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从高等植物叶片中制备淀粉和其他碳组分用于稳定碳同位素分析。

Preparation of starch and other carbon fractions from higher plant leaves for stable carbon isotope analysis.

作者信息

Wanek W, Heintel S, Richter A

机构信息

Chemical Physiology of Plants, Institute of Ecology and Conservation Biology, University of Vienna, Althanstrasse 14, A-1090 Vienna, Austria.

出版信息

Rapid Commun Mass Spectrom. 2001;15(14):1136-40. doi: 10.1002/rcm.353.

Abstract

The measurement of the carbon isotope composition of starch and cellulose still relies on chemical isolation of these water-insoluble plant constituents and subsequent elemental analysis by isotope ratio mass spectrometry (EA/IRMS) of the purified fractions, while delta(13)C values of low-molecular-weight organic compounds are now routinely measured by gas chromatography/combustion/isotope ratio mass spectrometry (GC/C/IRMS). Here we report a simple and reliable method for processing milligram quantities of dried plant material for the analysis of the carbon isotope composition of lipids, soluble sugars, starch and cellulose from the same sample. We evaluated three different starch preparation methods, namely (1) enzymatic hydrolysis by alpha-amylase, (2) solubilization by dimethyl sulfoxide (DMSO) followed by precipitation with ethanol, and (3) partial hydrolysis by HCl followed by precipitation of the resulting dextrins by ethanol. Starch recovery for three commercially available native starches (from potato, rice and wheat) varied from 48 to 81% for the techniques based on precipitation, whereas the enzymatic technique exhibited yields between 99 and 105%. In addition, the DMSO and HCl techniques introduced a significant (13)C fractionation of up to 1.9 per thousand, while the carbon isotope composition of native starches analyzed after enzymatic digestion did not show any significant difference from that of untreated samples. The enzymatic starch preparation method was then incorporated into a protocol for determination of delta(13)C signatures of lipids, soluble carbohydrates, starch and crude cellulose. The procedure is based on methanol/chloroform/water extraction of dried and ground leaf material. After recovery of the chloroform phase (lipid fraction), the methanol/water phase was deionized by ion exchange (soluble carbohydrate fraction) and the pellet treated with heat-stable alpha-amylase (starch fraction). The remaining insoluble material was subjected to solvolysis by diglyme (cellulose fraction). The method was shown to be applicable to foliar tissues of a variety of different plant species (spruce, erect brome, maize and soybean).

摘要

淀粉和纤维素碳同位素组成的测定仍然依赖于对这些水不溶性植物成分的化学分离,以及随后通过同位素比率质谱法(EA/IRMS)对纯化组分进行元素分析,而低分子量有机化合物的δ(13)C值现在通常通过气相色谱/燃烧/同位素比率质谱法(GC/C/IRMS)进行测量。在此,我们报告了一种简单可靠的方法,用于处理毫克量的干燥植物材料,以分析同一样品中脂质、可溶性糖、淀粉和纤维素的碳同位素组成。我们评估了三种不同的淀粉制备方法,即:(1)用α-淀粉酶进行酶促水解;(2)用二甲基亚砜(DMSO)溶解,然后用乙醇沉淀;(3)用HCl进行部分水解,然后用乙醇沉淀所得糊精。对于基于沉淀的技术,三种市售天然淀粉(来自马铃薯、大米和小麦)的淀粉回收率在48%至81%之间,而酶促技术的产率在99%至105%之间。此外,DMSO和HCl技术引入了高达1.9‰的显著(13)C分馏,而酶促消化后分析的天然淀粉的碳同位素组成与未处理样品相比没有显示出任何显著差异。然后,将酶促淀粉制备方法纳入用于测定脂质、可溶性碳水化合物、淀粉和粗纤维素的δ(13)C特征的方案中。该程序基于对干燥和研磨的叶片材料进行甲醇/氯仿/水提取。回收氯仿相(脂质部分)后,甲醇/水相通过离子交换进行去离子化(可溶性碳水化合物部分),沉淀用热稳定的α-淀粉酶处理(淀粉部分)。剩余的不溶性物质通过二甘醇甲醚进行溶剂分解(纤维素部分)。该方法已证明适用于多种不同植物物种(云杉、直立雀麦、玉米和大豆)的叶片组织。

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