Involvement of G proteins and cAMP in the production of chitinolytic enzymes by Trichoderma harzianum

Detalhes bibliográficos
Autor(a) principal: Firmino,Alexandre A.P.
Data de Publicação: 2002
Outros Autores: Ulhoa,Cirano J., Sousa,Marcelo V., Ferreira Filho,Edivaldo X., Ricart,Carlos A.O.
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=S1517-83822002000200015
Resumo: The effect of G protein modulators and cyclic AMP (cAMP) on N-acetylglucosaminidase (NAGase) production was investigated during 84 h of growth of a Trichoderma harzianum strain in chitin-containing medium. Caffeine (5 mM), N6--2'-O-dibutyryladenosine 3'5'-cyclic monophosphate sodium salt (dBcAMP) (1 mM) and 3-isobutyl-1-methylxanthine (IBMX) (2 mM) decreased extracellular NAGase activity by 80%, 77% and 37%, respectively. AlCl3/KF (100 µM/10 mM and 200 µM/ 20 mM) decreased the activity by 85% and 95%, respectively. Cholera (10 µ/mL) and pertussis (20 µ/mL) toxins also affected NAGase activity, causing a decrease of approximately 75%. Upon all treatments, protein bands of approximately 73 kDa, 68 kDa and 45 kDa had their signals diminished whilst a 50 kDa band was enhanced only by treatment with cholera and pertussis toxins. N-terminal sequencing analysis identified the 73 kDa and 68 kDa proteins as being T. harzianum NAGase in two different truncated forms whereas the 45 kDa band comprised a T. harzianum endochitinase. The 50 kDa protein showed sequence similarity to Coriolus vesicolor cellobiohydrolase. The above results suggest that a signaling pathway comprising G-proteins, adenylate cyclase and cAMP may be involved in the synthesis of T. harzianum chitinases.
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spelling Involvement of G proteins and cAMP in the production of chitinolytic enzymes by Trichoderma harzianumTrichodermaN-acetylglucosaminidasechitinasecAMPG proteinThe effect of G protein modulators and cyclic AMP (cAMP) on N-acetylglucosaminidase (NAGase) production was investigated during 84 h of growth of a Trichoderma harzianum strain in chitin-containing medium. Caffeine (5 mM), N6--2'-O-dibutyryladenosine 3'5'-cyclic monophosphate sodium salt (dBcAMP) (1 mM) and 3-isobutyl-1-methylxanthine (IBMX) (2 mM) decreased extracellular NAGase activity by 80%, 77% and 37%, respectively. AlCl3/KF (100 µM/10 mM and 200 µM/ 20 mM) decreased the activity by 85% and 95%, respectively. Cholera (10 µ/mL) and pertussis (20 µ/mL) toxins also affected NAGase activity, causing a decrease of approximately 75%. Upon all treatments, protein bands of approximately 73 kDa, 68 kDa and 45 kDa had their signals diminished whilst a 50 kDa band was enhanced only by treatment with cholera and pertussis toxins. N-terminal sequencing analysis identified the 73 kDa and 68 kDa proteins as being T. harzianum NAGase in two different truncated forms whereas the 45 kDa band comprised a T. harzianum endochitinase. The 50 kDa protein showed sequence similarity to Coriolus vesicolor cellobiohydrolase. The above results suggest that a signaling pathway comprising G-proteins, adenylate cyclase and cAMP may be involved in the synthesis of T. harzianum chitinases.Sociedade Brasileira de Microbiologia2002-06-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1517-83822002000200015Brazilian Journal of Microbiology v.33 n.2 2002reponame:Brazilian Journal of Microbiologyinstname:Sociedade Brasileira de Microbiologia (SBM)instacron:SBM10.1590/S1517-83822002000200015info:eu-repo/semantics/openAccessFirmino,Alexandre A.P.Ulhoa,Cirano J.Sousa,Marcelo V.Ferreira Filho,Edivaldo X.Ricart,Carlos A.O.eng2003-01-27T00:00:00Zoai:scielo:S1517-83822002000200015Revistahttps://www.scielo.br/j/bjm/ONGhttps://old.scielo.br/oai/scielo-oai.phpbjm@sbmicrobiologia.org.br||mbmartin@usp.br1678-44051517-8382opendoar:2003-01-27T00:00Brazilian Journal of Microbiology - Sociedade Brasileira de Microbiologia (SBM)false
dc.title.none.fl_str_mv Involvement of G proteins and cAMP in the production of chitinolytic enzymes by Trichoderma harzianum
title Involvement of G proteins and cAMP in the production of chitinolytic enzymes by Trichoderma harzianum
spellingShingle Involvement of G proteins and cAMP in the production of chitinolytic enzymes by Trichoderma harzianum
Firmino,Alexandre A.P.
Trichoderma
N-acetylglucosaminidase
chitinase
cAMP
G protein
title_short Involvement of G proteins and cAMP in the production of chitinolytic enzymes by Trichoderma harzianum
title_full Involvement of G proteins and cAMP in the production of chitinolytic enzymes by Trichoderma harzianum
title_fullStr Involvement of G proteins and cAMP in the production of chitinolytic enzymes by Trichoderma harzianum
title_full_unstemmed Involvement of G proteins and cAMP in the production of chitinolytic enzymes by Trichoderma harzianum
title_sort Involvement of G proteins and cAMP in the production of chitinolytic enzymes by Trichoderma harzianum
author Firmino,Alexandre A.P.
author_facet Firmino,Alexandre A.P.
Ulhoa,Cirano J.
Sousa,Marcelo V.
Ferreira Filho,Edivaldo X.
Ricart,Carlos A.O.
author_role author
author2 Ulhoa,Cirano J.
Sousa,Marcelo V.
Ferreira Filho,Edivaldo X.
Ricart,Carlos A.O.
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Firmino,Alexandre A.P.
Ulhoa,Cirano J.
Sousa,Marcelo V.
Ferreira Filho,Edivaldo X.
Ricart,Carlos A.O.
dc.subject.por.fl_str_mv Trichoderma
N-acetylglucosaminidase
chitinase
cAMP
G protein
topic Trichoderma
N-acetylglucosaminidase
chitinase
cAMP
G protein
description The effect of G protein modulators and cyclic AMP (cAMP) on N-acetylglucosaminidase (NAGase) production was investigated during 84 h of growth of a Trichoderma harzianum strain in chitin-containing medium. Caffeine (5 mM), N6--2'-O-dibutyryladenosine 3'5'-cyclic monophosphate sodium salt (dBcAMP) (1 mM) and 3-isobutyl-1-methylxanthine (IBMX) (2 mM) decreased extracellular NAGase activity by 80%, 77% and 37%, respectively. AlCl3/KF (100 µM/10 mM and 200 µM/ 20 mM) decreased the activity by 85% and 95%, respectively. Cholera (10 µ/mL) and pertussis (20 µ/mL) toxins also affected NAGase activity, causing a decrease of approximately 75%. Upon all treatments, protein bands of approximately 73 kDa, 68 kDa and 45 kDa had their signals diminished whilst a 50 kDa band was enhanced only by treatment with cholera and pertussis toxins. N-terminal sequencing analysis identified the 73 kDa and 68 kDa proteins as being T. harzianum NAGase in two different truncated forms whereas the 45 kDa band comprised a T. harzianum endochitinase. The 50 kDa protein showed sequence similarity to Coriolus vesicolor cellobiohydrolase. The above results suggest that a signaling pathway comprising G-proteins, adenylate cyclase and cAMP may be involved in the synthesis of T. harzianum chitinases.
publishDate 2002
dc.date.none.fl_str_mv 2002-06-01
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=S1517-83822002000200015
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1517-83822002000200015
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S1517-83822002000200015
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.33 n.2 2002
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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