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A High Performance Liquid Chromatography-Radio-Organic Acid Analyzer for Determining the Specific Activities of Radioactive Organic Acids

A High Performance Liquid Chromatography-Radio-Organic Acid Analyzer for Determining the Specific... Abstract To monitor rapidly the specific activity of radioactive organic acids, a high performance liquid chromatography (HPLC)-radioanalyzer was constructed. The instrument is a linear combination of an HPLC organic acid analyzer and a radioanalyzer. Organic acids are separated through a 100 cm column packed with Diaion-CK08S (H$type) resin. The organic acids were detected at 430 nm after reaction with bromocresol purple. The effluents from the HPLC are conduced to a U-type flow-cell packed with lithium-glass scintillator, which floresces in response to rrβ-rays. The instrument was utilized to investigate the assimilation of H14CO3− fixation in barley roots after 10 min uptake. Malate showed the highest specific activity, followed by citrate and aspartate. This content is only available as a PDF. Copyright © 1982. The Japanese Society of Plant Physiologists http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Plant and Cell Physiology Oxford University Press

A High Performance Liquid Chromatography-Radio-Organic Acid Analyzer for Determining the Specific Activities of Radioactive Organic Acids

Plant and Cell Physiology , Volume 23 (4) – Jun 1, 1982

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Publisher
Oxford University Press
Copyright
Copyright © 1982. The Japanese Society of Plant Physiologists
ISSN
0032-0781
eISSN
1471-9053
DOI
10.1093/oxfordjournals.pcp.a076399
Publisher site
See Article on Publisher Site

Abstract

Abstract To monitor rapidly the specific activity of radioactive organic acids, a high performance liquid chromatography (HPLC)-radioanalyzer was constructed. The instrument is a linear combination of an HPLC organic acid analyzer and a radioanalyzer. Organic acids are separated through a 100 cm column packed with Diaion-CK08S (H$type) resin. The organic acids were detected at 430 nm after reaction with bromocresol purple. The effluents from the HPLC are conduced to a U-type flow-cell packed with lithium-glass scintillator, which floresces in response to rrβ-rays. The instrument was utilized to investigate the assimilation of H14CO3− fixation in barley roots after 10 min uptake. Malate showed the highest specific activity, followed by citrate and aspartate. This content is only available as a PDF. Copyright © 1982. The Japanese Society of Plant Physiologists

Journal

Plant and Cell PhysiologyOxford University Press

Published: Jun 1, 1982

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