Serum-free suspension cultivation of PER.C6® cells and recombinant adenovirus production under different pH conditions
PER.C6® cell growth, metabolism, and adenovirus production were studied in head‐to‐head comparisons in stirred bioreactors under different pH conditions. Cell growth rate was found to be similar in the pH range of 7.1–7.6, while a long lag phase and a slower growth rate were observed at pH 6.8. The...
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Veröffentlicht in: | Biotechnology and bioengineering 2002-12, Vol.80 (5), p.569-579 |
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description | PER.C6® cell growth, metabolism, and adenovirus production were studied in head‐to‐head comparisons in stirred bioreactors under different pH conditions. Cell growth rate was found to be similar in the pH range of 7.1–7.6, while a long lag phase and a slower growth rate were observed at pH 6.8. The specific consumption rates of glucose and glutamine decreased rapidly over time during batch cell growth, as did the specific lactate and ammonium production rates. Cell metabolism in both infected and uninfected cultures was very sensitive to culture pH, resulting in dramatic differences in glucose/glutamine consumption and lactate/ammonium production under different pH conditions. It appeared that glucose metabolism was suppressed at low pH but the efficiency of energy production from glucose was enhanced. Adenovirus infection resulted in profound changes in cell growth and metabolism. Cell growth was largely arrested under all pH conditions, while glucose consumption and lactate production were elevated post virus infection. Virus infection induced a reduction in glutamine consumption at low pH but an increase at high pH. The optimal pH for adenovirus production was found to be 7.3 under the experimental conditions used in the study. Deviations from this optimum resulted in significant reductions of virus productivity. The results indicate that culture pH is a very critical process parameter in PER.C6® cell culture and adenovirus production. © 2002 Wiley Periodicals, Inc. Biotechnol Bioeng 80: 569–579, 2002. |
doi_str_mv | 10.1002/bit.10443 |
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Cell growth rate was found to be similar in the pH range of 7.1–7.6, while a long lag phase and a slower growth rate were observed at pH 6.8. The specific consumption rates of glucose and glutamine decreased rapidly over time during batch cell growth, as did the specific lactate and ammonium production rates. Cell metabolism in both infected and uninfected cultures was very sensitive to culture pH, resulting in dramatic differences in glucose/glutamine consumption and lactate/ammonium production under different pH conditions. It appeared that glucose metabolism was suppressed at low pH but the efficiency of energy production from glucose was enhanced. Adenovirus infection resulted in profound changes in cell growth and metabolism. Cell growth was largely arrested under all pH conditions, while glucose consumption and lactate production were elevated post virus infection. Virus infection induced a reduction in glutamine consumption at low pH but an increase at high pH. The optimal pH for adenovirus production was found to be 7.3 under the experimental conditions used in the study. Deviations from this optimum resulted in significant reductions of virus productivity. The results indicate that culture pH is a very critical process parameter in PER.C6® cell culture and adenovirus production. © 2002 Wiley Periodicals, Inc. Biotechnol Bioeng 80: 569–579, 2002.</description><identifier>ISSN: 0006-3592</identifier><identifier>EISSN: 1097-0290</identifier><identifier>DOI: 10.1002/bit.10443</identifier><identifier>PMID: 12355468</identifier><language>eng</language><publisher>New York: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Adenoviridae - growth & development ; adenovirus production ; bioreactor ; Bioreactors ; Cell Line ; Culture Media, Serum-Free ; culture pH ; Glucose - metabolism ; Glutamine - metabolism ; Humans ; Hydrogen-Ion Concentration ; Lactic Acid - metabolism ; metabolism ; PER.C6® cell culture ; Quality Control ; Quaternary Ammonium Compounds - metabolism ; Recombination, Genetic ; Reference Values ; Reproducibility of Results ; Retina - cytology ; Retina - embryology ; Retina - physiology ; Retina - virology ; Sensitivity and Specificity ; serum-free ; Stem Cells - physiology ; Virus Cultivation - methods</subject><ispartof>Biotechnology and bioengineering, 2002-12, Vol.80 (5), p.569-579</ispartof><rights>Copyright © 2002 Wiley Periodicals, Inc.</rights><rights>Copyright 2002 Wiley Periodicals, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4273-d5ddaf32fb3600b306490e02dc4d6dad88a40280fceb9dc2bef9f9a111703ad93</citedby><cites>FETCH-LOGICAL-c4273-d5ddaf32fb3600b306490e02dc4d6dad88a40280fceb9dc2bef9f9a111703ad93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fbit.10443$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fbit.10443$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12355468$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Xie, Liangzhi</creatorcontrib><creatorcontrib>Pilbrough, Warren</creatorcontrib><creatorcontrib>Metallo, Christian</creatorcontrib><creatorcontrib>Zhong, Tanya</creatorcontrib><creatorcontrib>Pikus, Lana</creatorcontrib><creatorcontrib>Leung, John</creatorcontrib><creatorcontrib>Auniņš, John G.</creatorcontrib><creatorcontrib>Zhou, Weichang</creatorcontrib><title>Serum-free suspension cultivation of PER.C6® cells and recombinant adenovirus production under different pH conditions</title><title>Biotechnology and bioengineering</title><addtitle>Biotechnol. Bioeng</addtitle><description>PER.C6® cell growth, metabolism, and adenovirus production were studied in head‐to‐head comparisons in stirred bioreactors under different pH conditions. Cell growth rate was found to be similar in the pH range of 7.1–7.6, while a long lag phase and a slower growth rate were observed at pH 6.8. The specific consumption rates of glucose and glutamine decreased rapidly over time during batch cell growth, as did the specific lactate and ammonium production rates. Cell metabolism in both infected and uninfected cultures was very sensitive to culture pH, resulting in dramatic differences in glucose/glutamine consumption and lactate/ammonium production under different pH conditions. It appeared that glucose metabolism was suppressed at low pH but the efficiency of energy production from glucose was enhanced. Adenovirus infection resulted in profound changes in cell growth and metabolism. Cell growth was largely arrested under all pH conditions, while glucose consumption and lactate production were elevated post virus infection. Virus infection induced a reduction in glutamine consumption at low pH but an increase at high pH. The optimal pH for adenovirus production was found to be 7.3 under the experimental conditions used in the study. Deviations from this optimum resulted in significant reductions of virus productivity. The results indicate that culture pH is a very critical process parameter in PER.C6® cell culture and adenovirus production. © 2002 Wiley Periodicals, Inc. Biotechnol Bioeng 80: 569–579, 2002.</description><subject>Adenoviridae - growth & development</subject><subject>adenovirus production</subject><subject>bioreactor</subject><subject>Bioreactors</subject><subject>Cell Line</subject><subject>Culture Media, Serum-Free</subject><subject>culture pH</subject><subject>Glucose - metabolism</subject><subject>Glutamine - metabolism</subject><subject>Humans</subject><subject>Hydrogen-Ion Concentration</subject><subject>Lactic Acid - metabolism</subject><subject>metabolism</subject><subject>PER.C6® cell culture</subject><subject>Quality Control</subject><subject>Quaternary Ammonium Compounds - metabolism</subject><subject>Recombination, Genetic</subject><subject>Reference Values</subject><subject>Reproducibility of Results</subject><subject>Retina - cytology</subject><subject>Retina - embryology</subject><subject>Retina - physiology</subject><subject>Retina - virology</subject><subject>Sensitivity and Specificity</subject><subject>serum-free</subject><subject>Stem Cells - physiology</subject><subject>Virus Cultivation - methods</subject><issn>0006-3592</issn><issn>1097-0290</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU1uFDEQhS0EIsPAggsgr5BYdFK2u-3uJYzyhyJASSBLy22XJUP_TOx2Qi7FIXKy9GQGWCFWVSV_76lcj5DXDPYZAD9owzQ3ZSmekAWDRhXAG3hKFgAgC1E1fI-8SOn7PKpayudkj3FRVaWsF-T2AmPuCx8RacppjUMK40Bt7qZwY6ZNP3r65fB8fyXvf1GLXZeoGRyNaMe-DYMZJmocDuNNiDnRdRxdto-6PDiM1AXvMeJMrU-oHQcXNo_pJXnmTZfw1a4uydejw8vVSXH2-fh09f6ssCVXonCVc8YL7lshAVoBsmwAgTtbOumMq2tTAq_BW2wbZ3mLvvGNYYwpEMY1Yknebn3nxa4zpkn3IW1-YQYcc9KKM1EBF_8FWa2YVPPhluTdFrRxTCmi1-sYehPvNAO9iUPPcejHOGb2zc40tz26v-Tu_jNwsAVuQ4d3_3bSH04vf1sWW0VIE_78ozDxh5ZKqEpffTrW50cX4uPVt5WuxAMINaZL</recordid><startdate>20021205</startdate><enddate>20021205</enddate><creator>Xie, Liangzhi</creator><creator>Pilbrough, Warren</creator><creator>Metallo, Christian</creator><creator>Zhong, Tanya</creator><creator>Pikus, Lana</creator><creator>Leung, John</creator><creator>Auniņš, John G.</creator><creator>Zhou, Weichang</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20021205</creationdate><title>Serum-free suspension cultivation of PER.C6® cells and recombinant adenovirus production under different pH conditions</title><author>Xie, Liangzhi ; Pilbrough, Warren ; Metallo, Christian ; Zhong, Tanya ; Pikus, Lana ; Leung, John ; Auniņš, John G. ; Zhou, Weichang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4273-d5ddaf32fb3600b306490e02dc4d6dad88a40280fceb9dc2bef9f9a111703ad93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Adenoviridae - growth & development</topic><topic>adenovirus production</topic><topic>bioreactor</topic><topic>Bioreactors</topic><topic>Cell Line</topic><topic>Culture Media, Serum-Free</topic><topic>culture pH</topic><topic>Glucose - metabolism</topic><topic>Glutamine - metabolism</topic><topic>Humans</topic><topic>Hydrogen-Ion Concentration</topic><topic>Lactic Acid - metabolism</topic><topic>metabolism</topic><topic>PER.C6® cell culture</topic><topic>Quality Control</topic><topic>Quaternary Ammonium Compounds - metabolism</topic><topic>Recombination, Genetic</topic><topic>Reference Values</topic><topic>Reproducibility of Results</topic><topic>Retina - cytology</topic><topic>Retina - embryology</topic><topic>Retina - physiology</topic><topic>Retina - virology</topic><topic>Sensitivity and Specificity</topic><topic>serum-free</topic><topic>Stem Cells - physiology</topic><topic>Virus Cultivation - methods</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Xie, Liangzhi</creatorcontrib><creatorcontrib>Pilbrough, Warren</creatorcontrib><creatorcontrib>Metallo, Christian</creatorcontrib><creatorcontrib>Zhong, Tanya</creatorcontrib><creatorcontrib>Pikus, Lana</creatorcontrib><creatorcontrib>Leung, John</creatorcontrib><creatorcontrib>Auniņš, John G.</creatorcontrib><creatorcontrib>Zhou, Weichang</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Biotechnology and bioengineering</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Xie, Liangzhi</au><au>Pilbrough, Warren</au><au>Metallo, Christian</au><au>Zhong, Tanya</au><au>Pikus, Lana</au><au>Leung, John</au><au>Auniņš, John G.</au><au>Zhou, Weichang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Serum-free suspension cultivation of PER.C6® cells and recombinant adenovirus production under different pH conditions</atitle><jtitle>Biotechnology and bioengineering</jtitle><addtitle>Biotechnol. Bioeng</addtitle><date>2002-12-05</date><risdate>2002</risdate><volume>80</volume><issue>5</issue><spage>569</spage><epage>579</epage><pages>569-579</pages><issn>0006-3592</issn><eissn>1097-0290</eissn><abstract>PER.C6® cell growth, metabolism, and adenovirus production were studied in head‐to‐head comparisons in stirred bioreactors under different pH conditions. Cell growth rate was found to be similar in the pH range of 7.1–7.6, while a long lag phase and a slower growth rate were observed at pH 6.8. The specific consumption rates of glucose and glutamine decreased rapidly over time during batch cell growth, as did the specific lactate and ammonium production rates. Cell metabolism in both infected and uninfected cultures was very sensitive to culture pH, resulting in dramatic differences in glucose/glutamine consumption and lactate/ammonium production under different pH conditions. It appeared that glucose metabolism was suppressed at low pH but the efficiency of energy production from glucose was enhanced. Adenovirus infection resulted in profound changes in cell growth and metabolism. Cell growth was largely arrested under all pH conditions, while glucose consumption and lactate production were elevated post virus infection. Virus infection induced a reduction in glutamine consumption at low pH but an increase at high pH. The optimal pH for adenovirus production was found to be 7.3 under the experimental conditions used in the study. Deviations from this optimum resulted in significant reductions of virus productivity. The results indicate that culture pH is a very critical process parameter in PER.C6® cell culture and adenovirus production. © 2002 Wiley Periodicals, Inc. Biotechnol Bioeng 80: 569–579, 2002.</abstract><cop>New York</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>12355468</pmid><doi>10.1002/bit.10443</doi><tpages>11</tpages></addata></record> |
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subjects | Adenoviridae - growth & development adenovirus production bioreactor Bioreactors Cell Line Culture Media, Serum-Free culture pH Glucose - metabolism Glutamine - metabolism Humans Hydrogen-Ion Concentration Lactic Acid - metabolism metabolism PER.C6® cell culture Quality Control Quaternary Ammonium Compounds - metabolism Recombination, Genetic Reference Values Reproducibility of Results Retina - cytology Retina - embryology Retina - physiology Retina - virology Sensitivity and Specificity serum-free Stem Cells - physiology Virus Cultivation - methods |
title | Serum-free suspension cultivation of PER.C6® cells and recombinant adenovirus production under different pH conditions |
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