Literature DB >> 1367426

Spin filter perfusion system for high density cell culture: production of recombinant urinary type plasminogen activator in CHO cells.

G C Avgerinos1, D Drapeau, J S Socolow, J I Mao, K Hsiao, R J Broeze.   

Abstract

We have used a 20 liter stirred tank fermentor, equipped with a 127 mesh ethylene-tetrafluoroethylene rotating screen for cell recycle, for the continuous production of recombinant single chain urokinase-type plasminogen activator (rscu-PA) from Chinese hamster ovary (CHO) cells. Viable cell densities between 60 and 74 million per ml were maintained at medium perfusion rates of 3.0 to 4.0 fermentor volumes per day. Cells were retained by the 120 micron nominal opening filter through the formation of "clumped" cell aggregates of 200 to 600 microns in size, which did not foul the filter. In 31 days of culture, a total of 51 grams of rscu-PA were produced in 1,000 liters of medium. The rscu-PA produced over the course of this continuous culture was purified and characterized both in vitro and in vivo and shown to be comparable to natural scu-PA produced from the transformed human kidney cell line, TCL-598.

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Year:  1990        PMID: 1367426     DOI: 10.1038/nbt0190-54

Source DB:  PubMed          Journal:  Biotechnology (N Y)        ISSN: 0733-222X


  15 in total

1.  Production of recombinant proteins in serum-free media.

Authors:  D Broad; R Boraston; M Rhodes
Journal:  Cytotechnology       Date:  1991-01       Impact factor: 2.058

2.  Formation of bridges and large cellular clumps in CHO-cell microcarrier cultures: effects of agitation, dimethyl sulfoxide and calf serum.

Authors:  M C Borys; E T Papoutsakis
Journal:  Cytotechnology       Date:  1992       Impact factor: 2.058

3.  The optimization of serum-free medium for the production of the scu-PA by the addition of algal extracts.

Authors:  H G Kim; K D Sung; M S Ham; K H Chung; K H Chung; H Y Lee
Journal:  Cytotechnology       Date:  1995-10       Impact factor: 2.058

4.  Engineering challenges in high density cell culture systems.

Authors:  S S Ozturk
Journal:  Cytotechnology       Date:  1996-01       Impact factor: 2.058

5.  Influence of alterations in culture condition and changes in perfusion parameters on the retention performance of a 20 mum spinfilter during a perfusion cultivation of a recombinant CHO cell line in pilot scale.

Authors:  K Iding; D Lütkemeyer; E Fraune; K Gerlach; J Lehmann
Journal:  Cytotechnology       Date:  2000-10       Impact factor: 2.058

6.  Dielectrophoretic forces can be safely used to retain viable cells in perfusion cultures of animal cells.

Authors:  A Docoslis; N Kalogerakis; L A Behie
Journal:  Cytotechnology       Date:  1999-07       Impact factor: 2.058

7.  Use of cell cycle analysis to characterise growth and interferon-gamma production in perfusion culture of CHO cells.

Authors:  V Leelavatcharamas; A N Emery; M Al-Rubeai
Journal:  Cytotechnology       Date:  1999-07       Impact factor: 2.058

8.  The evolution of recombinant thrombolytics: Current status and future directions.

Authors:  Yogender Pal Khasa
Journal:  Bioengineered       Date:  2016-10-03       Impact factor: 3.269

Review 9.  Perfusion culture apparatus for suspended mammalian cells.

Authors:  M Tokashiki; H Takamatsu
Journal:  Cytotechnology       Date:  1993       Impact factor: 2.058

10.  Stable production of recombinant pro-urokinase by human lymphoblastoid Namalwa KJM-1 cells: host-cell dependency of the expressed-protein stability.

Authors:  M Satoh; S Hosoi; H Miyaji; S Itoh; S Sato
Journal:  Cytotechnology       Date:  1993       Impact factor: 2.058

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