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Enzymic Assay of 10−7 to 10−14 Moles of Sucrose in Plant Tissues

机译:植物组织中蔗糖10−7至10−14摩尔的酶促测定

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摘要

Procedures are described for measuring sucrose in plant extracts or freeze-dried tissue in the range between 10−7 and 10−14 moles. The method is based on the destruction of pre-existing glucose and fructose, followed by the hydrolysis of sucrose and reduction of NADP+ by a series of coupled enzymic reactions. Depending on the sensitivity required, the NADPH is determined directly with a spectrophotometer or a fluorometer, or is amplified as much as 30,000 times before fluorometric assay. The procedures suggested for the macro level are simpler than current methods, and those suggested for microanalysis are several orders of magnitude more sensitive.With this technique, single palisade parenchyma cells and single spongy parenchyma cells of Vicia faba leaflets were each found to contain about 2.2 pmoles of sucrose.
机译:描述了测量植物提取物或冻干组织中蔗糖的摩尔数在10 -7 和10 -14 之间的程序。该方法基于破坏已有的葡萄糖和果糖,然后通过一系列偶合的酶促反应水解蔗糖和还原NADP + 。根据所需的灵敏度,可以使用分光光度计或荧光计直接测定NADPH,或者在进行荧光测定之前将其放大多达30,000次。宏观水平上建议的程序比当前方法更简单,微观分析建议的程序更敏感几个数量级。通过这种技术,发现蚕豆小叶的单个栅栏实质细胞和海绵状实质细胞分别包含约2.2一摩尔的蔗糖。

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