The production of D‐acetoin by a transgenic Escherichia coli
A 6 kbp SphI fragment encoding genes for the enzymes α‐acetolactate synthase (ALS), α‐acetolactate decarboxylase (ALDC) and meso‐2,3‐butanediol dehydrogenase (meso‐BDH), involved in the formation of meso‐2,3‐butanediol (meso‐BD) from pyruvic acid, was cloned into plasmid pUC118. When derivatives of...
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Veröffentlicht in: | Letters in applied microbiology 1998-04, Vol.26 (4), p.275-278 |
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creator | UI, S MIMURA, A OKUMA, M KUDO, T |
description | A 6 kbp SphI fragment encoding genes for the enzymes α‐acetolactate synthase (ALS), α‐acetolactate decarboxylase (ALDC) and meso‐2,3‐butanediol dehydrogenase (meso‐BDH), involved in the formation of meso‐2,3‐butanediol (meso‐BD) from pyruvic acid, was cloned into plasmid pUC118. When derivatives of this plasmid were introduced into Escherichia coli JM109, the transformants were able to produce
D‐acetoin (
D‐AC) without contamination with
L‐acetoin (
L‐AC). |
doi_str_mv | 10.1046/j.1472-765X.1998.00313.x |
format | Article |
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D‐acetoin (
D‐AC) without contamination with
L‐acetoin (
L‐AC).</description><identifier>ISSN: 0266-8254</identifier><identifier>EISSN: 1472-765X</identifier><identifier>DOI: 10.1046/j.1472-765X.1998.00313.x</identifier><identifier>PMID: 9633093</identifier><identifier>CODEN: LAMIE7</identifier><language>eng</language><publisher>Edinburgh, UK: Blackwell Science Ltd</publisher><subject>Acetoin - metabolism ; Acetolactate Synthase - genetics ; Alcohol Oxidoreductases - genetics ; Biological and medical sciences ; Biotechnology ; Carboxy-Lyases - genetics ; Chromatography, Gas ; Culture Media - chemistry ; Escherichia coli ; Escherichia coli - genetics ; Escherichia coli - metabolism ; Fundamental and applied biological sciences. Psychology ; Genetic engineering ; Genetic technics ; Methods. Procedures. Technologies ; Modification of gene expression level ; Time Factors ; Transformation, Bacterial</subject><ispartof>Letters in applied microbiology, 1998-04, Vol.26 (4), p.275-278</ispartof><rights>The Society for Applied Bacteriology, 1998</rights><rights>1998 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5103-e46282885ee696a4f2ef46f937a879fa54be6ae27fe988c3bccabdfcbc6f35b93</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1046%2Fj.1472-765X.1998.00313.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1046%2Fj.1472-765X.1998.00313.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>315,781,785,1418,27929,27930,45579,45580</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2265116$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9633093$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>UI, S</creatorcontrib><creatorcontrib>MIMURA, A</creatorcontrib><creatorcontrib>OKUMA, M</creatorcontrib><creatorcontrib>KUDO, T</creatorcontrib><title>The production of D‐acetoin by a transgenic Escherichia coli</title><title>Letters in applied microbiology</title><addtitle>Lett Appl Microbiol</addtitle><description>A 6 kbp SphI fragment encoding genes for the enzymes α‐acetolactate synthase (ALS), α‐acetolactate decarboxylase (ALDC) and meso‐2,3‐butanediol dehydrogenase (meso‐BDH), involved in the formation of meso‐2,3‐butanediol (meso‐BD) from pyruvic acid, was cloned into plasmid pUC118. When derivatives of this plasmid were introduced into Escherichia coli JM109, the transformants were able to produce
D‐acetoin (
D‐AC) without contamination with
L‐acetoin (
L‐AC).</description><subject>Acetoin - metabolism</subject><subject>Acetolactate Synthase - genetics</subject><subject>Alcohol Oxidoreductases - genetics</subject><subject>Biological and medical sciences</subject><subject>Biotechnology</subject><subject>Carboxy-Lyases - genetics</subject><subject>Chromatography, Gas</subject><subject>Culture Media - chemistry</subject><subject>Escherichia coli</subject><subject>Escherichia coli - genetics</subject><subject>Escherichia coli - metabolism</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Genetic engineering</subject><subject>Genetic technics</subject><subject>Methods. Procedures. Technologies</subject><subject>Modification of gene expression level</subject><subject>Time Factors</subject><subject>Transformation, Bacterial</subject><issn>0266-8254</issn><issn>1472-765X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkMtKAzEUhoMoWi-PIGQh7mbMZZJJQIRSr1Bxo-AuZNITmzKdqZMW252P4DP6JM7Y0q2ucuD_Ts7PhxCmJKUkkxeTlGY5S3IpXlOqtUoJ4ZSnyx3U2wa7qEeYlIliIjtAhzFOCCGKMr2P9rXknGjeQ1fPY8Czph4t3DzUFa49vv7-_LIO5nWocLHCFs8bW8U3qILDN9GNoQluHCx2dRmO0Z63ZYSTzXuEXm5vngf3yfDp7mHQHyZOUMITyCRTTCkBILW0mWfgM-k1z63KtbciK0BaYLkHrZTjhXO2GHlXOOm5KDQ_Qufrf9uq7wuIczMN0UFZ2grqRTS51pmUufwTpFII1nZpQbUGXVPH2IA3syZMbbMylJjOsZmYTqXpVJrOsfl1bJbt6unmxqKYwmi7uJHa5meb3EZnS9_qcyFuMcakoLSrernGPkIJq3-fN8P-YzvwH1OMmEI</recordid><startdate>199804</startdate><enddate>199804</enddate><creator>UI, S</creator><creator>MIMURA, A</creator><creator>OKUMA, M</creator><creator>KUDO, T</creator><general>Blackwell Science Ltd</general><general>Blackwell Science</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>7QL</scope><scope>7QO</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>199804</creationdate><title>The production of D‐acetoin by a transgenic Escherichia coli</title><author>UI, S ; MIMURA, A ; OKUMA, M ; KUDO, T</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5103-e46282885ee696a4f2ef46f937a879fa54be6ae27fe988c3bccabdfcbc6f35b93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Acetoin - metabolism</topic><topic>Acetolactate Synthase - genetics</topic><topic>Alcohol Oxidoreductases - genetics</topic><topic>Biological and medical sciences</topic><topic>Biotechnology</topic><topic>Carboxy-Lyases - genetics</topic><topic>Chromatography, Gas</topic><topic>Culture Media - chemistry</topic><topic>Escherichia coli</topic><topic>Escherichia coli - genetics</topic><topic>Escherichia coli - metabolism</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Genetic engineering</topic><topic>Genetic technics</topic><topic>Methods. Procedures. Technologies</topic><topic>Modification of gene expression level</topic><topic>Time Factors</topic><topic>Transformation, Bacterial</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>UI, S</creatorcontrib><creatorcontrib>MIMURA, A</creatorcontrib><creatorcontrib>OKUMA, M</creatorcontrib><creatorcontrib>KUDO, T</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>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Letters in applied microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>UI, S</au><au>MIMURA, A</au><au>OKUMA, M</au><au>KUDO, T</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The production of D‐acetoin by a transgenic Escherichia coli</atitle><jtitle>Letters in applied microbiology</jtitle><addtitle>Lett Appl Microbiol</addtitle><date>1998-04</date><risdate>1998</risdate><volume>26</volume><issue>4</issue><spage>275</spage><epage>278</epage><pages>275-278</pages><issn>0266-8254</issn><eissn>1472-765X</eissn><coden>LAMIE7</coden><abstract>A 6 kbp SphI fragment encoding genes for the enzymes α‐acetolactate synthase (ALS), α‐acetolactate decarboxylase (ALDC) and meso‐2,3‐butanediol dehydrogenase (meso‐BDH), involved in the formation of meso‐2,3‐butanediol (meso‐BD) from pyruvic acid, was cloned into plasmid pUC118. When derivatives of this plasmid were introduced into Escherichia coli JM109, the transformants were able to produce
D‐acetoin (
D‐AC) without contamination with
L‐acetoin (
L‐AC).</abstract><cop>Edinburgh, UK</cop><pub>Blackwell Science Ltd</pub><pmid>9633093</pmid><doi>10.1046/j.1472-765X.1998.00313.x</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record> |
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language | eng |
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source | MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Access via Wiley Online Library; Oxford University Press Journals All Titles (1996-Current); Alma/SFX Local Collection |
subjects | Acetoin - metabolism Acetolactate Synthase - genetics Alcohol Oxidoreductases - genetics Biological and medical sciences Biotechnology Carboxy-Lyases - genetics Chromatography, Gas Culture Media - chemistry Escherichia coli Escherichia coli - genetics Escherichia coli - metabolism Fundamental and applied biological sciences. Psychology Genetic engineering Genetic technics Methods. Procedures. Technologies Modification of gene expression level Time Factors Transformation, Bacterial |
title | The production of D‐acetoin by a transgenic Escherichia coli |
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