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稳定同位素标记的同时拉曼和红外光谱学。

Simultaneous Raman and Infrared Spectroscopy of Stable Isotope Labelled .

机构信息

Centre for Metabolomics Research, Department of Biochemistry and Systems Biology, Institute of Systems, Molecular and Integrative Biology, University of Liverpool, Liverpool L69 7ZB, UK.

出版信息

Sensors (Basel). 2022 May 22;22(10):3928. doi: 10.3390/s22103928.

Abstract

We report the use of a novel technology based on optical photothermal infrared (O-PTIR) spectroscopy for obtaining simultaneous infrared and Raman spectra from the same location of the sample allowing us to study bacterial metabolism by monitoring the incorporation of C- and N-labeled compounds. Infrared data obtained from bulk populations and single cells via O-PTIR spectroscopy were compared to conventional Fourier transform infrared (FTIR) spectroscopy in order to evaluate the reproducibility of the results achieved by all three approaches. Raman spectra acquired were concomitant with infrared data from bulk populations as well as infrared spectra collected from single cells, and were subjected to principal component analysis in order to evaluate any specific separation resulting from the isotopic incorporation. Similar clustering patterns were observed in infrared data acquired from single cells via O-PTIR spectroscopy as well as from bulk populations via FTIR and O-PTIR spectroscopies, indicating full incorporation of heavy isotopes by the bacteria. Satisfactory discrimination between unlabeled (. CN), CN- and CN-labeled bacteria was also obtained using Raman spectra from bulk populations. In this report, we also discuss the limitations of O-PTIR technology to acquire Raman data from single bacterial cells (with typical dimensions of 1 × 2 µm) as well as spectral artifacts induced by thermal damage when analyzing very small amounts of biomass (a bacterium tipically weighs ~ 1 pg).

摘要

我们报告了一种基于光热红外(O-PTIR)光谱的新技术的应用,该技术可从样品的同一位置同时获得红外和拉曼光谱,从而通过监测 C 和 N 标记化合物的掺入来研究细菌代谢。通过 O-PTIR 光谱从群体和单细胞获得的红外数据与常规傅里叶变换红外(FTIR)光谱进行了比较,以评估所有三种方法所获得结果的重现性。获得的拉曼光谱与群体的红外数据以及从单细胞收集的红外光谱同时进行,并且进行了主成分分析,以评估由于同位素掺入而导致的任何特定分离。通过 O-PTIR 光谱从单细胞获得的红外数据以及通过 FTIR 和 O-PTIR 光谱从群体获得的红外数据观察到相似的聚类模式,表明细菌完全掺入了重同位素。还使用群体的拉曼光谱获得了对未标记(.CN)、CN-和 CN-标记细菌的令人满意的区分。在本报告中,我们还讨论了 O-PTIR 技术从单个细菌细胞(典型尺寸为 1×2 µm)获取拉曼数据的局限性,以及在分析非常少量生物量(细菌通常重约 1 pg)时由热损伤引起的光谱伪影。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be1d/9145054/fc356ccef194/sensors-22-03928-g001.jpg

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