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Registro Completo |
Biblioteca(s): |
Embrapa Agropecuária Oeste; Embrapa Cerrados; Embrapa Rondônia; Embrapa Soja; Embrapa Trigo; Embrapa Unidades Centrais. |
Data corrente: |
17/11/1997 |
Data da última atualização: |
20/11/1997 |
Tipo da produção científica: |
Circular Técnica |
Autoria: |
HUNGRIA, M.; VARGAS, M. A. T.; CAMPO, R. J. |
Título: |
A inoculacao da soja. |
Ano de publicação: |
1997 |
Fonte/Imprenta: |
Londrina: EMBRAPA-CNPSo, 1997. |
Páginas: |
28P. |
Série: |
(EMBRAPA-CNPSo. Circular Tecnica, 17; EMBRAPA-CPAC. Circular Tecnica, 34). |
Idioma: |
Português |
Conteúdo: |
Como ocorre o processo de fixacao biologica do N2?; Quando e por quanto tempo a soja consegue fixar N2?; Por que e necessario inocular a soja em solos de primeiro cultivo?; Em area tradicionalmente cultivadas, vale a pena reinocular?; Os incrementos no rendimento obtidos pela reinoculacao compensam financeiramente?; Com deve ser o inoculante para a soja?; No campo, quais os principais fatores limitantes a fixacao biologica do N2?; Existem outros inoculantes biologicos para a cultura da soja?; Como saber mais sobre a fixacao biologica do N2?; Consideracoes finais. |
Palavras-Chave: |
Biological fixation; Bradyrhizobium elkanni; Bradyrhizobium elkanu; Brasil; CNPSo; CPAC; EMBRAPA; Fixação biológica; Fixacao biologica de nitrogenio; Fixacao biologica do nitrogenio; Inoculation; Parana. |
Thesagro: |
Bactéria; Bradyrhizobium Japonicum; Fixação de Nitrogênio; Glycine Max; Inoculação; Nitrogênio; Rhizobium; Soja. |
Thesaurus Nal: |
Bradyrhizobium elkanii; Brazil; inoculation methods; nitrogen; nitrogen fixation; soybeans. |
Categoria do assunto: |
-- X Pesquisa, Tecnologia e Engenharia |
URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/CNPSO/15723/1/circtec17.pdf
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Marc: |
LEADER 01803nam a2200469 a 4500 001 1553170 005 1997-11-20 008 1997 bl uuuu u0uu1 u #d 100 1 $aHUNGRIA, M. 245 $aA inoculacao da soja. 260 $aLondrina: EMBRAPA-CNPSo$c1997 300 $a28P. 490 $a(EMBRAPA-CNPSo. Circular Tecnica, 17; EMBRAPA-CPAC. Circular Tecnica, 34). 520 $aComo ocorre o processo de fixacao biologica do N2?; Quando e por quanto tempo a soja consegue fixar N2?; Por que e necessario inocular a soja em solos de primeiro cultivo?; Em area tradicionalmente cultivadas, vale a pena reinocular?; Os incrementos no rendimento obtidos pela reinoculacao compensam financeiramente?; Com deve ser o inoculante para a soja?; No campo, quais os principais fatores limitantes a fixacao biologica do N2?; Existem outros inoculantes biologicos para a cultura da soja?; Como saber mais sobre a fixacao biologica do N2?; Consideracoes finais. 650 $aBradyrhizobium elkanii 650 $aBrazil 650 $ainoculation methods 650 $anitrogen 650 $anitrogen fixation 650 $asoybeans 650 $aBactéria 650 $aBradyrhizobium Japonicum 650 $aFixação de Nitrogênio 650 $aGlycine Max 650 $aInoculação 650 $aNitrogênio 650 $aRhizobium 650 $aSoja 653 $aBiological fixation 653 $aBradyrhizobium elkanni 653 $aBradyrhizobium elkanu 653 $aBrasil 653 $aCNPSo 653 $aCPAC 653 $aEMBRAPA 653 $aFixação biológica 653 $aFixacao biologica de nitrogenio 653 $aFixacao biologica do nitrogenio 653 $aInoculation 653 $aParana 700 1 $aVARGAS, M. A. T. 700 1 $aCAMPO, R. J.
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Registro original: |
Embrapa Cerrados (CPAC) |
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Registro Completo
Biblioteca(s): |
Embrapa Recursos Genéticos e Biotecnologia; Embrapa Semiárido. |
Data corrente: |
18/04/2023 |
Data da última atualização: |
25/05/2023 |
Tipo da produção científica: |
Artigo em Periódico Indexado |
Circulação/Nível: |
A - 2 |
Autoria: |
VASQUEZ, D. D. N.; PINHEIRO, D. H.; TEIXEIRA, L. A.; MOREIRA-PINTO, C. E.; MACEDO, L. L. P. de; SALLES-FILHO, A. L. O.; SILVA, M. C. M. da; LOURENCO, I. T.; MORGANTE, C. V.; SILVA, L. P. da; SA, M. F. G. de. |
Afiliação: |
DANIEL D. N. VASQUEZ, Catholic University of Brasília; DANIELE H. PINHEIRO; LAYS A. TEIXEIRA, Catholic University of Brasília; CLIDIA E. MOREIRA-PINTO; LEONARDO LIMA PEPINO DE MACEDO, Cenargen; ALVARO L. O. SALLES-FILHO, Federal University of Paraná; MARIA CRISTINA MATTAR DA SILVA, Cenargen; ISABELA TRISTAN LOURENCO TESSUTTI, Cenargen; CAROLINA VIANNA MORGANTE, CPATSA; LUCIANO PAULINO DA SILVA, Cenargen; MARIA FATIMA GROSSI DE SA, Cenargen. |
Título: |
Simultaneous silencing of juvenile hormone metabolism genes through RNAi interrupts metamorphosis in the cotton boll weevil. |
Ano de publicação: |
2023 |
Fonte/Imprenta: |
Frontiers in Molecular Biosciences, v. 10, 2023. |
DOI: |
https://doi.org/10.3389/fmolb.2023.1073721 |
Idioma: |
Inglês |
Notas: |
Na publicação: Leonardo L. P. Macedo; Maria C. M. Silva; Isabela T. Lourenço-Tessutti; Luciano P. Silva; Maria F. Grossi-de-Sa. |
Conteúdo: |
The cotton boll weevil (CBW) (Anthonomus grandis) is one of the major insect pests of cotton in Brazil. Currently, CBW control is mainly achieved by insecticide application, which is costly and insufficient to ensure effective crop protection. RNA interference (RNAi) has been used in gene function analysis and the development of insect control methods. However, some insect species respond poorly to RNAi, limiting the widespread application of this approach. Therefore, nanoparticles have been explored as an option to increase RNAi efficiency in recalcitrant insects. Herein, we investigated the potential of chitosan?tripolyphosphate (CS-TPP) and polyethylenimine (PEI) nanoparticles as a dsRNA carrier system to improve RNAi efficiency in the CBW. Different formulations of the nanoparticles with dsRNAs targeting genes associated with juvenile hormone metabolism, such as juvenile hormone diol kinase (JHDK), juvenile hormone epoxide hydrolase (JHEH), and methyl farnesoate hydrolase (MFE), were tested. The formulations were delivered to CBW larvae through injection (0.05?2 ?g), and the expression of the target genes was evaluated using RT-qPCR. PEI nanoparticles increased targeted gene silencing compared with naked dsRNAs (up to 80%), whereas CS-TPP-dsRNA nanoparticles decreased gene silencing (0%?20%) or led to the same level of gene silencing as the naked dsRNAs (up to 50%). We next evaluated the effects of targeting a single gene orsimultaneously targeting two genes via the injection of naked dsRNAs or dsRNAs complexed with PEI (500 ng) on CBW survival and phenotypes. Overall, the gene expression analysis showed that the treatments with PEI targeting either a single gene or multiple genes induced greater gene silencing than naked dsRNA (~60%). In addition, the injection of dsJHEH/JHDK, either naked or complexed with PEI, significantly affected CBW survival (18% for PEI nanoparticles and 47% for naked dsRNA) and metamorphosis. Phenotypic alterations, such as uncompleted pupation or malformed pupae, suggested that JHEH and JHDK are involved in developmental regulation. Moreover, CBW larvae treated with dsJHEH/JHDK + PEI (1,000 ng/g) exhibited significantly lower survival rate (55%) than those that MenosThe cotton boll weevil (CBW) (Anthonomus grandis) is one of the major insect pests of cotton in Brazil. Currently, CBW control is mainly achieved by insecticide application, which is costly and insufficient to ensure effective crop protection. RNA interference (RNAi) has been used in gene function analysis and the development of insect control methods. However, some insect species respond poorly to RNAi, limiting the widespread application of this approach. Therefore, nanoparticles have been explored as an option to increase RNAi efficiency in recalcitrant insects. Herein, we investigated the potential of chitosan?tripolyphosphate (CS-TPP) and polyethylenimine (PEI) nanoparticles as a dsRNA carrier system to improve RNAi efficiency in the CBW. Different formulations of the nanoparticles with dsRNAs targeting genes associated with juvenile hormone metabolism, such as juvenile hormone diol kinase (JHDK), juvenile hormone epoxide hydrolase (JHEH), and methyl farnesoate hydrolase (MFE), were tested. The formulations were delivered to CBW larvae through injection (0.05?2 ?g), and the expression of the target genes was evaluated using RT-qPCR. PEI nanoparticles increased targeted gene silencing compared with naked dsRNAs (up to 80%), whereas CS-TPP-dsRNA nanoparticles decreased gene silencing (0%?20%) or led to the same level of gene silencing as the naked dsRNAs (up to 50%). We next evaluated the effects of targeting a single gene orsimultaneously targeting two genes via the inj... Mostrar Tudo |
Palavras-Chave: |
Bicudo do algodoeiro; Juvenile diol kinase; Juvenile hormone epoxide hydrolase; Polyethylenimine; Pragas do algodoeiro. |
Thesagro: |
Algodão; Anthonomus Grandis; Inseto; Praga. |
Thesaurus NAL: |
Chitosan; Cotton; Insect control; Insect pests. |
Categoria do assunto: |
-- O Insetos e Entomologia |
URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/doc/1153217/1/fmolb-10-1073721.pdf
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Marc: |
LEADER 03612naa a2200421 a 4500 001 2153271 005 2023-05-25 008 2023 bl uuuu u00u1 u #d 024 7 $ahttps://doi.org/10.3389/fmolb.2023.1073721$2DOI 100 1 $aVASQUEZ, D. D. N. 245 $aSimultaneous silencing of juvenile hormone metabolism genes through RNAi interrupts metamorphosis in the cotton boll weevil.$h[electronic resource] 260 $c2023 500 $aNa publicação: Leonardo L. P. Macedo; Maria C. M. Silva; Isabela T. Lourenço-Tessutti; Luciano P. Silva; Maria F. Grossi-de-Sa. 520 $aThe cotton boll weevil (CBW) (Anthonomus grandis) is one of the major insect pests of cotton in Brazil. Currently, CBW control is mainly achieved by insecticide application, which is costly and insufficient to ensure effective crop protection. RNA interference (RNAi) has been used in gene function analysis and the development of insect control methods. However, some insect species respond poorly to RNAi, limiting the widespread application of this approach. Therefore, nanoparticles have been explored as an option to increase RNAi efficiency in recalcitrant insects. Herein, we investigated the potential of chitosan?tripolyphosphate (CS-TPP) and polyethylenimine (PEI) nanoparticles as a dsRNA carrier system to improve RNAi efficiency in the CBW. Different formulations of the nanoparticles with dsRNAs targeting genes associated with juvenile hormone metabolism, such as juvenile hormone diol kinase (JHDK), juvenile hormone epoxide hydrolase (JHEH), and methyl farnesoate hydrolase (MFE), were tested. The formulations were delivered to CBW larvae through injection (0.05?2 ?g), and the expression of the target genes was evaluated using RT-qPCR. PEI nanoparticles increased targeted gene silencing compared with naked dsRNAs (up to 80%), whereas CS-TPP-dsRNA nanoparticles decreased gene silencing (0%?20%) or led to the same level of gene silencing as the naked dsRNAs (up to 50%). We next evaluated the effects of targeting a single gene orsimultaneously targeting two genes via the injection of naked dsRNAs or dsRNAs complexed with PEI (500 ng) on CBW survival and phenotypes. Overall, the gene expression analysis showed that the treatments with PEI targeting either a single gene or multiple genes induced greater gene silencing than naked dsRNA (~60%). In addition, the injection of dsJHEH/JHDK, either naked or complexed with PEI, significantly affected CBW survival (18% for PEI nanoparticles and 47% for naked dsRNA) and metamorphosis. Phenotypic alterations, such as uncompleted pupation or malformed pupae, suggested that JHEH and JHDK are involved in developmental regulation. Moreover, CBW larvae treated with dsJHEH/JHDK + PEI (1,000 ng/g) exhibited significantly lower survival rate (55%) than those that 650 $aChitosan 650 $aCotton 650 $aInsect control 650 $aInsect pests 650 $aAlgodão 650 $aAnthonomus Grandis 650 $aInseto 650 $aPraga 653 $aBicudo do algodoeiro 653 $aJuvenile diol kinase 653 $aJuvenile hormone epoxide hydrolase 653 $aPolyethylenimine 653 $aPragas do algodoeiro 700 1 $aPINHEIRO, D. H. 700 1 $aTEIXEIRA, L. A. 700 1 $aMOREIRA-PINTO, C. E. 700 1 $aMACEDO, L. L. P. de 700 1 $aSALLES-FILHO, A. L. O. 700 1 $aSILVA, M. C. M. da 700 1 $aLOURENCO, I. T. 700 1 $aMORGANTE, C. V. 700 1 $aSILVA, L. P. da 700 1 $aSA, M. F. G. de 773 $tFrontiers in Molecular Biosciences$gv. 10, 2023.
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