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采用甲磺酸水解和9-芴基甲基氯甲酸酯衍生化的高效液相色谱法进行氨基酸分析。

Amino acid analysis by high-performance liquid chromatography with methanesulfonic acid hydrolysis and 9-fluorenylmethylchloroformate derivatization.

作者信息

Malmer M F, Schroeder L A

机构信息

Department of Biological Sciences, Youngstown State University, OH 44555.

出版信息

J Chromatogr. 1990 Aug 29;514(2):227-39. doi: 10.1016/s0021-9673(01)89394-8.

Abstract

Experiments were undertaken to verify a method for complete amino acid analysis of plant and animal tissues and waste products from a single hydrolysis and high-performance liquid chromatographic run. Using methanesulfonic acid, hydrolysis of cytochrome c at 115 degrees C for 22 h yielded recoveries equal to or higher than hydrolysis at 115 degrees C for 70 h or at 150 degrees C for 22 h. Triple evacuation of the hydrolysis tube alternated with nitrogen flush gave recovery improvements over single evacuation. Refrigerated storage of samples under vacuum for up to 4 days between hydrolysis and further analysis was not different from immediate analysis. However, recoveries of several amino acids were reduced by refrigerated storage in air. Recoveries of individual amino acids were determined by hydrolysis of biological samples with and without added cytochrome c. Although recoveries from biological samples were lower for several amino acids, precision was sufficient to allow quantitation after correction for incomplete recoveries. Derivatization with 9-fluorenylmethylchloroformate (FMOC) was chosen because derivatives are formed with both primary and secondary amino acids, derivatives are quite stable, and detection may be either UV absorbance or fluorescence. Derivative yield is sensitive to the pH of the reaction mixture. A pH of 8.0 gave reproducible derivative yield for all physiological amino acids. Solvent extraction of excess FMOC, when compared to addition of amantadine to react with excess FMOC, gave both higher recoveries and greater precision. Following derivatization, samples could be kept at 4 degrees C for at least 24 h before high-performance liquid chromatographic analysis without loss of response. Derivative yield and detector response were constant across a wide range of molar ratio of FMOC to total amino acids. Gradient elution was required to separate FMOC derivatives on a reversed-phase column. The capability of the pumping system to produce exponential gradients permitted rapid and easy fine-tuning of the gradient.

摘要

进行了实验,以验证一种通过单次水解和高效液相色谱分析来完成动植物组织及废弃物中氨基酸分析的方法。使用甲磺酸,在115℃下水解细胞色素c 22小时,其回收率等于或高于在115℃下水解70小时或在150℃下水解22小时的回收率。水解管进行三次抽空并交替用氮气冲洗,其回收率比单次抽空有所提高。在水解和进一步分析之间,将样品在真空下冷藏保存长达4天,与立即分析没有差异。然而,在空气中冷藏保存会降低几种氨基酸的回收率。通过对添加和未添加细胞色素c的生物样品进行水解来测定单个氨基酸的回收率。尽管几种氨基酸在生物样品中的回收率较低,但精密度足以在校正不完全回收率后进行定量分析。选择用9-芴甲基氯甲酸酯(FMOC)进行衍生化,是因为它能与伯氨基酸和仲氨基酸都形成衍生物,衍生物相当稳定,并且检测既可以采用紫外吸收法也可以采用荧光法。衍生物产率对反应混合物的pH敏感。pH为8.0时,所有生理氨基酸的衍生物产率均可重现。与添加金刚烷与过量FMOC反应相比,用溶剂萃取过量的FMOC,回收率更高且精密度更高。衍生化后,样品在进行高效液相色谱分析前可在4℃下保存至少24小时而不会损失响应。在很宽的FMOC与总氨基酸摩尔比范围内,衍生物产率和检测器响应都是恒定的。在反相柱上分离FMOC衍生物需要梯度洗脱。泵系统产生指数梯度的能力允许对梯度进行快速且容易的微调。

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