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Development of a highly sensitive chemiluminescence flow-injection analysis sensor for phosphate-ion detection using maltose phosphorylase
A chemiluminescence flow-injection analysis biosensor has been constructed for phosphate-ion detection. This system is coenzymeless and employs a maltose phosphorylase, mutarotase, and glucose-oxidase (MP–MUT–GOD) reaction system combined with an Arthromyces ramosus peroxidase–luminol reaction syste...
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Published in: | Journal of biotechnology 1999-10, Vol.75 (2), p.127-133 |
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container_end_page | 133 |
container_issue | 2 |
container_start_page | 127 |
container_title | Journal of biotechnology |
container_volume | 75 |
creator | Nakamura, Hideaki Hasegawa, Mami Nomura, Yoko Arikawa, Yoshiko Matsukawa, Ritsuko Ikebukuro, Kazunori Karube, Isao |
description | A chemiluminescence flow-injection analysis biosensor has been constructed for phosphate-ion detection. This system is coenzymeless and employs a maltose phosphorylase, mutarotase, and glucose-oxidase (MP–MUT–GOD) reaction system combined with an
Arthromyces ramosus peroxidase–luminol reaction system. The system consists of a column packed with MP–MUT–GOD immobilized on
N-hydroxysuccinimide beads, a mixing joint for the chemiluminescence reaction, and a photomultiplier. The response provided by this system was linear, with a wide range between 10 nM and 30 μM phosphate ion, and a measuring time of 3 min per sample. Under the optimal condition, the sensor was able to detect 1.0 μM phosphate ion for at least 2 weeks. For a practical application, the determination of phosphate ion in river water was examined using ethylenediaminetetraacetic acid, and the results were estimated by comparing with the molybdenum-blue method. |
doi_str_mv | 10.1016/S0168-1656(99)00150-9 |
format | article |
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Arthromyces ramosus peroxidase–luminol reaction system. The system consists of a column packed with MP–MUT–GOD immobilized on
N-hydroxysuccinimide beads, a mixing joint for the chemiluminescence reaction, and a photomultiplier. The response provided by this system was linear, with a wide range between 10 nM and 30 μM phosphate ion, and a measuring time of 3 min per sample. Under the optimal condition, the sensor was able to detect 1.0 μM phosphate ion for at least 2 weeks. For a practical application, the determination of phosphate ion in river water was examined using ethylenediaminetetraacetic acid, and the results were estimated by comparing with the molybdenum-blue method.</description><identifier>ISSN: 0168-1656</identifier><identifier>EISSN: 1873-4863</identifier><identifier>DOI: 10.1016/S0168-1656(99)00150-9</identifier><identifier>CODEN: JBITD4</identifier><language>eng</language><publisher>Lausanne: Elsevier B.V</publisher><subject>Arthromyces ramosus peroxidase ; Biological and medical sciences ; Biosensors ; Biotechnology ; Chemiluminescence ; Enzyme immobilization ; Enzyme kinetics ; Flow-injection analysis ; Fundamental and applied biological sciences. Psychology ; Methods. Procedures. Technologies ; N-Hydroxysuccinimide beads ; Organic acids ; Phosphate sensor ; Phosphates ; Various methods and equipments</subject><ispartof>Journal of biotechnology, 1999-10, Vol.75 (2), p.127-133</ispartof><rights>1999 Elsevier Science B.V.</rights><rights>1999 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c464t-1191a106cbc0c490a08d6abf759d91a11020b334026aaf89d4738415337b54823</citedby><cites>FETCH-LOGICAL-c464t-1191a106cbc0c490a08d6abf759d91a11020b334026aaf89d4738415337b54823</cites></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&idt=1991684$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Nakamura, Hideaki</creatorcontrib><creatorcontrib>Hasegawa, Mami</creatorcontrib><creatorcontrib>Nomura, Yoko</creatorcontrib><creatorcontrib>Arikawa, Yoshiko</creatorcontrib><creatorcontrib>Matsukawa, Ritsuko</creatorcontrib><creatorcontrib>Ikebukuro, Kazunori</creatorcontrib><creatorcontrib>Karube, Isao</creatorcontrib><title>Development of a highly sensitive chemiluminescence flow-injection analysis sensor for phosphate-ion detection using maltose phosphorylase</title><title>Journal of biotechnology</title><description>A chemiluminescence flow-injection analysis biosensor has been constructed for phosphate-ion detection. This system is coenzymeless and employs a maltose phosphorylase, mutarotase, and glucose-oxidase (MP–MUT–GOD) reaction system combined with an
Arthromyces ramosus peroxidase–luminol reaction system. The system consists of a column packed with MP–MUT–GOD immobilized on
N-hydroxysuccinimide beads, a mixing joint for the chemiluminescence reaction, and a photomultiplier. The response provided by this system was linear, with a wide range between 10 nM and 30 μM phosphate ion, and a measuring time of 3 min per sample. Under the optimal condition, the sensor was able to detect 1.0 μM phosphate ion for at least 2 weeks. For a practical application, the determination of phosphate ion in river water was examined using ethylenediaminetetraacetic acid, and the results were estimated by comparing with the molybdenum-blue method.</description><subject>Arthromyces ramosus peroxidase</subject><subject>Biological and medical sciences</subject><subject>Biosensors</subject><subject>Biotechnology</subject><subject>Chemiluminescence</subject><subject>Enzyme immobilization</subject><subject>Enzyme kinetics</subject><subject>Flow-injection analysis</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Methods. Procedures. Technologies</subject><subject>N-Hydroxysuccinimide beads</subject><subject>Organic acids</subject><subject>Phosphate sensor</subject><subject>Phosphates</subject><subject>Various methods and equipments</subject><issn>0168-1656</issn><issn>1873-4863</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><recordid>eNqFkc2OFCEUhYnRxHb0EUxYGKOLUmigClbGjL_JJC7UNaGpW1NMKCi51W36FXxqqe6OLmdxuQu-wwnnEPKcszec8fbt93rohreqfWXMa8a4Yo15QDZcd6KRuhUPyeYf8pg8QbxjjEmj-Ib8-QAHiHmeIC00D9TRMdyO8UgREoYlHID6EaYQ91NIgB6SBzrE_LsJ6Q78EnKiLrl4xIAnTS50qDOPGefRLdCsRA_Lhd1jSLd0cnHJCBcql2N0CE_Jo8FFhGeXfUV-fvr44_pLc_Pt89fr9zeNl61cGs4Nd5y1fueZl4Y5pvvW7YZOmX694WzLdkJItm2dG7TpZSe05EqIbqek3oor8vL87lzyrz3gYqdQPxajS5D3aLdc1rCMuBfknVBaK15BdQZ9yYgFBjuXMLlytJzZtSJ7qsiu-Vtj7Kkia6ruxcXAoXdxKC75gP_FxlSVrNi7MwY1lUOAYtGHtYg-lBqr7XO4x-gvVCeoTg</recordid><startdate>19991008</startdate><enddate>19991008</enddate><creator>Nakamura, Hideaki</creator><creator>Hasegawa, Mami</creator><creator>Nomura, Yoko</creator><creator>Arikawa, Yoshiko</creator><creator>Matsukawa, Ritsuko</creator><creator>Ikebukuro, Kazunori</creator><creator>Karube, Isao</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope></search><sort><creationdate>19991008</creationdate><title>Development of a highly sensitive chemiluminescence flow-injection analysis sensor for phosphate-ion detection using maltose phosphorylase</title><author>Nakamura, Hideaki ; Hasegawa, Mami ; Nomura, Yoko ; Arikawa, Yoshiko ; Matsukawa, Ritsuko ; Ikebukuro, Kazunori ; Karube, Isao</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c464t-1191a106cbc0c490a08d6abf759d91a11020b334026aaf89d4738415337b54823</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Arthromyces ramosus peroxidase</topic><topic>Biological and medical sciences</topic><topic>Biosensors</topic><topic>Biotechnology</topic><topic>Chemiluminescence</topic><topic>Enzyme immobilization</topic><topic>Enzyme kinetics</topic><topic>Flow-injection analysis</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Methods. Procedures. Technologies</topic><topic>N-Hydroxysuccinimide beads</topic><topic>Organic acids</topic><topic>Phosphate sensor</topic><topic>Phosphates</topic><topic>Various methods and equipments</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nakamura, Hideaki</creatorcontrib><creatorcontrib>Hasegawa, Mami</creatorcontrib><creatorcontrib>Nomura, Yoko</creatorcontrib><creatorcontrib>Arikawa, Yoshiko</creatorcontrib><creatorcontrib>Matsukawa, Ritsuko</creatorcontrib><creatorcontrib>Ikebukuro, Kazunori</creatorcontrib><creatorcontrib>Karube, Isao</creatorcontrib><collection>Pascal-Francis</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><jtitle>Journal of biotechnology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nakamura, Hideaki</au><au>Hasegawa, Mami</au><au>Nomura, Yoko</au><au>Arikawa, Yoshiko</au><au>Matsukawa, Ritsuko</au><au>Ikebukuro, Kazunori</au><au>Karube, Isao</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Development of a highly sensitive chemiluminescence flow-injection analysis sensor for phosphate-ion detection using maltose phosphorylase</atitle><jtitle>Journal of biotechnology</jtitle><date>1999-10-08</date><risdate>1999</risdate><volume>75</volume><issue>2</issue><spage>127</spage><epage>133</epage><pages>127-133</pages><issn>0168-1656</issn><eissn>1873-4863</eissn><coden>JBITD4</coden><abstract>A chemiluminescence flow-injection analysis biosensor has been constructed for phosphate-ion detection. This system is coenzymeless and employs a maltose phosphorylase, mutarotase, and glucose-oxidase (MP–MUT–GOD) reaction system combined with an
Arthromyces ramosus peroxidase–luminol reaction system. The system consists of a column packed with MP–MUT–GOD immobilized on
N-hydroxysuccinimide beads, a mixing joint for the chemiluminescence reaction, and a photomultiplier. The response provided by this system was linear, with a wide range between 10 nM and 30 μM phosphate ion, and a measuring time of 3 min per sample. Under the optimal condition, the sensor was able to detect 1.0 μM phosphate ion for at least 2 weeks. For a practical application, the determination of phosphate ion in river water was examined using ethylenediaminetetraacetic acid, and the results were estimated by comparing with the molybdenum-blue method.</abstract><cop>Lausanne</cop><cop>Amsterdam</cop><cop>New York, NY</cop><pub>Elsevier B.V</pub><doi>10.1016/S0168-1656(99)00150-9</doi><tpages>7</tpages></addata></record> |
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language | eng |
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source | ScienceDirect Journals |
subjects | Arthromyces ramosus peroxidase Biological and medical sciences Biosensors Biotechnology Chemiluminescence Enzyme immobilization Enzyme kinetics Flow-injection analysis Fundamental and applied biological sciences. Psychology Methods. Procedures. Technologies N-Hydroxysuccinimide beads Organic acids Phosphate sensor Phosphates Various methods and equipments |
title | Development of a highly sensitive chemiluminescence flow-injection analysis sensor for phosphate-ion detection using maltose phosphorylase |
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