一种改进挥发性有机化合物体外分析的工程培养容器和流动系统。

Jarrett Eshima, Taylor R Pennington, Youssef Abdellatif, Angela Ponce Olea, Joel F Lusk, Benjamin D Ambrose, Ethan Marschall, Christopher Miranda, Paula Phan, Christina Aridi, Barbara S Smith
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引用次数: 0

摘要

挥发性有机化合物(VOCs)是生物代谢组的一个重要的生物学子集,但在实践中,用于分析这些小分子的体外技术差异很大,限制了研究结果的解释。在这里,我们提出了一种称为“Biodome”的工程培养工具,旨在通过集成动态顶空采样方法来从生物培养物中回收挥发性有机化合物,从而提高内源性分析物的回收率。我们利用哺乳动物细胞培养的计算建模和荧光成像验证了该装置在体外挥发性代谢组学中的功能。利用全面的二维气相色谱,加上飞行时间质谱仪和我们的工具提供的增强的采样能力,我们确定了14种具有统计意义的挥发性有机化合物,这些挥发性有机化合物不是在介质中发现的,也不是来自采样方法的外源,其中4种以前没有在体外报道过。为了证明在哺乳动物细胞培养之外的适用性,我们评估了耐氨苄西林DH5α大肠杆菌在生长的对数和固定阶段产生的挥发性有机化合物。我们鉴定出19种化合物,结果支持内源性生产,其中2种以前没有与大肠杆菌相关,3-辛酮和3-三甲酮。我们的研究结果强调了Biodome体外挥发性代谢组学的改进能力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An engineered culture vessel and flow system to improve the in vitro analysis of volatile organic compounds.

Volatile organic compounds (VOCs) are a biologically important subset of an organism's metabolome, yet in vitro techniques for the analysis of these small molecules vary substantially in practice, restricting the interpretation of study findings. Here, we present an engineered culture tool, termed the "Biodome", designed to enhance endogenous analyte recovery by integrating dynamic headspace sampling methodology for the recovery of VOCs from biological cultures. We validate the functionality of the device for in vitro volatile metabolomics utilizing computational modeling and fluorescent imaging of mammalian cell culture. Leveraging comprehensive two-dimensional gas chromatography coupled with a time-of-flight mass spectrometer and the enhanced sampling capabilities afforded by our tool, we identify 14 statistically significant VOCs not found in the media or exogenously derived from the sampling method, four of which have not been previously reported in vitro. To demonstrate applicability beyond mammalian cell culture, we assess the production of VOCs throughout the log and stationary phases of growth in ampicillin-resistant DH5α Escherichia coli. We identified 19 compounds with results supporting endogenous production, two of which had not previously associated with E. coli, 3-Octanone and 3-Tridecanone. Our findings emphasize the improved capabilities of the Biodome for in vitro volatile metabolomics.

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