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Characterization of bacterial fluorescence: insight into rapid detection of bacteria in water

Microbial contamination is one of the main risks affecting water safety. Traditional microbial detection methods tend to be time-consuming and labor-intensive. Thus, this study investigated a potential rapid and simple method for bacterial detection in water by excitation–emission matrix (EEM) fluor...

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Published in:Journal of water reuse and desalination 2021-12, Vol.11 (4), p.621-631
Main Authors: Mao, Yu, Chen, Xiao-Wen, Chen, Zhuo, Chen, Gen-Qiang, Lu, Yun, Wu, Yin-Hu, Hu, Hong-Ying
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cited_by cdi_FETCH-LOGICAL-c367t-d76de28711537129531631a9749705b8cd7ce095b8c987b1a5920770b9e583993
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container_title Journal of water reuse and desalination
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description Microbial contamination is one of the main risks affecting water safety. Traditional microbial detection methods tend to be time-consuming and labor-intensive. Thus, this study investigated a potential rapid and simple method for bacterial detection in water by excitation–emission matrix (EEM) fluorescence spectroscopy. Particularly, bacterial intrinsic fluorophores were divided into three regions, namely Region A (amino acids), Region N (NAD(P)H) and Region F (flavins). Afterwards, fluorescence characteristics of four pure bacterial species (Bacillus subtilis, Staphylococcus aureus, Escherichia coli and Pseudomonas aeruginosa) as well as indigenous bacteria in secondary effluent from two water reclamation plants were evaluated via fluorescence regional integration (FRI). Correlation analysis between fluorescence intensity (FI) integral and bacterial concentration was conducted, and principal component analysis (PCA) was applied to distinguish the fluorescence spectra of different bacteria. The results showed that most of the bacterial autofluorescence was emitted by amino acids and the FI integral of flavins had a good linear relationship (R2 > 0.9) with bacterial concentration. PCA could distinguish varied bacterial species and bacteria from different secondary effluents. This study indicated that FRI was helpful for the characterization of bacterial fluorescence and the quantification of bacteria in water.
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Traditional microbial detection methods tend to be time-consuming and labor-intensive. Thus, this study investigated a potential rapid and simple method for bacterial detection in water by excitation–emission matrix (EEM) fluorescence spectroscopy. Particularly, bacterial intrinsic fluorophores were divided into three regions, namely Region A (amino acids), Region N (NAD(P)H) and Region F (flavins). Afterwards, fluorescence characteristics of four pure bacterial species (Bacillus subtilis, Staphylococcus aureus, Escherichia coli and Pseudomonas aeruginosa) as well as indigenous bacteria in secondary effluent from two water reclamation plants were evaluated via fluorescence regional integration (FRI). Correlation analysis between fluorescence intensity (FI) integral and bacterial concentration was conducted, and principal component analysis (PCA) was applied to distinguish the fluorescence spectra of different bacteria. The results showed that most of the bacterial autofluorescence was emitted by amino acids and the FI integral of flavins had a good linear relationship (R2 &gt; 0.9) with bacterial concentration. PCA could distinguish varied bacterial species and bacteria from different secondary effluents. 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identifier ISSN: 2220-1319
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source Alma/SFX Local Collection
subjects Adenosine triphosphate
Amino acids
Analytical methods
Bacteria
bacterial detection
Biological contamination
Chemical compounds
Correlation analysis
Detection
E coli
Effluents
Fluorescence
fluorescence regional integration
Fluorescence spectroscopy
Fluorophores
Gram-positive bacteria
Labour
Methods
Microbial contamination
Microorganisms
NAD
Polymerase chain reaction
principal component analysis
Principal components analysis
Pseudomonas aeruginosa
Reclamation
Software
Spectrum analysis
Water pollution
Water reclamation
Water treatment
title Characterization of bacterial fluorescence: insight into rapid detection of bacteria in water
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