High-level expression of recombinant human soluble thrombomodulin in serum-free medium by CHO-K1 cells
Cultivation of gene-engineered Chinese hamster ovary (CHO-K1) cells that produce recombinant human soluble thrombomodulin (rsTM) was investigated to optimize conditions for high-level expression of the protein in a serum-free medium. For economic protein production, oxygenation of cultures with pure...
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Veröffentlicht in: | Applied microbiology and biotechnology 1993, Vol.38 (4), p.520-525 |
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creator | OGATA, M WAKITA, K.-I KIMURA, K MARUMOTO, Y OH-I, K SHIMIZU, S |
description | Cultivation of gene-engineered Chinese hamster ovary (CHO-K1) cells that produce recombinant human soluble thrombomodulin (rsTM) was investigated to optimize conditions for high-level expression of the protein in a serum-free medium. For economic protein production, oxygenation of cultures with pure O2 permitted sufficient cell growth for high rsTM production with only 1 g/l of microcarriers and a low foetal bovine serum concentration. A longer growth phase (over 5 days) with serum was important to establish sufficient growth of this cell line on the microcarriers for subsequent serum-free culture, and to support a long-term production phase (about 2 months). In the production phase, a high glucose concentration (6.15 g/l) in the serum-free medium was very effective for prolonging the harvest cycle interval. Under these conditions, up to 100 mg/l rsTM was expressed in the conditioned medium. The rates of glucose consumption (G) and lactate production (L) were measured periodically and their ratio (L/G ratio) correlated with rsTM productivity. When the average L/G ratio was lower, reflecting a lower lactate production rate due to appropriate oxygenation of the culture, the specific rsTM production rate increased. Thus it may be possible to estimate protein productivity from L/G ratios calculated from the glucose and lactate measurements. |
doi_str_mv | 10.1007/bf00242948 |
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For economic protein production, oxygenation of cultures with pure O2 permitted sufficient cell growth for high rsTM production with only 1 g/l of microcarriers and a low foetal bovine serum concentration. A longer growth phase (over 5 days) with serum was important to establish sufficient growth of this cell line on the microcarriers for subsequent serum-free culture, and to support a long-term production phase (about 2 months). In the production phase, a high glucose concentration (6.15 g/l) in the serum-free medium was very effective for prolonging the harvest cycle interval. Under these conditions, up to 100 mg/l rsTM was expressed in the conditioned medium. The rates of glucose consumption (G) and lactate production (L) were measured periodically and their ratio (L/G ratio) correlated with rsTM productivity. When the average L/G ratio was lower, reflecting a lower lactate production rate due to appropriate oxygenation of the culture, the specific rsTM production rate increased. Thus it may be possible to estimate protein productivity from L/G ratios calculated from the glucose and lactate measurements.</description><identifier>ISSN: 0175-7598</identifier><identifier>EISSN: 1432-0614</identifier><identifier>DOI: 10.1007/bf00242948</identifier><identifier>PMID: 7764042</identifier><identifier>CODEN: AMBIDG</identifier><language>eng</language><publisher>Berlin: Springer</publisher><subject>Animals ; Biological and medical sciences ; Biotechnology ; Cell Division ; CHO Cells ; Cloning, Molecular ; Cricetinae ; Culture Media, Serum-Free - pharmacology ; Fundamental and applied biological sciences. Psychology ; Genetic engineering ; Genetic technics ; Glucose - pharmacology ; Humans ; Methods. Procedures. Technologies ; Microspheres ; Modification of gene expression level ; Oxygen - pharmacology ; Receptors, Cell Surface - biosynthesis ; Receptors, Cell Surface - genetics ; Receptors, Thrombin ; Recombinant Proteins - biosynthesis ; Recombinant Proteins - genetics ; Time Factors</subject><ispartof>Applied microbiology and biotechnology, 1993, Vol.38 (4), p.520-525</ispartof><rights>1993 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c408t-1d0c05e2f4fac9020d9858e696f85e5e4a3a0ec2ce2e840aa3290a7dbc41660f3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,4024,27923,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=4629223$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7764042$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>OGATA, M</creatorcontrib><creatorcontrib>WAKITA, K.-I</creatorcontrib><creatorcontrib>KIMURA, K</creatorcontrib><creatorcontrib>MARUMOTO, Y</creatorcontrib><creatorcontrib>OH-I, K</creatorcontrib><creatorcontrib>SHIMIZU, S</creatorcontrib><title>High-level expression of recombinant human soluble thrombomodulin in serum-free medium by CHO-K1 cells</title><title>Applied microbiology and biotechnology</title><addtitle>Appl Microbiol Biotechnol</addtitle><description>Cultivation of gene-engineered Chinese hamster ovary (CHO-K1) cells that produce recombinant human soluble thrombomodulin (rsTM) was investigated to optimize conditions for high-level expression of the protein in a serum-free medium. For economic protein production, oxygenation of cultures with pure O2 permitted sufficient cell growth for high rsTM production with only 1 g/l of microcarriers and a low foetal bovine serum concentration. A longer growth phase (over 5 days) with serum was important to establish sufficient growth of this cell line on the microcarriers for subsequent serum-free culture, and to support a long-term production phase (about 2 months). In the production phase, a high glucose concentration (6.15 g/l) in the serum-free medium was very effective for prolonging the harvest cycle interval. Under these conditions, up to 100 mg/l rsTM was expressed in the conditioned medium. The rates of glucose consumption (G) and lactate production (L) were measured periodically and their ratio (L/G ratio) correlated with rsTM productivity. When the average L/G ratio was lower, reflecting a lower lactate production rate due to appropriate oxygenation of the culture, the specific rsTM production rate increased. Thus it may be possible to estimate protein productivity from L/G ratios calculated from the glucose and lactate measurements.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Biotechnology</subject><subject>Cell Division</subject><subject>CHO Cells</subject><subject>Cloning, Molecular</subject><subject>Cricetinae</subject><subject>Culture Media, Serum-Free - pharmacology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Genetic engineering</subject><subject>Genetic technics</subject><subject>Glucose - pharmacology</subject><subject>Humans</subject><subject>Methods. Procedures. Technologies</subject><subject>Microspheres</subject><subject>Modification of gene expression level</subject><subject>Oxygen - pharmacology</subject><subject>Receptors, Cell Surface - biosynthesis</subject><subject>Receptors, Cell Surface - genetics</subject><subject>Receptors, Thrombin</subject><subject>Recombinant Proteins - biosynthesis</subject><subject>Recombinant Proteins - genetics</subject><subject>Time Factors</subject><issn>0175-7598</issn><issn>1432-0614</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1993</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE1LxDAURYMoOn5s3AtZiAuh-pImabrUwXHEATe6Lmn64lTSZkym4vx7K45uhQd3cQ-XxyHklMEVAyiuawfABS-F3iETJnKegWJil0yAFTIrZKkPyGFKbwCMa6X2yX5RKAGCT4ibt6_LzOMHeoqfq4gptaGnwdGINnR125t-TZdDZ3qagh9qj3S9jGMTutAMvu3peAnj0GUuItIOm3boaL2h0_lT9sioRe_TMdlzxic82eYReZndPU_n2eLp_mF6s8isAL3OWAMWJHInnLElcGhKLTWqUjktUaIwuQG03CJHLcCYnJdgiqa2gikFLj8iFz-7qxjeB0zrqmvT9wemxzCkqpBSM635vyBTolSSqxG8_AFtDClFdNUqtp2Jm4pB9W2_up392h_hs-3qUI8i_tCt7rE_3_YmWeNdNL1t0x8mFC85z_MvPS6MLg</recordid><startdate>1993</startdate><enddate>1993</enddate><creator>OGATA, M</creator><creator>WAKITA, K.-I</creator><creator>KIMURA, K</creator><creator>MARUMOTO, Y</creator><creator>OH-I, K</creator><creator>SHIMIZU, S</creator><general>Springer</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>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>1993</creationdate><title>High-level expression of recombinant human soluble thrombomodulin in serum-free medium by CHO-K1 cells</title><author>OGATA, M ; WAKITA, K.-I ; KIMURA, K ; MARUMOTO, Y ; OH-I, K ; SHIMIZU, S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c408t-1d0c05e2f4fac9020d9858e696f85e5e4a3a0ec2ce2e840aa3290a7dbc41660f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1993</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Biotechnology</topic><topic>Cell Division</topic><topic>CHO Cells</topic><topic>Cloning, Molecular</topic><topic>Cricetinae</topic><topic>Culture Media, Serum-Free - pharmacology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Genetic engineering</topic><topic>Genetic technics</topic><topic>Glucose - pharmacology</topic><topic>Humans</topic><topic>Methods. Procedures. Technologies</topic><topic>Microspheres</topic><topic>Modification of gene expression level</topic><topic>Oxygen - pharmacology</topic><topic>Receptors, Cell Surface - biosynthesis</topic><topic>Receptors, Cell Surface - genetics</topic><topic>Receptors, Thrombin</topic><topic>Recombinant Proteins - biosynthesis</topic><topic>Recombinant Proteins - genetics</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>OGATA, M</creatorcontrib><creatorcontrib>WAKITA, K.-I</creatorcontrib><creatorcontrib>KIMURA, K</creatorcontrib><creatorcontrib>MARUMOTO, Y</creatorcontrib><creatorcontrib>OH-I, K</creatorcontrib><creatorcontrib>SHIMIZU, S</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>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>Applied microbiology and biotechnology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>OGATA, M</au><au>WAKITA, K.-I</au><au>KIMURA, K</au><au>MARUMOTO, Y</au><au>OH-I, K</au><au>SHIMIZU, S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>High-level expression of recombinant human soluble thrombomodulin in serum-free medium by CHO-K1 cells</atitle><jtitle>Applied microbiology and biotechnology</jtitle><addtitle>Appl Microbiol Biotechnol</addtitle><date>1993</date><risdate>1993</risdate><volume>38</volume><issue>4</issue><spage>520</spage><epage>525</epage><pages>520-525</pages><issn>0175-7598</issn><eissn>1432-0614</eissn><coden>AMBIDG</coden><abstract>Cultivation of gene-engineered Chinese hamster ovary (CHO-K1) cells that produce recombinant human soluble thrombomodulin (rsTM) was investigated to optimize conditions for high-level expression of the protein in a serum-free medium. For economic protein production, oxygenation of cultures with pure O2 permitted sufficient cell growth for high rsTM production with only 1 g/l of microcarriers and a low foetal bovine serum concentration. A longer growth phase (over 5 days) with serum was important to establish sufficient growth of this cell line on the microcarriers for subsequent serum-free culture, and to support a long-term production phase (about 2 months). In the production phase, a high glucose concentration (6.15 g/l) in the serum-free medium was very effective for prolonging the harvest cycle interval. Under these conditions, up to 100 mg/l rsTM was expressed in the conditioned medium. The rates of glucose consumption (G) and lactate production (L) were measured periodically and their ratio (L/G ratio) correlated with rsTM productivity. When the average L/G ratio was lower, reflecting a lower lactate production rate due to appropriate oxygenation of the culture, the specific rsTM production rate increased. Thus it may be possible to estimate protein productivity from L/G ratios calculated from the glucose and lactate measurements.</abstract><cop>Berlin</cop><pub>Springer</pub><pmid>7764042</pmid><doi>10.1007/bf00242948</doi><tpages>6</tpages></addata></record> |
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subjects | Animals Biological and medical sciences Biotechnology Cell Division CHO Cells Cloning, Molecular Cricetinae Culture Media, Serum-Free - pharmacology Fundamental and applied biological sciences. Psychology Genetic engineering Genetic technics Glucose - pharmacology Humans Methods. Procedures. Technologies Microspheres Modification of gene expression level Oxygen - pharmacology Receptors, Cell Surface - biosynthesis Receptors, Cell Surface - genetics Receptors, Thrombin Recombinant Proteins - biosynthesis Recombinant Proteins - genetics Time Factors |
title | High-level expression of recombinant human soluble thrombomodulin in serum-free medium by CHO-K1 cells |
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