Liu Xin, Li Dian-Fan, Wang Yun, Lu Ying-Tang
Key Laboratory of MOE for Plant Developmental Biology, College of Life Sciences, Wuhan University, Wuhan 430072, PR China.
J Chromatogr A. 2004 Dec 17;1061(1):99-104. doi: 10.1016/j.chroma.2004.10.067.
A rapid and sensitive method for the determination of 1-aminocyclopropane-1-carboxylic acid (ACC) in apple tissues has been described. This method is based on the derivatization of ACC with 3-(2-furoyl)quinoline-2-carboxaldehyde (FQ), and separation and quantification of the resulting FQ-ACC derivative by capillary electrophoresis coupled to laser-induced fluorescence detection (CE-LIF). Our results indicated that ACC derivatized with FQ could be well separated from other interfering amino acids using 20 mM borate buffer (pH 9.35) containing 40 mM sodium dodecyl sulfate and 10 mM Brij 35. The linearity of ACC was determined in the range from 0.05 to 5 microM with a correlation of 0.9967. The concentration detection limit for ACC was 10 nM (signal-to-noise = 3). The sensitivity and selectivity of this described method allows the analysis of ACC in crude apple extracts without extra purification and enrichment procedure.
本文描述了一种快速灵敏地测定苹果组织中1-氨基环丙烷-1-羧酸(ACC)的方法。该方法基于ACC与3-(2-呋喃甲酰基)喹啉-2-甲醛(FQ)的衍生化反应,并通过毛细管电泳-激光诱导荧光检测(CE-LIF)对生成的FQ-ACC衍生物进行分离和定量。我们的结果表明,使用含有40 mM十二烷基硫酸钠和10 mM Brij 35的20 mM硼酸盐缓冲液(pH 9.35),用FQ衍生化的ACC可以与其他干扰氨基酸很好地分离。ACC的线性范围为0.05至5 microM,相关性为0.9967。ACC的浓度检测限为10 nM(信噪比=3)。所述方法的灵敏度和选择性使得无需额外的纯化和富集步骤即可分析粗苹果提取物中的ACC。