Recuperação do nitrogênio da mistura de uréia e sulfato de amônio por plantas do milho

A mistura de uréia com fertilizantes de características ácidas aplicada ao solo pode aumentar a concentração de íons H+ próximos do grânulo e promover a redução da perda de N por volatilização. O experimento foi desenvolvido em vasos com 15 kg de Latossolo Vermelho textura média, sob túnel plástico, em Botucatu (SP), nos quais foram crescidas plantas de milho (duas plantas por vaso) até o pendoamento (66 dias após a emergência - DAE). Como tratamentos foi realizada a adubação (100 mg dm-3 N), no estádio de cinco folhas (30 DAE) utilizando os seguintes fertilizantes ou misturas físicas: (1) uréia (UR), enriquecida com 15N; (2) sulfato de amônio (SA), enriquecido com 15N; (3) sulfnitro (80% de N-UR e 20% de N-SA no mesmo grânulo); (4) mistura de UR (80% N) e SA (20% N e enriquecido com 15N); (5) mistura de UR (50% N) e SA (50% N), enriquecidos com 15N; (6) mistura de UR (50% N) e SA (50% N e enriquecido com 15N), (7) mistura de UR (50% N) e SA (50% N), enriquecido com 15N, diluídos em água (solução contendo 3% de N) e mais um tratamento que não recebeu N. A mistura de UR e SA não promoveu aumento na recuperação do N da uréia na planta de milho. do total de 15N-fertilizante aplicado, aproximadamente, 67% foram recuperados pela planta de milho (29% nas folhas, 25% no caule e 13% nas raízes) e 6% no solo, com uma perda estimada de 27%. O 15N da uréia foi recuperado em menor quantidade no caule em relação ao N do sulfato de amônio.

Production and action pattern of inulinase from Aspergillus Niger-245: hydrolysis of inulin from several sources

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

Purification and characterization of β-Fructosidase with inulinase activity from Aspergillus niger - 245

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

Fontes e doses de nitrogênio em cobertura no feijoeiro de inverno irrigado no sistema plantio direto

The common bean is a leguminous of great importance in the Brazilian economy and nitrogen is the taken up nutrient in larger amount. Nitrogen fertilization management is of extreme importance to offer larger economical viability, besides increasing the efficiency of plant in the use of the available resources. The objective this study was to evaluate the effect of sources and doses of sidedressing nitrogen in the development and yield of winter common bean in no tillage system, as well as evaluate its economical viability. A randomized blocks design was used, in a factorial scheme 3x3 with 9 treatments constituted by three sources of nitrogen (ammonium sulphate, urea and ammonium sulphate 1/2 of N + urea 1/2 of N, applied at V(4-3) stadium) and different doses of sidedressing nitrogen (0, 40, 80 kg ha(-1)) in four replications. The study was conducted in Selviria county, MS State in 2004 in no season crop period, in a dystrophic Haplustox soil. The conclusion: independent of nitrogen source, nitrogen fertilization increasing provides increment in yield of winter common bean up to dose 80 kg/ha, and this provides, on average, an increase of 20% in yield compared with control (without sidedressing nitrogen). The urea is the nitrogen source of larger economical efficiency.

Fontes, doses e modo de aplicação de nitrogênio em feijoeiro no sistema plantio direto

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

The Use of Response Surface Methodology in Optimization of Lactic Acid Production: Focus on Medium Supplementation, Temperature and pH Control

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

Purification and properties of an acid beta-xylosidase from Penicillium sclerotiorum

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

Purification and Characterization of the alpha-Glucosidase Produced by Thermophilic Fungus Thermoascus aurantiacus CBMAI 756

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

Very high gravity sucrose fermentation by Brazilian industrial yeast strains: effect of nitrogen supplementation

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

Kinetic aspects of rat (Rattus-norvegicus albinus) submandibular glands lactic-dehydrogenase

Submandibular glands of male rats were homogenized with 33 mM sodium potassium phosphate buffer, pH 6.5, containing 1 mM MgCl2 and 0.1 mM DTT and purified with ammonium sulphate, phosphocellulose chromatography, eluted with KC1 0.5 M, followed by Blue Sepharose CL-6B chromatography, eluted with NADH 0.5 mM. The enzyme kepts stable for 60 days when stored at -15-degrees-C in 33 mM phosphate buffer. In other experiment the enzyme was purified by oxamate-agarose chromatography from a crude extract of submandibular gland and the results obtained were better than by phosphocellulose and Sepharose CL-6B chromatography. The Km values for pyruvate. NADH, lactate and NAD+ were established. Sodium oxamate at 0.1 and 0.9 mM concentrations inhibited the LDH activity by 40 and 85%, respectively (competitive); with sodium oxalate the inhibition was of 30% (uncompetitive) and with 3-acetyl pyridine adenine dinucleotide was 80%.

Qualidade da água para a irrigação de plantas em viveiros: utilização de descargas elétricas sem efeito térmico e de campos de energia no controle de Meloidogyne incognita Raça 1

The effect of electrical discharges without thermic effect and of energy field on Meloidogyne incognita Rara 1 larvae elimination in weir water was tested. on an average, 63,22% of larvae were killed by electrical discharges, in comparison with 53,12% of dead larvae in the control (water that received only ammonium sulphate) as an electrolyte. Water exposed to energy fields presented higher percentages of dead larvae (50,01% for electromagnetic field, 43,78% for variable electric field and 40,48% for static electric field) in comparison with control, represented by water without exposition to any energy field and without ammonium sulphate (34,27%).

Partial purification, heat stability and kinetic characterization of the pectinmethylesterase from Brazilian guava, Paluma cultivars

Pectinmethylesterase (PME) was extracted from guava fruit (Psidium guajava L.), cultivar Paluma, by 70% ammonium sulphate saturation and partially purified by gel filtration on Sephadex G100. Gel filtration showed PME isoenzymes with different values of molecular mass. Two samples were examined: concPME (70% saturation by ammonium sulphate) and Iso4 PME (one of the isoforms from gel filtration with the greatest specific activity). Optimum pH of the enzyme (for both samples) was 8.5 and optimum temperature ranged from 75 and 85 degrees C. The optimum sodium chloride concentration was 0.15 M. The K-M and V-max ranged from 0.32 to 0.23 mg m1(-1) and 244 to 53.2 mu mol/min, respectively, for concPME and Iso4PME. The activation energies (E-a) were 64.5 and 103 kJ/mol, respectively, for concPME and Iso4PME. Guava PME, cv Paluma, is a very thermostable enzyme, showing great heat stability at all temperatures studied. (c) 2005 Elsevier Ltd. All rights reserved.

Purification and characterization of beta-fructosidase with inulinase activity from Aspergillus niger-245

Aspergillus niger - 245 a strain isolated from soil samples showed good beta -fructosidase activity when inoculated in medium formulated with dahlia extract tubers. The enzyme was purified by precipitation in ammonium sulphate and percolated in DEAE-Sephadex A-50 and CM-cellulose columns, witch showed a single peack in all the purification steps, maintaining the I/S ratio between 0.32 to, 0.39. Optimum pH for inulinase activity (I) was between 4.0 - 4.5 and for invertase activity (S) between 2.5 and 50. The optimum temperature was 60 degrees .C for both activities and no loss in activity was observed when it was maintained at this temperature for 30 min. The K-m value was 1.44 and 5.0 respectively, for I and S and V-m value 10.48 and 30.55 respectively. The I activity was strongly inhibited by Hg2+ and Ag+ and 2 x 10(-3) M of glucose, but not by fructose at the same concentration. The enzyme showed an exo-action mechanism acting on the inulin of different origins. In assay conditions total hydrolysis of all the frutans was obtained although it has shown larger activity on the chicory inulin than that one from artichoke Jerusalem and dahlia, in the first 30 min. The obtained results suggested that the enzyme presented good potential for industrial application in the preparing the fructose syrups.

Properties of a polynucleotide synthesized by strain 74a of Neurospora crassa

A polynucleotide (or a fragment of RNA) was purified to apparent homogeneity by HPLC from mycelium of the wild strain 74A of the mould Neurospora crassa, after growth on sucrose and in the presence of saturating amounts of inorganic phosphate (Pi) for 72 hr at 30 degrees. The M(r) was ca 20000 as determined by HPLC at pH 6.8. Polynucleotide synthesis ranged from 4.0 to 6.5 mu g polynucleotide per mg dry mycelium in mycelium of the wild strain 74A and the various phosphorus regulatory and structural mutant strains of the mould N. crassa. Kinetic data showed that the polynucleotide interacts with mycelial Pi-repressible alkaline phosphatase by inhibiting its p-nitrophenylphosphatase activity and by protecting the enzyme against thermal inactivation in the presence of high concentrations of ammonium sulphate.

Soluble and bound peroxidases from papaya fruit

Soluble and bound peroxidases were isolated from the pulp of ripening papaya fruit. During papaya ripening, soluble and bound peroxidase activities increased 2.5- and 4.2-fold, respectively. Soluble peroxidase was purified 59-fold by ammonium sulphate precipitation and chromatography on Sephadex G-25, DEAE-cellulose and Sephadex G-100. Bound peroxidase was purified 140-fold by ammonium sulphate precipitation and chromatography on Sephadex G-100 and DEAE-cellulose. Polyacrylamide gel electrophoresis of the purified preparations revealed that both enzymes were highly purified by the procedures adopted. The soluble and bound forms had a Mr of 41 000 and 54 000, respectively. Soluble and bound peroxidases showed optimum activity at pH 6.0 and 5.5, respectively, and were inhibited by p-chloromercuribenzoate, iodoacetamide, N-ethylmaleimide, potassium cyanide and Fe2+. Soluble peroxidase was activated by ammonium sulphate and this activation was prevented by cyanide. © 1990.