New chemiluminescence assay for linamarin
A new chemiluminescence assay was developed for the quantitative determination of linamarin, a cyanogenic glucoside present in cassava. The assay involved hydrolysis of linamarin by a specific enzyme, linamarase, to release glucose, which was then quantitated by a chemiluminescence system consisting...
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th-mahidol.253252018-09-07T15:48:12Z New chemiluminescence assay for linamarin Sutarnthip Ruengprapavut Montri Chulavatnatol Mahidol University Biochemistry, Genetics and Molecular Biology A new chemiluminescence assay was developed for the quantitative determination of linamarin, a cyanogenic glucoside present in cassava. The assay involved hydrolysis of linamarin by a specific enzyme, linamarase, to release glucose, which was then quantitated by a chemiluminescence system consisting of glucose oxidase-peroxidase-luminol. The new assay was more sensitive than the conventional spectrophotometric method for quantitating linamarin in cassava extracts. However, the following agents were found to interfere with the new assay: Vanadate, Mg2+, and Cu2+, were inhibitory to the luminescence of the H2O2-peroxidase-luminol system used in the coupling reaction, whereas EDTA and EGTA activated the system. In addition, Hg2+, which inhibits glucose oxidase, and Tris ion, which inhibits linamarase, both interfered with the new assay. 2018-09-07T08:48:12Z 2018-09-07T08:48:12Z 1999-11-17 Article IUBMB Life. Vol.48, No.2 (1999), 219-223 10.1080/152165499307260 15216543 2-s2.0-0032749988 https://repository.li.mahidol.ac.th/handle/123456789/25325 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0032749988&origin=inward |
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Biochemistry, Genetics and Molecular Biology Sutarnthip Ruengprapavut Montri Chulavatnatol New chemiluminescence assay for linamarin |
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A new chemiluminescence assay was developed for the quantitative determination of linamarin, a cyanogenic glucoside present in cassava. The assay involved hydrolysis of linamarin by a specific enzyme, linamarase, to release glucose, which was then quantitated by a chemiluminescence system consisting of glucose oxidase-peroxidase-luminol. The new assay was more sensitive than the conventional spectrophotometric method for quantitating linamarin in cassava extracts. However, the following agents were found to interfere with the new assay: Vanadate, Mg2+, and Cu2+, were inhibitory to the luminescence of the H2O2-peroxidase-luminol system used in the coupling reaction, whereas EDTA and EGTA activated the system. In addition, Hg2+, which inhibits glucose oxidase, and Tris ion, which inhibits linamarase, both interfered with the new assay. |
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Mahidol University |
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Mahidol University Sutarnthip Ruengprapavut Montri Chulavatnatol |
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Sutarnthip Ruengprapavut Montri Chulavatnatol |
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Sutarnthip Ruengprapavut |
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New chemiluminescence assay for linamarin |
title_short |
New chemiluminescence assay for linamarin |
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New chemiluminescence assay for linamarin |
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New chemiluminescence assay for linamarin |
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New chemiluminescence assay for linamarin |
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new chemiluminescence assay for linamarin |
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2018 |
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https://repository.li.mahidol.ac.th/handle/123456789/25325 |
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1763487888730750976 |