Effect of Ca2+ and Mg2+ concentration in culture medium on the activation of recombinant factor IX produced in Chinese hamster ovary cells
Factor IX (FIX) plays an important role in the blood coagulation cascade. When Chinese hamster ovary (CHO) cells producing recombinant human FIX were cultivated using a serum-free medium (SFM) containing 1.12 mM of Ca(2+) and 0.82 mM of Mg(2+), a significant amount of active FIX (aFIX) was converted...
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Veröffentlicht in: | Journal of biotechnology 2009-07, Vol.142 (3-4), p.275-278 |
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description | Factor IX (FIX) plays an important role in the blood coagulation cascade. When Chinese hamster ovary (CHO) cells producing recombinant human FIX were cultivated using a serum-free medium (SFM) containing 1.12 mM of Ca(2+) and 0.82 mM of Mg(2+), a significant amount of active FIX (aFIX) was converted into undesirable activated FIX (FIXa) in the later phase of batch culture. In an effort to improve aFIX production from CHO cells, the effect of Ca(2+) and Mg(2+) concentrations in the culture medium on the activation of aFIX to FIXa was investigated using SFM with various concentrations of Ca(2+) and Mg(2+) in the range of 0-1.0 mM. The highest aFIX concentration of 1.36 IU/mL was obtained at 1.0 mM Ca(2+) and 1.0 mM Mg(2+), but the activation of aFIX to FIXa in the later phase of culture was rapid and significant. In contrast, at 0.5 mM Ca(2+) and 1.0 mM Mg(2+), the aFIX concentration of 1.33 IU/mL was obtained and did not decrease significantly in the later phase of culture. Taken together, lowering Ca(2+) concentration from 1.0 to 0.5 mM inhibits the activation of aFIX to FIXa in the later phase of culture, fortifying the robustness of downstream bioprocessing. |
doi_str_mv | 10.1016/j.jbiotec.2009.06.001 |
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When Chinese hamster ovary (CHO) cells producing recombinant human FIX were cultivated using a serum-free medium (SFM) containing 1.12 mM of Ca(2+) and 0.82 mM of Mg(2+), a significant amount of active FIX (aFIX) was converted into undesirable activated FIX (FIXa) in the later phase of batch culture. In an effort to improve aFIX production from CHO cells, the effect of Ca(2+) and Mg(2+) concentrations in the culture medium on the activation of aFIX to FIXa was investigated using SFM with various concentrations of Ca(2+) and Mg(2+) in the range of 0-1.0 mM. The highest aFIX concentration of 1.36 IU/mL was obtained at 1.0 mM Ca(2+) and 1.0 mM Mg(2+), but the activation of aFIX to FIXa in the later phase of culture was rapid and significant. In contrast, at 0.5 mM Ca(2+) and 1.0 mM Mg(2+), the aFIX concentration of 1.33 IU/mL was obtained and did not decrease significantly in the later phase of culture. Taken together, lowering Ca(2+) concentration from 1.0 to 0.5 mM inhibits the activation of aFIX to FIXa in the later phase of culture, fortifying the robustness of downstream bioprocessing.</description><identifier>ISSN: 0168-1656</identifier><identifier>EISSN: 1873-4863</identifier><identifier>DOI: 10.1016/j.jbiotec.2009.06.001</identifier><identifier>PMID: 19523499</identifier><identifier>CODEN: JBITD4</identifier><language>eng</language><publisher>Amsterdam: Elsevier</publisher><subject>Animals ; Biological and medical sciences ; Biotechnology ; Calcium - pharmacology ; Cell Survival ; CHO Cells ; Cricetinae ; Cricetulus ; Culture Media, Serum-Free - chemistry ; Culture Media, Serum-Free - metabolism ; Edetic Acid - chemistry ; Factor IX - biosynthesis ; Factor IX - genetics ; Factor IX - metabolism ; Female ; Fundamental and applied biological sciences. Psychology ; Magnesium - pharmacology ; Ovary - drug effects ; Ovary - metabolism ; Recombinant Proteins - biosynthesis ; Recombinant Proteins - genetics ; Recombinant Proteins - metabolism</subject><ispartof>Journal of biotechnology, 2009-07, Vol.142 (3-4), p.275-278</ispartof><rights>2009 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c333t-3bf9013982cca0b651c1eef9c9af7c4302873a2b594dd42372216527340765b63</citedby><cites>FETCH-LOGICAL-c333t-3bf9013982cca0b651c1eef9c9af7c4302873a2b594dd42372216527340765b63</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=21770074$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19523499$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>WON HEE KIM</creatorcontrib><creatorcontrib>LIM, Jung-Seop</creatorcontrib><creatorcontrib>YOON, Yeup</creatorcontrib><creatorcontrib>GYUN MIN LEE</creatorcontrib><title>Effect of Ca2+ and Mg2+ concentration in culture medium on the activation of recombinant factor IX produced in Chinese hamster ovary cells</title><title>Journal of biotechnology</title><addtitle>J Biotechnol</addtitle><description>Factor IX (FIX) plays an important role in the blood coagulation cascade. When Chinese hamster ovary (CHO) cells producing recombinant human FIX were cultivated using a serum-free medium (SFM) containing 1.12 mM of Ca(2+) and 0.82 mM of Mg(2+), a significant amount of active FIX (aFIX) was converted into undesirable activated FIX (FIXa) in the later phase of batch culture. In an effort to improve aFIX production from CHO cells, the effect of Ca(2+) and Mg(2+) concentrations in the culture medium on the activation of aFIX to FIXa was investigated using SFM with various concentrations of Ca(2+) and Mg(2+) in the range of 0-1.0 mM. The highest aFIX concentration of 1.36 IU/mL was obtained at 1.0 mM Ca(2+) and 1.0 mM Mg(2+), but the activation of aFIX to FIXa in the later phase of culture was rapid and significant. In contrast, at 0.5 mM Ca(2+) and 1.0 mM Mg(2+), the aFIX concentration of 1.33 IU/mL was obtained and did not decrease significantly in the later phase of culture. Taken together, lowering Ca(2+) concentration from 1.0 to 0.5 mM inhibits the activation of aFIX to FIXa in the later phase of culture, fortifying the robustness of downstream bioprocessing.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Biotechnology</subject><subject>Calcium - pharmacology</subject><subject>Cell Survival</subject><subject>CHO Cells</subject><subject>Cricetinae</subject><subject>Cricetulus</subject><subject>Culture Media, Serum-Free - chemistry</subject><subject>Culture Media, Serum-Free - metabolism</subject><subject>Edetic Acid - chemistry</subject><subject>Factor IX - biosynthesis</subject><subject>Factor IX - genetics</subject><subject>Factor IX - metabolism</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Magnesium - pharmacology</subject><subject>Ovary - drug effects</subject><subject>Ovary - metabolism</subject><subject>Recombinant Proteins - biosynthesis</subject><subject>Recombinant Proteins - genetics</subject><subject>Recombinant Proteins - metabolism</subject><issn>0168-1656</issn><issn>1873-4863</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkc2OFCEUhYnROO3oI2jY6MZUyV9BszSdUScZ40YTd4S6BTadKhiBmsRXmKeWTld0BYHvnntyDkKvKekpofLDqT-NIVUHPSNE90T2hNAnaEf3indiL_lTtGvcvqNykFfoRSknQojQA32OrqgeGBda79DjjfcOKk4eHyx7j22c8Ndf7QIpgos12xpSxCFiWOe6ZocXN4V1we2xHh22UMPDhWkS2UFaxhBtrNi3r5Tx7U98n9O0gpvOKodjiK44fLRLqS7j9GDzHwxunstL9MzbubhX23mNfny6-X740t19-3x7-HjXAee8dnz0mlCu9wzAklEOFKhzXoO2XoHghLUELBsHLaZJMK4YaxEwxQVRchglv0bvLrrN1-_VlWqWUM4ObHRpLUYqoVtUtIHDBYScSsnOm_sclubXUGLOJZiT2Uow5xIMkeYy92ZbsI4trf9TW-oNeLsBtoCdfbYRQvnHMaoUIUrwv606kjo</recordid><startdate>20090715</startdate><enddate>20090715</enddate><creator>WON HEE KIM</creator><creator>LIM, Jung-Seop</creator><creator>YOON, Yeup</creator><creator>GYUN MIN LEE</creator><general>Elsevier</general><scope>IQODW</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>7X8</scope></search><sort><creationdate>20090715</creationdate><title>Effect of Ca2+ and Mg2+ concentration in culture medium on the activation of recombinant factor IX produced in Chinese hamster ovary cells</title><author>WON HEE KIM ; LIM, Jung-Seop ; YOON, Yeup ; GYUN MIN LEE</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c333t-3bf9013982cca0b651c1eef9c9af7c4302873a2b594dd42372216527340765b63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Biotechnology</topic><topic>Calcium - pharmacology</topic><topic>Cell Survival</topic><topic>CHO Cells</topic><topic>Cricetinae</topic><topic>Cricetulus</topic><topic>Culture Media, Serum-Free - chemistry</topic><topic>Culture Media, Serum-Free - metabolism</topic><topic>Edetic Acid - chemistry</topic><topic>Factor IX - biosynthesis</topic><topic>Factor IX - genetics</topic><topic>Factor IX - metabolism</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Magnesium - pharmacology</topic><topic>Ovary - drug effects</topic><topic>Ovary - metabolism</topic><topic>Recombinant Proteins - biosynthesis</topic><topic>Recombinant Proteins - genetics</topic><topic>Recombinant Proteins - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>WON HEE KIM</creatorcontrib><creatorcontrib>LIM, Jung-Seop</creatorcontrib><creatorcontrib>YOON, Yeup</creatorcontrib><creatorcontrib>GYUN MIN LEE</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of biotechnology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>WON HEE KIM</au><au>LIM, Jung-Seop</au><au>YOON, Yeup</au><au>GYUN MIN LEE</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effect of Ca2+ and Mg2+ concentration in culture medium on the activation of recombinant factor IX produced in Chinese hamster ovary cells</atitle><jtitle>Journal of biotechnology</jtitle><addtitle>J Biotechnol</addtitle><date>2009-07-15</date><risdate>2009</risdate><volume>142</volume><issue>3-4</issue><spage>275</spage><epage>278</epage><pages>275-278</pages><issn>0168-1656</issn><eissn>1873-4863</eissn><coden>JBITD4</coden><abstract>Factor IX (FIX) plays an important role in the blood coagulation cascade. When Chinese hamster ovary (CHO) cells producing recombinant human FIX were cultivated using a serum-free medium (SFM) containing 1.12 mM of Ca(2+) and 0.82 mM of Mg(2+), a significant amount of active FIX (aFIX) was converted into undesirable activated FIX (FIXa) in the later phase of batch culture. In an effort to improve aFIX production from CHO cells, the effect of Ca(2+) and Mg(2+) concentrations in the culture medium on the activation of aFIX to FIXa was investigated using SFM with various concentrations of Ca(2+) and Mg(2+) in the range of 0-1.0 mM. The highest aFIX concentration of 1.36 IU/mL was obtained at 1.0 mM Ca(2+) and 1.0 mM Mg(2+), but the activation of aFIX to FIXa in the later phase of culture was rapid and significant. In contrast, at 0.5 mM Ca(2+) and 1.0 mM Mg(2+), the aFIX concentration of 1.33 IU/mL was obtained and did not decrease significantly in the later phase of culture. Taken together, lowering Ca(2+) concentration from 1.0 to 0.5 mM inhibits the activation of aFIX to FIXa in the later phase of culture, fortifying the robustness of downstream bioprocessing.</abstract><cop>Amsterdam</cop><pub>Elsevier</pub><pmid>19523499</pmid><doi>10.1016/j.jbiotec.2009.06.001</doi><tpages>4</tpages></addata></record> |
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subjects | Animals Biological and medical sciences Biotechnology Calcium - pharmacology Cell Survival CHO Cells Cricetinae Cricetulus Culture Media, Serum-Free - chemistry Culture Media, Serum-Free - metabolism Edetic Acid - chemistry Factor IX - biosynthesis Factor IX - genetics Factor IX - metabolism Female Fundamental and applied biological sciences. Psychology Magnesium - pharmacology Ovary - drug effects Ovary - metabolism Recombinant Proteins - biosynthesis Recombinant Proteins - genetics Recombinant Proteins - metabolism |
title | Effect of Ca2+ and Mg2+ concentration in culture medium on the activation of recombinant factor IX produced in Chinese hamster ovary cells |
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