Trypsin-catalyzed Oligomerization of L-Lysine Esters
The oligomerization of L-lysine esters with a free α-amino group was done using trypsin as a catalyst in aqueous media, and some reaction parameters were examined. The pH-dependence of the reaction suggested that aminolysis by the substrate species having non-protonated α- and ɛ-amino groups was a d...
Gespeichert in:
Veröffentlicht in: | Bioscience, biotechnology, and biochemistry biotechnology, and biochemistry, 1992, Vol.56 (5), p.755-758 |
---|---|
Hauptverfasser: | , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 758 |
---|---|
container_issue | 5 |
container_start_page | 755 |
container_title | Bioscience, biotechnology, and biochemistry |
container_volume | 56 |
creator | Aso, Keiichi Kodaka, Hiroaki |
description | The oligomerization of L-lysine esters with a free α-amino group was done using trypsin as a catalyst in aqueous media, and some reaction parameters were examined. The pH-dependence of the reaction suggested that aminolysis by the substrate species having non-protonated α- and ɛ-amino groups was a dominant factor governing the reaction progress. At the beginning of the reaction lysine oligomers containing up to 8 residues were observed, but much of the dimer was accumulated during prolonged incubation due to secondary hydrolysis of highly polymerized products. The reaction yield depended on the ratio of enzyme and substrate; an overall reaction yield higher than 70% was attained after 2 hr of reaction when 1,000 mM of L-lysine ethyl ester was treated with 200 μM of trypsin at pH 10.0. The oligomerization was apparently enhanced by an addition of NaCl and by using the longer alkyl esters. |
doi_str_mv | 10.1271/bbb.56.755 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmed_primary_27286202</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>3121572691</sourcerecordid><originalsourceid>FETCH-LOGICAL-c591t-21f0dc50674e88835d5d934636625b64d8e8fbde840873c785630adf61724ac13</originalsourceid><addsrcrecordid>eNpt0ElLAzEUB_Agiq3Vix9ACnoQYWr25SilLlDopZ5DJsnIlJlJTabI9NM7pctBPD14_N7CH4BbBCcIC_Sc5_mE8Ylg7AwMEaEi44qKczCECvFMUoYG4CqlFYR9g6FLMMACS44hHgK6jN06lU1mTWuqbuvdeFGVX6H2sdyatgzNOBTjeTbveuTHs9T6mK7BRWGq5G8OdQQ-X2fL6Xs2X7x9TF_mmWUKtRlGBXSWQS6ol1IS5phThHLCOWY5p056WeTOSwqlIFZIxgk0ruBIYGosIiPwuN-7juF741Or6zJZX1Wm8WGTNBKKc0kE29H7P3QVNrHpv9OIUkUUxUr16mmvbAwpRV_odSxrEzuNoN5lqfssNeO6z7LHd4eVm7z27kSP4fXg4QBMsqYqomlsmU6OKkwY2h1le1Y2RYi1-Qmxcro1XRXicYb8c_8XovOLjA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1449394299</pqid></control><display><type>article</type><title>Trypsin-catalyzed Oligomerization of L-Lysine Esters</title><source>J-STAGE Free</source><source>Freely Accessible Japanese Titles</source><source>EZB-FREE-00999 freely available EZB journals</source><source>Free Full-Text Journals in Chemistry</source><creator>Aso, Keiichi ; Kodaka, Hiroaki</creator><creatorcontrib>Aso, Keiichi ; Kodaka, Hiroaki</creatorcontrib><description>The oligomerization of L-lysine esters with a free α-amino group was done using trypsin as a catalyst in aqueous media, and some reaction parameters were examined. The pH-dependence of the reaction suggested that aminolysis by the substrate species having non-protonated α- and ɛ-amino groups was a dominant factor governing the reaction progress. At the beginning of the reaction lysine oligomers containing up to 8 residues were observed, but much of the dimer was accumulated during prolonged incubation due to secondary hydrolysis of highly polymerized products. The reaction yield depended on the ratio of enzyme and substrate; an overall reaction yield higher than 70% was attained after 2 hr of reaction when 1,000 mM of L-lysine ethyl ester was treated with 200 μM of trypsin at pH 10.0. The oligomerization was apparently enhanced by an addition of NaCl and by using the longer alkyl esters.</description><identifier>ISSN: 0916-8451</identifier><identifier>EISSN: 1347-6947</identifier><identifier>DOI: 10.1271/bbb.56.755</identifier><identifier>PMID: 27286202</identifier><language>eng</language><publisher>Tokyo: Taylor & Francis</publisher><subject>Bioconversions. Hemisynthesis ; Biological and medical sciences ; Biotechnology ; Fundamental and applied biological sciences. Psychology ; Methods. Procedures. Technologies</subject><ispartof>Bioscience, biotechnology, and biochemistry, 1992, Vol.56 (5), p.755-758</ispartof><rights>Copyright 1992 Taylor and Francis Group LLC 1992</rights><rights>1993 INIST-CNRS</rights><rights>Copyright Japan Science and Technology Agency 1992</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c591t-21f0dc50674e88835d5d934636625b64d8e8fbde840873c785630adf61724ac13</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,4014,27914,27915,27916</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=4923519$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27286202$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Aso, Keiichi</creatorcontrib><creatorcontrib>Kodaka, Hiroaki</creatorcontrib><title>Trypsin-catalyzed Oligomerization of L-Lysine Esters</title><title>Bioscience, biotechnology, and biochemistry</title><addtitle>Biosci Biotechnol Biochem</addtitle><description>The oligomerization of L-lysine esters with a free α-amino group was done using trypsin as a catalyst in aqueous media, and some reaction parameters were examined. The pH-dependence of the reaction suggested that aminolysis by the substrate species having non-protonated α- and ɛ-amino groups was a dominant factor governing the reaction progress. At the beginning of the reaction lysine oligomers containing up to 8 residues were observed, but much of the dimer was accumulated during prolonged incubation due to secondary hydrolysis of highly polymerized products. The reaction yield depended on the ratio of enzyme and substrate; an overall reaction yield higher than 70% was attained after 2 hr of reaction when 1,000 mM of L-lysine ethyl ester was treated with 200 μM of trypsin at pH 10.0. The oligomerization was apparently enhanced by an addition of NaCl and by using the longer alkyl esters.</description><subject>Bioconversions. Hemisynthesis</subject><subject>Biological and medical sciences</subject><subject>Biotechnology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Methods. Procedures. Technologies</subject><issn>0916-8451</issn><issn>1347-6947</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1992</creationdate><recordtype>article</recordtype><recordid>eNpt0ElLAzEUB_Agiq3Vix9ACnoQYWr25SilLlDopZ5DJsnIlJlJTabI9NM7pctBPD14_N7CH4BbBCcIC_Sc5_mE8Ylg7AwMEaEi44qKczCECvFMUoYG4CqlFYR9g6FLMMACS44hHgK6jN06lU1mTWuqbuvdeFGVX6H2sdyatgzNOBTjeTbveuTHs9T6mK7BRWGq5G8OdQQ-X2fL6Xs2X7x9TF_mmWUKtRlGBXSWQS6ol1IS5phThHLCOWY5p056WeTOSwqlIFZIxgk0ruBIYGosIiPwuN-7juF741Or6zJZX1Wm8WGTNBKKc0kE29H7P3QVNrHpv9OIUkUUxUr16mmvbAwpRV_odSxrEzuNoN5lqfssNeO6z7LHd4eVm7z27kSP4fXg4QBMsqYqomlsmU6OKkwY2h1le1Y2RYi1-Qmxcro1XRXicYb8c_8XovOLjA</recordid><startdate>1992</startdate><enddate>1992</enddate><creator>Aso, Keiichi</creator><creator>Kodaka, Hiroaki</creator><general>Taylor & Francis</general><general>Japan Society for Bioscience Biotechnology and Agrochemistry</general><general>Oxford University Press</general><scope>IQODW</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>1992</creationdate><title>Trypsin-catalyzed Oligomerization of L-Lysine Esters</title><author>Aso, Keiichi ; Kodaka, Hiroaki</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c591t-21f0dc50674e88835d5d934636625b64d8e8fbde840873c785630adf61724ac13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1992</creationdate><topic>Bioconversions. Hemisynthesis</topic><topic>Biological and medical sciences</topic><topic>Biotechnology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Methods. Procedures. Technologies</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Aso, Keiichi</creatorcontrib><creatorcontrib>Kodaka, Hiroaki</creatorcontrib><collection>Pascal-Francis</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Bioscience, biotechnology, and biochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Aso, Keiichi</au><au>Kodaka, Hiroaki</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Trypsin-catalyzed Oligomerization of L-Lysine Esters</atitle><jtitle>Bioscience, biotechnology, and biochemistry</jtitle><addtitle>Biosci Biotechnol Biochem</addtitle><date>1992</date><risdate>1992</risdate><volume>56</volume><issue>5</issue><spage>755</spage><epage>758</epage><pages>755-758</pages><issn>0916-8451</issn><eissn>1347-6947</eissn><abstract>The oligomerization of L-lysine esters with a free α-amino group was done using trypsin as a catalyst in aqueous media, and some reaction parameters were examined. The pH-dependence of the reaction suggested that aminolysis by the substrate species having non-protonated α- and ɛ-amino groups was a dominant factor governing the reaction progress. At the beginning of the reaction lysine oligomers containing up to 8 residues were observed, but much of the dimer was accumulated during prolonged incubation due to secondary hydrolysis of highly polymerized products. The reaction yield depended on the ratio of enzyme and substrate; an overall reaction yield higher than 70% was attained after 2 hr of reaction when 1,000 mM of L-lysine ethyl ester was treated with 200 μM of trypsin at pH 10.0. The oligomerization was apparently enhanced by an addition of NaCl and by using the longer alkyl esters.</abstract><cop>Tokyo</cop><pub>Taylor & Francis</pub><pmid>27286202</pmid><doi>10.1271/bbb.56.755</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0916-8451 |
ispartof | Bioscience, biotechnology, and biochemistry, 1992, Vol.56 (5), p.755-758 |
issn | 0916-8451 1347-6947 |
language | eng |
recordid | cdi_pubmed_primary_27286202 |
source | J-STAGE Free; Freely Accessible Japanese Titles; EZB-FREE-00999 freely available EZB journals; Free Full-Text Journals in Chemistry |
subjects | Bioconversions. Hemisynthesis Biological and medical sciences Biotechnology Fundamental and applied biological sciences. Psychology Methods. Procedures. Technologies |
title | Trypsin-catalyzed Oligomerization of L-Lysine Esters |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-14T23%3A44%3A41IST&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=Trypsin-catalyzed%20Oligomerization%20of%20L-Lysine%20Esters&rft.jtitle=Bioscience,%20biotechnology,%20and%20biochemistry&rft.au=Aso,%20Keiichi&rft.date=1992&rft.volume=56&rft.issue=5&rft.spage=755&rft.epage=758&rft.pages=755-758&rft.issn=0916-8451&rft.eissn=1347-6947&rft_id=info:doi/10.1271/bbb.56.755&rft_dat=%3Cproquest_pubme%3E3121572691%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=1449394299&rft_id=info:pmid/27286202&rfr_iscdi=true |