Fatty Acid Analysis by Capillary Electrophoresis and Contactless Conductivity Detection for Future Life Detection Missions.

IF 3 3区 生物学 Q2 BIOCHEMICAL RESEARCH METHODS
Miranda G M Kok, Maria F Mora
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Abstract

Future life-detection missions will likely search for biosignatures within a wide range of organic compounds, including fatty acids. In order to determine such biosignatures, it is necessary to identify and quantify individual fatty acids present within a sample. In this study, we present a method using capillary electrophoresis coupled to contactless conductivity detection (CE-C4D) for the separation and detection of both saturated and unsaturated fatty acids after derivatization with N,N-diethylethylenediamine, triethylamine, and 2-chloro-1-methylpyridinium iodide at 40°C for 10 min. Operating conditions (background electrolyte, separation voltage, and temperature) were optimized to provide maximum separation of fatty acids, thereby allowing their identification and quantification. Using a background electrolyte of 2 M acetic acid in 45% acetonitrile, an optimal separation was obtained with a separation voltage of 10 kV and a capillary temperature of 15°C. The optimized CE-C4D method was used to analyze samples of the cyanobacterium Spirulina. Multiple fatty acids were detected in the samples, showing the potential of this method for detection of fatty acid biosignatures during future spaceflight missions.

利用毛细管电泳和非接触式电导检测进行脂肪酸分析,用于未来的生命探测任务。
未来的生命探测任务可能会在包括脂肪酸在内的各种有机化合物中寻找生物特征。为了确定此类生物特征,有必要对样品中的单个脂肪酸进行识别和量化。本研究采用毛细管电泳结合非接触式电导检测法(CE-C4D),在 40°C 下用 N,N-二乙基乙二胺、三乙胺和 2-氯-1-甲基碘化吡啶衍生 10 分钟后,对饱和脂肪酸和不饱和脂肪酸进行分离和检测。对操作条件(背景电解质、分离电压和温度)进行了优化,以最大限度地分离脂肪酸,从而对其进行鉴定和定量。背景电解质为 2 M 乙酸加 45% 乙腈,分离电压为 10 kV,毛细管温度为 15°C,分离效果最佳。优化后的 CE-C4D 方法用于分析蓝藻样品。样品中检测到了多种脂肪酸,显示了该方法在未来太空飞行任务中检测脂肪酸生物特征的潜力。
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来源期刊
ELECTROPHORESIS
ELECTROPHORESIS 生物-分析化学
CiteScore
6.30
自引率
13.80%
发文量
244
审稿时长
1.9 months
期刊介绍: ELECTROPHORESIS is an international journal that publishes original manuscripts on all aspects of electrophoresis, and liquid phase separations (e.g., HPLC, micro- and nano-LC, UHPLC, micro- and nano-fluidics, liquid-phase micro-extractions, etc.). Topics include new or improved analytical and preparative methods, sample preparation, development of theory, and innovative applications of electrophoretic and liquid phase separations methods in the study of nucleic acids, proteins, carbohydrates natural products, pharmaceuticals, food analysis, environmental species and other compounds of importance to the life sciences. Papers in the areas of microfluidics and proteomics, which are not limited to electrophoresis-based methods, will also be accepted for publication. Contributions focused on hyphenated and omics techniques are also of interest. Proteomics is within the scope, if related to its fundamentals and new technical approaches. Proteomics applications are only considered in particular cases. Papers describing the application of standard electrophoretic methods will not be considered. Papers on nanoanalysis intended for publication in ELECTROPHORESIS should focus on one or more of the following topics: • Nanoscale electrokinetics and phenomena related to electric double layer and/or confinement in nano-sized geometry • Single cell and subcellular analysis • Nanosensors and ultrasensitive detection aspects (e.g., involving quantum dots, "nanoelectrodes" or nanospray MS) • Nanoscale/nanopore DNA sequencing (next generation sequencing) • Micro- and nanoscale sample preparation • Nanoparticles and cells analyses by dielectrophoresis • Separation-based analysis using nanoparticles, nanotubes and nanowires.
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