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Registro Completo |
Biblioteca(s): |
Embrapa Florestas. |
Data corrente: |
09/02/2022 |
Data da última atualização: |
24/02/2022 |
Autoria: |
CARVALHO, P. E. R. |
Afiliação: |
PAULO ERNANI RAMALHO CARVALHO, CNPF. |
Título: |
Braúna-preta: Melanoxylon brauna. |
Ano de publicação: |
2010 |
Fonte/Imprenta: |
In: CARVALHO, P. E. R. Espécies arbóreas brasileiras. Brasília, DF: Embrapa Informação Tecnológica; Colombo: Embrapa Florestas, 2010. v. 4, p. 87-94. |
Série: |
(Coleção espécies arbóreas brasileiras, v. 4). |
Idioma: |
Português |
Conteúdo: |
NOMES VULGARES POR UNIDADES DA FEDERAÇÃO: na Bahia, baraúna-preta, baraúna-verdadeira, braúna, braúna-da-mata, braúna-parda, braúna-preta, coração-de-negro e pau-ferro; no Espírito Santo, braúna-parda, braúna-preta, graúna e maria-preta; em Goiás, braúma; no Paraná, brauna; no Estado do Rio de Janeiro, baraúna, braúna e graúna. NOTA: nos seguintes nomes vulgares, não foi encontrada a devida correspondência com as Unidades da Federação: árvore-da-chuva, baraúna, baraúna-parda, canela-amarela, garaúna, guaraúna, guiraúna, ibiraúna, ibiráuva, maria-preta-da- mata, maria-preta-do-campo, muiraúna, paravoúna, rabo-de- macaco. |
Palavras-Chave: |
Descrição; Ocorrência; Uso. |
Thesagro: |
Brauna Preta; Crescimento; Espécie Nativa; Madeira; Melanoxylon Brauna; Nomenclatura; Taxonomia. |
Categoria do assunto: |
K Ciência Florestal e Produtos de Origem Vegetal |
URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/item/231893/1/Especies-Arboreas-Brasileiras-vol-4-Brauna-Preta.pdf
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Marc: |
LEADER 01426naa a2200253 a 4500 001 2139836 005 2022-02-24 008 2010 bl uuuu u00u1 u #d 100 1 $aCARVALHO, P. E. R. 245 $aBraúna-preta$bMelanoxylon brauna. 260 $c2010 490 $a(Coleção espécies arbóreas brasileiras, v. 4). 520 $aNOMES VULGARES POR UNIDADES DA FEDERAÇÃO: na Bahia, baraúna-preta, baraúna-verdadeira, braúna, braúna-da-mata, braúna-parda, braúna-preta, coração-de-negro e pau-ferro; no Espírito Santo, braúna-parda, braúna-preta, graúna e maria-preta; em Goiás, braúma; no Paraná, brauna; no Estado do Rio de Janeiro, baraúna, braúna e graúna. NOTA: nos seguintes nomes vulgares, não foi encontrada a devida correspondência com as Unidades da Federação: árvore-da-chuva, baraúna, baraúna-parda, canela-amarela, garaúna, guaraúna, guiraúna, ibiraúna, ibiráuva, maria-preta-da- mata, maria-preta-do-campo, muiraúna, paravoúna, rabo-de- macaco. 650 $aBrauna Preta 650 $aCrescimento 650 $aEspécie Nativa 650 $aMadeira 650 $aMelanoxylon Brauna 650 $aNomenclatura 650 $aTaxonomia 653 $aDescrição 653 $aOcorrência 653 $aUso 773 $tIn: CARVALHO, P. E. R. Espécies arbóreas brasileiras. Brasília, DF: Embrapa Informação Tecnológica; Colombo: Embrapa Florestas, 2010.$gv. 4, p. 87-94.
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Registro original: |
Embrapa Florestas (CNPF) |
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Biblioteca(s): |
Embrapa Trigo. |
Data corrente: |
06/12/2021 |
Data da última atualização: |
06/12/2021 |
Tipo da produção científica: |
Artigo em Periódico Indexado |
Circulação/Nível: |
A - 1 |
Autoria: |
DIMKIĆ, I.; BHARDWAJ, V.; CARPENTIERI-PIPOLO, V.; KUZMANOVIĆ, N.; DEGRASSI, G. |
Afiliação: |
IVICA DIMKIĆ, Department of Biochemistry and Molecular Biology, University of Belgrade – Faculty of Biology, Belgrade, Serbia; VIBHA BHARDWAJ, Ras Al Khaimah Municipality Department, Director Environment Laboratories, Dubai, United Arab Emirate; VALERIA CARPENTIERI PIPOLO, CNPT; NEMANJA KUZMANOVIĆ, Federal Research Centre for Cultivated Plants (JKI), Institute for Plant Protection in Horticulture and Forests, Julius Ku¨ hn-Institut, Braunschweig, Germany; GIULIANO DEGRASSI, Industrial Biotechnology Group, International Centre for Genetic Engineering and Biotechnology (ICGEB), Buenos Aires, Argentina. |
Título: |
The chitinolytic activity of the Curtobacterium sp. isolated from field-grown soybean and analysis of its genome sequence. |
Ano de publicação: |
2021 |
Fonte/Imprenta: |
Plos One, v. 16, n.11, e0259465 Jan. 2021. |
DOI: |
https://doi.org/10.1371/journal. pone.0259465 |
Idioma: |
Inglês |
Conteúdo: |
Curtobacterium sp. GD1 was isolated from leaves of conventionally grown soybean in Brazil. It was noteworthy that among all bacteria previously isolated from the same origin, only Curtobacterium sp. GD1 showed a strong chitinase activity. The enzyme was secreted and its production was induced by the presence of colloidal chitin in the medium. The chitinase was partially purified and characterized: molecular weight was approximately 37 kDa and specific activity 90.8 U/mg. Furthermore, Curtobacterium sp. GD1 genome was sequenced and analyzed. Our isolate formed a phylogenetic cluster with four other Curtobacterium spp. strains, with ANIb/ANIm � 98%, representing a new, still non described Curtobacterium species. The circular genome visualization and comparison of genome sequences of strains forming new cluster indicated that most regions within their genomes were highly conserved. The gene associated with chitinase production was identified and the distribution pattern of glycosyl hydrolases genes was assessed. Also, genes associated with catabolism of structural carbohydrates such as oligosaccharides, mixed polysaccharides, plant and animal polysaccharides, as well as genes or gene clusters associated with resistance to antibiotics, toxic compounds and auxin biosynthesis subsystem products were identified. The abundance of putative glycosyl hydrolases in the genome of Curtobacterium sp. GD1 suggests that it has the tools for the hydrolysis of different polysaccharides. Therefore, Curtobacterium sp. GD1 isolated from soybean might be a bioremediator, biocontrol agent, an elicitor of the plant defense responses or simply degrader. MenosCurtobacterium sp. GD1 was isolated from leaves of conventionally grown soybean in Brazil. It was noteworthy that among all bacteria previously isolated from the same origin, only Curtobacterium sp. GD1 showed a strong chitinase activity. The enzyme was secreted and its production was induced by the presence of colloidal chitin in the medium. The chitinase was partially purified and characterized: molecular weight was approximately 37 kDa and specific activity 90.8 U/mg. Furthermore, Curtobacterium sp. GD1 genome was sequenced and analyzed. Our isolate formed a phylogenetic cluster with four other Curtobacterium spp. strains, with ANIb/ANIm � 98%, representing a new, still non described Curtobacterium species. The circular genome visualization and comparison of genome sequences of strains forming new cluster indicated that most regions within their genomes were highly conserved. The gene associated with chitinase production was identified and the distribution pattern of glycosyl hydrolases genes was assessed. Also, genes associated with catabolism of structural carbohydrates such as oligosaccharides, mixed polysaccharides, plant and animal polysaccharides, as well as genes or gene clusters associated with resistance to antibiotics, toxic compounds and auxin biosynthesis subsystem products were identified. The abundance of putative glycosyl hydrolases in the genome of Curtobacterium sp. GD1 suggests that it has the tools for the hydrolysis of different polysaccharides.... Mostrar Tudo |
Palavras-Chave: |
Curtobacterium sp; Enzyme; GD1. |
Thesaurus NAL: |
Soybeans. |
Categoria do assunto: |
F Plantas e Produtos de Origem Vegetal |
URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/item/228529/1/journal.pone.0259465-PLOSONE-2021.pdf
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Marc: |
LEADER 02369naa a2200229 a 4500 001 2137133 005 2021-12-06 008 2021 bl uuuu u00u1 u #d 024 7 $ahttps://doi.org/10.1371/journal. pone.0259465$2DOI 100 1 $aDIMKIĆ, I. 245 $aThe chitinolytic activity of the Curtobacterium sp. isolated from field-grown soybean and analysis of its genome sequence.$h[electronic resource] 260 $c2021 520 $aCurtobacterium sp. GD1 was isolated from leaves of conventionally grown soybean in Brazil. It was noteworthy that among all bacteria previously isolated from the same origin, only Curtobacterium sp. GD1 showed a strong chitinase activity. The enzyme was secreted and its production was induced by the presence of colloidal chitin in the medium. The chitinase was partially purified and characterized: molecular weight was approximately 37 kDa and specific activity 90.8 U/mg. Furthermore, Curtobacterium sp. GD1 genome was sequenced and analyzed. Our isolate formed a phylogenetic cluster with four other Curtobacterium spp. strains, with ANIb/ANIm � 98%, representing a new, still non described Curtobacterium species. The circular genome visualization and comparison of genome sequences of strains forming new cluster indicated that most regions within their genomes were highly conserved. The gene associated with chitinase production was identified and the distribution pattern of glycosyl hydrolases genes was assessed. Also, genes associated with catabolism of structural carbohydrates such as oligosaccharides, mixed polysaccharides, plant and animal polysaccharides, as well as genes or gene clusters associated with resistance to antibiotics, toxic compounds and auxin biosynthesis subsystem products were identified. The abundance of putative glycosyl hydrolases in the genome of Curtobacterium sp. GD1 suggests that it has the tools for the hydrolysis of different polysaccharides. Therefore, Curtobacterium sp. GD1 isolated from soybean might be a bioremediator, biocontrol agent, an elicitor of the plant defense responses or simply degrader. 650 $aSoybeans 653 $aCurtobacterium sp 653 $aEnzyme 653 $aGD1 700 1 $aBHARDWAJ, V. 700 1 $aCARPENTIERI-PIPOLO, V. 700 1 $aKUZMANOVIĆ, N. 700 1 $aDEGRASSI, G. 773 $tPlos One$gv. 16, n.11, e0259465 Jan. 2021.
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