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Registro Completo |
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Biblioteca(s): |
Embrapa Gado de Leite. |
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Data corrente: |
24/03/2009 |
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Data da última atualização: |
16/02/2024 |
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Tipo da produção científica: |
Artigo em Periódico Indexado |
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Autoria: |
MARCELINO, F. C.; GUIMARÃES, M. F. M.; BARROS, E. G. |
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Afiliação: |
Francismar Correa Marcelino, Embrapa Soja; Marta Fonseca Martins Guimaraes, Embrapa Gado de Leite; Everaldo Gonçalves de Barros, Bioagro / UFV. |
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Título: |
Detection and quantification of Roundup Ready soybean residues in sausage samples by conventional and real-time PCR. |
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Ano de publicação: |
2008 |
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Fonte/Imprenta: |
Ciência e Tecnologia de Alimentos, Campinas, v. 28, p. 38-45, 2008. |
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DOI: |
https://doi.org/10.1590/S0101-20612008000500007 |
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Idioma: |
Inglês |
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Notas: |
Supl. |
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Conteúdo: |
The increasing presence of products derived from genetically modified (GM) plants in human and animal diets has led to the development of detection methods to distinguish biotechnology-derived foods from conventional ones. The conventional and real-time PCR have been used, respectively, to detect and quantify GM residues in highly processed foods. DNA extraction is a critical step during the analysis process. Some factors such as DNA degradation, matrix effects, and the presence of PCR inhibitors imply that a detection or quantification limit, established for a given method, is restricted to a matrix used during validation and cannot be projected to any other matrix outside the scope of the method. In Brazil, sausage samples were the main class of processed products in which Roundup Ready® (RR) soybean residues were detected. Thus, the validation of methodologies for the detection and quantification of those residues is absolutely necessary. Sausage samples were submitted to two different methods of DNA extraction: modified Wizard and the CTAB method. The yield and quality were compared for both methods. DNA samples were analyzed by conventional and real-time PCR for the detection and quantification of Roundup Ready® soybean in the samples. At least 200 ng of total sausage DNA was necessary for a reliable quantification. Reactions containing DNA amounts below this value led to large variations on the expected GM percentage value. In conventional PCR, the detection limit varied from 1.0 to 500 ng, depending on the GM soybean content in the sample. The precision, performance, and linearity were relatively high indicating that the method used for analysis was satisfactory. MenosThe increasing presence of products derived from genetically modified (GM) plants in human and animal diets has led to the development of detection methods to distinguish biotechnology-derived foods from conventional ones. The conventional and real-time PCR have been used, respectively, to detect and quantify GM residues in highly processed foods. DNA extraction is a critical step during the analysis process. Some factors such as DNA degradation, matrix effects, and the presence of PCR inhibitors imply that a detection or quantification limit, established for a given method, is restricted to a matrix used during validation and cannot be projected to any other matrix outside the scope of the method. In Brazil, sausage samples were the main class of processed products in which Roundup Ready® (RR) soybean residues were detected. Thus, the validation of methodologies for the detection and quantification of those residues is absolutely necessary. Sausage samples were submitted to two different methods of DNA extraction: modified Wizard and the CTAB method. The yield and quality were compared for both methods. DNA samples were analyzed by conventional and real-time PCR for the detection and quantification of Roundup Ready® soybean in the samples. At least 200 ng of total sausage DNA was necessary for a reliable quantification. Reactions containing DNA amounts below this value led to large variations on the expected GM percentage value. In conventional PCR, the detection limit vari... Mostrar Tudo |
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Palavras-Chave: |
GMO; PCR quantitative; Sausage; Transgenic residues. |
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Categoria do assunto: |
-- |
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URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/doc/596463/1/Detection-and-quantification-of-Roundup-Ready-soybean.pdf
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Marc: |
LEADER 02405naa a2200217 a 4500
001 1596463
005 2024-02-16
008 2008 bl uuuu u00u1 u #d
024 7 $ahttps://doi.org/10.1590/S0101-20612008000500007$2DOI
100 1 $aMARCELINO, F. C.
245 $aDetection and quantification of Roundup Ready soybean residues in sausage samples by conventional and real-time PCR.$h[electronic resource]
260 $c2008
500 $aSupl.
520 $aThe increasing presence of products derived from genetically modified (GM) plants in human and animal diets has led to the development of detection methods to distinguish biotechnology-derived foods from conventional ones. The conventional and real-time PCR have been used, respectively, to detect and quantify GM residues in highly processed foods. DNA extraction is a critical step during the analysis process. Some factors such as DNA degradation, matrix effects, and the presence of PCR inhibitors imply that a detection or quantification limit, established for a given method, is restricted to a matrix used during validation and cannot be projected to any other matrix outside the scope of the method. In Brazil, sausage samples were the main class of processed products in which Roundup Ready® (RR) soybean residues were detected. Thus, the validation of methodologies for the detection and quantification of those residues is absolutely necessary. Sausage samples were submitted to two different methods of DNA extraction: modified Wizard and the CTAB method. The yield and quality were compared for both methods. DNA samples were analyzed by conventional and real-time PCR for the detection and quantification of Roundup Ready® soybean in the samples. At least 200 ng of total sausage DNA was necessary for a reliable quantification. Reactions containing DNA amounts below this value led to large variations on the expected GM percentage value. In conventional PCR, the detection limit varied from 1.0 to 500 ng, depending on the GM soybean content in the sample. The precision, performance, and linearity were relatively high indicating that the method used for analysis was satisfactory.
653 $aGMO
653 $aPCR quantitative
653 $aSausage
653 $aTransgenic residues
700 1 $aGUIMARÃES, M. F. M.
700 1 $aBARROS, E. G.
773 $tCiência e Tecnologia de Alimentos, Campinas$gv. 28, p. 38-45, 2008.
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Registro original: |
Embrapa Gado de Leite (CNPGL) |
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Registro Completo
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Biblioteca(s): |
Embrapa Mandioca e Fruticultura. |
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Data corrente: |
09/09/2021 |
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Data da última atualização: |
09/09/2021 |
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Tipo da produção científica: |
Resumo em Anais de Congresso |
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Autoria: |
SANTANA, A. N.; SOUZA, T. R. de; GÓES, N. da H.; SILVA, M. dos S.; AMORIM, E. P.; SEREJO, J. A. dos S. |
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Afiliação: |
ADRIELE NASCIMENTO SANTANA, UFRB; THAISE RAMOS DE SOUZA, UFRB; NAIALA DA HORA GÓES, UFRB; MANASSÉS DOS SANTOS SILVA, UEFS; EDSON PERITO AMORIM, CNPMF; JANAY ALMEIDA DOS SANTOS SEREJO, CNPMF. |
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Título: |
Fertilização em diferentes estágios de maturação da inflorescência em bananeira 'Grande Naine'. |
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Ano de publicação: |
2020 |
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Fonte/Imprenta: |
In: JORNADA CIENTÍFICA EMBRAPA MANDIOCA E FRUTICULTURA, 14., 2020. Ciência em tempos de crise: resumos. Cruz das Almas, BA: Embrapa Mandioca e Fruticultura, 2020. 112 p. il. |
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Idioma: |
Português |
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Thesagro: |
Banana. |
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Categoria do assunto: |
-- |
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URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/item/225812/1/p21.pdf
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Marc: |
LEADER 00679nam a2200169 a 4500
001 2134176
005 2021-09-09
008 2020 bl uuuu u00u1 u #d
100 1 $aSANTANA, A. N.
245 $aFertilização em diferentes estágios de maturação da inflorescência em bananeira 'Grande Naine'.$h[electronic resource]
260 $aIn: JORNADA CIENTÍFICA EMBRAPA MANDIOCA E FRUTICULTURA, 14., 2020. Ciência em tempos de crise: resumos. Cruz das Almas, BA: Embrapa Mandioca e Fruticultura, 2020. 112 p. il.$c2020
650 $aBanana
700 1 $aSOUZA, T. R. de
700 1 $aGÓES, N. da H.
700 1 $aSILVA, M. dos S.
700 1 $aAMORIM, E. P.
700 1 $aSEREJO, J. A. dos S.
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Embrapa Mandioca e Fruticultura (CNPMF) |
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