首页 | 本学科首页   官方微博 | 高级检索  
     


Analysis by reverse-phase high-pressure liquid chromatography of phenylisothiocyanate-derivatized 1-aminocyclopropane-1-carboxylic acid in apple extracts
Authors:D Lanneluc-Sanson  C T Phan  R L Granger
Affiliation:1. Biomedical Engineering Department, Faculty of Engineering, University of Malaya, 50603 Kuala Lumpur, Malaysia;2. Mechanical Engineering Department, Faculty of Engineering, University of Malaya, 50603 Kuala Lumpur, Malaysia;3. School of Chemical and Materials Engineering, National University of Sciences and Technology, H-12, Islamabad, Pakistan;4. Department of Materials Science and Engineering, The Ohio State University, Columbus, OH 43210, USA;5. Centre for Ionics, University of Malaya, 50603 Kuala Lumpur, Malaysia
Abstract:A rapid and sensitive method for the determination of 1-aminocyclopropane-1-carboxylic acid (ACC) in apple tissues is described. This method is based on the derivatization of ACC with phenylisothiocyanate, and the subsequent separation and quantification of the resulting phenylthiocarbamyl-ACC by reverse-phase high-pressure liquid chromatography. Phenylthiocarbamylation of ACC (and other amino acids) in apple extracts is complete within 20 min at room temperature. After removing solvents and reagent, the phenylthiocarbamyl derivatives are separated on an octadecyl reverse-phase column, eluted with a mixture of acetonitrile and sodium acetate buffer at pH 4.6, and monitored with a uv detector set at 254 nm. An analysis of apple extract can thus be achieved in 23 min and detect quantities as low as 1 pmol. Assays have been done to compare the efficiency of this method with that of a method using an ion-exchange amino acid analyzer and with that of Lizada and Yang's method [(1979), Anal. Biochem. 100, 140-145]. The latter method proved to yield markedly less accurate results than the other two, but the derivatization-HPLC method was preferred because of simplicity of operation and a better separation of ACC.
Keywords:
本文献已被 ScienceDirect 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号