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Registro Completo |
Biblioteca(s): |
Embrapa Amapá. |
Data corrente: |
22/11/2018 |
Data da última atualização: |
16/06/2023 |
Tipo da produção científica: |
Artigo em Anais de Congresso |
Autoria: |
TOMAZI, R.; YOKOMIZO, G. K. I.; ALMEIDA, S. S. M. da S. de. |
Afiliação: |
ROSANA TOMAZI, IFAP; GILBERTO KEN ITI YOKOMIZO, CPAF-AP; SHEYLLA SUSAN MOREIRA DA SILVA DE ALMEIDA, Unifap. |
Título: |
A potencialidade da produção de mangabeiras (Hancornia speciosa Gomes) para o desenvolvimento do Amapá: caracterizações físicas, físico-químicas e químicas. |
Ano de publicação: |
2018 |
Fonte/Imprenta: |
In: ENGINEERING, SCIENCE AND TECHNOLOGY CONFERENCE, 6th., 2017, Panama. Proceedings... Panama: Universidad Tecnologica de Panama, 2018. p. 48-60. |
ISBN: |
978-85-5707-303-6 |
Idioma: |
Português |
Conteúdo: |
O Estado do Amapá possui um quantitativo de recursos vegetais naturais expressivo, no entanto pouco explorado. Um desses recursos é a mangabeira (Hancornia speciosa Gomes), cujo plantio e exploração são ações viáveis para a região, com atrativo principalmente devido o seu potencial nutricional, vitamínico e econômico, podendo representar uma alternativa de renda para as famílias que utilizam os meios de agricultura como forma de subsistência. Informações estas que podem ser obtidas nas progênies da coleção de trabalho da EMBRAPA AMAPÁ, onde existem plantas procedentes da Paraíba e nativas do Amapá. |
Thesagro: |
Cadeia produtiva; Conservação; Fruta tropical; Plantio. |
Categoria do assunto: |
K Ciência Florestal e Produtos de Origem Vegetal |
URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/item/186693/1/CPAF-AP-2018-A-potencialidade-da-producao-de-mangabeiras.pdf
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Marc: |
LEADER 01395nam a2200193 a 4500 001 2099823 005 2023-06-16 008 2018 bl uuuu u00u1 u #d 020 $a978-85-5707-303-6 100 1 $aTOMAZI, R. 245 $aA potencialidade da produção de mangabeiras (Hancornia speciosa Gomes) para o desenvolvimento do Amapá$bcaracterizações físicas, físico-químicas e químicas.$h[electronic resource] 260 $aIn: ENGINEERING, SCIENCE AND TECHNOLOGY CONFERENCE, 6th., 2017, Panama. Proceedings... Panama: Universidad Tecnologica de Panama, 2018. p. 48-60.$c2018 520 $aO Estado do Amapá possui um quantitativo de recursos vegetais naturais expressivo, no entanto pouco explorado. Um desses recursos é a mangabeira (Hancornia speciosa Gomes), cujo plantio e exploração são ações viáveis para a região, com atrativo principalmente devido o seu potencial nutricional, vitamínico e econômico, podendo representar uma alternativa de renda para as famílias que utilizam os meios de agricultura como forma de subsistência. Informações estas que podem ser obtidas nas progênies da coleção de trabalho da EMBRAPA AMAPÁ, onde existem plantas procedentes da Paraíba e nativas do Amapá. 650 $aCadeia produtiva 650 $aConservação 650 $aFruta tropical 650 $aPlantio 700 1 $aYOKOMIZO, G. K. I. 700 1 $aALMEIDA, S. S. M. da S. de
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Embrapa Amapá (CPAF-AP) |
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Registro Completo
Biblioteca(s): |
Embrapa Soja. |
Data corrente: |
02/12/2005 |
Data da última atualização: |
21/08/2009 |
Autoria: |
BELINTANI, P.; GASPAR, J. O.; ALMEIDA, A. M. R. |
Título: |
Sequencing of the triple gene block of Cole latent virus. |
Ano de publicação: |
2005 |
Fonte/Imprenta: |
Virus Reviews & Research, Rio de Janeiro, v. 10, p. 142, Nov. 2005. Supplement, ref. P-197. |
Idioma: |
Inglês |
Notas: |
Edição dos Resumos da XVI National Meeting of Virology, nov. 2005. |
Conteúdo: |
Cole latent virus (ColLV) was first detected in Brassica oleracea var. acephala in São Paulo State, Brazil. The virus is transmitted mechanically and also inefficiently in a non-psersistent manner by Myzus persicae. Some molecular properties os CoLV has been determined (Belintani et al. J. Phytpathol. 150:330-333, 2002). and the coat protein gene sequenced (Belintani et al. GeneBank AY340584). As a consequence, recently the virus was designate as a definitive species in the genus (Carlavirus by the International Committee on Taxanomy of Viruses (Mayo. Arch. Virol. 150:189-198, 2005). Here, we describe the sequencing of the Triple Gene Block (TGB) of Cole latent virus. The RNA was extracted from purified virus particles and used to generate genomic library, making use of the Universal RiboClone cDNA Synthesis System (Promega). Several overlapping clones were generated and their nucleotide sequences were determined in both strands and analyzed by the BLAST program. Sequences of carlaviruses for comparisons were obtained from the GeneBank Database. The sequence of the TGB showed three overlapping ORFs predicting proteins of 25K, 12K and 7 K, an organization conserved among carlaviruses and potexviruses. The 25K and 12K proteins share amino acids identity of 50-66% with Hop latent virus AB032469), Potato virus M(AF023877), Aconitum latent virus (AB56118) and Potato virus S (D00461). The 7 K protein showed amino acids identity of 24-40% with the same viruses. However, the Cole latent virus coat protein gene has a higher identity with Potato virus M (Belintani et al. Fitopatol. Bras. 28:288, 2003). and probably they are closely related viruses yet distinct. Our results support the classification of CoLV as a distinct species of the Carlavirus genus. MenosCole latent virus (ColLV) was first detected in Brassica oleracea var. acephala in São Paulo State, Brazil. The virus is transmitted mechanically and also inefficiently in a non-psersistent manner by Myzus persicae. Some molecular properties os CoLV has been determined (Belintani et al. J. Phytpathol. 150:330-333, 2002). and the coat protein gene sequenced (Belintani et al. GeneBank AY340584). As a consequence, recently the virus was designate as a definitive species in the genus (Carlavirus by the International Committee on Taxanomy of Viruses (Mayo. Arch. Virol. 150:189-198, 2005). Here, we describe the sequencing of the Triple Gene Block (TGB) of Cole latent virus. The RNA was extracted from purified virus particles and used to generate genomic library, making use of the Universal RiboClone cDNA Synthesis System (Promega). Several overlapping clones were generated and their nucleotide sequences were determined in both strands and analyzed by the BLAST program. Sequences of carlaviruses for comparisons were obtained from the GeneBank Database. The sequence of the TGB showed three overlapping ORFs predicting proteins of 25K, 12K and 7 K, an organization conserved among carlaviruses and potexviruses. The 25K and 12K proteins share amino acids identity of 50-66% with Hop latent virus AB032469), Potato virus M(AF023877), Aconitum latent virus (AB56118) and Potato virus S (D00461). The 7 K protein showed amino acids identity of 24-40% with the same viruses. However, the Cole la... Mostrar Tudo |
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Marc: |
LEADER 02295naa a2200157 a 4500 001 1468610 005 2009-08-21 008 2005 bl --- 0-- u #d 100 1 $aBELINTANI, P. 245 $aSequencing of the triple gene block of Cole latent virus. 260 $c2005 500 $aEdição dos Resumos da XVI National Meeting of Virology, nov. 2005. 520 $aCole latent virus (ColLV) was first detected in Brassica oleracea var. acephala in São Paulo State, Brazil. The virus is transmitted mechanically and also inefficiently in a non-psersistent manner by Myzus persicae. Some molecular properties os CoLV has been determined (Belintani et al. J. Phytpathol. 150:330-333, 2002). and the coat protein gene sequenced (Belintani et al. GeneBank AY340584). As a consequence, recently the virus was designate as a definitive species in the genus (Carlavirus by the International Committee on Taxanomy of Viruses (Mayo. Arch. Virol. 150:189-198, 2005). Here, we describe the sequencing of the Triple Gene Block (TGB) of Cole latent virus. The RNA was extracted from purified virus particles and used to generate genomic library, making use of the Universal RiboClone cDNA Synthesis System (Promega). Several overlapping clones were generated and their nucleotide sequences were determined in both strands and analyzed by the BLAST program. Sequences of carlaviruses for comparisons were obtained from the GeneBank Database. The sequence of the TGB showed three overlapping ORFs predicting proteins of 25K, 12K and 7 K, an organization conserved among carlaviruses and potexviruses. The 25K and 12K proteins share amino acids identity of 50-66% with Hop latent virus AB032469), Potato virus M(AF023877), Aconitum latent virus (AB56118) and Potato virus S (D00461). The 7 K protein showed amino acids identity of 24-40% with the same viruses. However, the Cole latent virus coat protein gene has a higher identity with Potato virus M (Belintani et al. Fitopatol. Bras. 28:288, 2003). and probably they are closely related viruses yet distinct. Our results support the classification of CoLV as a distinct species of the Carlavirus genus. 700 1 $aGASPAR, J. O. 700 1 $aALMEIDA, A. M. R. 773 $tVirus Reviews & Research, Rio de Janeiro$gv. 10, p. 142, Nov. 2005. Supplement, ref. P-197.
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