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Electrical Retrieval of Living Microorganisms from Cryopreserved Marine Sponges Using a Potential-Controlled Electrode
The purpose of this study was to develop a novel electrical retrieval method (ER method) for living sponge-associated microorganisms from marine sponges frozen at −80 °C. A −0.3-V vs. Ag/AgCl constant potential applied for 2 h at 9 °C induced the attachment of the sponge-associated microorganisms to...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4540769/ https://www.ncbi.nlm.nih.gov/pubmed/26242755 http://dx.doi.org/10.1007/s10126-015-9651-y |
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author | Koyama, Sumihiro Nishi, Shinro Tokuda, Maki Uemura, Moeka Ishikawa, Yoichi Seya, Takeshi Chow, Seinen Ise, Yuji Hatada, Yuji Fujiwara, Yoshihiro Tsubouchi, Taishi |
author_facet | Koyama, Sumihiro Nishi, Shinro Tokuda, Maki Uemura, Moeka Ishikawa, Yoichi Seya, Takeshi Chow, Seinen Ise, Yuji Hatada, Yuji Fujiwara, Yoshihiro Tsubouchi, Taishi |
author_sort | Koyama, Sumihiro |
collection | PubMed |
description | The purpose of this study was to develop a novel electrical retrieval method (ER method) for living sponge-associated microorganisms from marine sponges frozen at −80 °C. A −0.3-V vs. Ag/AgCl constant potential applied for 2 h at 9 °C induced the attachment of the sponge-associated microorganisms to an indium tin oxide/glass (ITO) or a gallium-doped zinc oxide/glass (GZO) working electrode. The electrically attached microorganisms from homogenized Spirastrella insignis tissues had intact cell membranes and showed intracellular dehydrogenase activity. Dead microorganisms were not attracted to the electrode when the homogenized tissues were autoclaved for 15 min at 121 °C before use. The electrically attached microorganisms included cultivable microorganisms retrieved after detachment from the electrode by application of a 9-MHz sine-wave potential. Using the ER method, we obtained 32 phyla and 72 classes of bacteria and 3 archaea of Crenarchaeota thermoprotei, Marine Group I, and Thaumarchaeota incertae sedis from marine sponges S. insignis and Callyspongia confoederata. Employment of the ER method for extraction and purification of the living microorganisms holds potential of single-cell cultivation for genome, transcriptome, proteome, and metabolome analyses of bioactive compounds producing sponge-associated microorganisms. |
format | Online Article Text |
id | pubmed-4540769 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-45407692015-08-21 Electrical Retrieval of Living Microorganisms from Cryopreserved Marine Sponges Using a Potential-Controlled Electrode Koyama, Sumihiro Nishi, Shinro Tokuda, Maki Uemura, Moeka Ishikawa, Yoichi Seya, Takeshi Chow, Seinen Ise, Yuji Hatada, Yuji Fujiwara, Yoshihiro Tsubouchi, Taishi Mar Biotechnol (NY) Original Article The purpose of this study was to develop a novel electrical retrieval method (ER method) for living sponge-associated microorganisms from marine sponges frozen at −80 °C. A −0.3-V vs. Ag/AgCl constant potential applied for 2 h at 9 °C induced the attachment of the sponge-associated microorganisms to an indium tin oxide/glass (ITO) or a gallium-doped zinc oxide/glass (GZO) working electrode. The electrically attached microorganisms from homogenized Spirastrella insignis tissues had intact cell membranes and showed intracellular dehydrogenase activity. Dead microorganisms were not attracted to the electrode when the homogenized tissues were autoclaved for 15 min at 121 °C before use. The electrically attached microorganisms included cultivable microorganisms retrieved after detachment from the electrode by application of a 9-MHz sine-wave potential. Using the ER method, we obtained 32 phyla and 72 classes of bacteria and 3 archaea of Crenarchaeota thermoprotei, Marine Group I, and Thaumarchaeota incertae sedis from marine sponges S. insignis and Callyspongia confoederata. Employment of the ER method for extraction and purification of the living microorganisms holds potential of single-cell cultivation for genome, transcriptome, proteome, and metabolome analyses of bioactive compounds producing sponge-associated microorganisms. Springer US 2015-08-05 2015 /pmc/articles/PMC4540769/ /pubmed/26242755 http://dx.doi.org/10.1007/s10126-015-9651-y Text en © The Author(s) 2015 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Article Koyama, Sumihiro Nishi, Shinro Tokuda, Maki Uemura, Moeka Ishikawa, Yoichi Seya, Takeshi Chow, Seinen Ise, Yuji Hatada, Yuji Fujiwara, Yoshihiro Tsubouchi, Taishi Electrical Retrieval of Living Microorganisms from Cryopreserved Marine Sponges Using a Potential-Controlled Electrode |
title | Electrical Retrieval of Living Microorganisms from Cryopreserved Marine Sponges Using a Potential-Controlled Electrode |
title_full | Electrical Retrieval of Living Microorganisms from Cryopreserved Marine Sponges Using a Potential-Controlled Electrode |
title_fullStr | Electrical Retrieval of Living Microorganisms from Cryopreserved Marine Sponges Using a Potential-Controlled Electrode |
title_full_unstemmed | Electrical Retrieval of Living Microorganisms from Cryopreserved Marine Sponges Using a Potential-Controlled Electrode |
title_short | Electrical Retrieval of Living Microorganisms from Cryopreserved Marine Sponges Using a Potential-Controlled Electrode |
title_sort | electrical retrieval of living microorganisms from cryopreserved marine sponges using a potential-controlled electrode |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4540769/ https://www.ncbi.nlm.nih.gov/pubmed/26242755 http://dx.doi.org/10.1007/s10126-015-9651-y |
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