Rapid yeast DNA extraction by boiling and freeze-thawing without using chemical reagents and DNA purification.
Autor(a) principal: | |
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Data de Publicação: | 2012 |
Outros Autores: | , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da EMBRAPA (Repository Open Access to Scientific Information from EMBRAPA - Alice) |
Texto Completo: | http://www.alice.cnptia.embrapa.br/alice/handle/doc/925175 |
Resumo: | The purpose of this work was to study a rapid yeast DNA extraction by boiling and freeze-thawing processes without using chemical reagents or any purification procedures, to obtain a high grade PCR-product. A specific DNA fragment of the 18S region of Dekkera bruxellensis and Saccharomyces cerevisiae was chosen. The described boiling and freeze-thawing protocols generated the PCR-grade product preparations and could be used to process many samples. The amplification of the fragments could be observed after 30 and 35 cycles. These processes of extraction without using any kind of chemical reagents, especial water, and purification procedures proved to be efficient, reproducible, simple, fast, and inexpensive. |
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Rapid yeast DNA extraction by boiling and freeze-thawing without using chemical reagents and DNA purification.Gelo-degeloEbuliçãoExtração de DNAMetodologiaMicrobiologiaDNASaccharomyces CerevisiaeDekkera bruxellensisThe purpose of this work was to study a rapid yeast DNA extraction by boiling and freeze-thawing processes without using chemical reagents or any purification procedures, to obtain a high grade PCR-product. A specific DNA fragment of the 18S region of Dekkera bruxellensis and Saccharomyces cerevisiae was chosen. The described boiling and freeze-thawing protocols generated the PCR-grade product preparations and could be used to process many samples. The amplification of the fragments could be observed after 30 and 35 cycles. These processes of extraction without using any kind of chemical reagents, especial water, and purification procedures proved to be efficient, reproducible, simple, fast, and inexpensive.GILDO ALMEIDA DA SILVA, CNPUV; Taís Letícia Bernardi, CNPUV (BOLSISTA); Patrícia Dayane Carvalho Schaker, CNPUV (BOLSISTA); Morgana Menegotto, CNPUV (BOLSISTA); Patricia Valente, UFRGS.SILVA, G. A. daBERNARDI, T. L.SCHAKER, P. D. C.MENEGOTTO, M.VALENTE, P.2012-05-22T11:11:11Z2012-05-22T11:11:11Z2012-05-22T11:11:11Z2012-05-22T11:11:11Z2012-05-2220122012-05-22T11:11:11Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleBrazilian Archives of Biology and Technology, Curitiba, v. 55, n. 2, p. 319-327, mar./abr. 2012.http://www.alice.cnptia.embrapa.br/alice/handle/doc/925175enginfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da EMBRAPA (Repository Open Access to Scientific Information from EMBRAPA - Alice)instname:Empresa Brasileira de Pesquisa Agropecuária (Embrapa)instacron:EMBRAPA2017-08-15T23:46:15Zoai:www.alice.cnptia.embrapa.br:doc/925175Repositório InstitucionalPUBhttps://www.alice.cnptia.embrapa.br/oai/requestopendoar:21542017-08-15T23:46:15falseRepositório InstitucionalPUBhttps://www.alice.cnptia.embrapa.br/oai/requestcg-riaa@embrapa.bropendoar:21542017-08-15T23:46:15Repositório Institucional da EMBRAPA (Repository Open Access to Scientific Information from EMBRAPA - Alice) - Empresa Brasileira de Pesquisa Agropecuária (Embrapa)false |
dc.title.none.fl_str_mv |
Rapid yeast DNA extraction by boiling and freeze-thawing without using chemical reagents and DNA purification. |
title |
Rapid yeast DNA extraction by boiling and freeze-thawing without using chemical reagents and DNA purification. |
spellingShingle |
Rapid yeast DNA extraction by boiling and freeze-thawing without using chemical reagents and DNA purification. SILVA, G. A. da Gelo-degelo Ebulição Extração de DNA Metodologia Microbiologia DNA Saccharomyces Cerevisiae Dekkera bruxellensis |
title_short |
Rapid yeast DNA extraction by boiling and freeze-thawing without using chemical reagents and DNA purification. |
title_full |
Rapid yeast DNA extraction by boiling and freeze-thawing without using chemical reagents and DNA purification. |
title_fullStr |
Rapid yeast DNA extraction by boiling and freeze-thawing without using chemical reagents and DNA purification. |
title_full_unstemmed |
Rapid yeast DNA extraction by boiling and freeze-thawing without using chemical reagents and DNA purification. |
title_sort |
Rapid yeast DNA extraction by boiling and freeze-thawing without using chemical reagents and DNA purification. |
author |
SILVA, G. A. da |
author_facet |
SILVA, G. A. da BERNARDI, T. L. SCHAKER, P. D. C. MENEGOTTO, M. VALENTE, P. |
author_role |
author |
author2 |
BERNARDI, T. L. SCHAKER, P. D. C. MENEGOTTO, M. VALENTE, P. |
author2_role |
author author author author |
dc.contributor.none.fl_str_mv |
GILDO ALMEIDA DA SILVA, CNPUV; Taís Letícia Bernardi, CNPUV (BOLSISTA); Patrícia Dayane Carvalho Schaker, CNPUV (BOLSISTA); Morgana Menegotto, CNPUV (BOLSISTA); Patricia Valente, UFRGS. |
dc.contributor.author.fl_str_mv |
SILVA, G. A. da BERNARDI, T. L. SCHAKER, P. D. C. MENEGOTTO, M. VALENTE, P. |
dc.subject.por.fl_str_mv |
Gelo-degelo Ebulição Extração de DNA Metodologia Microbiologia DNA Saccharomyces Cerevisiae Dekkera bruxellensis |
topic |
Gelo-degelo Ebulição Extração de DNA Metodologia Microbiologia DNA Saccharomyces Cerevisiae Dekkera bruxellensis |
description |
The purpose of this work was to study a rapid yeast DNA extraction by boiling and freeze-thawing processes without using chemical reagents or any purification procedures, to obtain a high grade PCR-product. A specific DNA fragment of the 18S region of Dekkera bruxellensis and Saccharomyces cerevisiae was chosen. The described boiling and freeze-thawing protocols generated the PCR-grade product preparations and could be used to process many samples. The amplification of the fragments could be observed after 30 and 35 cycles. These processes of extraction without using any kind of chemical reagents, especial water, and purification procedures proved to be efficient, reproducible, simple, fast, and inexpensive. |
publishDate |
2012 |
dc.date.none.fl_str_mv |
2012-05-22T11:11:11Z 2012-05-22T11:11:11Z 2012-05-22T11:11:11Z 2012-05-22T11:11:11Z 2012-05-22 2012 2012-05-22T11:11:11Z |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/publishedVersion info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
Brazilian Archives of Biology and Technology, Curitiba, v. 55, n. 2, p. 319-327, mar./abr. 2012. http://www.alice.cnptia.embrapa.br/alice/handle/doc/925175 |
identifier_str_mv |
Brazilian Archives of Biology and Technology, Curitiba, v. 55, n. 2, p. 319-327, mar./abr. 2012. |
url |
http://www.alice.cnptia.embrapa.br/alice/handle/doc/925175 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.source.none.fl_str_mv |
reponame:Repositório Institucional da EMBRAPA (Repository Open Access to Scientific Information from EMBRAPA - Alice) instname:Empresa Brasileira de Pesquisa Agropecuária (Embrapa) instacron:EMBRAPA |
instname_str |
Empresa Brasileira de Pesquisa Agropecuária (Embrapa) |
instacron_str |
EMBRAPA |
institution |
EMBRAPA |
reponame_str |
Repositório Institucional da EMBRAPA (Repository Open Access to Scientific Information from EMBRAPA - Alice) |
collection |
Repositório Institucional da EMBRAPA (Repository Open Access to Scientific Information from EMBRAPA - Alice) |
repository.name.fl_str_mv |
Repositório Institucional da EMBRAPA (Repository Open Access to Scientific Information from EMBRAPA - Alice) - Empresa Brasileira de Pesquisa Agropecuária (Embrapa) |
repository.mail.fl_str_mv |
cg-riaa@embrapa.br |
_version_ |
1794503363416555520 |