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Chemical lysis of cyanobacteria

We have developed a mixture of enzymes and chemicals that completely lyse cyanobacteria. Since the treatment involves only readily-available chemicals and simple proteins that degrade the components of the cyanobacterial cell wall, it can easily be used in high-throughput applications requiring lysi...

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Detalles Bibliográficos
Autores principales: Mehta, Kunal K., Evitt, Niklaus H., Swartz, James R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4478636/
https://www.ncbi.nlm.nih.gov/pubmed/26110017
http://dx.doi.org/10.1186/s13036-015-0007-y
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author Mehta, Kunal K.
Evitt, Niklaus H.
Swartz, James R.
author_facet Mehta, Kunal K.
Evitt, Niklaus H.
Swartz, James R.
author_sort Mehta, Kunal K.
collection PubMed
description We have developed a mixture of enzymes and chemicals that completely lyse cyanobacteria. Since the treatment involves only readily-available chemicals and simple proteins that degrade the components of the cyanobacterial cell wall, it can easily be used in high-throughput applications requiring lysis for subsequent intracellular measurements. Our lysis technique consistently enables complete lysis of several different cyanobacterial strains, and we demonstrated that DNA, mRNA, and proteins are preserved in the lysates. Chemical lysis can be superior to existing techniques because of its convenience, reliability, and amenability to a variety of downstream applications. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13036-015-0007-y) contains supplementary material, which is available to authorized users.
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spelling pubmed-44786362015-06-25 Chemical lysis of cyanobacteria Mehta, Kunal K. Evitt, Niklaus H. Swartz, James R. J Biol Eng Methodology We have developed a mixture of enzymes and chemicals that completely lyse cyanobacteria. Since the treatment involves only readily-available chemicals and simple proteins that degrade the components of the cyanobacterial cell wall, it can easily be used in high-throughput applications requiring lysis for subsequent intracellular measurements. Our lysis technique consistently enables complete lysis of several different cyanobacterial strains, and we demonstrated that DNA, mRNA, and proteins are preserved in the lysates. Chemical lysis can be superior to existing techniques because of its convenience, reliability, and amenability to a variety of downstream applications. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13036-015-0007-y) contains supplementary material, which is available to authorized users. BioMed Central 2015-06-05 /pmc/articles/PMC4478636/ /pubmed/26110017 http://dx.doi.org/10.1186/s13036-015-0007-y Text en © Mehta et al. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Methodology
Mehta, Kunal K.
Evitt, Niklaus H.
Swartz, James R.
Chemical lysis of cyanobacteria
title Chemical lysis of cyanobacteria
title_full Chemical lysis of cyanobacteria
title_fullStr Chemical lysis of cyanobacteria
title_full_unstemmed Chemical lysis of cyanobacteria
title_short Chemical lysis of cyanobacteria
title_sort chemical lysis of cyanobacteria
topic Methodology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4478636/
https://www.ncbi.nlm.nih.gov/pubmed/26110017
http://dx.doi.org/10.1186/s13036-015-0007-y
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