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Biblioteca(s): |
Embrapa Agrobiologia. |
Data corrente: |
09/11/2021 |
Data da última atualização: |
09/11/2021 |
Tipo da produção científica: |
Artigo em Periódico Indexado |
Autoria: |
SOARES, I. C.; PACHECO, R. S.; SILVA, C. G. N. da; SANTOS, R. S.; BALDANI, J. I.; URQUIAGA, S.; VIDAL, M. S.; ARAUJO, J. L. S. de. |
Afiliação: |
ISIS CAPELLA SOARES, UFRRJ; RAFAEL SANCHES PACHECO, UFRRJ; CLEUDISON GABRIEL NASCIMENTO DA SILVA, UFLA; RAFAEL SALAZAR SANTOS, UFRRJ; JOSE IVO BALDANI, CNPAB; SEGUNDO SACRAMENTO U CABALLERO, CNPAB; MARCIA SOARES VIDAL, CNPAB; JEAN LUIZ SIMOES DE ARAUJO, CNPAB. |
Título: |
Real-time PCR method to quantify Sp245 strain of Azospirillum baldaniorum on Brachiaria grasses under field conditions. |
Ano de publicação: |
2021 |
Fonte/Imprenta: |
Plant and Soil, 06 September 2021 |
ISSN: |
0032-079X |
DOI: |
https://doi.org/10.1007/s11104-021-05137-y |
Idioma: |
Inglês |
Conteúdo: |
Bacterial quantification by qPCR is considered the gold standard for microbial molecular diagnosis. However, a fundamental pre-requisite in this methodology is the designing of specific primers for the bacterium of interest. With the increase in bacterial genome sequencing data in the recent years, it has become possible to design specific primers that can be used to quantify different strains of the same bacterial species. Methods: To develop a real-time PCR (qPCR) protocol for the specific quantification of Azospirillum baldaniorum Sp245 strain (old Azospirillum brasilense), the Sp245 genome sequence was fragmented into small contigs with 500 base pairs each, and analyzed for similarity against the NCBI non-redundant database. A. baldaniorum-specific contigs were used to design the primers. The best pair of primers was used to quantify these bacteria after inoculation in different cultivars of Brachiaria, grown under field conditions. Results: Our results showed that the primer pair Sp245p10 was highly specific for the Sp245 strain in the Brachiaria root and shoot field under different conditions. The qPCR assay using these primers showed differences among cultivars in the number of bacteria detected in plants after inoculation. Additionally, the number of bacteria observed in the roots was higher than that in the shoots. Conclusion: The qPCR methodology using a Sp245 strain-specific primer may be used to monitor A. baldaniorum inoculated into other plants and may find potential application in field experiments. MenosBacterial quantification by qPCR is considered the gold standard for microbial molecular diagnosis. However, a fundamental pre-requisite in this methodology is the designing of specific primers for the bacterium of interest. With the increase in bacterial genome sequencing data in the recent years, it has become possible to design specific primers that can be used to quantify different strains of the same bacterial species. Methods: To develop a real-time PCR (qPCR) protocol for the specific quantification of Azospirillum baldaniorum Sp245 strain (old Azospirillum brasilense), the Sp245 genome sequence was fragmented into small contigs with 500 base pairs each, and analyzed for similarity against the NCBI non-redundant database. A. baldaniorum-specific contigs were used to design the primers. The best pair of primers was used to quantify these bacteria after inoculation in different cultivars of Brachiaria, grown under field conditions. Results: Our results showed that the primer pair Sp245p10 was highly specific for the Sp245 strain in the Brachiaria root and shoot field under different conditions. The qPCR assay using these primers showed differences among cultivars in the number of bacteria detected in plants after inoculation. Additionally, the number of bacteria observed in the roots was higher than that in the shoots. Conclusion: The qPCR methodology using a Sp245 strain-specific primer may be used to monitor A. baldaniorum inoculated into other plants and may find pot... Mostrar Tudo |
Palavras-Chave: |
Azospirillum baldanioru; Plant growth promoting bacteria; Quantification; Signal grass. |
Categoria do assunto: |
S Ciências Biológicas |
Marc: |
LEADER 02397naa a2200277 a 4500 001 2135952 005 2021-11-09 008 2021 bl uuuu u00u1 u #d 022 $a0032-079X 024 7 $ahttps://doi.org/10.1007/s11104-021-05137-y$2DOI 100 1 $aSOARES, I. C. 245 $aReal-time PCR method to quantify Sp245 strain of Azospirillum baldaniorum on Brachiaria grasses under field conditions.$h[electronic resource] 260 $c2021 520 $aBacterial quantification by qPCR is considered the gold standard for microbial molecular diagnosis. However, a fundamental pre-requisite in this methodology is the designing of specific primers for the bacterium of interest. With the increase in bacterial genome sequencing data in the recent years, it has become possible to design specific primers that can be used to quantify different strains of the same bacterial species. Methods: To develop a real-time PCR (qPCR) protocol for the specific quantification of Azospirillum baldaniorum Sp245 strain (old Azospirillum brasilense), the Sp245 genome sequence was fragmented into small contigs with 500 base pairs each, and analyzed for similarity against the NCBI non-redundant database. A. baldaniorum-specific contigs were used to design the primers. The best pair of primers was used to quantify these bacteria after inoculation in different cultivars of Brachiaria, grown under field conditions. Results: Our results showed that the primer pair Sp245p10 was highly specific for the Sp245 strain in the Brachiaria root and shoot field under different conditions. The qPCR assay using these primers showed differences among cultivars in the number of bacteria detected in plants after inoculation. Additionally, the number of bacteria observed in the roots was higher than that in the shoots. Conclusion: The qPCR methodology using a Sp245 strain-specific primer may be used to monitor A. baldaniorum inoculated into other plants and may find potential application in field experiments. 653 $aAzospirillum baldanioru 653 $aPlant growth promoting bacteria 653 $aQuantification 653 $aSignal grass 700 1 $aPACHECO, R. S. 700 1 $aSILVA, C. G. N. da 700 1 $aSANTOS, R. S. 700 1 $aBALDANI, J. I. 700 1 $aURQUIAGA, S. 700 1 $aVIDAL, M. S. 700 1 $aARAUJO, J. L. S. de 773 $tPlant and Soil, 06 September 2021
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Embrapa Agrobiologia (CNPAB) |
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Biblioteca(s): |
Embrapa Unidades Centrais. |
Data corrente: |
16/11/2010 |
Data da última atualização: |
16/11/2010 |
Tipo da produção científica: |
Resumo em Anais de Congresso |
Autoria: |
GOMES, E. G.; SOUZA, G. da S. e; GAZZOLA, R.; AVILA, A. F. D. |
Afiliação: |
ELIANE GONCALVES GOMES, SGE; GERALDO DA SILVA E SOUZA, SGE; ROSAURA GAZZOLA, SGE; ANTONIO FLAVIO DIAS AVILA, SGE. |
Título: |
Effects of ecucation and investment in research in agricultural production in Brazil. |
Ano de publicação: |
2010 |
Fonte/Imprenta: |
In: EUROPEAN CONFERENCE ON OPERATIONAL RESEARCH, 24., 2010, Lisboa, Portugal. Proceedings. ... |
Idioma: |
Português |
Conteúdo: |
We use census data (1996 and 2006) to model the agricultural production at state level in Brazil. Cost efficiency measurements are computed using data envelopment analysis and the response is assessed via censored regressions. We study the effects of region, education and investment in agricultural research on the economic efficiency. Education has a strong significant effect, as well as investment in research. The intensity of the effects varies over regions for education, and is statistically the same for investment in research. |
Palavras-Chave: |
Model the agricultural. |
Categoria do assunto: |
-- |
URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/item/23577/1/Effects-of-education.pdf
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Marc: |
LEADER 01079nam a2200157 a 4500 001 1867015 005 2010-11-16 008 2010 bl uuuu u00u1 u #d 100 1 $aGOMES, E. G. 245 $aEffects of ecucation and investment in research in agricultural production in Brazil.$h[electronic resource] 260 $aIn: EUROPEAN CONFERENCE ON OPERATIONAL RESEARCH, 24., 2010, Lisboa, Portugal. Proceedings. ...$c2010 520 $aWe use census data (1996 and 2006) to model the agricultural production at state level in Brazil. Cost efficiency measurements are computed using data envelopment analysis and the response is assessed via censored regressions. We study the effects of region, education and investment in agricultural research on the economic efficiency. Education has a strong significant effect, as well as investment in research. The intensity of the effects varies over regions for education, and is statistically the same for investment in research. 653 $aModel the agricultural 700 1 $aSOUZA, G. da S. e 700 1 $aGAZZOLA, R. 700 1 $aAVILA, A. F. D.
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