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1.
J Appl Microbiol ; 123(4): 861-874, 2017 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-28792661

RESUMO

AIMS: To evaluate the antibiofilm potential of water-soluble Moringa oleifera seed lectin (WSMoL) on Serratia marcescens and Bacillus sp. METHODS AND RESULTS: WSMoL inhibited biofilm formation by S. marcescens at concentrations lower than 2·6 µg ml-1 and impaired bacterial growth at higher concentrations, avoiding biofilm formation. For Bacillus sp., the lectin inhibited bacterial growth at all concentrations. The antibiofilm action of WSMoL is associated with damage to bacterial cells. WSMoL did not disrupt preformed S. marcescens biofilms but was able to damage cells inside them. On the other hand, the lectin reduced the number of cells in Bacillus sp. biofilm treated with it. WSMoL was able to control biofilm formation when immobilized on glass surface (116 µg cm-2 ), damaging S. marcescens cells and avoiding adherence of Bacillus sp. cells on glass. The Bacillus sp. isolate is member of Bacillus subtilis species complex and closely related to species of the conspecific 'amyloliquefaciens' group. CONCLUSION: WSMoL prevented biofilm development by S. marcescens and Bacillus sp. and the antibiofilm effect is also observed when the lectin is immobilized on glass. SIGNIFICANCE AND IMPACT OF THE STUDY: Taking together, our results provide support to the potential use of WSMoL for controlling biofilm formation by bacteria.


Assuntos
Antibacterianos/farmacologia , Bacillus/efeitos dos fármacos , Biofilmes/efeitos dos fármacos , Lectinas/farmacologia , Moringa oleifera/química , Extratos Vegetais/farmacologia , Serratia marcescens/efeitos dos fármacos , Antibacterianos/isolamento & purificação , Bacillus/fisiologia , Lectinas/isolamento & purificação , Extratos Vegetais/isolamento & purificação , Sementes/química , Serratia marcescens/fisiologia
2.
Genet Mol Res ; 14(3): 8181-200, 2015 Jul 27.
Artigo em Inglês | MEDLINE | ID: mdl-26345744

RESUMO

Gene expression related to drought response in the leaf tissues of two Brazilian upland cultivars, the drought-tolerant Douradão and the drought-sensitive Primavera, was analyzed. RNA-seq identified 27,618 transcripts in the Douradão cultivar, with 24,090 (87.2%) homologous to the rice database, and 27,221 transcripts in the Primavera cultivar, with 23,663 (86.9%) homologous to the rice database. Gene-expression analysis between control and water-deficient treatments revealed 493 and 1154 differentially expressed genes in Douradão and Primavera cultivars, respectively. Genes exclusively expressed under drought were identified for Douradão, including two genes of particular interest coding for the protein peroxidase precursor, which is involved in three distinct metabolic pathways. Comparisons between the two drought-exposed cultivars revealed 2314 genes were differentially expressed (978 upregulated, 1336 downregulated in Douradão). Six genes distributed across 4 different transcription factor families (bHLH, MYB, NAC, and WRKY) were identified, all of which were upregulated in Douradão compared to Primavera during drought. Most of the genes identified in Douradão activate metabolic pathways responsible for production of secondary metabolites and genes coding for enzymatically active signaling receptors. Quantitative PCR validation showed that most gene expression was in agreement with computational prediction of these transcripts. The transcripts identified here will define molecular markers for identification of Cis-acting elements to search for allelic variants of these genes through analysis of polymorphic SNPs in GenBank accessions of upland rice, aiming to develop cultivars with the best combination of these alleles, resulting in materials with high yield potential in the event of drought during the reproductive phase.


Assuntos
Adaptação Fisiológica/genética , Secas , Ecótipo , Regulação da Expressão Gênica de Plantas , Genes de Plantas , Oryza/genética , Oryza/fisiologia , Clima Tropical , Sequência de Bases , Regulação para Baixo/genética , Perfilação da Expressão Gênica , Ontologia Genética , Redes e Vias Metabólicas/genética , Anotação de Sequência Molecular , Folhas de Planta/genética , Reação em Cadeia da Polimerase em Tempo Real , Reprodutibilidade dos Testes , Análise de Sequência de RNA , Estresse Fisiológico/genética , Fatores de Transcrição/metabolismo , Regulação para Cima/genética
3.
Lett Appl Microbiol ; 48(5): 611-7, 2009 May.
Artigo em Inglês | MEDLINE | ID: mdl-19291207

RESUMO

AIMS: To develop a polymerase chain reaction (PCR)-based approach for the detection of nifH gene-containing Paenibacillus in environmental samples. METHODS AND RESULTS: The primers, nifHPAENf and nifHPAENr, were designed and tested with DNA from: (i) strains of different nitrogen-fixing Paenibacillus species, (ii) strains of other nitrogen-fixing genera and (iii) rhizosphere of sorghum sown in Cerrado soil amended with either 12 or 120 kg ha(-1) of nitrogen fertilizer. All nitrogen-fixing Paenibacillus strains tested and the DNA samples from rhizosphere soil were amplified when these primers were used, generating a 280 bp fragment. When the PCR products obtained from both sorghum rhizospheres were cloned and sequenced, the majority of the clones analysed could be identified as Paenibacillus durus. Moreover, a greater diversity in the nifH sequences could be observed in the rhizosphere treated with a high amount of nitrogen fertilizer. CONCLUSIONS: Nitrogen fertilization slightly influenced the structure of the nifH gene-containing Paenibacillus community in sorghum rhizospheres cultivated in Cerrado soil. SIGNIFICANCE AND IMPACT OF THE STUDY: The PCR detection method developed is adequate to assess the presence of nifH gene-containing Paenibacillus in the environment and can be used in future to determine the ecological role of this group of micro-organisms for the nitrogen input to the plants.


Assuntos
Bactérias/genética , Bactérias/isolamento & purificação , Proteínas de Bactérias/genética , Oxirredutases/genética , Raízes de Plantas/microbiologia , Microbiologia do Solo , Sorghum/microbiologia , Bactérias/enzimologia , Biodiversidade , Dados de Sequência Molecular
4.
Genet Mol Res ; 7(2): 498-508, 2008.
Artigo em Inglês | MEDLINE | ID: mdl-18561383

RESUMO

The texture of corn grains is a fundamental characteristic for the industry as well as for grain producers and processors. To further understand the mechanisms involved in grain hardness, contrasting corn cultivars for grain hardness and protein quality were evaluated. The cultivars were Cateto L237/67 (hard endosperm and low protein value), QPM BR 451 (semi-hard endosperm and high protein value); Bolivia-2 (floury endosperm and low protein value), and Opaque-2 (floury endosperm and high protein value). Evaluations were carried out at 10, 20, 30, 40, 50, and 60 days after pollination in developing corn grains and in the mature grain. In developing grains, evaluation consisted in the determination of the area, percentage of starch granules, distribution of starch granules, and protein bodies in the endosperm. In mature corn grains, the parameters evaluated were: density, percentage of total proteins, levels of lysine and tryptophan, and banding pattern of zeins. The results indicate that the higher physical resistance of corn grains from the cultivars analyzed is influenced by the high percentage of total proteins, high synthesis of 27-kDa zeins, presence of protein bodies, and perfect organization of starch granules in the endosperm, independent of their sizes.


Assuntos
Grão Comestível/metabolismo , Zea mays/metabolismo , Proteínas de Ligação a DNA/metabolismo , Grão Comestível/crescimento & desenvolvimento , Grão Comestível/normas , Peso Molecular , Proteínas de Plantas/metabolismo , Sementes/metabolismo , Amido/metabolismo , Fatores de Transcrição/metabolismo , Zea mays/crescimento & desenvolvimento , Zea mays/normas , Zeína/química , Zeína/metabolismo
5.
Genet. mol. res. (Online) ; 7(2): 498-508, 2008. tab, ilus
Artigo em Inglês | LILACS | ID: lil-640988

RESUMO

The texture of corn grains is a fundamental characteristic for the industry as well as for grain producers and processors. To further understand the mechanisms involved in grain hardness, contrasting corn cultivars for grain hardness and protein quality were evaluated. The cultivars were Cateto L237/67 (hard endosperm and low protein value), QPM BR 451 (semi-hard endosperm and high protein value); Bolivia-2 (floury endosperm and low protein value), and Opaque-2 (floury endosperm and high protein value). Evaluations were carried out at 10, 20, 30, 40, 50, and 60 days after pollination in developing corn grains and in the mature grain. In developing grains, evaluation consisted in the determination of the area, percentage of starch granules, distribution of starch granules, and protein bodies in the endosperm. In mature corn grains, the parameters evaluated were: density, percentage of total proteins, levels of lysine and tryptophan, and banding pattern of zeins. The results indicate that the higher physical resistance of corn grains from the cultivars analyzed is influenced by the high percentage of total proteins, high synthesis of 27-kDa zeins, presence of protein bodies, and perfect organization of starch granules in the endosperm, independent of their sizes.


Assuntos
Grão Comestível/metabolismo , Zea mays/metabolismo , Amido/metabolismo , Grão Comestível/crescimento & desenvolvimento , Grão Comestível/normas , Fatores de Transcrição/metabolismo , Peso Molecular , Proteínas de Plantas , Proteínas de Ligação a DNA/metabolismo , Sementes/metabolismo , Zea mays/crescimento & desenvolvimento , Zea mays/normas , Zeína/metabolismo , Zeína/química
6.
Proc Natl Acad Sci U S A ; 96(7): 4180-5, 1999 Mar 30.
Artigo em Inglês | MEDLINE | ID: mdl-10097184

RESUMO

We report the characterization of a maize Wee1 homologue and its expression in developing endosperm. Using a 0.8-kb cDNA from an expressed sequence tag project, we isolated a 1.6-kb cDNA (ZmWee1), which encodes a protein of 403 aa with a calculated molecular size of 45.6 kDa. The deduced amino acid sequence shows 50% identity to the protein kinase domain of human Wee1. Overexpression of ZmWee1 in Schizosaccharomyces pombe inhibited cell division and caused the cells to enlarge significantly. Recombinant ZmWee1 obtained from Escherichia coli is able to inhibit the activity of p13(suc1)-adsorbed cyclin-dependent kinase from maize. ZmWee1 is encoded by a single gene at a locus on the long arm of chromosome 4. RNA gel blots showed the ZmWee1 transcript is about 2.4 kb in length and that its abundance reaches a maximum 15 days after pollination in endosperm tissue. High levels of expression of ZmWee1 at this stage of endosperm development imply that ZmWee1 plays a role in endoreduplication. Our results show that control of cyclin-dependent kinase activity by Wee1 is conserved among eukaryotes, from fungi to animals and plants.


Assuntos
Proteínas de Ciclo Celular , Proteínas Tirosina Quinases/genética , Proteínas Tirosina Quinases/metabolismo , Zea mays/fisiologia , Sequência de Aminoácidos , Animais , Sequência de Bases , Clonagem Molecular , Drosophila , Escherichia coli , Etiquetas de Sequências Expressas , Regulação da Expressão Gênica de Plantas , Humanos , Dados de Sequência Molecular , Proteínas Nucleares/química , Proteínas Nucleares/genética , Proteínas Nucleares/metabolismo , Filogenia , Proteínas Tirosina Quinases/química , Proteínas Recombinantes/biossíntese , Proteínas Recombinantes/química , Proteínas Recombinantes/metabolismo , Schizosaccharomyces , Proteínas de Schizosaccharomyces pombe , Transcrição Gênica , Zea mays/genética , Zea mays/crescimento & desenvolvimento
7.
Plant Mol Biol ; 41(6): 801-13, 1999 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-10737145

RESUMO

eEF1A appears to be a multifunctional protein in eukaryotes, where it serves as a protein synthesis factor as well as a cytoskeletal protein. In maize endosperm, the eEF1A concentration is highly correlated with lysine content, and eEF1A synthesis is increased in opaque2 mutants compared to wild type. To investigate the basis for the increased synthesis of eEF1A in opaque2, we characterized the genes encoding this protein and measured their relative level of expression in endosperm and other tissues. Maize contains 10 to 15 eEF1A genes that are nearly identical in nucleotide and amino acid sequences. However, these genes can be distinguished based on their 3' non-coding sequences, which are less conserved. By screening endosperm and seedling cDNA libraries, we show that most of the maize eEF1A genes are expressed, and the relative level of their transcripts varies in different tissues. At least five genes are transcribed in the endosperm, and two account for ca. 80% of the RNA transcripts. The expression of several genes is enhanced in opaque2 endosperm, although the significance of this is unclear.


Assuntos
Fator 1 de Elongação de Peptídeos/genética , Sementes/genética , Zea mays/genética , Sequência de Aminoácidos , Sequência de Bases , DNA Complementar/química , DNA Complementar/genética , DNA de Plantas/genética , Dosagem de Genes , Regulação da Expressão Gênica no Desenvolvimento , Regulação da Expressão Gênica de Plantas , Dados de Sequência Molecular , Plantas/genética , RNA de Plantas/genética , RNA de Plantas/metabolismo , Alinhamento de Sequência , Análise de Sequência de DNA , Homologia de Sequência de Aminoácidos , Homologia de Sequência do Ácido Nucleico , Distribuição Tecidual , Zea mays/crescimento & desenvolvimento
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