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Registro Completo |
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Biblioteca(s): |
Embrapa Recursos Genéticos e Biotecnologia. |
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Data corrente: |
09/12/2015 |
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Data da última atualização: |
20/03/2023 |
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Tipo da produção científica: |
Artigo em Periódico Indexado |
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Autoria: |
TELFER, E. J.; STOVOLD, G. T.; LI, Y.; SILVA JUNIOR, O. B. da; GRATTAPAGLIA, D.; DUNGEY, H. S. |
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Afiliação: |
EMILY J. TELFER, SCION (NEW ZEALAND FOREST RESEARCH INSTITUTE LTD.), NEW ZEALAND; GRAHAME T. STOVOLD, SCION (NEW ZEALAND FOREST RESEARCH INSTITUTE LTD.), NEW ZEALAND; YONGJUN LI, SCION (NEW ZEALAND FOREST RESEARCH INSTITUTE LTD.), NEW ZEALAND; ORZENIL BONFIM DA SILVA JUNIOR, CENARGEN; DARIO GRATTAPAGLIA, CENARGEN; HEIDI S. DUNGEY, SCION (NEW ZEALAND FOREST RESEARCH INSTITUTE LTD.), NEW ZEALAND. |
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Título: |
Parentage reconstruction in eucalyptus nitens using SNPs and microsatellite markers: a comparative analysis of marker data power and robustness. |
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Ano de publicação: |
2015 |
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Fonte/Imprenta: |
Plos One, July 9, 2015. (Open Access) |
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DOI: |
10.1371/journal.pone.013060 |
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Idioma: |
Inglês |
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Thesaurus Nal: |
Eucalyptus; Eucalyptus nitens. |
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Categoria do assunto: |
-- |
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URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/item/181968/1/journal.pone.0130601.PDF
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Marc: |
LEADER 00677naa a2200205 a 4500
001 2031232
005 2023-03-20
008 2015 bl uuuu u00u1 u #d
024 7 $a10.1371/journal.pone.013060$2DOI
100 1 $aTELFER, E. J.
245 $aParentage reconstruction in eucalyptus nitens using SNPs and microsatellite markers$ba comparative analysis of marker data power and robustness.$h[electronic resource]
260 $c2015
650 $aEucalyptus
650 $aEucalyptus nitens
700 1 $aSTOVOLD, G. T.
700 1 $aLI, Y.
700 1 $aSILVA JUNIOR, O. B. da
700 1 $aGRATTAPAGLIA, D.
700 1 $aDUNGEY, H. S.
773 $tPlos One, July 9, 2015. (Open Access)
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Registro original: |
Embrapa Recursos Genéticos e Biotecnologia (CENARGEN) |
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Registro Completo
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Biblioteca(s): |
Embrapa Uva e Vinho. |
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Data corrente: |
20/12/2023 |
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Data da última atualização: |
20/12/2023 |
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Tipo da produção científica: |
Resumo em Anais de Congresso |
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Autoria: |
AGUSTINI, B. C.; CORREA, O. L. dos S.; OSTER, A. H.; SILVA, G. A. |
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Afiliação: |
BRUNA CARLA AGUSTINI, CNPUV; ODINELI LOUZADA DOS SANTOS CORREA, CNPUV; ANDREIA HANSEN OSTER, CNPUV; GILDO ALMEIDA SILVA, EMBRAPA UVA E VINHO. |
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Título: |
Yeast as a biological agent in the control of botrytis cinerea. |
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Ano de publicação: |
2023 |
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Fonte/Imprenta: |
In: CONGRESSO BRASILEIRO DE MICROBIOLOGIA, 32., 2023, Foz do Iguaçú, PR. Anais... FOz do Iguaçú: SBM, 18 a 22 de out. 2023. p. 1487-2. |
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Idioma: |
Inglês |
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Conteúdo: |
Gray mold of grapes, also called Botrytis bunch rot is caused by the fungus Botrytis cinerea and is found in practically all vineyards in the world, causing serious reductions in the quality and quantity of grapes produced. The control of this disease is based on chemical fungicides applications associated with grapevine management techniques. However, during grape maturation, the use of chemical fungicides is restricted due to the pre-harvest interval. Hence, an alternative product for controlling these pests would provide relief for producers. The use of biological control agents may be a promising option to attend the growing demands for healthy products and sustainable management techniques that respect the environment and reduce the use of pesticides. In previous work, the antagonism of a Saccharomyces cerevisiae strain, present in the CMIA Collection of Embrapa Grape and Wine, against B. cinerea has already been demonstrated by the production of diffusible substances in solid culture medium. In order to understand the mechanisms involved in this biocontrol, the present work had the objective of growing this yeast strain in liquid medium and evaluate its supernatant without active cells against the same fungus. To this end, the S. cerevisiae strain was grown in a complex medium for 96 hours at 28°C and three treatments (in duplicate) were carried out: A) Medium was centrifuged and its supernatant was autoclaved; B) Medium was centrifuged and the supernatant was filtered at 0.22µm; C) Full medium (without centrifugation) was autoclaved. As positive control, the target fungi were inoculated into the same culture medium used for yeast growth. Each of the treatments was inoculated with two discs (0.5 cm each) of the fungus mycelium. After inoculation, mycelial growth was observed daily by visual inspection for 96 hours. The results indicate that the biocontrol compound appears to be thermolabile, once 48 hours after the start of the test, the fungus began to grow in the treatments A and C, while treatment B did not show proliferation until 96 hours. This outcome reinforces the need for characterization and identification of the metabolites produced by the yeast to unravel the mechanisms of action involved in the biocontrol observed and, consequently, support new bioinput development. MenosGray mold of grapes, also called Botrytis bunch rot is caused by the fungus Botrytis cinerea and is found in practically all vineyards in the world, causing serious reductions in the quality and quantity of grapes produced. The control of this disease is based on chemical fungicides applications associated with grapevine management techniques. However, during grape maturation, the use of chemical fungicides is restricted due to the pre-harvest interval. Hence, an alternative product for controlling these pests would provide relief for producers. The use of biological control agents may be a promising option to attend the growing demands for healthy products and sustainable management techniques that respect the environment and reduce the use of pesticides. In previous work, the antagonism of a Saccharomyces cerevisiae strain, present in the CMIA Collection of Embrapa Grape and Wine, against B. cinerea has already been demonstrated by the production of diffusible substances in solid culture medium. In order to understand the mechanisms involved in this biocontrol, the present work had the objective of growing this yeast strain in liquid medium and evaluate its supernatant without active cells against the same fungus. To this end, the S. cerevisiae strain was grown in a complex medium for 96 hours at 28°C and three treatments (in duplicate) were carried out: A) Medium was centrifuged and its supernatant was autoclaved; B) Medium was centrifuged and the supernatant was filtered... Mostrar Tudo |
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Palavras-Chave: |
Bionput; Grapevine; Yeast. |
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Thesagro: |
Botrytis Cinerea. |
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Categoria do assunto: |
-- |
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URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/doc/1160133/1/Agustini-CBM-2023-1487-2.pdf
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Marc: |
LEADER 02962nam a2200193 a 4500
001 2160133
005 2023-12-20
008 2023 bl uuuu u00u1 u #d
100 1 $aAGUSTINI, B. C.
245 $aYeast as a biological agent in the control of botrytis cinerea.$h[electronic resource]
260 $aIn: CONGRESSO BRASILEIRO DE MICROBIOLOGIA, 32., 2023, Foz do Iguaçú, PR. Anais... FOz do Iguaçú: SBM, 18 a 22 de out. 2023. p. 1487-2.$c1487
520 $aGray mold of grapes, also called Botrytis bunch rot is caused by the fungus Botrytis cinerea and is found in practically all vineyards in the world, causing serious reductions in the quality and quantity of grapes produced. The control of this disease is based on chemical fungicides applications associated with grapevine management techniques. However, during grape maturation, the use of chemical fungicides is restricted due to the pre-harvest interval. Hence, an alternative product for controlling these pests would provide relief for producers. The use of biological control agents may be a promising option to attend the growing demands for healthy products and sustainable management techniques that respect the environment and reduce the use of pesticides. In previous work, the antagonism of a Saccharomyces cerevisiae strain, present in the CMIA Collection of Embrapa Grape and Wine, against B. cinerea has already been demonstrated by the production of diffusible substances in solid culture medium. In order to understand the mechanisms involved in this biocontrol, the present work had the objective of growing this yeast strain in liquid medium and evaluate its supernatant without active cells against the same fungus. To this end, the S. cerevisiae strain was grown in a complex medium for 96 hours at 28°C and three treatments (in duplicate) were carried out: A) Medium was centrifuged and its supernatant was autoclaved; B) Medium was centrifuged and the supernatant was filtered at 0.22µm; C) Full medium (without centrifugation) was autoclaved. As positive control, the target fungi were inoculated into the same culture medium used for yeast growth. Each of the treatments was inoculated with two discs (0.5 cm each) of the fungus mycelium. After inoculation, mycelial growth was observed daily by visual inspection for 96 hours. The results indicate that the biocontrol compound appears to be thermolabile, once 48 hours after the start of the test, the fungus began to grow in the treatments A and C, while treatment B did not show proliferation until 96 hours. This outcome reinforces the need for characterization and identification of the metabolites produced by the yeast to unravel the mechanisms of action involved in the biocontrol observed and, consequently, support new bioinput development.
650 $aBotrytis Cinerea
653 $aBionput
653 $aGrapevine
653 $aYeast
700 1 $aCORREA, O. L. dos S.
700 1 $aOSTER, A. H.
700 1 $aSILVA, G. A.
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Embrapa Uva e Vinho (CNPUV) |
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