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Fully integrated L-phenylalanine separation and concentration using reactive-extraction with liquid-liquid centrifuges in a fed-batch process with E. coli
Authors:N.?Rüffer,U.?Heidersdorf,I.?Kretzers,G.?A.?Sprenger,L.?Raeven,R.?Takors  author-information"  >  author-information__contact u-icon-before"  >  mailto:r.takors@fz-juelich.de"   title="  r.takors@fz-juelich.de"   itemprop="  email"   data-track="  click"   data-track-action="  Email author"   data-track-label="  "  >Email author
Affiliation:(1) Institute of Biotechnology, Forschungszentrum Jülich GmbH, 52425 Jülich, Germany;(2) Institute of Microbiology, University of Stuttgart, Allmandring 31, 70569 Stuttgart, Germany;(3) DSM Biotech GmbH, Karl-Heinz Beckurts Str. 13, 52428 Jülich, Germany
Abstract:A novel in situ product recovery (ISPR) approach for the (fully) integrated separation of L-phenylalanine (L-phe) from a 20 l fed-batch process with the recombinant L-tyrosine auxotrophic strain E. coli F-4/pF81 is presented. The strain was rationally constructed for the production of the aromatic amino acid. Glucose and tyrosine control is used. A reactive extraction system consisting of kerosene, the cation-selective carrier D2EHPA and sulphuric acid, all circulating in liquid-liquid centrifuges, is applied for the on-line L-phe separation from cell- and protein-free permeate. Permeate is drained off from the bioreactor bypass. Using the novel ISPR approach, a significantly extended product formation period at 0.25 mmol/(g*h) together with a reduced by-product formation and a 28% relative glucose/L-phe yield increase is observed. Thus, the ISPR approach is superior to the reference non-ISPR process and even offers extraction rates approximately three times higher than the published membrane-based process.
Keywords:L-phenylalanine (L-phe)  Reactive extraction  Liquid-liquid centrifuge  E. coli
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