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用于诊断应用的近紫外/可见光大肠杆菌(pYAC4)、枯草芽孢杆菌(PY79)和绿色面包霉菌荧光的定量光谱表征。

Quantitative Spectroscopic Characterization of Near-UV/visible E. coli (pYAC4), B. subtilis (PY79), and Green Bread Mold Fungus Fluorescence for Diagnostic Applications.

作者信息

Herzog Joshua M, Sick Volker

机构信息

Department of Mechanical Engineering, University of Michigan, 2350 Hayward St., Ann Arbor, MI 48109, USA.

出版信息

J Fluoresc. 2023 Sep;33(5):1813-1825. doi: 10.1007/s10895-023-03183-6. Epub 2023 Feb 27.

Abstract

Ultraviolet (UV)-excited visible fluorescence is an attractive option for low-cost, low-complexity, rapid imaging of bacterial and fungal samples for imaging diagnostics in the biomedical community. While several studies have shown there is potential for identification of microbial samples, very little quantitative information is available in the literature for the purposes of diagnostic design. In this work, two non-pathogenic bacteria samples (E. coli pYAC4, and B. subtilis PY79) and a wild-cultivated green bread mold fungus sample are characterized spectroscopically for the purpose of diagnostic design. For each sample, fluorescence spectra excited with low-power near-UV continuous wave (CW) sources, and extinction and elastic scattering spectra are captured and compared. Absolute fluorescence intensity per cell excited at 340 nm is estimated from imaging measurements of aqueous samples. The results are used to estimate detection limits for a prototypical imaging experiment. It was found that fluorescence imaging is feasible for as few as 35 bacteria cells (or [Formula: see text]30 µm of bacteria) per pixel, and that the fluorescence intensity per unit volume is similar for the three samples tested here. A discussion and model of the mechanism of bacterial fluorescence in E. coli is provided.

摘要

紫外线(UV)激发的可见荧光是一种颇具吸引力的选择,可用于生物医学领域低成本、低复杂度的细菌和真菌样本快速成像诊断。虽然多项研究表明微生物样本的识别具有潜力,但文献中关于诊断设计目的的定量信息却非常少。在这项工作中,为了诊断设计的目的,对两种非致病性细菌样本(大肠杆菌pYAC4和枯草芽孢杆菌PY79)以及一种野生培养的绿色面包霉菌样本进行了光谱表征。对于每个样本,捕获并比较了由低功率近紫外连续波(CW)光源激发的荧光光谱、消光光谱和弹性散射光谱。通过对水性样本的成像测量估计了在340 nm激发下每个细胞的绝对荧光强度。结果用于估计典型成像实验的检测限。发现对于每像素低至35个细菌细胞(或30 µm的细菌),荧光成像都是可行的,并且此处测试的三个样本的单位体积荧光强度相似。本文还提供了大肠杆菌中细菌荧光机制的讨论和模型。

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