Use of Bioscreen C for growth of Mucor hiemalis in different carbon and nitrogen sources

Detalhes bibliográficos
Autor(a) principal: Tauk-Tornisielo,Sâmia Maria
Data de Publicação: 2007
Outros Autores: Vieira,Joelma Maurício, Govone,José Silvio
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Brazilian Journal of Microbiology
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1517-83822007000100024
Resumo: The automated Bioscreen C system was used for growth of four Mucor hiemalis strains isolated from the soil in the Juréia-Itatins Ecology Station (JIES), São Paulo state, in liquid culture media containing different carbon (2%) and nitrogen (1%) sources, pH 5.0, at 25ºC, and agitated at 150 rpm for 5 days. The medium containing only one nitrogen source had been added with 2% glucose. The readings were taken at lambda = 540 nm, at 2-hour intervals, up to five days. The results were compared using the Friedman Test (alpha = 5%). The best growth was obtained for strains M1, M2 and M3, reaching the log phase in 60 hours. The best carbon sources varied according to the strain, and yeast extract proved to be the best nitrogen source. Sodium acetate inhibited the growth of the four strains, being the M3 strain the most affected. The use of the automated system was very convenient for cultures in liquid media, as it is rapid and automated, providing a good technique for determination of the optimal environmental factors for growth of the filamentous fungi.
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spelling Use of Bioscreen C for growth of Mucor hiemalis in different carbon and nitrogen sourcesMucor hiemaliszygomycetesautomated systemscarbon and nitrogen sourcesThe automated Bioscreen C system was used for growth of four Mucor hiemalis strains isolated from the soil in the Juréia-Itatins Ecology Station (JIES), São Paulo state, in liquid culture media containing different carbon (2%) and nitrogen (1%) sources, pH 5.0, at 25ºC, and agitated at 150 rpm for 5 days. The medium containing only one nitrogen source had been added with 2% glucose. The readings were taken at lambda = 540 nm, at 2-hour intervals, up to five days. The results were compared using the Friedman Test (alpha = 5%). The best growth was obtained for strains M1, M2 and M3, reaching the log phase in 60 hours. The best carbon sources varied according to the strain, and yeast extract proved to be the best nitrogen source. Sodium acetate inhibited the growth of the four strains, being the M3 strain the most affected. The use of the automated system was very convenient for cultures in liquid media, as it is rapid and automated, providing a good technique for determination of the optimal environmental factors for growth of the filamentous fungi.Sociedade Brasileira de Microbiologia2007-03-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1517-83822007000100024Brazilian Journal of Microbiology v.38 n.1 2007reponame:Brazilian Journal of Microbiologyinstname:Sociedade Brasileira de Microbiologia (SBM)instacron:SBM10.1590/S1517-83822007000100024info:eu-repo/semantics/openAccessTauk-Tornisielo,Sâmia MariaVieira,Joelma MaurícioGovone,José Silvioeng2007-04-24T00:00:00Zoai:scielo:S1517-83822007000100024Revistahttps://www.scielo.br/j/bjm/ONGhttps://old.scielo.br/oai/scielo-oai.phpbjm@sbmicrobiologia.org.br||mbmartin@usp.br1678-44051517-8382opendoar:2007-04-24T00:00Brazilian Journal of Microbiology - Sociedade Brasileira de Microbiologia (SBM)false
dc.title.none.fl_str_mv Use of Bioscreen C for growth of Mucor hiemalis in different carbon and nitrogen sources
title Use of Bioscreen C for growth of Mucor hiemalis in different carbon and nitrogen sources
spellingShingle Use of Bioscreen C for growth of Mucor hiemalis in different carbon and nitrogen sources
Tauk-Tornisielo,Sâmia Maria
Mucor hiemalis
zygomycetes
automated systems
carbon and nitrogen sources
title_short Use of Bioscreen C for growth of Mucor hiemalis in different carbon and nitrogen sources
title_full Use of Bioscreen C for growth of Mucor hiemalis in different carbon and nitrogen sources
title_fullStr Use of Bioscreen C for growth of Mucor hiemalis in different carbon and nitrogen sources
title_full_unstemmed Use of Bioscreen C for growth of Mucor hiemalis in different carbon and nitrogen sources
title_sort Use of Bioscreen C for growth of Mucor hiemalis in different carbon and nitrogen sources
author Tauk-Tornisielo,Sâmia Maria
author_facet Tauk-Tornisielo,Sâmia Maria
Vieira,Joelma Maurício
Govone,José Silvio
author_role author
author2 Vieira,Joelma Maurício
Govone,José Silvio
author2_role author
author
dc.contributor.author.fl_str_mv Tauk-Tornisielo,Sâmia Maria
Vieira,Joelma Maurício
Govone,José Silvio
dc.subject.por.fl_str_mv Mucor hiemalis
zygomycetes
automated systems
carbon and nitrogen sources
topic Mucor hiemalis
zygomycetes
automated systems
carbon and nitrogen sources
description The automated Bioscreen C system was used for growth of four Mucor hiemalis strains isolated from the soil in the Juréia-Itatins Ecology Station (JIES), São Paulo state, in liquid culture media containing different carbon (2%) and nitrogen (1%) sources, pH 5.0, at 25ºC, and agitated at 150 rpm for 5 days. The medium containing only one nitrogen source had been added with 2% glucose. The readings were taken at lambda = 540 nm, at 2-hour intervals, up to five days. The results were compared using the Friedman Test (alpha = 5%). The best growth was obtained for strains M1, M2 and M3, reaching the log phase in 60 hours. The best carbon sources varied according to the strain, and yeast extract proved to be the best nitrogen source. Sodium acetate inhibited the growth of the four strains, being the M3 strain the most affected. The use of the automated system was very convenient for cultures in liquid media, as it is rapid and automated, providing a good technique for determination of the optimal environmental factors for growth of the filamentous fungi.
publishDate 2007
dc.date.none.fl_str_mv 2007-03-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1517-83822007000100024
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1517-83822007000100024
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S1517-83822007000100024
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Sociedade Brasileira de Microbiologia
publisher.none.fl_str_mv Sociedade Brasileira de Microbiologia
dc.source.none.fl_str_mv Brazilian Journal of Microbiology v.38 n.1 2007
reponame:Brazilian Journal of Microbiology
instname:Sociedade Brasileira de Microbiologia (SBM)
instacron:SBM
instname_str Sociedade Brasileira de Microbiologia (SBM)
instacron_str SBM
institution SBM
reponame_str Brazilian Journal of Microbiology
collection Brazilian Journal of Microbiology
repository.name.fl_str_mv Brazilian Journal of Microbiology - Sociedade Brasileira de Microbiologia (SBM)
repository.mail.fl_str_mv bjm@sbmicrobiologia.org.br||mbmartin@usp.br
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