ciccarelli.   

Abstract

A fermentation process in Escherichia coli for production of supercoiled plasmid DNA for use as a DNA vaccine was developed using an automated feed-back control nutrient feeding strategy based on dissolved oxygen (DO) and pH. The process was further automated through a computer-aided data processing system to regulate the cell growth rate by controlling interactively both the nutrient feed rate and agitation speed based on DO. The process increased the total yield of the plasmid DNA by approximately 10-fold as compared to a manual fed-batch culture. The final cell yield from the automated process reached 60 g L-1 of dry cell weight (OD600 = 120) within 24 h. A plasmid DNA yield of 100 mg L-1 (1.7 mg g-1 cell weight) was achieved by using an alkaline cell lysis method. Plasmid yield was confirmed using High Performance Liquid Chromatography (HPLC) analysis. Because cells had been grown under carbon-limiting conditions in the automated process, acetic acid production was minimal (below 0.01 g L-1) throughout the fed-batch stage. In contrast, in the manual process, an acid accumulation rate as high as 0.36 g L-1 was observed, presumably due to the high nutrient feed rates used to maintain a maximum growth rate. The manual fed-batch process produced a low cell density averaging 10-12 g L-1 (OD600 = 25-30) and plasmid yields of 5-8 mg L-1 (approximately 0.7 mg g-1 cells). The improved plasmid DNA yields in the DO- and pH-based feed-back controlled process were assumed to be a result of a combination of increased cell density, reduced growth rate (mu) from 0.69 h-1 to 0.13 h-1 and the carbon/nitrogen limitation in the fed-batch stage. The DO- and pH-based feed-back control, fed-batch process has proven itself to be advantageous in regulating cell growth rate to achieve both high cell density and plasmid yield without having to use pure oxygen. The process was reproducible in triplicate fermentations at both 7-L and 80-L scales.

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Year:  1997        PMID: 9079287     DOI: 10.1038/sj.jim.2900355

Source DB:  PubMed          Journal:  J Ind Microbiol Biotechnol        ISSN: 1367-5435            Impact factor:   3.346


  7 in total

1.  Ultra-high expression of a thermally responsive recombinant fusion protein in E. coli.

Authors:  Dominic C Chow; Matthew R Dreher; Kimberly Trabbic-Carlson; Ashutosh Chilkoti
Journal:  Biotechnol Prog       Date:  2006 May-Jun

2.  DNA plasmid production in different host strains of Escherichia coli.

Authors:  Adam Singer; Mark A Eiteman; Elliot Altman
Journal:  J Ind Microbiol Biotechnol       Date:  2009-01-10       Impact factor: 3.346

3.  Overproduction of lipopeptide biosurfactant by Aneurinibacillus thermoaerophilus HAK01 in various fed-batch modes under thermophilic conditions.

Authors:  Hamidreza Hajfarajollah; Babak Mokhtarani; Azadeh Tohidi; Shayesteh Bazsefidpar; Kambiz Akbari Noghabi
Journal:  RSC Adv       Date:  2019-09-25       Impact factor: 4.036

4.  In situ pH management for microbial culture in shake flasks and its application to increase plasmid yield.

Authors:  Reenu Sanil; Vishwanathgouda Maralingannavar; Mugdha Gadgil
Journal:  J Ind Microbiol Biotechnol       Date:  2014-01-30       Impact factor: 3.346

Review 5.  Bioprocess engineering issues that would be faced in producing a DNA vaccine at up to 100 m3 fermentation scale for an influenza pandemic.

Authors:  Mike Hoare; M Susana Levy; Daniel G Bracewell; Steven D Doig; Simyee Kong; Nigel Titchener-Hooker; John M Ward; Peter Dunnill
Journal:  Biotechnol Prog       Date:  2005 Nov-Dec

6.  Enhanced plasmid production in miniaturized high-cell-density cultures of Escherichia coli supported with perfluorinated oxygen carrier.

Authors:  Maciej Pilarek; Eva Brand; Friederike Hillig; Mirja Krause; Peter Neubauer
Journal:  Bioprocess Biosyst Eng       Date:  2012-11-23       Impact factor: 3.210

7.  High-level fed-batch fermentative expression of an engineered Staphylococcal protein A based ligand in E. coli: purification and characterization.

Authors:  Martin Kangwa; Vikas Yelemane; Ayse Nur Polat; Kanaka Durga Devi Gorrepati; Mariano Grasselli; Marcelo Fernández-Lahore
Journal:  AMB Express       Date:  2015-11-10       Impact factor: 3.298

  7 in total

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