Literature DB >> 18612985

Expression of epoxide hydrolase in insect cells: a focus on the infected cell.

M Y Wang1, V Vakharia, W E Bentley.   

Abstract

Insect cell culture and the baculovirus vector expression system have emerged to be a promising production technique for heterologous proteins. In this article, expression characteristics for membrane-bound epoxide hydrolase are examined. A generic process is presented whereby cells are grown in serum-free media supplemented with serum and then resuspended in serum-free media to simplify purification after infection. The infected cells retain significant metabolic activity during the postinfection stage. Thus, maintaining nutrient supply during the postinfection period is critical, and a low stirring rate will result in oxygen depletion and shift the metabolism of the infected cells toward lactate production which then lowers product yield. This is the first report indicating that glucose is supplied from sucrose decomposition and then metabolized for viral DNA and recombinant protein production in recombinant baculovirus insect expression system. (c) 1993 John Wiley & Sons, Inc.

Entities:  

Year:  1993        PMID: 18612985     DOI: 10.1002/bit.260420212

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


  10 in total

1.  Insect cell physiology.

Authors:  R Bhatia; G Jesionowski; J Ferrance; M M Ataai
Journal:  Cytotechnology       Date:  1997-05       Impact factor: 2.058

2.  Insect cell physiology.

Authors:  R Bhatia; G Jesionowski; J Ferrance; M M Ataai
Journal:  Cytotechnology       Date:  1996-01       Impact factor: 2.058

3.  Insect cell bioreactors.

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

4.  Continuous insect cell (Sf-9) culture with aeration through sparging.

Authors:  M Y Wang; W E Bentley
Journal:  Appl Microbiol Biotechnol       Date:  1994-05       Impact factor: 4.813

5.  Maximization of recombinant protein yield in the insect cell/baculovirus system by one-time addition of nutrients to high-density batch cultures.

Authors:  C Bédard; A Kamen; R Tom; B Massie
Journal:  Cytotechnology       Date:  1994       Impact factor: 2.058

6.  Improved yields of the extracellular domain of the epidermal growth factor receptor produced using the baculovirus expression system by medium replacement following infection.

Authors:  R L Tom; M T Debanne; C Bédard; A W Caron; B Massie; A A Kamen
Journal:  Appl Microbiol Biotechnol       Date:  1995-12       Impact factor: 4.813

7.  Evaluation of monitoring approaches and effects of culture conditions on recombinant protein production in baculovirus-infected insect cells.

Authors:  W T Hensler; S N Agathos
Journal:  Cytotechnology       Date:  1994       Impact factor: 2.058

8.  Induction of a metabolic switch in insect cells by substrate-limited fed batch cultures.

Authors:  L Ohman; J Ljunggren; L Häggström
Journal:  Appl Microbiol Biotechnol       Date:  1995-11       Impact factor: 4.813

9.  Growth, viral production and metabolism of a Helicoverpa zea cell line in serum-free culture.

Authors:  Linda H L Lua; Steven Reid
Journal:  Cytotechnology       Date:  2003-09       Impact factor: 2.058

10.  Development of an efficient bioprocess for poultry vaccines using high-density insect cell culture.

Authors:  W E Bentley; M Y Wang; V Vakharia
Journal:  Ann N Y Acad Sci       Date:  1994-11-30       Impact factor: 5.691

  10 in total

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