Efficient coupled transcription/translation from PCR template by a hollow-fiber membrane bioreactor
A novel bioreactor using a hollow‐fiber membrane was developed for the coupled transcription/translation system using T7 RNA polymerase and Escherichia coli S30 extract. The large surface area per the reaction volume of the reactor assured rapid mass transfers of substrates into the reaction mixture...
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Veröffentlicht in: | Biotechnology and bioengineering 1999-07, Vol.64 (2), p.194-199 |
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creator | Nakano, Hideo Shinbata, Tomoya Okumura, Reiko Sekiguchi, Satoshi Fujishiro, Masatoshi Yamane, Tsuneo |
description | A novel bioreactor using a hollow‐fiber membrane was developed for the coupled transcription/translation system using T7 RNA polymerase and Escherichia coli S30 extract. The large surface area per the reaction volume of the reactor assured rapid mass transfers of substrates into the reaction mixture and of wastes out from it across the membrane by their molecular diffusion. The flux was large enough to maintain nucleotide concentrations for more than 3 h, which increased the protein synthesis greatly. In addition, the T7 terminator sequence downstream from the reporter genes was found to increase the synthesized protein significantly, especially when the product of polymerase chain reaction (PCR) was used as a template. Implementation of this finding and use of the bioreactor developed multiplied the productivity of protein by the in vitro direct expression from PCR template. © 1999 John Wiley & Sons, Inc. Biotechnol Bioeng 64: 194–199, 1999. |
doi_str_mv | 10.1002/(SICI)1097-0290(19990720)64:2<194::AID-BIT8>3.0.CO;2-5 |
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Biotechnol Bioeng 64: 194–199, 1999.</description><identifier>ISSN: 0006-3592</identifier><identifier>EISSN: 1097-0290</identifier><identifier>DOI: 10.1002/(SICI)1097-0290(19990720)64:2<194::AID-BIT8>3.0.CO;2-5</identifier><identifier>PMID: 10397855</identifier><identifier>CODEN: BIBIAU</identifier><language>eng</language><publisher>New York: John Wiley & Sons, Inc</publisher><subject>Base Sequence ; Biological and medical sciences ; Biological membranes ; bioreactor ; Bioreactors ; Biosynthesis ; Biotechnology ; coupled transcription/translation ; DNA-Directed RNA Polymerases - metabolism ; Enzymes ; Escherichia coli ; Escherichia coli - genetics ; Fibrous membranes ; Fundamental and applied biological sciences. Psychology ; hollow-fiber membrane ; Mass transfer ; Methods. Procedures. Technologies ; Molecular Sequence Data ; Phage T7 ; polymerase chain reaction ; Polymerase Chain Reaction - methods ; Protein Biosynthesis ; Substrates ; T7 terminator ; Time Factors ; Transcription, Genetic ; Various methods and equipments ; Viral Proteins</subject><ispartof>Biotechnology and bioengineering, 1999-07, Vol.64 (2), p.194-199</ispartof><rights>Copyright © 1999 John Wiley & Sons, Inc.</rights><rights>1999 INIST-CNRS</rights><rights>Copyright 1999 John Wiley & Sons, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c5978-12dff5ed178b67cb6bb50e0e51beea90367f6456f5c3fabe65d3fad027dd15dd3</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%2F%28SICI%291097-0290%2819990720%2964%3A2%3C194%3A%3AAID-BIT8%3E3.0.CO%3B2-5$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2F%28SICI%291097-0290%2819990720%2964%3A2%3C194%3A%3AAID-BIT8%3E3.0.CO%3B2-5$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1853205$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10397855$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Nakano, Hideo</creatorcontrib><creatorcontrib>Shinbata, Tomoya</creatorcontrib><creatorcontrib>Okumura, Reiko</creatorcontrib><creatorcontrib>Sekiguchi, Satoshi</creatorcontrib><creatorcontrib>Fujishiro, Masatoshi</creatorcontrib><creatorcontrib>Yamane, Tsuneo</creatorcontrib><title>Efficient coupled transcription/translation from PCR template by a hollow-fiber membrane bioreactor</title><title>Biotechnology and bioengineering</title><addtitle>Biotechnol. Bioeng</addtitle><description>A novel bioreactor using a hollow‐fiber membrane was developed for the coupled transcription/translation system using T7 RNA polymerase and Escherichia coli S30 extract. The large surface area per the reaction volume of the reactor assured rapid mass transfers of substrates into the reaction mixture and of wastes out from it across the membrane by their molecular diffusion. The flux was large enough to maintain nucleotide concentrations for more than 3 h, which increased the protein synthesis greatly. In addition, the T7 terminator sequence downstream from the reporter genes was found to increase the synthesized protein significantly, especially when the product of polymerase chain reaction (PCR) was used as a template. Implementation of this finding and use of the bioreactor developed multiplied the productivity of protein by the in vitro direct expression from PCR template. © 1999 John Wiley & Sons, Inc. Biotechnol Bioeng 64: 194–199, 1999.</description><subject>Base Sequence</subject><subject>Biological and medical sciences</subject><subject>Biological membranes</subject><subject>bioreactor</subject><subject>Bioreactors</subject><subject>Biosynthesis</subject><subject>Biotechnology</subject><subject>coupled transcription/translation</subject><subject>DNA-Directed RNA Polymerases - metabolism</subject><subject>Enzymes</subject><subject>Escherichia coli</subject><subject>Escherichia coli - genetics</subject><subject>Fibrous membranes</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>hollow-fiber membrane</subject><subject>Mass transfer</subject><subject>Methods. Procedures. Technologies</subject><subject>Molecular Sequence Data</subject><subject>Phage T7</subject><subject>polymerase chain reaction</subject><subject>Polymerase Chain Reaction - methods</subject><subject>Protein Biosynthesis</subject><subject>Substrates</subject><subject>T7 terminator</subject><subject>Time Factors</subject><subject>Transcription, Genetic</subject><subject>Various methods and equipments</subject><subject>Viral Proteins</subject><issn>0006-3592</issn><issn>1097-0290</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkVFv0zAUhSMEYmXwF1AeENoe0l3bsR0XNGnLRldpoggKSLxYjmMLQ9IUO9XWf4-zlg0JpD5dn-vjoyN_SXKKYIwA8MnRp1k5O0YgeAZYwBESQgDHcMzyCX6LRD6ZnM0usvPZojglYxiX8zc4o4-S0f2Tx8kIAFhGqMAHybMQfkTJC8aeJgcIiOAFpaNEX1rrtDPLPtXdetWYOu29Wgbt3ap33fLkTjVqOKfWd236ofyY9qZdxZ1Jq02q0u9d03Q3mXWV8Wlr2io-iVeu80bpvvPPkydWNcG82M3D5PO7y0V5lV3Pp7Py7DrTNLbJEK6tpaZGvKgY1xWrKgoGDEWVMUoAYdyynDJLNbGqMozWcdaAeV0jWtfkMHm9zV357tfahF62LmjTNLFOtw6SiaJAnIq9RoxyKFC-34g4AUoKFo1ftkbtuxC8sXLlXav8RiKQA1ApB6ByoCMHOvIPUMlyiaPKpYxA5QBUEgmynMc1jcEvdw3WVWvqv2K3BKPh1c6gglaNjX-vXXjwFZRgoA8Fb1xjNv-021vuP93udAzOtsEu9Ob2Plj5n5Jxwqn8-n4qr75N8eKiFLIkvwFBp9i6</recordid><startdate>19990720</startdate><enddate>19990720</enddate><creator>Nakano, Hideo</creator><creator>Shinbata, Tomoya</creator><creator>Okumura, Reiko</creator><creator>Sekiguchi, Satoshi</creator><creator>Fujishiro, Masatoshi</creator><creator>Yamane, Tsuneo</creator><general>John Wiley & Sons, Inc</general><general>Wiley</general><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>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>19990720</creationdate><title>Efficient coupled transcription/translation from PCR template by a hollow-fiber membrane bioreactor</title><author>Nakano, Hideo ; Shinbata, Tomoya ; Okumura, Reiko ; Sekiguchi, Satoshi ; Fujishiro, Masatoshi ; Yamane, Tsuneo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5978-12dff5ed178b67cb6bb50e0e51beea90367f6456f5c3fabe65d3fad027dd15dd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Base Sequence</topic><topic>Biological and medical sciences</topic><topic>Biological membranes</topic><topic>bioreactor</topic><topic>Bioreactors</topic><topic>Biosynthesis</topic><topic>Biotechnology</topic><topic>coupled transcription/translation</topic><topic>DNA-Directed RNA Polymerases - metabolism</topic><topic>Enzymes</topic><topic>Escherichia coli</topic><topic>Escherichia coli - genetics</topic><topic>Fibrous membranes</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>hollow-fiber membrane</topic><topic>Mass transfer</topic><topic>Methods. Procedures. Technologies</topic><topic>Molecular Sequence Data</topic><topic>Phage T7</topic><topic>polymerase chain reaction</topic><topic>Polymerase Chain Reaction - methods</topic><topic>Protein Biosynthesis</topic><topic>Substrates</topic><topic>T7 terminator</topic><topic>Time Factors</topic><topic>Transcription, Genetic</topic><topic>Various methods and equipments</topic><topic>Viral Proteins</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nakano, Hideo</creatorcontrib><creatorcontrib>Shinbata, Tomoya</creatorcontrib><creatorcontrib>Okumura, Reiko</creatorcontrib><creatorcontrib>Sekiguchi, Satoshi</creatorcontrib><creatorcontrib>Fujishiro, Masatoshi</creatorcontrib><creatorcontrib>Yamane, Tsuneo</creatorcontrib><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>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>Nakano, Hideo</au><au>Shinbata, Tomoya</au><au>Okumura, Reiko</au><au>Sekiguchi, Satoshi</au><au>Fujishiro, Masatoshi</au><au>Yamane, Tsuneo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Efficient coupled transcription/translation from PCR template by a hollow-fiber membrane bioreactor</atitle><jtitle>Biotechnology and bioengineering</jtitle><addtitle>Biotechnol. Bioeng</addtitle><date>1999-07-20</date><risdate>1999</risdate><volume>64</volume><issue>2</issue><spage>194</spage><epage>199</epage><pages>194-199</pages><issn>0006-3592</issn><eissn>1097-0290</eissn><coden>BIBIAU</coden><abstract>A novel bioreactor using a hollow‐fiber membrane was developed for the coupled transcription/translation system using T7 RNA polymerase and Escherichia coli S30 extract. The large surface area per the reaction volume of the reactor assured rapid mass transfers of substrates into the reaction mixture and of wastes out from it across the membrane by their molecular diffusion. The flux was large enough to maintain nucleotide concentrations for more than 3 h, which increased the protein synthesis greatly. In addition, the T7 terminator sequence downstream from the reporter genes was found to increase the synthesized protein significantly, especially when the product of polymerase chain reaction (PCR) was used as a template. 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subjects | Base Sequence Biological and medical sciences Biological membranes bioreactor Bioreactors Biosynthesis Biotechnology coupled transcription/translation DNA-Directed RNA Polymerases - metabolism Enzymes Escherichia coli Escherichia coli - genetics Fibrous membranes Fundamental and applied biological sciences. Psychology hollow-fiber membrane Mass transfer Methods. Procedures. Technologies Molecular Sequence Data Phage T7 polymerase chain reaction Polymerase Chain Reaction - methods Protein Biosynthesis Substrates T7 terminator Time Factors Transcription, Genetic Various methods and equipments Viral Proteins |
title | Efficient coupled transcription/translation from PCR template by a hollow-fiber membrane bioreactor |
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