Coupling of metabolism and bioconversion: microbial esterification of citronellol with acetyl coenzyme A produced via metabolism of glucose in an interface bioreactor

Microbial esterification of citronellol with acetyl coenzyme A (acetyl-CoA) produced via metabolism of glucose was performed with Hansenula saturnus IFO 0809 in an interface bioreactor by using a hydrophilic carrier (an agar plate or an agar-coated filter pad) and a hydrophobic organic solvent (deca...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Applied and Environmental Microbiology 1996-07, Vol.62 (7), p.2216-2220
Hauptverfasser: Oda, S.O. (Kansai Paint Co., Ltd., Hiratsuka, Kanagawa.), Inada, Y, Kobayashi, A, Kato, A, Matsudomi, N, Ohta, H
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 2220
container_issue 7
container_start_page 2216
container_title Applied and Environmental Microbiology
container_volume 62
creator Oda, S.O. (Kansai Paint Co., Ltd., Hiratsuka, Kanagawa.)
Inada, Y
Kobayashi, A
Kato, A
Matsudomi, N
Ohta, H
description Microbial esterification of citronellol with acetyl coenzyme A (acetyl-CoA) produced via metabolism of glucose was performed with Hansenula saturnus IFO 0809 in an interface bioreactor by using a hydrophilic carrier (an agar plate or an agar-coated filter pad) and a hydrophobic organic solvent (decane). An increase in the glucose concentration on an agar plate led to a decrease in oxidation of citronellol and an increase in the amount of citronellyl acetate. Fed-batch addition of citronellol efficiently alleviated substrate toxicity and resulted in the accumulation of high levels of citronellyl acetate. Furthermore, triple coupling of acetyl-CoA formation, microbial reduction of citronellal to citronellol, and esterification of the resulting citronellol with acetyl-CoA was also an efficient way to prepare citronellyl acetate. By using coupling systems, citronellyl acetate could be efficiently produced without any acetyl donor
doi_str_mv 10.1128/AEM.62.7.2216-2220.1996
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmed_primary_16535347</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>733446751</sourcerecordid><originalsourceid>FETCH-LOGICAL-c600t-27759ebc2c9cf12d0832454b46a4277e7283f884fed21890c491ab1c51317853</originalsourceid><addsrcrecordid>eNp9ks2O0zAUhS0EYkrhBViAQQhWLf6LY7NAqqrhRxrEgmFtOY7TeuTYHTvpqDwQz4mjVsMMC7yIpdzvnnNzcwB4idESYyLer86_LTlZ1ktCMF8QQsp7KfkDMMNIikVFKX8IZghJWYoMnYEnOV8hhBji4jE4w7yiFWX1DPxex3HnXdjA2MHeDrqJ3uUe6tDCxkUTw96m7GL4AHtnUmyc9tDmwSbXOaOHUpk6jRtSDNb76OGNG7ZQGzscPDTRhl-H3sIV3KXYjsa2cO_0XafSvfGjidlCF4pveRb1rghMAySrzRDTU_Co0z7bZ6d7Di4_nV-uvywuvn_-ul5dLAxHaFiQuq6kbQwx0nSYtEhQwirWMK5ZqdmaCNoJwTrbEiwkMkxi3WBTYYprUdE5-HiU3Y1Nb1tjw5C0V7vkep0OKmqn7leC26pN3CtMRTmTwLuTQIrXY9mT6l02ZS862DhmVVPKGK-L3xy8_S-JK04kkbyAr_8Br-KYQtmCIqiSRY9NavURKr8o52S725kxUlNilLa94kTVakqMmhKjpsSUzhd3P_lv3ykiBXhzAnQ22ndJB-PyLUexYBWdsFdHbOs22xuXrNK5v-9amOdHptNR6U0qMj9_SE6Kj6R_AGSx4Mc</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>205934441</pqid></control><display><type>article</type><title>Coupling of metabolism and bioconversion: microbial esterification of citronellol with acetyl coenzyme A produced via metabolism of glucose in an interface bioreactor</title><source>American Society for Microbiology</source><source>PubMed Central</source><source>Alma/SFX Local Collection</source><creator>Oda, S.O. (Kansai Paint Co., Ltd., Hiratsuka, Kanagawa.) ; Inada, Y ; Kobayashi, A ; Kato, A ; Matsudomi, N ; Ohta, H</creator><creatorcontrib>Oda, S.O. (Kansai Paint Co., Ltd., Hiratsuka, Kanagawa.) ; Inada, Y ; Kobayashi, A ; Kato, A ; Matsudomi, N ; Ohta, H</creatorcontrib><description>Microbial esterification of citronellol with acetyl coenzyme A (acetyl-CoA) produced via metabolism of glucose was performed with Hansenula saturnus IFO 0809 in an interface bioreactor by using a hydrophilic carrier (an agar plate or an agar-coated filter pad) and a hydrophobic organic solvent (decane). An increase in the glucose concentration on an agar plate led to a decrease in oxidation of citronellol and an increase in the amount of citronellyl acetate. Fed-batch addition of citronellol efficiently alleviated substrate toxicity and resulted in the accumulation of high levels of citronellyl acetate. Furthermore, triple coupling of acetyl-CoA formation, microbial reduction of citronellal to citronellol, and esterification of the resulting citronellol with acetyl-CoA was also an efficient way to prepare citronellyl acetate. By using coupling systems, citronellyl acetate could be efficiently produced without any acetyl donor</description><identifier>ISSN: 0099-2240</identifier><identifier>EISSN: 1098-5336</identifier><identifier>DOI: 10.1128/AEM.62.7.2216-2220.1996</identifier><identifier>PMID: 16535347</identifier><identifier>CODEN: AEMIDF</identifier><language>eng</language><publisher>Washington, DC: American Society for Microbiology</publisher><subject>ACETATE (ESTER) ; ACETATOS (ESTERES) ; ACTIVIDAD ENZIMATICA ; ACTIVITE ENZYMATIQUE ; ALCOHOLES ; ALCOOL ; Bioconversions. Hemisynthesis ; Biological and medical sciences ; BIOREACTEUR ; BIORREACTORES ; BIOSINTESIS ; BIOSYNTHESE ; Biotechnology ; COENZIMAS ; COENZYME ; Enzymes ; Fundamental and applied biological sciences. Psychology ; GLUCOSA ; GLUCOSE ; HANSENULA ; Metabolism ; METABOLISME DES GLUCIDES ; METABOLISMO DE CARBOHIDRATOS ; Methods. Procedures. Technologies ; Microbiology ; Microorganisms ; REACCIONES QUIMICAS ; REACTION CHIMIQUE ; TRIACILGLICEROL LIPASA ; TRIACYLGLYCEROL LIPASE</subject><ispartof>Applied and Environmental Microbiology, 1996-07, Vol.62 (7), p.2216-2220</ispartof><rights>1996 INIST-CNRS</rights><rights>Copyright American Society for Microbiology Jul 1996</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c600t-27759ebc2c9cf12d0832454b46a4277e7283f884fed21890c491ab1c51317853</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1388885/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1388885/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,3175,3176,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=3184537$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16535347$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Oda, S.O. (Kansai Paint Co., Ltd., Hiratsuka, Kanagawa.)</creatorcontrib><creatorcontrib>Inada, Y</creatorcontrib><creatorcontrib>Kobayashi, A</creatorcontrib><creatorcontrib>Kato, A</creatorcontrib><creatorcontrib>Matsudomi, N</creatorcontrib><creatorcontrib>Ohta, H</creatorcontrib><title>Coupling of metabolism and bioconversion: microbial esterification of citronellol with acetyl coenzyme A produced via metabolism of glucose in an interface bioreactor</title><title>Applied and Environmental Microbiology</title><addtitle>Appl Environ Microbiol</addtitle><description>Microbial esterification of citronellol with acetyl coenzyme A (acetyl-CoA) produced via metabolism of glucose was performed with Hansenula saturnus IFO 0809 in an interface bioreactor by using a hydrophilic carrier (an agar plate or an agar-coated filter pad) and a hydrophobic organic solvent (decane). An increase in the glucose concentration on an agar plate led to a decrease in oxidation of citronellol and an increase in the amount of citronellyl acetate. Fed-batch addition of citronellol efficiently alleviated substrate toxicity and resulted in the accumulation of high levels of citronellyl acetate. Furthermore, triple coupling of acetyl-CoA formation, microbial reduction of citronellal to citronellol, and esterification of the resulting citronellol with acetyl-CoA was also an efficient way to prepare citronellyl acetate. By using coupling systems, citronellyl acetate could be efficiently produced without any acetyl donor</description><subject>ACETATE (ESTER)</subject><subject>ACETATOS (ESTERES)</subject><subject>ACTIVIDAD ENZIMATICA</subject><subject>ACTIVITE ENZYMATIQUE</subject><subject>ALCOHOLES</subject><subject>ALCOOL</subject><subject>Bioconversions. Hemisynthesis</subject><subject>Biological and medical sciences</subject><subject>BIOREACTEUR</subject><subject>BIORREACTORES</subject><subject>BIOSINTESIS</subject><subject>BIOSYNTHESE</subject><subject>Biotechnology</subject><subject>COENZIMAS</subject><subject>COENZYME</subject><subject>Enzymes</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>GLUCOSA</subject><subject>GLUCOSE</subject><subject>HANSENULA</subject><subject>Metabolism</subject><subject>METABOLISME DES GLUCIDES</subject><subject>METABOLISMO DE CARBOHIDRATOS</subject><subject>Methods. Procedures. Technologies</subject><subject>Microbiology</subject><subject>Microorganisms</subject><subject>REACCIONES QUIMICAS</subject><subject>REACTION CHIMIQUE</subject><subject>TRIACILGLICEROL LIPASA</subject><subject>TRIACYLGLYCEROL LIPASE</subject><issn>0099-2240</issn><issn>1098-5336</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><recordid>eNp9ks2O0zAUhS0EYkrhBViAQQhWLf6LY7NAqqrhRxrEgmFtOY7TeuTYHTvpqDwQz4mjVsMMC7yIpdzvnnNzcwB4idESYyLer86_LTlZ1ktCMF8QQsp7KfkDMMNIikVFKX8IZghJWYoMnYEnOV8hhBji4jE4w7yiFWX1DPxex3HnXdjA2MHeDrqJ3uUe6tDCxkUTw96m7GL4AHtnUmyc9tDmwSbXOaOHUpk6jRtSDNb76OGNG7ZQGzscPDTRhl-H3sIV3KXYjsa2cO_0XafSvfGjidlCF4pveRb1rghMAySrzRDTU_Co0z7bZ6d7Di4_nV-uvywuvn_-ul5dLAxHaFiQuq6kbQwx0nSYtEhQwirWMK5ZqdmaCNoJwTrbEiwkMkxi3WBTYYprUdE5-HiU3Y1Nb1tjw5C0V7vkep0OKmqn7leC26pN3CtMRTmTwLuTQIrXY9mT6l02ZS862DhmVVPKGK-L3xy8_S-JK04kkbyAr_8Br-KYQtmCIqiSRY9NavURKr8o52S725kxUlNilLa94kTVakqMmhKjpsSUzhd3P_lv3ykiBXhzAnQ22ndJB-PyLUexYBWdsFdHbOs22xuXrNK5v-9amOdHptNR6U0qMj9_SE6Kj6R_AGSx4Mc</recordid><startdate>19960701</startdate><enddate>19960701</enddate><creator>Oda, S.O. (Kansai Paint Co., Ltd., Hiratsuka, Kanagawa.)</creator><creator>Inada, Y</creator><creator>Kobayashi, A</creator><creator>Kato, A</creator><creator>Matsudomi, N</creator><creator>Ohta, H</creator><general>American Society for Microbiology</general><scope>FBQ</scope><scope>IQODW</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7QO</scope><scope>7SN</scope><scope>7SS</scope><scope>7ST</scope><scope>7T7</scope><scope>7TM</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>SOI</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>19960701</creationdate><title>Coupling of metabolism and bioconversion: microbial esterification of citronellol with acetyl coenzyme A produced via metabolism of glucose in an interface bioreactor</title><author>Oda, S.O. (Kansai Paint Co., Ltd., Hiratsuka, Kanagawa.) ; Inada, Y ; Kobayashi, A ; Kato, A ; Matsudomi, N ; Ohta, H</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c600t-27759ebc2c9cf12d0832454b46a4277e7283f884fed21890c491ab1c51317853</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1996</creationdate><topic>ACETATE (ESTER)</topic><topic>ACETATOS (ESTERES)</topic><topic>ACTIVIDAD ENZIMATICA</topic><topic>ACTIVITE ENZYMATIQUE</topic><topic>ALCOHOLES</topic><topic>ALCOOL</topic><topic>Bioconversions. Hemisynthesis</topic><topic>Biological and medical sciences</topic><topic>BIOREACTEUR</topic><topic>BIORREACTORES</topic><topic>BIOSINTESIS</topic><topic>BIOSYNTHESE</topic><topic>Biotechnology</topic><topic>COENZIMAS</topic><topic>COENZYME</topic><topic>Enzymes</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>GLUCOSA</topic><topic>GLUCOSE</topic><topic>HANSENULA</topic><topic>Metabolism</topic><topic>METABOLISME DES GLUCIDES</topic><topic>METABOLISMO DE CARBOHIDRATOS</topic><topic>Methods. Procedures. Technologies</topic><topic>Microbiology</topic><topic>Microorganisms</topic><topic>REACCIONES QUIMICAS</topic><topic>REACTION CHIMIQUE</topic><topic>TRIACILGLICEROL LIPASA</topic><topic>TRIACYLGLYCEROL LIPASE</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Oda, S.O. (Kansai Paint Co., Ltd., Hiratsuka, Kanagawa.)</creatorcontrib><creatorcontrib>Inada, Y</creatorcontrib><creatorcontrib>Kobayashi, A</creatorcontrib><creatorcontrib>Kato, A</creatorcontrib><creatorcontrib>Matsudomi, N</creatorcontrib><creatorcontrib>Ohta, H</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Environment Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>Environment Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Applied and Environmental Microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Oda, S.O. (Kansai Paint Co., Ltd., Hiratsuka, Kanagawa.)</au><au>Inada, Y</au><au>Kobayashi, A</au><au>Kato, A</au><au>Matsudomi, N</au><au>Ohta, H</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Coupling of metabolism and bioconversion: microbial esterification of citronellol with acetyl coenzyme A produced via metabolism of glucose in an interface bioreactor</atitle><jtitle>Applied and Environmental Microbiology</jtitle><addtitle>Appl Environ Microbiol</addtitle><date>1996-07-01</date><risdate>1996</risdate><volume>62</volume><issue>7</issue><spage>2216</spage><epage>2220</epage><pages>2216-2220</pages><issn>0099-2240</issn><eissn>1098-5336</eissn><coden>AEMIDF</coden><abstract>Microbial esterification of citronellol with acetyl coenzyme A (acetyl-CoA) produced via metabolism of glucose was performed with Hansenula saturnus IFO 0809 in an interface bioreactor by using a hydrophilic carrier (an agar plate or an agar-coated filter pad) and a hydrophobic organic solvent (decane). An increase in the glucose concentration on an agar plate led to a decrease in oxidation of citronellol and an increase in the amount of citronellyl acetate. Fed-batch addition of citronellol efficiently alleviated substrate toxicity and resulted in the accumulation of high levels of citronellyl acetate. Furthermore, triple coupling of acetyl-CoA formation, microbial reduction of citronellal to citronellol, and esterification of the resulting citronellol with acetyl-CoA was also an efficient way to prepare citronellyl acetate. By using coupling systems, citronellyl acetate could be efficiently produced without any acetyl donor</abstract><cop>Washington, DC</cop><pub>American Society for Microbiology</pub><pmid>16535347</pmid><doi>10.1128/AEM.62.7.2216-2220.1996</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0099-2240
ispartof Applied and Environmental Microbiology, 1996-07, Vol.62 (7), p.2216-2220
issn 0099-2240
1098-5336
language eng
recordid cdi_pubmed_primary_16535347
source American Society for Microbiology; PubMed Central; Alma/SFX Local Collection
subjects ACETATE (ESTER)
ACETATOS (ESTERES)
ACTIVIDAD ENZIMATICA
ACTIVITE ENZYMATIQUE
ALCOHOLES
ALCOOL
Bioconversions. Hemisynthesis
Biological and medical sciences
BIOREACTEUR
BIORREACTORES
BIOSINTESIS
BIOSYNTHESE
Biotechnology
COENZIMAS
COENZYME
Enzymes
Fundamental and applied biological sciences. Psychology
GLUCOSA
GLUCOSE
HANSENULA
Metabolism
METABOLISME DES GLUCIDES
METABOLISMO DE CARBOHIDRATOS
Methods. Procedures. Technologies
Microbiology
Microorganisms
REACCIONES QUIMICAS
REACTION CHIMIQUE
TRIACILGLICEROL LIPASA
TRIACYLGLYCEROL LIPASE
title Coupling of metabolism and bioconversion: microbial esterification of citronellol with acetyl coenzyme A produced via metabolism of glucose in an interface bioreactor
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-04T20%3A09%3A34IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Coupling%20of%20metabolism%20and%20bioconversion:%20microbial%20esterification%20of%20citronellol%20with%20acetyl%20coenzyme%20A%20produced%20via%20metabolism%20of%20glucose%20in%20an%20interface%20bioreactor&rft.jtitle=Applied%20and%20Environmental%20Microbiology&rft.au=Oda,%20S.O.%20(Kansai%20Paint%20Co.,%20Ltd.,%20Hiratsuka,%20Kanagawa.)&rft.date=1996-07-01&rft.volume=62&rft.issue=7&rft.spage=2216&rft.epage=2220&rft.pages=2216-2220&rft.issn=0099-2240&rft.eissn=1098-5336&rft.coden=AEMIDF&rft_id=info:doi/10.1128/AEM.62.7.2216-2220.1996&rft_dat=%3Cproquest_pubme%3E733446751%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=205934441&rft_id=info:pmid/16535347&rfr_iscdi=true