Bedoukian   RussellIPM   RussellIPM   Piezoelectric Micro-Sprayer


Home
Animal Taxa
Plant Taxa
Semiochemicals
Floral Compounds
Semiochemical Detail
Semiochemicals & Taxa
Synthesis
Control
Invasive spp.
References

Abstract

Guide

Alphascents
Pherobio
InsectScience
E-Econex
Counterpart-Semiochemicals
Print
Email to a Friend
Kindly Donate for The Pherobase

« Previous AbstractDetection of volatile organic compounds as biomarkers in breath analysis by different analytical techniques    Next AbstractThe effect of biosilver nanoparticles on different bacterial strains' metabolism reflected in their VOCs profiles »

Electrophoresis


Title:Investigation of bacterial viability from incubated saliva by application of flow cytometry and hyphenated separation techniques
Author(s):Buszewski B; Milanowski M; Ligor T; Pomastowski P;
Address:"Department of Environmental Chemistry and Bioanalytics, Faculty of Chemistry, Nicolaus Copernicus University, Torun, Poland. Interdisciplinary Centre of Modern Technologies, Nicolaus Copernicus University, Torun, Poland"
Journal Title:Electrophoresis
Year:2017
Volume:20170515
Issue:16
Page Number:2081 - 2088
DOI: 10.1002/elps.201700057
ISSN/ISBN:1522-2683 (Electronic) 0173-0835 (Linking)
Abstract:"The aim of the study was determination of bacterial viability in saliva samples and finding a correlation between microbiological and volatile profiles of saliva depending on incubation time. Bacteria colonizing healthy oral cavities were also identified. Twelve healthy adults donated unstimulated saliva samples. Flow cytometry, optical density measurements and colony-forming unit (CFU) counting method were employed for analyses of native and inoculated saliva after 0, 1, 2, 24, and 48 h of incubation. Volatile profiles were acquired using headspace-solid phase microextraction-gas chromatography/mass spectrometry (HS-SPME-GC/MS). Oral bacteria were the most viable within 2 h after collection of saliva. Extension of incubation time to 48 h caused considerable decrease in live bacteria counts and sharp increase in dead bacteria counts. The most prevalent strain was Sphingomonas paucimobilis (26.67%). The number of volatiles raised from 5 to 27 with incubation time and most of them were putrefaction products, such as methanethiol, indole and pyrrole. HS-SPME-GC/MS method is insufficient for volatile profiling of 'fresh' saliva and should be directed rather to investigation of bacterial metabolites"
Keywords:Adult Bacteria/*isolation & purification Cell Culture Techniques Flow Cytometry Gas Chromatography-Mass Spectrometry Humans Metabolome *Microbial Viability Saliva/*microbiology Solid Phase Microextraction Volatile Organic Compounds/*analysis Bacteria Hs-s;
Notes:"MedlineBuszewski, Boguslaw Milanowski, Maciej Ligor, Tomasz Pomastowski, Pawel eng Germany 2017/04/22 Electrophoresis. 2017 Aug; 38(16):2081-2088. doi: 10.1002/elps.201700057. Epub 2017 May 15"

 
Back to top
 
Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
© 2003-2024 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
Page created on 26-12-2024