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Spiking a Silty-Sand Reference Soil with Bacterial DNA: Limits and Pitfalls in the Discrimination of Live and Dead Cells When Applying Ethidium Monoazide (EMA) Treatment
by
Illmer, Paul
, Wagner, Andreas O
, Praeg, Nadine
in
Cell differentiation
/ Deoxyribonucleic acid
/ Dilution
/ DNA
/ Ecological monitoring
/ Heat treatment
/ Listeria
/ Listeria monocytogenes
/ Microorganisms
/ Sand
/ Soil microorganisms
/ Soils
2019
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Spiking a Silty-Sand Reference Soil with Bacterial DNA: Limits and Pitfalls in the Discrimination of Live and Dead Cells When Applying Ethidium Monoazide (EMA) Treatment
by
Illmer, Paul
, Wagner, Andreas O
, Praeg, Nadine
in
Cell differentiation
/ Deoxyribonucleic acid
/ Dilution
/ DNA
/ Ecological monitoring
/ Heat treatment
/ Listeria
/ Listeria monocytogenes
/ Microorganisms
/ Sand
/ Soil microorganisms
/ Soils
2019
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While trying to remove the title from your shelf something went wrong :( Kindly try again later!
Do you wish to request the book?
Spiking a Silty-Sand Reference Soil with Bacterial DNA: Limits and Pitfalls in the Discrimination of Live and Dead Cells When Applying Ethidium Monoazide (EMA) Treatment
by
Illmer, Paul
, Wagner, Andreas O
, Praeg, Nadine
in
Cell differentiation
/ Deoxyribonucleic acid
/ Dilution
/ DNA
/ Ecological monitoring
/ Heat treatment
/ Listeria
/ Listeria monocytogenes
/ Microorganisms
/ Sand
/ Soil microorganisms
/ Soils
2019
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Spiking a Silty-Sand Reference Soil with Bacterial DNA: Limits and Pitfalls in the Discrimination of Live and Dead Cells When Applying Ethidium Monoazide (EMA) Treatment
Journal Article
Spiking a Silty-Sand Reference Soil with Bacterial DNA: Limits and Pitfalls in the Discrimination of Live and Dead Cells When Applying Ethidium Monoazide (EMA) Treatment
2019
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Overview
In the present study, EMA (ethidium monoazide) treatment was applied to a silty-sand reference soil prior to DNA extraction to enable a differentiation between dead and living cells. For this purpose, a reference soil was spiked with Listeria monocytogenes cells or cell equivalents, respectively. With the purpose of evaluating optimum treatment conditions, different EMA concentrations have been tested. However, the results remained largely inconclusive. Furthermore, varied dark incubation periods allowing EMA to penetrate dead cells did not allow the selective removal of DNA from membrane-compromised cells in downstream analyses. In contrast to undiluted soil, an effect of EMA treatment during DNA extraction could be observed when using a 1:10 dilution of the reference soil; however, the effect has not been sufficiently selective to act on heat-treated cells only. Although the application of EMA to soil requires further evaluation, the procedure harbors future potential for improving DNA-based approaches in microbial ecology studies.
Publisher
Springer Nature B.V
Subject
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