Literature DB >> 19002977

The use of peptones as medium additives for the production of a recombinant therapeutic protein in high density perfusion cultures of mammalian cells.

R Heidemann1, C Zhang, H Qi, J Larrick Rule, C Rozales, S Park, S Chuppa, M Ray, J Michaels, K Konstantinov, D Naveh.   

Abstract

Protein hydrolysates as substitutes for serum havebeen employed by many in cell culture mediumformulation, especially with the shift to low proteinor protein-free media. More recently, vegetablehydrolysates have also been added as nutritionalsupplements to fortify the amino acid content in smallpeptide form for batch and fed-batch fermentations. Several of these new hydrolysates (peptones of soy,rice, wheat gluten etc.) were tested as protein-freemedium supplements for the production of a recombinanttherapeutic protein. Multiple peptone-supplemented,continuous perfusion bioreactor experiments wereconducted, varying dilution rates and basal mediumcomposition over the various runs. Cell specificrates and product quality studies were obtained forthe various peptones and compared with peptone-freemedium. The potential for peptones to decreaseintrinsic and proteolytic degradation of the productwas also investigated.It was found that peptones confer a nutritionalbenefit, especially at low dilution rates, for therecombinant BHK cell line used in this investigation.The specific productivity increased 20-30% comparedto the peptone-free controls. However, this benefitwas also fully delivered by using fortified medium inplace of the peptone-enriched media. Therefore, whilepeptones may be considered as useful medium additiveswhen development time is limited, their addition maybe avoided by systematic medium development ifpermitted by the time line of the project.

Entities:  

Year:  2000        PMID: 19002977      PMCID: PMC3449690          DOI: 10.1023/A:1008196521213

Source DB:  PubMed          Journal:  Cytotechnology        ISSN: 0920-9069            Impact factor:   2.058


  24 in total

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3.  Fermentor temperature as a tool for control of high-density perfusion cultures of mammalian cells.

Authors:  S Chuppa; Y S Tsai; S Yoon; S Shackleford; C Rozales; R Bhat; G Tsay; C Matanguihan; K Konstantinov; D Naveh
Journal:  Biotechnol Bioeng       Date:  1997-07-20       Impact factor: 4.530

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7.  Peptone, a low-cost growth-promoting nutrient for intensive animal cell culture.

Authors:  D C Jan; S J Jones; A N Emery; M al-Rubeai
Journal:  Cytotechnology       Date:  1994       Impact factor: 2.058

8.  Identification of a renal cell line that constitutively expresses the kidney-specific high-affinity H+/peptide cotransporter.

Authors:  M Brandsch; C Brandsch; P D Prasad; V Ganapathy; U Hopfer; F H Leibach
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9.  H(+)-peptide cotransport in Madin-Darby canine kidney cells: expression and calmodulin-dependent regulation.

Authors:  M Brandsch; V Ganapathy; F H Leibach
Journal:  Am J Physiol       Date:  1995-03

10.  Proton/peptide cotransporter (PEPT 2) from human kidney: functional characterization and chromosomal localization.

Authors:  S Ramamoorthy; W Liu; Y Y Ma; T L Yang-Feng; V Ganapathy; F H Leibach
Journal:  Biochim Biophys Acta       Date:  1995-11-22
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  23 in total

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3.  Optimization and control of perfusion cultures using a viable cell probe and cell specific perfusion rates.

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6.  A T-flask based screening platform for evaluating and identifying plant hydrolysates for a fed-batch cell culture process.

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9.  Elucidating the impact of cottonseed hydrolysates on CHO cell culture performance through transcriptomic analysis.

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10.  Combination of temperature shift and hydrolysate addition regulates anti-IgE monoclonal antibody charge heterogeneity in Chinese hamster ovary cell fed-batch culture.

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