Bramanti Emilia, Toncelli Daniel, Morelli Elisabetta, Lampugnani Leonardo, Zamboni Roberto, Miller Keith E, Zemetra Joseph, D'Ulivo Alessandro
Italian National Research Council, CNR-Istituto per i Processi Chimico-Fisici, Laboratory of Instrumental Analytical Chemistry, Via G. Moruzzi 1, 56124 Pisa, Italy.
J Chromatogr A. 2006 Nov 10;1133(1-2):195-203. doi: 10.1016/j.chroma.2006.08.045. Epub 2006 Sep 8.
Liquid chromatography (LC) coupled on line with UV/visible diode array detector (DAD) and cold vapour generation atomic fluorescence spectrometry (CVGAFS) has been developed for the speciation, determination and characterization of phytochelatins (PCs). The method is based on a bidimensional approach, e.g. on the analysis of synthetic PC solutions (apo-PCs and Cd(2+)-complexed PCs) (i) by size exclusion chromatography coupled to UV diode array detector (SEC-DAD); (ii) by the derivatization of PC -SH groups in SEC fractions by p-hydroxymercurybenzoate (PHMB) and the indirect detection of PC-PHMB complexes by reversed phase liquid chromatography coupled to atomic fluorescence detector (RPLC-CVGAFS). MALDI-TOF/MS (matrix assisted laser desorption ionization time of flight mass spectrometry) analysis of underivatized synthetic PC samples was performed in order have a qualitative information of their composition. Quantitative analysis of synthetic PC solutions has been performed on the basis of peak area of PC-PHMB complexes of the mercury specific chromatogram and calibration curve of standard solution of glutathione (GSH) complexed to PHMB (GS-PHMB). The limit of quantitation (LOQ) in terms of GS-PHMB complex was 90 nM (CV 5%) with an injection volume of 35 microL, corresponding to 3.2 pmol (0.97 ng) of GSH. The method has been applied to analysis of extracts of cell cultures from Phaeodactylum tricornutum grown in Cd-containing nutrient solutions, analysed by SEC-DAD-CVGAFS and RPLC-DAD-CVGAFS.
已开发出液相色谱(LC)与紫外/可见二极管阵列检测器(DAD)和冷蒸气发生原子荧光光谱法(CVGAFS)在线联用的方法,用于植物螯合肽(PCs)的形态分析、测定和表征。该方法基于二维方法,例如对合成PC溶液(脱辅基PCs和Cd(2+)络合的PCs)进行分析:(i)通过尺寸排阻色谱与紫外二极管阵列检测器联用(SEC-DAD);(ii)通过对SEC馏分中的PC -SH基团用对羟基汞苯甲酸(PHMB)进行衍生化,并通过反相液相色谱与原子荧光检测器联用(RPLC-CVGAFS)间接检测PC-PHMB络合物。对未衍生化的合成PC样品进行了基质辅助激光解吸电离飞行时间质谱(MALDI-TOF/MS)分析,以便获得其组成的定性信息。基于汞特异性色谱图中PC-PHMB络合物的峰面积和与PHMB络合的谷胱甘肽(GSH)标准溶液的校准曲线,对合成PC溶液进行了定量分析。以GS-PHMB络合物计,定量限(LOQ)为90 nM(CV 5%),进样体积为35 μL,相当于3.2 pmol(0.97 ng)的GSH。该方法已应用于对在含镉营养液中生长的三角褐指藻细胞培养物提取物的分析,采用SEC-DAD-CVGAFS和RPLC-DAD-CVGAFS进行分析。