Real-time in situ detection and quantification of bacteria in the Arctic environment

At present, there are no methods that determine the total microbial load on an abiotic substrate in real time. The utility of such a capability ranges from sterilization and medical diagnostics to the search for new microorganisms in the environment and study of their ecological niches. We report th...

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Main Authors: Linda Powers, Walther R. Ellis, Christopher R. Lloyd
Format: Article
Language:English
Published: World Scientific Publishing 2014-03-01
Series:Journal of Innovative Optical Health Sciences
Subjects:
Online Access:http://www.worldscientific.com/doi/pdf/10.1142/S1793545813500387
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spelling doaj-c5e68ca26a8a48c2b6a824d31d72c0382020-11-24T23:24:44ZengWorld Scientific PublishingJournal of Innovative Optical Health Sciences1793-54581793-72052014-03-01721350038-11350038-1110.1142/S179354581350038710.1142/S1793545813500387Real-time in situ detection and quantification of bacteria in the Arctic environmentLinda Powers0Walther R. Ellis1Christopher R. Lloyd2Department of Electrical and Computer Engineering, Department of Biomedical Engineering, University of Arizona, Tucson, AZ 85721, USADepartment of Biomedical Engineering, University of Arizona, Tucson, AZ 85721, USAMicroBioSystems of Arizona, 1665 E 18th St., Suite 204, Tucson, AZ 85719, USAAt present, there are no methods that determine the total microbial load on an abiotic substrate in real time. The utility of such a capability ranges from sterilization and medical diagnostics to the search for new microorganisms in the environment and study of their ecological niches. We report the development of a hand-held, fluorescence detection device and demonstrate its applicability to the field detection of Arctic bacteria. This technology is based on the early pioneering work of Britton Chance which elucidated the intrinsic fluorescence of a number of metabolites and protein cofactors in cells, including reduced pyridine nucleotides, cytochromes and flavins. A PDA controls the device (fluorescence excitation and data collection) and processes the multiwavelength signals to yield bacterial cell counts, including estimates of live cells, dead cells and endospores. Unlike existing methods for cell counting, this method requires no sample contact or addition of reagents. The use of this technology is demonstrated with in situ measurements of two sub-glacial microbial communities at sites in Palander and colonized surface rocks in the Bockfjord Volcanic Complex during AMASE 2008 (Arctic Mars Analog Svalbard Expedition). The total bacterial load on the interrogated sample surfaces ranged from < 20 cells/cm2 to > 109 cells/cm2.http://www.worldscientific.com/doi/pdf/10.1142/S1793545813500387Intrinsic fluorescencemicrobial sensoroptical detectionamplitude modulationSvalbard Archipelago
collection DOAJ
language English
format Article
sources DOAJ
author Linda Powers
Walther R. Ellis
Christopher R. Lloyd
spellingShingle Linda Powers
Walther R. Ellis
Christopher R. Lloyd
Real-time in situ detection and quantification of bacteria in the Arctic environment
Journal of Innovative Optical Health Sciences
Intrinsic fluorescence
microbial sensor
optical detection
amplitude modulation
Svalbard Archipelago
author_facet Linda Powers
Walther R. Ellis
Christopher R. Lloyd
author_sort Linda Powers
title Real-time in situ detection and quantification of bacteria in the Arctic environment
title_short Real-time in situ detection and quantification of bacteria in the Arctic environment
title_full Real-time in situ detection and quantification of bacteria in the Arctic environment
title_fullStr Real-time in situ detection and quantification of bacteria in the Arctic environment
title_full_unstemmed Real-time in situ detection and quantification of bacteria in the Arctic environment
title_sort real-time in situ detection and quantification of bacteria in the arctic environment
publisher World Scientific Publishing
series Journal of Innovative Optical Health Sciences
issn 1793-5458
1793-7205
publishDate 2014-03-01
description At present, there are no methods that determine the total microbial load on an abiotic substrate in real time. The utility of such a capability ranges from sterilization and medical diagnostics to the search for new microorganisms in the environment and study of their ecological niches. We report the development of a hand-held, fluorescence detection device and demonstrate its applicability to the field detection of Arctic bacteria. This technology is based on the early pioneering work of Britton Chance which elucidated the intrinsic fluorescence of a number of metabolites and protein cofactors in cells, including reduced pyridine nucleotides, cytochromes and flavins. A PDA controls the device (fluorescence excitation and data collection) and processes the multiwavelength signals to yield bacterial cell counts, including estimates of live cells, dead cells and endospores. Unlike existing methods for cell counting, this method requires no sample contact or addition of reagents. The use of this technology is demonstrated with in situ measurements of two sub-glacial microbial communities at sites in Palander and colonized surface rocks in the Bockfjord Volcanic Complex during AMASE 2008 (Arctic Mars Analog Svalbard Expedition). The total bacterial load on the interrogated sample surfaces ranged from < 20 cells/cm2 to > 109 cells/cm2.
topic Intrinsic fluorescence
microbial sensor
optical detection
amplitude modulation
Svalbard Archipelago
url http://www.worldscientific.com/doi/pdf/10.1142/S1793545813500387
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