Chromogenic analogues of penicillin dihydroF and penicillin K for the continuous spectrophotometric determination of aliphatic penicillin acylase activity

The synthesis of 2-nitro-5-[(hexanoyl)-amino]-benzoic acid and 2-nitro-5-[(octanoyl)-amino]-benzoic acid as chromogenic substrates for the determination of aliphatic penicillin acylase activity is described. During enzymatic hydrolysis, the released chromophore, 2-nitro-5-amino-benzoic acid, was det...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Biotechnology letters 2002-07, Vol.24 (13), p.1045-1048
Hauptverfasser: ARROYO, Miguel, TORRES-GUZMAN, Raquel, TORRES-BACETE, Jesus, DE LA MATA, Isabel, CASTILLON, Maria Pilar, ACEBAL, Carmen
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1048
container_issue 13
container_start_page 1045
container_title Biotechnology letters
container_volume 24
creator ARROYO, Miguel
TORRES-GUZMAN, Raquel
TORRES-BACETE, Jesus
DE LA MATA, Isabel
CASTILLON, Maria Pilar
ACEBAL, Carmen
description The synthesis of 2-nitro-5-[(hexanoyl)-amino]-benzoic acid and 2-nitro-5-[(octanoyl)-amino]-benzoic acid as chromogenic substrates for the determination of aliphatic penicillin acylase activity is described. During enzymatic hydrolysis, the released chromophore, 2-nitro-5-amino-benzoic acid, was detected at 405 nm. Penicillin acylase from Streptomyces lavendulae had an appreciable activity towards these substrates, which can then be used to detect penicillin acylases able to cleave hexanoyl and octanoyl residues off synthetic amides as well as penicillin dihydroF and penicillin K, their natural analogues.[PUBLICATION ABSTRACT]
doi_str_mv 10.1023/A:1016096111453
format Article
fullrecord <record><control><sourceid>proquest_pasca</sourceid><recordid>TN_cdi_proquest_miscellaneous_18460027</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2100898401</sourcerecordid><originalsourceid>FETCH-LOGICAL-p241t-e0df2bf50dae925cf78e9564c0530032f74c75bf79ab53067c8a19ad77af22563</originalsourceid><addsrcrecordid>eNpdkEtLLDEQRoMoOD7WbhtBd31vHp1k4k4GH5cruNF1U5NO7Eg6aZOMMH_FX2sGXYirj_o4HKoKoTOC_xBM2d_rK4KJwEoQQjrO9tCCcMlaIaXYRwtMOtLyTtFDdJTzK8ZYSSwX6GM1pjjFFxOcbiCAjy8bk5tom3lXOe9daAY3bocUbysw_Oz_Nzampoym0TEUFzZxk5s8G11SnMdY4mRKqt7BFJMmF6C4GHZu8G4e66R_2kBvPWRTs7h3V7Yn6MCCz-b0O4_R8-3N0-q-fXi8-7e6fmhn2pHSGjxYurYcD2AU5drKpVFcdBpzhjGjVnZa8rWVCta1EVIvgSgYpARLKRfsGF1-eecU3-rxpZ9c1sZ7CKYe1JNlJzCmsoLnv8DXuEn1Z7mXrFsqIdUOuviGIGvwNkHQLvdzchOkbU-YFIzW1T4BCdCIPg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>734896797</pqid></control><display><type>article</type><title>Chromogenic analogues of penicillin dihydroF and penicillin K for the continuous spectrophotometric determination of aliphatic penicillin acylase activity</title><source>SpringerNature Journals</source><creator>ARROYO, Miguel ; TORRES-GUZMAN, Raquel ; TORRES-BACETE, Jesus ; DE LA MATA, Isabel ; CASTILLON, Maria Pilar ; ACEBAL, Carmen</creator><creatorcontrib>ARROYO, Miguel ; TORRES-GUZMAN, Raquel ; TORRES-BACETE, Jesus ; DE LA MATA, Isabel ; CASTILLON, Maria Pilar ; ACEBAL, Carmen</creatorcontrib><description>The synthesis of 2-nitro-5-[(hexanoyl)-amino]-benzoic acid and 2-nitro-5-[(octanoyl)-amino]-benzoic acid as chromogenic substrates for the determination of aliphatic penicillin acylase activity is described. During enzymatic hydrolysis, the released chromophore, 2-nitro-5-amino-benzoic acid, was detected at 405 nm. Penicillin acylase from Streptomyces lavendulae had an appreciable activity towards these substrates, which can then be used to detect penicillin acylases able to cleave hexanoyl and octanoyl residues off synthetic amides as well as penicillin dihydroF and penicillin K, their natural analogues.[PUBLICATION ABSTRACT]</description><identifier>ISSN: 0141-5492</identifier><identifier>EISSN: 1573-6776</identifier><identifier>DOI: 10.1023/A:1016096111453</identifier><identifier>CODEN: BILED3</identifier><language>eng</language><publisher>Dordrecht: Springer</publisher><subject>Amides ; Biological and medical sciences ; Biotechnology ; Enzyme engineering ; Fundamental and applied biological sciences. Psychology ; Methods. Procedures. Technologies ; Miscellaneous ; Penicillin</subject><ispartof>Biotechnology letters, 2002-07, Vol.24 (13), p.1045-1048</ispartof><rights>2002 INIST-CNRS</rights><rights>Kluwer Academic Publishers 2002</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=13763205$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>ARROYO, Miguel</creatorcontrib><creatorcontrib>TORRES-GUZMAN, Raquel</creatorcontrib><creatorcontrib>TORRES-BACETE, Jesus</creatorcontrib><creatorcontrib>DE LA MATA, Isabel</creatorcontrib><creatorcontrib>CASTILLON, Maria Pilar</creatorcontrib><creatorcontrib>ACEBAL, Carmen</creatorcontrib><title>Chromogenic analogues of penicillin dihydroF and penicillin K for the continuous spectrophotometric determination of aliphatic penicillin acylase activity</title><title>Biotechnology letters</title><description>The synthesis of 2-nitro-5-[(hexanoyl)-amino]-benzoic acid and 2-nitro-5-[(octanoyl)-amino]-benzoic acid as chromogenic substrates for the determination of aliphatic penicillin acylase activity is described. During enzymatic hydrolysis, the released chromophore, 2-nitro-5-amino-benzoic acid, was detected at 405 nm. Penicillin acylase from Streptomyces lavendulae had an appreciable activity towards these substrates, which can then be used to detect penicillin acylases able to cleave hexanoyl and octanoyl residues off synthetic amides as well as penicillin dihydroF and penicillin K, their natural analogues.[PUBLICATION ABSTRACT]</description><subject>Amides</subject><subject>Biological and medical sciences</subject><subject>Biotechnology</subject><subject>Enzyme engineering</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Methods. Procedures. Technologies</subject><subject>Miscellaneous</subject><subject>Penicillin</subject><issn>0141-5492</issn><issn>1573-6776</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNpdkEtLLDEQRoMoOD7WbhtBd31vHp1k4k4GH5cruNF1U5NO7Eg6aZOMMH_FX2sGXYirj_o4HKoKoTOC_xBM2d_rK4KJwEoQQjrO9tCCcMlaIaXYRwtMOtLyTtFDdJTzK8ZYSSwX6GM1pjjFFxOcbiCAjy8bk5tom3lXOe9daAY3bocUbysw_Oz_Nzampoym0TEUFzZxk5s8G11SnMdY4mRKqt7BFJMmF6C4GHZu8G4e66R_2kBvPWRTs7h3V7Yn6MCCz-b0O4_R8-3N0-q-fXi8-7e6fmhn2pHSGjxYurYcD2AU5drKpVFcdBpzhjGjVnZa8rWVCta1EVIvgSgYpARLKRfsGF1-eecU3-rxpZ9c1sZ7CKYe1JNlJzCmsoLnv8DXuEn1Z7mXrFsqIdUOuviGIGvwNkHQLvdzchOkbU-YFIzW1T4BCdCIPg</recordid><startdate>20020701</startdate><enddate>20020701</enddate><creator>ARROYO, Miguel</creator><creator>TORRES-GUZMAN, Raquel</creator><creator>TORRES-BACETE, Jesus</creator><creator>DE LA MATA, Isabel</creator><creator>CASTILLON, Maria Pilar</creator><creator>ACEBAL, Carmen</creator><general>Springer</general><general>Springer Nature B.V</general><scope>IQODW</scope><scope>3V.</scope><scope>7QL</scope><scope>7QR</scope><scope>7T7</scope><scope>7TB</scope><scope>7U5</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>L6V</scope><scope>L7M</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PTHSS</scope><scope>Q9U</scope><scope>7QO</scope></search><sort><creationdate>20020701</creationdate><title>Chromogenic analogues of penicillin dihydroF and penicillin K for the continuous spectrophotometric determination of aliphatic penicillin acylase activity</title><author>ARROYO, Miguel ; TORRES-GUZMAN, Raquel ; TORRES-BACETE, Jesus ; DE LA MATA, Isabel ; CASTILLON, Maria Pilar ; ACEBAL, Carmen</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p241t-e0df2bf50dae925cf78e9564c0530032f74c75bf79ab53067c8a19ad77af22563</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Amides</topic><topic>Biological and medical sciences</topic><topic>Biotechnology</topic><topic>Enzyme engineering</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Methods. Procedures. Technologies</topic><topic>Miscellaneous</topic><topic>Penicillin</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>ARROYO, Miguel</creatorcontrib><creatorcontrib>TORRES-GUZMAN, Raquel</creatorcontrib><creatorcontrib>TORRES-BACETE, Jesus</creatorcontrib><creatorcontrib>DE LA MATA, Isabel</creatorcontrib><creatorcontrib>CASTILLON, Maria Pilar</creatorcontrib><creatorcontrib>ACEBAL, Carmen</creatorcontrib><collection>Pascal-Francis</collection><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Chemoreception Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Mechanical &amp; Transportation Engineering Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Materials Science &amp; Engineering Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>ProQuest Engineering Collection</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>ProQuest Biological Science Collection</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Engineering Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>Engineering Collection</collection><collection>ProQuest Central Basic</collection><collection>Biotechnology Research Abstracts</collection><jtitle>Biotechnology letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>ARROYO, Miguel</au><au>TORRES-GUZMAN, Raquel</au><au>TORRES-BACETE, Jesus</au><au>DE LA MATA, Isabel</au><au>CASTILLON, Maria Pilar</au><au>ACEBAL, Carmen</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Chromogenic analogues of penicillin dihydroF and penicillin K for the continuous spectrophotometric determination of aliphatic penicillin acylase activity</atitle><jtitle>Biotechnology letters</jtitle><date>2002-07-01</date><risdate>2002</risdate><volume>24</volume><issue>13</issue><spage>1045</spage><epage>1048</epage><pages>1045-1048</pages><issn>0141-5492</issn><eissn>1573-6776</eissn><coden>BILED3</coden><abstract>The synthesis of 2-nitro-5-[(hexanoyl)-amino]-benzoic acid and 2-nitro-5-[(octanoyl)-amino]-benzoic acid as chromogenic substrates for the determination of aliphatic penicillin acylase activity is described. During enzymatic hydrolysis, the released chromophore, 2-nitro-5-amino-benzoic acid, was detected at 405 nm. Penicillin acylase from Streptomyces lavendulae had an appreciable activity towards these substrates, which can then be used to detect penicillin acylases able to cleave hexanoyl and octanoyl residues off synthetic amides as well as penicillin dihydroF and penicillin K, their natural analogues.[PUBLICATION ABSTRACT]</abstract><cop>Dordrecht</cop><pub>Springer</pub><doi>10.1023/A:1016096111453</doi><tpages>4</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0141-5492
ispartof Biotechnology letters, 2002-07, Vol.24 (13), p.1045-1048
issn 0141-5492
1573-6776
language eng
recordid cdi_proquest_miscellaneous_18460027
source SpringerNature Journals
subjects Amides
Biological and medical sciences
Biotechnology
Enzyme engineering
Fundamental and applied biological sciences. Psychology
Methods. Procedures. Technologies
Miscellaneous
Penicillin
title Chromogenic analogues of penicillin dihydroF and penicillin K for the continuous spectrophotometric determination of aliphatic penicillin acylase activity
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-04T03%3A50%3A57IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pasca&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Chromogenic%20analogues%20of%20penicillin%20dihydroF%20and%20penicillin%20K%20for%20the%20continuous%20spectrophotometric%20determination%20of%20aliphatic%20penicillin%20acylase%20activity&rft.jtitle=Biotechnology%20letters&rft.au=ARROYO,%20Miguel&rft.date=2002-07-01&rft.volume=24&rft.issue=13&rft.spage=1045&rft.epage=1048&rft.pages=1045-1048&rft.issn=0141-5492&rft.eissn=1573-6776&rft.coden=BILED3&rft_id=info:doi/10.1023/A:1016096111453&rft_dat=%3Cproquest_pasca%3E2100898401%3C/proquest_pasca%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=734896797&rft_id=info:pmid/&rfr_iscdi=true