Production of functional killer protein in batch cultures upon a shift from aerobic to anaerobic conditions
Autor(a) principal: | |
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Data de Publicação: | 2011 |
Outros Autores: | , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Brazilian Archives of Biology and Technology |
Texto Completo: | http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-89132011000300022 |
Resumo: | The aim of this work was to study the production of functional protein in yeast culture. The cells of Saccharomyces cerevisiae Embrapa 1B (K+R+) killed a strain of Saccharomyces cerevisiae Embrapa 26B (K-R-)in grape must and YEPD media. The lethal effect of toxin-containing supernatant and the effect of aeration upon functional killer production and the correlation between the products of anaerobic metabolism and the functional toxin formation were evaluated. The results showed that at low sugar concentration, the toxin of the killer strain of Sacch. cerevisiae was only produced under anaerobic conditions . The system of killer protein production showed to be regulated by Pasteur and Crabtree effects. As soon as the ethanol was formed, the functional killer toxin was produced. The synthesis of the active killer toxin seemed to be somewhat associated with the switch to fermentation process and with concomitant alcohol dehydrogenase (ADH) activity. |
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Brazilian Archives of Biology and Technology |
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Production of functional killer protein in batch cultures upon a shift from aerobic to anaerobic conditionsKiller yeastCrabtree effectPasteur effectinhibitionmycocinogenic strainThe aim of this work was to study the production of functional protein in yeast culture. The cells of Saccharomyces cerevisiae Embrapa 1B (K+R+) killed a strain of Saccharomyces cerevisiae Embrapa 26B (K-R-)in grape must and YEPD media. The lethal effect of toxin-containing supernatant and the effect of aeration upon functional killer production and the correlation between the products of anaerobic metabolism and the functional toxin formation were evaluated. The results showed that at low sugar concentration, the toxin of the killer strain of Sacch. cerevisiae was only produced under anaerobic conditions . The system of killer protein production showed to be regulated by Pasteur and Crabtree effects. As soon as the ethanol was formed, the functional killer toxin was produced. The synthesis of the active killer toxin seemed to be somewhat associated with the switch to fermentation process and with concomitant alcohol dehydrogenase (ADH) activity.Instituto de Tecnologia do Paraná - Tecpar2011-06-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-89132011000300022Brazilian Archives of Biology and Technology v.54 n.3 2011reponame:Brazilian Archives of Biology and Technologyinstname:Instituto de Tecnologia do Paraná (Tecpar)instacron:TECPAR10.1590/S1516-89132011000300022info:eu-repo/semantics/openAccessSilva,Gildo Almeida daPoli,Jandora SeveroPoletto,Carolina MadalozzoSchaker,Patricia Dayane CarvalhoValente,Patriciaeng2011-06-13T00:00:00Zoai:scielo:S1516-89132011000300022Revistahttps://www.scielo.br/j/babt/https://old.scielo.br/oai/scielo-oai.phpbabt@tecpar.br||babt@tecpar.br1678-43241516-8913opendoar:2011-06-13T00:00Brazilian Archives of Biology and Technology - Instituto de Tecnologia do Paraná (Tecpar)false |
dc.title.none.fl_str_mv |
Production of functional killer protein in batch cultures upon a shift from aerobic to anaerobic conditions |
title |
Production of functional killer protein in batch cultures upon a shift from aerobic to anaerobic conditions |
spellingShingle |
Production of functional killer protein in batch cultures upon a shift from aerobic to anaerobic conditions Silva,Gildo Almeida da Killer yeast Crabtree effect Pasteur effect inhibition mycocinogenic strain |
title_short |
Production of functional killer protein in batch cultures upon a shift from aerobic to anaerobic conditions |
title_full |
Production of functional killer protein in batch cultures upon a shift from aerobic to anaerobic conditions |
title_fullStr |
Production of functional killer protein in batch cultures upon a shift from aerobic to anaerobic conditions |
title_full_unstemmed |
Production of functional killer protein in batch cultures upon a shift from aerobic to anaerobic conditions |
title_sort |
Production of functional killer protein in batch cultures upon a shift from aerobic to anaerobic conditions |
author |
Silva,Gildo Almeida da |
author_facet |
Silva,Gildo Almeida da Poli,Jandora Severo Poletto,Carolina Madalozzo Schaker,Patricia Dayane Carvalho Valente,Patricia |
author_role |
author |
author2 |
Poli,Jandora Severo Poletto,Carolina Madalozzo Schaker,Patricia Dayane Carvalho Valente,Patricia |
author2_role |
author author author author |
dc.contributor.author.fl_str_mv |
Silva,Gildo Almeida da Poli,Jandora Severo Poletto,Carolina Madalozzo Schaker,Patricia Dayane Carvalho Valente,Patricia |
dc.subject.por.fl_str_mv |
Killer yeast Crabtree effect Pasteur effect inhibition mycocinogenic strain |
topic |
Killer yeast Crabtree effect Pasteur effect inhibition mycocinogenic strain |
description |
The aim of this work was to study the production of functional protein in yeast culture. The cells of Saccharomyces cerevisiae Embrapa 1B (K+R+) killed a strain of Saccharomyces cerevisiae Embrapa 26B (K-R-)in grape must and YEPD media. The lethal effect of toxin-containing supernatant and the effect of aeration upon functional killer production and the correlation between the products of anaerobic metabolism and the functional toxin formation were evaluated. The results showed that at low sugar concentration, the toxin of the killer strain of Sacch. cerevisiae was only produced under anaerobic conditions . The system of killer protein production showed to be regulated by Pasteur and Crabtree effects. As soon as the ethanol was formed, the functional killer toxin was produced. The synthesis of the active killer toxin seemed to be somewhat associated with the switch to fermentation process and with concomitant alcohol dehydrogenase (ADH) activity. |
publishDate |
2011 |
dc.date.none.fl_str_mv |
2011-06-01 |
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=S1516-89132011000300022 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-89132011000300022 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1590/S1516-89132011000300022 |
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 |
Instituto de Tecnologia do Paraná - Tecpar |
publisher.none.fl_str_mv |
Instituto de Tecnologia do Paraná - Tecpar |
dc.source.none.fl_str_mv |
Brazilian Archives of Biology and Technology v.54 n.3 2011 reponame:Brazilian Archives of Biology and Technology instname:Instituto de Tecnologia do Paraná (Tecpar) instacron:TECPAR |
instname_str |
Instituto de Tecnologia do Paraná (Tecpar) |
instacron_str |
TECPAR |
institution |
TECPAR |
reponame_str |
Brazilian Archives of Biology and Technology |
collection |
Brazilian Archives of Biology and Technology |
repository.name.fl_str_mv |
Brazilian Archives of Biology and Technology - Instituto de Tecnologia do Paraná (Tecpar) |
repository.mail.fl_str_mv |
babt@tecpar.br||babt@tecpar.br |
_version_ |
1750318274771419136 |