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作 者:安子涵 张宏宇 殷佳欣 张攀 姚敏 黄康俊 AN Zihan;ZHANG Hongyu;YIN Jiaxin;ZHANG Pan;YAO Min;HUANG Kangjun(State Key Laboratory of Continental Dynamics,Department of Geology,Northwest University,Xi’an 710069,China;State Key Laboratory of Isotope Geochemistry,Guangzhou Institute of Geochemistry,Chinese Academy of Sciences,Guangzhou 510640,China)
机构地区:[1]西北大学地质学系,大陆动力学国家重点实验室,陕西西安710069 [2]中国科学院广州地球化学研究所,同位素地球化学国家重点实验室,广东广州510640
出 处:《岩矿测试》2024年第3期476-486,共11页Rock and Mineral Analysis
基 金:国家自然科学基金项目(42373061,41890845)。
摘 要:叶绿素a和叶绿素b是植物光合作用时吸收光能的主要色素,其中叶绿素b能帮助叶绿素a扩展吸收光谱促使其吸收更多光能,叶绿素a和叶绿素b比例的改变有助于植物适应光照变化。准确测定叶绿素a和叶绿素b的镁同位素值对研究叶绿素形成过程中镁的生物合成路径等问题具有重要意义,其中将叶绿素a和叶绿素b分离并收集是使用多接收电感耦合等离子体质谱仪(MC-ICP-MS)准确测定两者镁同位素值的关键。高效液相色谱(HPLC)是分离叶绿素的常用仪器,但目前HPLC分离叶绿素的方法主要聚焦于细菌和藻类叶绿素分离。因此,需开发一套能将植物叶绿素a和叶绿素b分离的方法,且该方法分离的样品适用于MC-ICP-MS的镁同位素测定。本文基于665nm检测波长和C18色谱柱(7.6mm×250mm,5μm),以三因素三水平正交设计优化HPLC条件,分析影响样品运行因素间的关系,得出符合要求的参数条件。经过优化的HPLC方法柱温为25℃,流速为1mL/min,流动相为甲醇-丙酮(80∶20,V/V)。结果表明:通过外标法定量分析叶绿素a和叶绿素b所得标准曲线在5~50mg/L浓度范围内的相关系数均大于0.9996,检测限为0.40~1.09mg/L,定量限为1.22~3.31mg/L,相对标准偏差(RSD)小于8.10%,样品加标回收率介于91.92%~111.11%。采用该方法对样品进行分离后,再利用MC-ICP-MS对前处理后的样品进行镁同位素测定,标准-样品间插法测定的数据表明镁同位素测试结果可靠,证明本文建立的方法为植物叶绿素a和叶绿素b的分离提供了技术支撑,且分离样品可用于镁同位素测定。The accurate determination of magnesium isotope values of chlorophyll a and chlorophyll b is particularly important for the study of magnesium biosynthesis pathways during chlorophyll formation.HPLC is required before MC-ICP-MS can be utilized,but HPLC lacks a method for separating chlorophylls.Therefore,it is necessary to develop a set of methods for separating plant chlorophyll a and chlorophyll b.The samples separated by this method are suitable for magnesium isotope determination by MC-ICP-MS.Based on the detection wavelength of 665nm and C18 column(7.6mm×250mm,5μm),the HPLC conditions were optimized by three-factor and three-level orthogonal design to obtain the required parameters.The correlation coefficients of chlorophyll a and chlorophyll b standard curves in the concentration range of 5−50mg/L were greater than 0.9996,the detection limits were 0.40−1.09mg/L,the quantification limits were 1.22−3.31mg/L,the relative standard deviation was less than 8.10%,and the recoveries were 91.92%−111.11%.The magnesium isotope data of the isolated samples also showed that the column temperature of 25℃,flow rate of 1mL/min,and methanol-acetone(80∶20,V/V)mobile phase were reliable as HPLC separation conditions.The method established in this paper provides technical support for the separation of chlorophyll a and chlorophyll b in plants,and the separated samples can be used for magnesium isotope determination.
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