Production of human α-1-antitrypsin from transgenic rice cell culture in a membrane bioreactor
Transgenic plant cell cultures offer a number of advantages over alternative host expression systems, but so far relatively low product concentrations have been achieved. In this study, transgenic rice cells are used in a two‐compartment membrane bioreactor (CELLine 350, Integra Biosciences) for the...
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Veröffentlicht in: | Biotechnology progress 2005-05, Vol.21 (3), p.728-734 |
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creator | McDonald, K.A Hong, L.M Trombly, D.M Xie, Q Jackman, A.P |
description | Transgenic plant cell cultures offer a number of advantages over alternative host expression systems, but so far relatively low product concentrations have been achieved. In this study, transgenic rice cells are used in a two‐compartment membrane bioreactor (CELLine 350, Integra Biosciences) for the production of recombinant α‐1‐antitrypsin (rAAT). Expression of rAAT is controlled by the rice α‐amylase (RAmy3D) promoter, which is induced in the absence of sugar. The extracellular product is retained in the bioreactorapos;s relatively small cell compartment, thereby increasing product concentration. Due to the packed nature of the cell aggregates in the cell compartment, a clarified product solution can be withdrawn from the bioreactor. Active rAAT reached levels of 100–247 mg/L (4–10% of the total extracellular protein) in the cell compartment at 5–6 days postinduction, and multiple inductions of the RAmy3D promoter were demonstrated. |
doi_str_mv | 10.1021/bp0496676 |
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In this study, transgenic rice cells are used in a two‐compartment membrane bioreactor (CELLine 350, Integra Biosciences) for the production of recombinant α‐1‐antitrypsin (rAAT). Expression of rAAT is controlled by the rice α‐amylase (RAmy3D) promoter, which is induced in the absence of sugar. The extracellular product is retained in the bioreactorapos;s relatively small cell compartment, thereby increasing product concentration. Due to the packed nature of the cell aggregates in the cell compartment, a clarified product solution can be withdrawn from the bioreactor. Active rAAT reached levels of 100–247 mg/L (4–10% of the total extracellular protein) in the cell compartment at 5–6 days postinduction, and multiple inductions of the RAmy3D promoter were demonstrated.</description><identifier>ISSN: 8756-7938</identifier><identifier>EISSN: 1520-6033</identifier><identifier>DOI: 10.1021/bp0496676</identifier><identifier>PMID: 15932249</identifier><identifier>CODEN: BIPRET</identifier><language>eng</language><publisher>USA: American Chemical Society</publisher><subject>Acetylcholine receptors ; alpha -Amylase ; alpha 1-Antitrypsin - biosynthesis ; alpha 1-Antitrypsin - genetics ; alpha-1-antitrypsin ; artificial membranes ; Biological and medical sciences ; Bioreactors ; Biotechnology ; blood proteins ; Cell culture ; Cell Culture Techniques - instrumentation ; Cell Culture Techniques - methods ; Cell Line ; Equipment Design ; Equipment Failure Analysis ; Fundamental and applied biological sciences. Psychology ; Humans ; Membranes, Artificial ; Oryza - physiology ; Oryza sativa ; Plants, Genetically Modified - growth & development ; Plants, Genetically Modified - metabolism ; promoter regions ; Promoters ; Protein Engineering - instrumentation ; Protein Engineering - methods ; protein synthesis ; Q1 ; Q2 ; recombinant DNA ; recombinant proteins ; Recombinant Proteins - biosynthesis ; rice ; Sugar ; Transgenic plants ; trypsin inhibitors</subject><ispartof>Biotechnology progress, 2005-05, Vol.21 (3), p.728-734</ispartof><rights>Copyright © 2005 American Institute of Chemical Engineers (AIChE)</rights><rights>2005 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4496-3f1f5d2bae9eb17aaed54acad0513d51809f1365ebb779438a758d327d4eacab3</citedby><cites>FETCH-LOGICAL-c4496-3f1f5d2bae9eb17aaed54acad0513d51809f1365ebb779438a758d327d4eacab3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1021%2Fbp0496676$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1021%2Fbp0496676$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=16843516$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15932249$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>McDonald, K.A</creatorcontrib><creatorcontrib>Hong, L.M</creatorcontrib><creatorcontrib>Trombly, D.M</creatorcontrib><creatorcontrib>Xie, Q</creatorcontrib><creatorcontrib>Jackman, A.P</creatorcontrib><title>Production of human α-1-antitrypsin from transgenic rice cell culture in a membrane bioreactor</title><title>Biotechnology progress</title><addtitle>Biotechnol Progress</addtitle><description>Transgenic plant cell cultures offer a number of advantages over alternative host expression systems, but so far relatively low product concentrations have been achieved. In this study, transgenic rice cells are used in a two‐compartment membrane bioreactor (CELLine 350, Integra Biosciences) for the production of recombinant α‐1‐antitrypsin (rAAT). Expression of rAAT is controlled by the rice α‐amylase (RAmy3D) promoter, which is induced in the absence of sugar. The extracellular product is retained in the bioreactorapos;s relatively small cell compartment, thereby increasing product concentration. Due to the packed nature of the cell aggregates in the cell compartment, a clarified product solution can be withdrawn from the bioreactor. Active rAAT reached levels of 100–247 mg/L (4–10% of the total extracellular protein) in the cell compartment at 5–6 days postinduction, and multiple inductions of the RAmy3D promoter were demonstrated.</description><subject>Acetylcholine receptors</subject><subject>alpha -Amylase</subject><subject>alpha 1-Antitrypsin - biosynthesis</subject><subject>alpha 1-Antitrypsin - genetics</subject><subject>alpha-1-antitrypsin</subject><subject>artificial membranes</subject><subject>Biological and medical sciences</subject><subject>Bioreactors</subject><subject>Biotechnology</subject><subject>blood proteins</subject><subject>Cell culture</subject><subject>Cell Culture Techniques - instrumentation</subject><subject>Cell Culture Techniques - methods</subject><subject>Cell Line</subject><subject>Equipment Design</subject><subject>Equipment Failure Analysis</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Humans</subject><subject>Membranes, Artificial</subject><subject>Oryza - physiology</subject><subject>Oryza sativa</subject><subject>Plants, Genetically Modified - growth & development</subject><subject>Plants, Genetically Modified - metabolism</subject><subject>promoter regions</subject><subject>Promoters</subject><subject>Protein Engineering - instrumentation</subject><subject>Protein Engineering - methods</subject><subject>protein synthesis</subject><subject>Q1</subject><subject>Q2</subject><subject>recombinant DNA</subject><subject>recombinant proteins</subject><subject>Recombinant Proteins - biosynthesis</subject><subject>rice</subject><subject>Sugar</subject><subject>Transgenic plants</subject><subject>trypsin inhibitors</subject><issn>8756-7938</issn><issn>1520-6033</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp90M1u1DAUBWALUdGhsOAFwBtAXQTsOP5b0im0FVWpoBUSG-vGcYppEg92IpjH4kV4pnqU0XQFK2--e-_xQegZJW8oKenbekUqLYQUD9CC8pIUgjD2EC2U5KKQmql99DilH4QQRUT5CO1TrllZVnqBzGUMzWRHHwYcWvx96mHAf_8UtIBh9GNcr5IfcBtDj8cIQ7pxg7c4euuwdV2H7dSNU3Q4I8C96-uMHK59iA7sGOITtNdCl9zT7XuArj-8v1qeFuefTs6W784LW-XoBWtpy5uyBqddTSWAa3gFFhrCKWs4VUS3lAnu6lpKXTEFkquGlbKp8h2o2QF6Pe9dxfBzcmk0vU-bhDlOmJKRFRdEUqqyfPVfKaTSVGie4eEMbQwpRdeaVfQ9xLWhxGx6N7ves32-XTrVvWvu5bboDF5uASQLXZtrsj7dO6EqxulmEZ3dL9-59b8vmqOry8-748U849Pofu9mIN7mzzDJzdeLE3N88fHbKT9emqPsX8y-hWDgJuYc119KQhmhhGhFKnYHZDuy6g</recordid><startdate>20050501</startdate><enddate>20050501</enddate><creator>McDonald, K.A</creator><creator>Hong, L.M</creator><creator>Trombly, D.M</creator><creator>Xie, Q</creator><creator>Jackman, A.P</creator><general>American Chemical Society</general><general>American Institute of Chemical Engineers</general><scope>FBQ</scope><scope>BSCLL</scope><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>20050501</creationdate><title>Production of human α-1-antitrypsin from transgenic rice cell culture in a membrane bioreactor</title><author>McDonald, K.A ; Hong, L.M ; Trombly, D.M ; Xie, Q ; Jackman, A.P</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4496-3f1f5d2bae9eb17aaed54acad0513d51809f1365ebb779438a758d327d4eacab3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Acetylcholine receptors</topic><topic>alpha -Amylase</topic><topic>alpha 1-Antitrypsin - biosynthesis</topic><topic>alpha 1-Antitrypsin - genetics</topic><topic>alpha-1-antitrypsin</topic><topic>artificial membranes</topic><topic>Biological and medical sciences</topic><topic>Bioreactors</topic><topic>Biotechnology</topic><topic>blood proteins</topic><topic>Cell culture</topic><topic>Cell Culture Techniques - instrumentation</topic><topic>Cell Culture Techniques - methods</topic><topic>Cell Line</topic><topic>Equipment Design</topic><topic>Equipment Failure Analysis</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Humans</topic><topic>Membranes, Artificial</topic><topic>Oryza - physiology</topic><topic>Oryza sativa</topic><topic>Plants, Genetically Modified - growth & development</topic><topic>Plants, Genetically Modified - metabolism</topic><topic>promoter regions</topic><topic>Promoters</topic><topic>Protein Engineering - instrumentation</topic><topic>Protein Engineering - methods</topic><topic>protein synthesis</topic><topic>Q1</topic><topic>Q2</topic><topic>recombinant DNA</topic><topic>recombinant proteins</topic><topic>Recombinant Proteins - biosynthesis</topic><topic>rice</topic><topic>Sugar</topic><topic>Transgenic plants</topic><topic>trypsin inhibitors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>McDonald, K.A</creatorcontrib><creatorcontrib>Hong, L.M</creatorcontrib><creatorcontrib>Trombly, D.M</creatorcontrib><creatorcontrib>Xie, Q</creatorcontrib><creatorcontrib>Jackman, A.P</creatorcontrib><collection>AGRIS</collection><collection>Istex</collection><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>Biotechnology progress</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>McDonald, K.A</au><au>Hong, L.M</au><au>Trombly, D.M</au><au>Xie, Q</au><au>Jackman, A.P</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Production of human α-1-antitrypsin from transgenic rice cell culture in a membrane bioreactor</atitle><jtitle>Biotechnology progress</jtitle><addtitle>Biotechnol Progress</addtitle><date>2005-05-01</date><risdate>2005</risdate><volume>21</volume><issue>3</issue><spage>728</spage><epage>734</epage><pages>728-734</pages><issn>8756-7938</issn><eissn>1520-6033</eissn><coden>BIPRET</coden><abstract>Transgenic plant cell cultures offer a number of advantages over alternative host expression systems, but so far relatively low product concentrations have been achieved. In this study, transgenic rice cells are used in a two‐compartment membrane bioreactor (CELLine 350, Integra Biosciences) for the production of recombinant α‐1‐antitrypsin (rAAT). Expression of rAAT is controlled by the rice α‐amylase (RAmy3D) promoter, which is induced in the absence of sugar. The extracellular product is retained in the bioreactorapos;s relatively small cell compartment, thereby increasing product concentration. Due to the packed nature of the cell aggregates in the cell compartment, a clarified product solution can be withdrawn from the bioreactor. Active rAAT reached levels of 100–247 mg/L (4–10% of the total extracellular protein) in the cell compartment at 5–6 days postinduction, and multiple inductions of the RAmy3D promoter were demonstrated.</abstract><cop>USA</cop><pub>American Chemical Society</pub><pmid>15932249</pmid><doi>10.1021/bp0496676</doi><tpages>7</tpages></addata></record> |
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subjects | Acetylcholine receptors alpha -Amylase alpha 1-Antitrypsin - biosynthesis alpha 1-Antitrypsin - genetics alpha-1-antitrypsin artificial membranes Biological and medical sciences Bioreactors Biotechnology blood proteins Cell culture Cell Culture Techniques - instrumentation Cell Culture Techniques - methods Cell Line Equipment Design Equipment Failure Analysis Fundamental and applied biological sciences. Psychology Humans Membranes, Artificial Oryza - physiology Oryza sativa Plants, Genetically Modified - growth & development Plants, Genetically Modified - metabolism promoter regions Promoters Protein Engineering - instrumentation Protein Engineering - methods protein synthesis Q1 Q2 recombinant DNA recombinant proteins Recombinant Proteins - biosynthesis rice Sugar Transgenic plants trypsin inhibitors |
title | Production of human α-1-antitrypsin from transgenic rice cell culture in a membrane bioreactor |
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