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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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 |
work_keys_str_mv |
AT lindapowers realtimeinsitudetectionandquantificationofbacteriainthearcticenvironment AT waltherrellis realtimeinsitudetectionandquantificationofbacteriainthearcticenvironment AT christopherrlloyd realtimeinsitudetectionandquantificationofbacteriainthearcticenvironment |
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1725559129938853888 |