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Determination of Amino Acids in Cell Culture and Fermentation Broth Media Using Anion-Exchange Chromatography with Integrated Pulsed Amperometric Detection

机译:阴离子交换色谱-积分脉冲安培检测法测定细胞培养液和发酵液中的氨基酸

摘要

Anion-exchange chromatography with integrated pulsed amperometric detection (AE-IPAD) separates and directly detects amino acids, carbohydrates, alditols, and glycols in the same injection without pre- or post-column derivatization. These separations use a combination of NaOH and NaOH/sodium acetate eluents. We previously published the successful use of this technique, also known as AAA-Direct, to determine free amino acids in cell culture and fermentation broth media. We showed that retention of carbohydrates varies with eluent NaOH concentration differently than amino acids, and thus separations can be optimized by varying the initial NaOH concentration and its duration. Unfortunately, some amino acids eluting in the acetate gradient portion of the method were not completely resolved from system-related peaks and from unknown peaks in complex cell culture and fermentation media. In this article, we present changes in method that improve amino acid resolution and system ruggedness. The success of these changes and their compatibility with the separations previously designed for fermentation and cell culture are demonstrated with yeast extract-peptone-dextrose broth, M199, Dulbecco’s modified Eagle’s (with F-12), L-15 (Leibovitz), and McCoy’s 5A cell culture media.
机译:带有集成脉冲安培检测器(AE-IPAD)的阴离子交换色谱法可分离并直接检测同一进样中的氨基酸,碳水化合物,醛糖醇和乙二醇,而无需进行柱前或柱后衍生。这些分离使用NaOH和NaOH /乙酸钠洗脱液的组合。我们先前已成功发布了该技术(也称为AAA-Direct)的成功使用,以确定细胞培养和发酵液培养基中的游离氨基酸。我们表明,碳水化合物的保留量随洗脱液NaOH浓度的变化而不同于氨基酸,因此可以通过改变初始NaOH浓度及其持续时间来优化分离。不幸的是,该方法的乙酸盐梯度部分洗脱的某些氨基酸无法从系统相关峰以及复杂细胞培养和发酵培养基中的未知峰中完全分离出来。在本文中,我们提出了改善氨基酸分辨率和系统耐用性的方法更改。这些变化的成功及其与先前设计用于发酵和细胞培养的分离液的相容性通过酵母提取物-蛋白pe-葡萄糖肉汤,M199,Dulbecco改良的Eagle's(配F-12),L-15(Leibovitz)和McCoy's证明。 5A细胞培养基。

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