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Registro Completo |
Biblioteca(s): |
Embrapa Agrobiologia. |
Data corrente: |
18/12/2023 |
Data da última atualização: |
18/12/2023 |
Tipo da produção científica: |
Artigo em Periódico Indexado |
Autoria: |
SILVA, C. G. N. da; MONTEIRO, E. de C.; DINIZ, P. P.; TERRA, L. A.; SCHWAB, S.; REIS, V. M.; ARAUJO, J. L. S. de; URQUIAGA, S. |
Afiliação: |
CLEUDISON GABRIEL NASCIMENTO DA SILVA, UFRRJ; EDEVALDO DE CASTRO MONTEIRO, UFRRJ; PRISCILA PEREIRA DINIZ, UFRRJ; LEONARDO ARAUJO TERRA, UFRRJ; STEFAN SCHWAB, CNPAB; VERONICA MASSENA REIS, CNPAB; JEAN LUIZ SIMOES DE ARAUJO, CNPAB; SEGUNDO SACRAMENTO U CABALLERO, CNPAB. |
Título: |
Designing and validation of specifc primers for the quantitative detection of bacteria in sugarcane inoculant. |
Ano de publicação: |
2023 |
Fonte/Imprenta: |
Brazilian Journal of Microbiology, v. 54, p. 2627–2640, 2023. |
ISSN: |
1678-4405 |
Idioma: |
Inglês |
Conteúdo: |
Endophytic diazotrophic plant growth-promoting bacteria Herbaspirillum rubrisubalbicans (HCC103), Herbaspirillum seropedicae (HRC54), Paraburkholderia tropica (Ppe8T), Gluconacetobacter diazotrophicus (Pal5T), and Nitrospirillum amazonense (CBAmC) have been used as inoculants for sugarcane. The genome sequences of these strains were used to design a set of specifc primers for the real-time PCR (qPCR) assay. Primer specifcity was confrmed by conventional PCR using the genomic DNAs of 25 related bacterial species and the fve target strains. The qPCR assays were conducted using root and shoot samples from two sugarcane varieties (RB867515 and RB92579). These samples were collected both with and without inoculation, using the target strains specifed in this study. The sugarcane plants were grown in a greenhouse, utilizing a substrate composed of sterile sand and vermiculite in a 2:1 ratio, for a duration of 55 days. The primers designed for this study successfully amplifed target DNA fragments from each of the bacterial species, enabling their diferentiation at the species level. The total bacterial population present in the sugarcane quantifed using qPCR was on average 105.2 cells g−1 of fresh tissue. Across both evaluated varieties, it was observed that the population of inoculated bacteria tended to decrease over time and became more concentrated in the sugarcane roots compared to the aerial parts. The qPCR results suggest that both the host and the microbes infuence the endophytic population and the bacterial number decreases with plant age. MenosEndophytic diazotrophic plant growth-promoting bacteria Herbaspirillum rubrisubalbicans (HCC103), Herbaspirillum seropedicae (HRC54), Paraburkholderia tropica (Ppe8T), Gluconacetobacter diazotrophicus (Pal5T), and Nitrospirillum amazonense (CBAmC) have been used as inoculants for sugarcane. The genome sequences of these strains were used to design a set of specifc primers for the real-time PCR (qPCR) assay. Primer specifcity was confrmed by conventional PCR using the genomic DNAs of 25 related bacterial species and the fve target strains. The qPCR assays were conducted using root and shoot samples from two sugarcane varieties (RB867515 and RB92579). These samples were collected both with and without inoculation, using the target strains specifed in this study. The sugarcane plants were grown in a greenhouse, utilizing a substrate composed of sterile sand and vermiculite in a 2:1 ratio, for a duration of 55 days. The primers designed for this study successfully amplifed target DNA fragments from each of the bacterial species, enabling their diferentiation at the species level. The total bacterial population present in the sugarcane quantifed using qPCR was on average 105.2 cells g−1 of fresh tissue. Across both evaluated varieties, it was observed that the population of inoculated bacteria tended to decrease over time and became more concentrated in the sugarcane roots compared to the aerial parts. The qPCR results suggest that both the host and the microbes infuence the endo... Mostrar Tudo |
Palavras-Chave: |
Diazotrophic bacteria; DPGPB quantifcation; Primers; Real Time PCR. |
Thesagro: |
Saccharum Officinarum. |
Categoria do assunto: |
S Ciências Biológicas |
Marc: |
LEADER 02399naa a2200277 a 4500 001 2159851 005 2023-12-18 008 2023 bl uuuu u00u1 u #d 022 $a1678-4405 100 1 $aSILVA, C. G. N. da 245 $aDesigning and validation of specifc primers for the quantitative detection of bacteria in sugarcane inoculant.$h[electronic resource] 260 $c2023 520 $aEndophytic diazotrophic plant growth-promoting bacteria Herbaspirillum rubrisubalbicans (HCC103), Herbaspirillum seropedicae (HRC54), Paraburkholderia tropica (Ppe8T), Gluconacetobacter diazotrophicus (Pal5T), and Nitrospirillum amazonense (CBAmC) have been used as inoculants for sugarcane. The genome sequences of these strains were used to design a set of specifc primers for the real-time PCR (qPCR) assay. Primer specifcity was confrmed by conventional PCR using the genomic DNAs of 25 related bacterial species and the fve target strains. The qPCR assays were conducted using root and shoot samples from two sugarcane varieties (RB867515 and RB92579). These samples were collected both with and without inoculation, using the target strains specifed in this study. The sugarcane plants were grown in a greenhouse, utilizing a substrate composed of sterile sand and vermiculite in a 2:1 ratio, for a duration of 55 days. The primers designed for this study successfully amplifed target DNA fragments from each of the bacterial species, enabling their diferentiation at the species level. The total bacterial population present in the sugarcane quantifed using qPCR was on average 105.2 cells g−1 of fresh tissue. Across both evaluated varieties, it was observed that the population of inoculated bacteria tended to decrease over time and became more concentrated in the sugarcane roots compared to the aerial parts. The qPCR results suggest that both the host and the microbes infuence the endophytic population and the bacterial number decreases with plant age. 650 $aSaccharum Officinarum 653 $aDiazotrophic bacteria 653 $aDPGPB quantifcation 653 $aPrimers 653 $aReal Time PCR 700 1 $aMONTEIRO, E. de C. 700 1 $aDINIZ, P. P. 700 1 $aTERRA, L. A. 700 1 $aSCHWAB, S. 700 1 $aREIS, V. M. 700 1 $aARAUJO, J. L. S. de 700 1 $aURQUIAGA, S. 773 $tBrazilian Journal of Microbiology$gv. 54, p. 2627–2640, 2023.
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Embrapa Agrobiologia (CNPAB) |
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Biblioteca(s): |
Embrapa Rondônia; Embrapa Unidades Centrais. |
Data corrente: |
01/07/2019 |
Data da última atualização: |
27/01/2020 |
Tipo da produção científica: |
Artigo em Periódico Indexado |
Circulação/Nível: |
A - 2 |
Autoria: |
BARBERENA, I. M.; ESPINDULA, M. C.; ARAÚJO, L. F. B. de; MARCOLAN, A. L. |
Afiliação: |
MARCELO CURITIBA ESPINDULA, CPAF-RO; ALAERTO LUIZ MARCOLAN, CPAF-RO. |
Título: |
Use of urease inhibitors to reduce ammonia volatilization in Amazonian soils. |
Ano de publicação: |
2019 |
Fonte/Imprenta: |
Pesquisa Agropecuária Brasileira, v. 54, e00253, 2019. |
Idioma: |
Inglês |
Conteúdo: |
The objective of this work was to evaluate urease inhibitors for the reduction of ammonia volatilization in Amazonian soils. The work was carried out on a clayey yellow Oxisol, a clayey red Oxisol, and on a light silty Ultisol. Each experiment was conducted in split plots, using standard urea, urea + a benzimidazole-type urease inhibitor (BZI1), urea + a benzoylthiourea-type urease inhibitor (RTB68), urea + N-(n-butyl) triamide thiophosphate (NBPT), or a fertilizer-free control. Volatilized ammonia was collected at 48, 96, 144, 192, 240, 288, 336, and 384 hours after fertilization. Ammonia volatilization reached a maximum at 144 hours in the urea, urea + benzimidazole, and urea + benzoylthiourea treatments. A peak level was reached at 192 and 288 hours in the urea + N-(n-butyl) triamide thiophosphate treatment. In yellow Oxisols, benzimidazole and benzoylthiourea reduced the ammonia losses by 22 and 10%, respectively, in soils without urease inhibitors. However, neither of these agents significantly reduced ammonia volatilization at the rate determined for standard urea in red Oxisols or Ultisols. N-(n-butyl) triamide thiophosphate is the most efficient urease inhibitor for the soils of southwestern Amazonia. |
Palavras-Chave: |
Benzoylthiourea; Inibidor de urease; Plintossolo. |
Thesagro: |
Benzimidazol; Latossolo. |
Thesaurus NAL: |
Benzimidazole; Oxisols; Plinthosols; Urease inhibitors. |
Categoria do assunto: |
-- |
URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/item/209268/1/Barberena-et-al.-2019.pdf
https://ainfo.cnptia.embrapa.br/digital/bitstream/item/198928/1/Use-of-urease-inhibitors-to-reduce.pdf
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Marc: |
LEADER 01978naa a2200265 a 4500 001 2119109 005 2020-01-27 008 2019 bl uuuu u00u1 u #d 100 1 $aBARBERENA, I. M. 245 $aUse of urease inhibitors to reduce ammonia volatilization in Amazonian soils.$h[electronic resource] 260 $c2019 520 $aThe objective of this work was to evaluate urease inhibitors for the reduction of ammonia volatilization in Amazonian soils. The work was carried out on a clayey yellow Oxisol, a clayey red Oxisol, and on a light silty Ultisol. Each experiment was conducted in split plots, using standard urea, urea + a benzimidazole-type urease inhibitor (BZI1), urea + a benzoylthiourea-type urease inhibitor (RTB68), urea + N-(n-butyl) triamide thiophosphate (NBPT), or a fertilizer-free control. Volatilized ammonia was collected at 48, 96, 144, 192, 240, 288, 336, and 384 hours after fertilization. Ammonia volatilization reached a maximum at 144 hours in the urea, urea + benzimidazole, and urea + benzoylthiourea treatments. A peak level was reached at 192 and 288 hours in the urea + N-(n-butyl) triamide thiophosphate treatment. In yellow Oxisols, benzimidazole and benzoylthiourea reduced the ammonia losses by 22 and 10%, respectively, in soils without urease inhibitors. However, neither of these agents significantly reduced ammonia volatilization at the rate determined for standard urea in red Oxisols or Ultisols. N-(n-butyl) triamide thiophosphate is the most efficient urease inhibitor for the soils of southwestern Amazonia. 650 $aBenzimidazole 650 $aOxisols 650 $aPlinthosols 650 $aUrease inhibitors 650 $aBenzimidazol 650 $aLatossolo 653 $aBenzoylthiourea 653 $aInibidor de urease 653 $aPlintossolo 700 1 $aESPINDULA, M. C. 700 1 $aARAÚJO, L. F. B. de 700 1 $aMARCOLAN, A. L. 773 $tPesquisa Agropecuária Brasileira$gv. 54, e00253, 2019.
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