Department of Food Science and Technology, Food Chemistry Laboratory, BOKU-University of Natural Resources and Life Sciences Vienna, Muthgasse 11, A-1190 Vienna, Austria.
J Chromatogr B Analyt Technol Biomed Life Sci. 2011 May 15;879(17-18):1353-60. doi: 10.1016/j.jchromb.2011.02.003. Epub 2011 Mar 1.
The AccQ.Tag™ method, as a well-established protocol for amino acid analysis combining derivatization procedure, dedicated HPLC separation and fluorescence detection, was properly transferred and accordingly optimized for the application on ultra performance liquid chromatography (UPLC™) and UV detection. Capitalizing on sub-2 μm particles, this newly established UV-UPLC™ technique facilitated efficient chromatographic separation of 21 amino acid derivatives within 12 min. In addition, UPLC™ demonstrated significant improvements due to superior performance and reduced run times compared with the former 35 min of the original HPLC protocol. Using UV instead of fluorescence detection, amino acid quantification after pre-column derivatization with 6-aminoquinolyl-N-hydroxysuccinimidyl carbamate (AQC) yielded appropriate sensitivities within the low pmol range with corresponding detection limits varying from 0.11 to 0.57 pmol per injection. Moreover, the UPLC™ method was applied to characterize changes in the free (FAA) as well as total amino acid (TAA) profiles specific to culture media at three distinctive stages of fermentation: fresh medium, fermentation broth after cell mass production prior to induction and after product expression at the end of fermentation. Amino acid profiles intrinsic to the fresh, sterilized medium indicated free, hence more bioavailable, amino acids at a FAA/TAA ratio of 40%, whereas ongoing fermentation implied a rather specific, successive decline in selective FAA concentrations. Thereby, the most distinctive variations in FAAs were highlighted by aspartic acid, serine and threonine, each exhibiting an almost complete uptake from the culture media (-96% to -99%), with remaining FAA/TAA ratios of 1%, 8%, and 1%, respectively. This indeed may indicate limitations and shortages within the nutrient broth. Thus, amino acid monitoring utilizing high-throughput chromatography, such as UPLC™, can be considered as a valuable tool to facilitate rapid adjustments of fermentation broths and to optimize culture media to specific requirements.
AccQ.Tag™ 方法是一种成熟的氨基酸分析方法,结合衍生化程序、专用 HPLC 分离和荧光检测,经过适当的转移和优化,可应用于超高效液相色谱 (UPLC™) 和紫外检测。利用亚 2μm 颗粒,新建立的 UV-UPLC™ 技术可在 12 分钟内高效分离 21 种氨基酸衍生物。此外,与原始 HPLC 方法的 35 分钟相比,UPLC™ 由于性能优越且运行时间缩短,因此显著提高了分析效率。使用紫外检测代替荧光检测,用 6-氨基喹啉-N-羟基琥珀酰亚胺基甲酸酯 (AQC) 进行柱前衍生化后对氨基酸进行定量,在低 pmol 范围内可获得适当的灵敏度,相应的检测限为 0.11 至 0.57 pmol/进样。此外,该 UPLC™ 方法还用于在发酵的三个不同阶段(新鲜培养基、细胞量生产后发酵液和发酵结束时产物表达后)中,对特定于培养基的游离(FAA)和总氨基酸(TAA)谱的变化进行特征描述。新鲜、灭菌培养基中的氨基酸谱表明游离(即更具生物利用度)氨基酸的 FAA/TAA 比例为 40%,而持续发酵则暗示选择性 FAA 浓度呈特定的、连续下降。因此,天冬氨酸、丝氨酸和苏氨酸的 FAA 变化最为显著,每种氨基酸几乎都从培养基中完全吸收(96%至 99%),剩余的 FAA/TAA 比例分别为 1%、8%和 1%。这确实可能表明营养肉汤存在局限性和短缺。因此,利用高通量色谱(如 UPLC™)进行氨基酸监测可被视为一种有价值的工具,可促进发酵液的快速调整,并优化培养基以满足特定需求。