Germinação e aspectos morfológicos de sementes de Archontophoenix cunninghamii H. Wendl. & Drude (Arecaceae)

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

Bases fisiológicas para a conservação a longo prazo de sementes Cariniana legalis (Mart.) O. Kuntze

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

Teste de tetrazólio para avaliação da qualidade de sementes de Tabebuia roseoalba (Ridl.) Sandwith - bignoniaceae, submetidas ao armazenamento

The species of Tabebuia are propagated sexually, and the use of high-quality seeds is crucial to achieving success in restoration of degraded areas, timber and medicinal production. Thus, the use of rapid tests in programs to control seed quality is an essential tool for the assessment of their physiological quality. The objectives of the present study were to establish the methodology for conducting the tetrazolium test in seeds of T. roseoalba and verify seed viability as a function of storage time, evaluating germination parameters and comparing them with the results of the tetrazolium test. The fruits were manually harvested at the opening, and fresh seeds and seeds stored up to 24 months were evaluated by tetrazolium test, germination, emergence, length and dry weight of seedlings. The tetrazolium at a concentration of 0.05% at 36 ° C for 24 hours is indicated to assess the viability of T. roseoalba, and during storage germination, length and dry weight of the seedlings are reduced and the germination in nursery is sharply reduced with seed storage in 24 months.

Propagação do pinhão manso por estaquia, enxertia e sementes

Pós-graduação em Agronomia - FEIS

Viabilidade e longevidade de sementes de tabebuia aurea benth. & hook. submetidas a diferentes métodos de armazenamento

Seeds Tabebuia aurea (syn. Handroanthus aureus Mattos), The seeds of Tabebuia aurea (syn. Handroanthus Mattos aureus), have low metabolic rates, which favors their storage conditions and freezing temperatures when stored at room temperature, there is a progressive decline in viability. Therefore, this study aims to determine the viability and longevity of seeds of Tabebuia aurea subjected to different storage methods. There were used 6100 seeds. In 2400 seeds were stored refrigerator, which in 1200 placed in transparent plastic bag and 1200 in Kraft paper bags. 3600 Other seeds were placed in room temperature and 1200 seeds in clear plastic bag, 1200 in Kraft paper bags and tray open in 1200. For each treatment, four replicates of 25 seeds for 12 months, with design was completely randomized. The average germination, normal seedlings and speed germination index were transformed into (x+1)(-1/2). The data were submitted to ANOVA and means compared by Tukey test at 5%. Also regressions polynomials were modeled for the variables study in function of the periods of storage of the seeds. The seeds stored in the refrigerator at 13 C maintained a high germination rate and normal seedling germination rate during the 360 days of evaluation. The method suitable for the seed storage of Tabebuia aurea is in the refrigerator at 13 degrees C, both in plastic and paper.

Structure, organization, and expression of the alpha prolamin multigenic family bring new insights into the evolutionary relationships among grasses

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Crystal structure of mature 2S albumin from Moringa oleifera seeds

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Hypocholesterolaemic effect of rat-administered oral doses of the isolated 7S globulins from cowpeas and adzuki beans

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Structural insights regarding an insecticidal Talisia esculenta protein and its biotechnological potential for Diatraea saccharalis larval control

Talisin is a seed-storage protein from Talisia esculenta that presents lectin-like activities, as well as proteinase-inhibitor properties. The present study aims to provide new in vitro and in silico biochemical information about this protein, shedding some light on its mechanistic inhibitory strategies. A theoretical three-dimensional structure of Talisin bound to trypsin was constructed in order to determine the relative interaction mode. Since the structure of non-competitive inhibition has not been elucidated, Talisin-trypsin docking was carried out using Hex v5.1, since the structure of non-competitive inhibition has not been elucidated. The predicted non-coincidence of the trypsin binding site is completely different from that previously proposed for Kunitz-type inhibitors, which demonstrate a substitution of an Arg(64) for the Glu(64) residue. Data, therefore, provide more information regarding the mechanisms of non-competitive plant proteinase inhibitors. Bioassays with Talisin also presented a strong insecticide effect on the larval development of Diatraea saccharalis, demonstrating LD50 and ED50 of ca. 2.0% and 1.5%, respectively. (C) 2011 Elsevier Inc. All rights reserved.

Variación del peso de la semilla de Nim y sus componentes durante su almacenamiento

En el presente trabajo se muestran los resultados de las investigaciones realizadas en el Instituto de Investigaciones Fundamentales en Agricultura Tropical (INIFAT), acerca de la acción del almacenamiento sobre la semilla de Nim y sus componentes. Se pudo determinar que durante el proceso de beneficio de los frutos de Nim cosechados sólo una cuarta parte del volumen de los frutos se convierte en semillas, definiéndose además que el peso de un fruto maduro es de 1.8 g y de una semilla seca 0.4 g. Por otra parte, se pudo conocer que en el proceso de almacenamiento de la semilla seca de Nim se produce una disminución notable del peso de la misma y sus componentes (almendra, aceite, torta y residuo), dada por la influencia del tiempo de almacenamiento y factores ambientales tales como humedad relativa y temperatura. Además, se observó de igual forma, que la mayor pérdida de peso de la semilla se produjo durante los dos primeros meses de almacenadas, que incluyen el período de envejecimiento fisiológico.

Cultivares de Pisum Sativum L. : caracterización e identificación por electroforesis de proteínas seminales totales

Se realizó el estudio electroforético de proteínas seminales totales de 13 cultivares de arveja (Pisum sativum L.) en geles de poliacrilamida con Sodio Dodecil Sulfato. Se logró fraccionar 53 bandas proteicas, de las cuales 36 mostraron diferencias en sus movilidades. De esta manera se obtuvieron modelos electroforéticos diferentes para cada cultivar y mediante análisis de conglomerados (método UPGMA) se obtuvo un dendrograma que mostró la distinción entre cultivares en dicho carácter, permitiendo expresar las diferencias entre ellos.

A maize zinc-finger protein binds the prolamin box in zein gene promoters and interacts with the basic leucine zipper transcriptional activator Opaque2

The prolamin box (P-box) is a highly conserved 7-bp sequence element (5′-TGTAAAG-3′) found in the promoters of many cereal seed storage protein genes. Nuclear factors from maize endosperm specifically interact with the P-box present in maize prolamin genes (zeins). The presence of the P-box in all zein gene promoters suggests that interactions between endosperm DNA binding proteins and the P-box may play an important role in the coordinate activation of zein gene expression during endosperm development. We have cloned an endosperm-specific maize cDNA, named prolamin-box binding factor (PBF), that encodes a member of the recently described Dof class of plant Cys2-Cys2 zinc-finger DNA binding proteins. When tested in gel shift assays, PBF exhibits the same sequence-specific binding to the P-box as factors present in maize endosperm nuclei. Additionally, PBF interacts in vitro with the basic leucine zipper protein Opaque2, a known transcriptional activator of zein gene expression whose target site lies 20 bp downstream of the P-box in the 22-kDa zein gene promoter. The isolation of the PBF gene provides an essential tool to further investigate the functional role of the highly conserved P-box in regulating cereal storage protein gene expression.

Isolation and characterization of neutral-lipid-containing organelles and globuli-filled plastids from Brassica napus tapetum

The monolayer tapetum cells of the maturing flowers of Brassica napus contain abundant subcellular globuli-filled plastids and special lipid particles, both enriched with lipids that are supposed to be discharged and deposited onto the surface of adjacent maturing pollen. We separated the two organelles by flotation density gradient centrifugation and identified them by electron microscopy. The globuli-filled plastids had a morphology similar to those described in other plant species and tissues. They had an equilibrium density of 1.02 g/cm3 and contained neutral esters and unique polypeptides. The lipid particles contained patches of osmiophilic materials situated among densely packed vesicles and did not have an enclosing membrane. They exhibited osmotic properties, presumably exerted by the individual vesicles. They had an equilibrium density of 1.05 g/cm3 and possessed triacylglycerols and unique polypeptides. Several of these polypeptides were identified, by their N-terminal sequences or antibody cross-reactivity, as oleosins, proteins known to be associated with seed storage oil bodies. The morphological and biochemical characteristics of the lipid particles indicate that they are novel organelles in eukaryotes that have not been previously isolated and studied. After lysis of the tapetum cells at a late stage of floral development, only the major plastid neutral ester was recovered, whereas the other abundant lipids and proteins of the two tapetum organelles were present in fragmented forms or absent on the pollen surface.

3-Methylcrotonyl-Coenzyme A Carboxylase Is a Component of the Mitochondrial Leucine Catabolic Pathway in Plants1

3-Methylcrotonyl-coenzyme A carboxylase (MCCase) is a mitochondrial biotin-containing enzyme whose metabolic function is not well understood in plants. In soybean (Glycine max) seedlings the organ-specific and developmentally induced changes in MCCase expression are regulated by mechanisms that control the accumulation of MCCase mRNA and the activity of the enzyme. During soybean cotyledon development, when seed-storage proteins are degraded, leucine (Leu) accumulation peaks transiently at 8 d after planting. The coincidence between peak MCCase expression and the decline in Leu content provides correlative evidence that MCCase is involved in the mitochondrial catabolism of Leu. Direct evidence for this conclusion was obtained from radiotracer metabolic studies using extracts from isolated mitochondria. These experiments traced the metabolic fate of [U-14C]Leu and NaH14CO3, the latter of which was incorporated into methylglutaconyl-coenzyme A (CoA) via MCCase. These studies directly demonstrate that plant mitochondria can catabolize Leu via the following scheme: Leu → α-ketoisocaproate → isovaleryl-CoA → 3-methylcrotonyl-CoA → 3-methylglutaconyl-CoA → 3-hydroxy-3-methylglutaryl-CoA → acetoacetate + acetyl-CoA. These findings demonstrate for the first time, to our knowledge, that the enzymes responsible for Leu catabolism are present in plant mitochondria. We conclude that a primary metabolic role of MCCase in plants is the catabolism of Leu.

A novel cis-acting element, ESP, contributes to high-level endosperm-specific expression in an oat globulin promoter

To examine the genetic controls of endosperm (ES) specificity, several cereal seed storage protein (SSP) promoters were isolated and studied using a transient expression analysis system. An oat globulin promoter (AsGlo1) capable of driving strong ES-specific expression in barley and wheat was identified. Progressive 5' deletions and cis element mutations demonstrated that the mechanism of specificity in the AsGlo1 promoter was distinct from that observed in glutelin and prolamin promoters. A novel interrupted palindromic sequence, ACATGTCAT-CATGT, was required for ES specificity and substantially contributed to expression strength of the AsGlo1 promoter. This sequence was termed the endosperm specificity palindrome (ESP) element. The GCN4 element, which has previously been shown to be required for ES specificity in cereal SSP promoters, had a quantitative role but was not required for tissue specificity. The 960-bp AsGlo1 promoter and a 251-bp deletion containing the ESP element also drove ES-specific expression in stably transformed barley. Reporter gene protein accumulated at very high levels (10% of total soluble protein) in ES tissues of plants transformed with an AsGlo1:GFP construct. Expression strength and tissue specificity were maintained over five transgenic generations. These attributes make the AsGlo1 promoter an ideal promoter for biotechnology applications. In conjunction with previous findings, our data demonstrate that there is more than one genetically distinct mechanism by which ES specificity can be achieved in cereal SSP promoters, and also suggest that there is redundancy between transcriptional and post-transcriptional tissue specificity mechanisms in cereal globulin genes.