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Registro Completo |
Biblioteca(s): |
Embrapa Acre; Embrapa Rondônia. |
Data corrente: |
02/09/2019 |
Data da última atualização: |
11/11/2019 |
Tipo da produção científica: |
Artigo em Periódico Indexado |
Autoria: |
AZÊVEDO, H. S. F. da S.; RUFINO, P. B.; AZEVEDO, J. M. A. de; SILVA, L. M. da; WADT, L. H. de O.; CAMPOS, T. de. |
Afiliação: |
LUCIELIO MANOEL DA SILVA, CPAF-AC; LUCIA HELENA DE OLIVEIRA WADT, CPAF-RO; TATIANA DE CAMPOS, CPAF-AC. |
Título: |
Preservation and maceration of amazon açai leaflet Tissue to obtain genomic DNA. |
Ano de publicação: |
2019 |
Fonte/Imprenta: |
Bioscience Journal, Uberlândia, v. 35, n. 4, p. 1188-1197, July/Aug. 2019. |
Idioma: |
Inglês Português |
Conteúdo: |
The objective of this study was to test the efficiency of preservation and maceration methods for Euterpe precatoria leaflet tissue to obtain genomic DNA for molecular studies. The leaflets of E. precatoria were collected in an experimental field at Embrapa Acre, Brazil. The study was conducted in a completely randomized design with 10 replicates, in a 12 × 2 factorial structure, with 12 storage treatments (fresh; lyophiliser 3 days; refrigerator 3, 5, and 7 days; silica gel 7, 10, 20, and 30 days; and transport buffer 3, 5, and 7 days) and two leaf tissue maceration methods (liquid nitrogen and the TissueLyser®). Statistically significant differences in the obtained DNA concentration were found between the maceration and storage treatments. The TissueLyser® macerator produced higher DNA concentrations when compared to liquid nitrogen. For the storage treatments, five groups were formed based on DNA concentration when macerated with the TissueLyser® and two groups when macerated with liquid nitrogen. The DNA concentrations ranged from 285.00 ng/uL (7 days in transport buffer) to 702.00 ng/uL (30 days in silica gel) when the leaflets were macerated with liquid nitrogen, and from 572.73 ng/uL (30 days in silica gel) to 2,850.00 ng/uL (3 days in lyophiliser) using the TissueLyser® macerator. The DNA purity (A260/A280 nm) varied from 1.30 to 1.70 when the leaflets were macerated with liquid nitrogen and from 1.30 to 1.90 with the TissueLyser® macerator. Despite the variations in leaf tissue preservation and DNA concentration, all treatments were effective for DNA isolation and it was possible to amplify genomic regions of microsatellite markers by PCR. It was concluded that leaflets of E. precatoria stored in a lyophiliser and processed with an automatic macerator resulted in satisfactory DNA for molecular studies. MenosThe objective of this study was to test the efficiency of preservation and maceration methods for Euterpe precatoria leaflet tissue to obtain genomic DNA for molecular studies. The leaflets of E. precatoria were collected in an experimental field at Embrapa Acre, Brazil. The study was conducted in a completely randomized design with 10 replicates, in a 12 × 2 factorial structure, with 12 storage treatments (fresh; lyophiliser 3 days; refrigerator 3, 5, and 7 days; silica gel 7, 10, 20, and 30 days; and transport buffer 3, 5, and 7 days) and two leaf tissue maceration methods (liquid nitrogen and the TissueLyser®). Statistically significant differences in the obtained DNA concentration were found between the maceration and storage treatments. The TissueLyser® macerator produced higher DNA concentrations when compared to liquid nitrogen. For the storage treatments, five groups were formed based on DNA concentration when macerated with the TissueLyser® and two groups when macerated with liquid nitrogen. The DNA concentrations ranged from 285.00 ng/uL (7 days in transport buffer) to 702.00 ng/uL (30 days in silica gel) when the leaflets were macerated with liquid nitrogen, and from 572.73 ng/uL (30 days in silica gel) to 2,850.00 ng/uL (3 days in lyophiliser) using the TissueLyser® macerator. The DNA purity (A260/A280 nm) varied from 1.30 to 1.70 when the leaflets were macerated with liquid nitrogen and from 1.30 to 1.90 with the TissueLyser® macerator. Despite the variations in... Mostrar Tudo |
Palavras-Chave: |
Açaí-solteiro; Acre; Amazonia Occidental; Amazônia Ocidental; CTAB method; DNA isolation; Embrapa Acre; Extracción; Hojas; Leaflet; Maceración; Rio Branco; Western Amazon. |
Thesagro: |
Açaí; Campo Experimental; DNA; Extração; Folha; Maceração. |
Thesaurus Nal: |
Euterpe precatoria; Extraction; Leaves; Maceration. |
Categoria do assunto: |
-- G Melhoramento Genético |
URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/item/201498/1/Azevedo-et-al-2019-PresMacAcaiLeaflet.pdf
https://ainfo.cnptia.embrapa.br/digital/bitstream/item/209322/1/26962.pdf
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Marc: |
LEADER 03064naa a2200457 a 4500 001 2111807 005 2019-11-11 008 2019 bl uuuu u00u1 u #d 100 1 $aAZÊVEDO, H. S. F. da S. 245 $aPreservation and maceration of amazon açai leaflet Tissue to obtain genomic DNA.$h[electronic resource] 260 $c2019 520 $aThe objective of this study was to test the efficiency of preservation and maceration methods for Euterpe precatoria leaflet tissue to obtain genomic DNA for molecular studies. The leaflets of E. precatoria were collected in an experimental field at Embrapa Acre, Brazil. The study was conducted in a completely randomized design with 10 replicates, in a 12 × 2 factorial structure, with 12 storage treatments (fresh; lyophiliser 3 days; refrigerator 3, 5, and 7 days; silica gel 7, 10, 20, and 30 days; and transport buffer 3, 5, and 7 days) and two leaf tissue maceration methods (liquid nitrogen and the TissueLyser®). Statistically significant differences in the obtained DNA concentration were found between the maceration and storage treatments. The TissueLyser® macerator produced higher DNA concentrations when compared to liquid nitrogen. For the storage treatments, five groups were formed based on DNA concentration when macerated with the TissueLyser® and two groups when macerated with liquid nitrogen. The DNA concentrations ranged from 285.00 ng/uL (7 days in transport buffer) to 702.00 ng/uL (30 days in silica gel) when the leaflets were macerated with liquid nitrogen, and from 572.73 ng/uL (30 days in silica gel) to 2,850.00 ng/uL (3 days in lyophiliser) using the TissueLyser® macerator. The DNA purity (A260/A280 nm) varied from 1.30 to 1.70 when the leaflets were macerated with liquid nitrogen and from 1.30 to 1.90 with the TissueLyser® macerator. Despite the variations in leaf tissue preservation and DNA concentration, all treatments were effective for DNA isolation and it was possible to amplify genomic regions of microsatellite markers by PCR. It was concluded that leaflets of E. precatoria stored in a lyophiliser and processed with an automatic macerator resulted in satisfactory DNA for molecular studies. 650 $aEuterpe precatoria 650 $aExtraction 650 $aLeaves 650 $aMaceration 650 $aAçaí 650 $aCampo Experimental 650 $aDNA 650 $aExtração 650 $aFolha 650 $aMaceração 653 $aAçaí-solteiro 653 $aAcre 653 $aAmazonia Occidental 653 $aAmazônia Ocidental 653 $aCTAB method 653 $aDNA isolation 653 $aEmbrapa Acre 653 $aExtracción 653 $aHojas 653 $aLeaflet 653 $aMaceración 653 $aRio Branco 653 $aWestern Amazon 700 1 $aRUFINO, P. B. 700 1 $aAZEVEDO, J. M. A. de 700 1 $aSILVA, L. M. da 700 1 $aWADT, L. H. de O. 700 1 $aCAMPOS, T. de 773 $tBioscience Journal, Uberlândia$gv. 35, n. 4, p. 1188-1197, July/Aug. 2019.
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Embrapa Rondônia (CPAF-RO) |
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1. | | AZÊVEDO, H. S. F. da S.; RUFINO, P. B.; AZEVEDO, J. M. A. de; SILVA, L. M. da; WADT, L. H. de O.; CAMPOS, T. de. Preservation and maceration of amazon açai leaflet Tissue to obtain genomic DNA. Bioscience Journal, Uberlândia, v. 35, n. 4, p. 1188-1197, July/Aug. 2019.Tipo: Artigo em Periódico Indexado | Circulação/Nível: A - 2 |
Biblioteca(s): Embrapa Acre; Embrapa Rondônia. |
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