Avaliação de progênies de mamona (Ricinus communis L.) para produção e rendimento de semente em condições de safrinha no Estado de São Paulo.

Foi instalado um ensaio de avaliação de 73 progênies do Programa de Melhoramento de mamona do Instituto Agronômico para dias para florescimento dos racemos, produção de grãos e rendimento de grãos, em Campinas-SP, em fevereiro, e avaliado na safrinha de 2007, em blocos casualisados com três repetições, incluindo sete testemunhas comerciais. A análise de variância e a distribuição de médias para produção de grãos evidenciaram a larga variabilidade e o potencial dos materiais para o melhoramento. As progênies mais produtivas foram: PB72II com 804,07 g; PB05II com 755,20 g; TS38 com 716,13 g; PB08II com 714,67 g e PB48 com 698,00 g, e não foram melhores que a testemunha mais produtiva, IAC 2028 com 1019,67 g. Os rendimentos no processamento das sementes foram bastante variados e refletiram a ocorrência de déficits hídricos de severidade moderada, com alto número de sementes chochas ou não granadas. Os resultados mostraram o elevado potencial para o melhoramento do conjunto de progênies estudado e a possibilidade de plantio da cultura da mamona em condição de safrinha no Sudeste do Brasil.

Caracterização de progênies de mamona (Ricinus communis L.) para arquitetura de planta em condições de safrinha no Estado de São Paulo.

A arquitetura da mamoneira é bastante variável, constituída por caracteres que apresentam, geralmente, herança independente que se encontram distribuídos pelo germoplasma da espécie. Variações nos padrões de arquitetura das plantas de mamona possibilitam novas distribuições espaciais na implantação da cultura, viabilizando diferentes métodos de cultivo e novas épocas de semeadura para a espécie. Foi instalado um ensaio de avaliação com 73 progênies do Programa de Melhoramento de Mamona do Instituto Agronômico - IAC e sete materiais comerciais como testemunhas intercalares. O delineamento experimental foi em blocos casualisados com três repetições e as parcelas foram semeadas em fevereiro de 2007, em Campinas, SP. Foram avaliados os caracteres: altura da planta, altura do racemo primário, altura do racemo secundário, diâmetro do caule, número de entrenós e tamanho de entrenós. Os resultados da análise de variância e a distribuição de médias para os caracteres avaliados evidenciaram a larga variabilidade e o potencial dos materiais para o melhoramento, além da possibilidade de cultivo da mamona em condição de safrinha no Sudeste do Brasil.

Avaliação da arquitetura dos racemos e produção de progênies de mamona (Ricinus communis L.) em condições de safrinha no Estado de São Paulo.

Foi instalado um ensaio de avaliação com 73 progênies do Programa de Melhoramento de Mamona do Instituto Agronômico - IAC e sete materiais comerciais como testemunhas intercalares. O delineamento experimental foi em blocos casualisados com três repetições e as parcelas foram plantadas em fevereiro de 2007, em Campinas, SP. Foram avaliadas as características dos racemos primários e secundários: quanto ao comprimento (CRP e CRS, em centímetros), número de frutos (NFRP e NFRS), produção de grãos (PRP e PRS, em gramas) e rendimento no descascamento (RRP e RRS, em %) de cinco plantas de 73 progênies de mamona desenvolvidas pelo Programa de Melhoramento. Foram conduzidas análises de variâncias sendo as progênies separadas pelo grupo de seleção sendo 42 da seleção PBII, 15 da seleção PB e 16 da seleção TS. Embora as condições ambientais não favoráveis da safrinha tenham contribuído para o elevado coeficiente de variação observado para alguns caracteres, quadrados médios altamente significativos, para caracteres do racemo primário, foram encontrados para diferença entre médias de Genótipos, Genótipos dentro de PBII e entre Seleções, exceto para número de frutos que foi não significativo. Nos caracteres do racemo secundário, foram encontrados testes F altamente significativos (P<0,01) para diferenças entre Genótipos e entre Genótipos dentro do grupo PBII. Diferenças não significativas foram detectadas entre Seleções e entre Genótipos dentro do Grupo PB, exceto para rendimento no descascamento que apresentou P<0,05. São apresentadas as distribuições de médias para os caracteres.

Activity of Ricinus communis (Euphorbiaceae) and ricinine against the leaf-cutting ant Atta sexdens rubropilosa (Hymenoptera : Formicidae) and the symbiotic fungus Leucoagaricus gongylophorus

The focus of this study was the identification of compounds from plant extracts for use in crop protection. This paper reports on the toxic activity of fractions of leaf extracts of Ricinus communis L (Euphorbiaceae) and isolated active compounds in the leaf-cutting ant Atta sexdens rubropilosa Forel and its symbiotic fungus Leucoagaricus gongylophorus (Singer) Moller. The main compounds responsible for activity against the fungus and ant in leaf extracts of R communis were found to be fatty acids for the former and ricinine for the ants. (C) 2004 Society of Chemical Industry.

Activity of Ricinus communis (Euphorbiaceae) and ricinine against the leaf-cutting ant Atta sexdens rubropilosa (Hymenoptera : Formicidae) and the symbiotic fungus Leucoagaricus gongylophorus

The focus of this study was the identification of compounds from plant extracts for use in crop protection. This paper reports on the toxic activity of fractions of leaf extracts of Ricinus communis L (Euphorbiaceae) and isolated active compounds in the leaf-cutting ant Atta sexdens rubropilosa Forel and its symbiotic fungus Leucoagaricus gongylophorus (Singer) Moller. The main compounds responsible for activity against the fungus and ant in leaf extracts of R communis were found to be fatty acids for the former and ricinine for the ants. (C) 2004 Society of Chemical Industry.

Ricinus communis treatment of denture stomatitis in institutionalised elderly

This study compared the effectiveness of Ricinus communis (RC) with Nystatin (NYS) and Miconazole (MIC) in the treatment of institutionalised elderly with denture stomatitis (DS). They (n = 30) were randomly distributed into three groups: MIC, NYS or RC. Clinical and mycological evaluations were performed prior to the use of the antifungal (baseline) and repeated after 15 and 30 days of treatment. The sample was clinically examined for oral mucosal conditions. Standard photographs were taken of the palate, and the oral candidiasis was classified (Newton's criteria). Mycological investigation was performed by swabbing the palatal mucosa, and Candida spp. were quantified by counting the number of colony-forming units (cfu mL-1). The clinical and mycological data were analysed, respectively by Wilcoxon and Student's t-test (α = 0·05). Significant improvement in the clinical appearance of DS in the MIC and RC groups was observed between the 1st and 3rd collections (MIC - P = 0·018; RC - P = 0·011) as well as between the 2nd and 3rd collections (MIC - P = 0·018; RC - P = 0·011). Neither groups showed a statistically significant reduction in cfu mL-1 at any time. Although none of the treatments decreased the cfu mL-1, it was concluded that Ricinus communis can improve the clinical condition of denture stomatitis in institutionalised elderly patients, showing similar results to Miconazole. © 2013 Blackwell Publishing Ltd.

Fluorescence-polarization studies on binding of 4-methylumbelliferyl beta-D-galactopyranoside to Ricinus communis (castor-bean) agglutinin

The binding of Ricinus communis (castor-bean) agglutinin 1 to saccharides was studied by equilibrium dialysis and fluorescence polarization by using the fluorescently labelled sugar 4-methylumbelliferyl beta-D-galactopyranoside. No appreciable change in ligand fluorescence of 4-methylumbelliferyl beta-D-galactopyranoside was considerably polarized on its binding to the lectin. The association constants obtained by Scatchard analysis of equilibrium-dialysis and fluorescence-polarization data do not differ much from each other, and at 25 degrees C, Ka = 2.4 (+/- 0.2) X 10(4)M-1. These values agree reasonably well with that reported in the literature for Ricinus agglutinin 1. The number of binding sites obtained by the different experimental procedures is 1.94 +/- 0.1 per molecule of 120 000 daltons and is equal to the reported value of 2. The consistency in the values of Ka and number of binding sites indicate the absence of additional subsites on Ricinus agglutinin 1 for its specific sugars. In addition, the excellent agreement between the binding parameters obtained by equilibrium dialysis and fluorescence polarization indicate the potential of ligand-fluorescence-polarization measurements in the investigation of lectin-sugar interactions.

Chemical Modification Studies On Ricinus-Communis (Castor Bean) Agglutinin

Ricinus communis agglutinin was subjected to various chemical treatments and the effect on its hemagglutinating and saccharide-binding properties was studied. Acetylation, succinylation and citraconylation led to a complete loss in the activity of the agglutinin, whereas reductive methylation had no effect on the activity, showing that charged amino groups were involved in the hemagglutinating and saccharide-binding activity of Ricinus agglutinin. Modification of tryptophyl, arginyl and carboxyl-group-containing residues did not lead to any loss in the activity of the agglutinin. Acetylation of tyrosyl groups with N-acetylimidazole strongly reduced the hemagglutinating and saccharide-binding property of Ricinus agglutinin. The loss in activity was restored on deacetylation of the tyrosyl groups. Modification of tyrosyl residues also led to a change in the immunological properties of the agglutinin. The initial rate of modification of tyrosyl and amino groups and the concomitant loss of activity was reduced in the presence of lactose.

On the Specificity of Carbohydrate-Lectin Recognition The Interaction of a Lectin from Ricinus communis Beans with Simple Saccharides and Concanavalin A

A galactose-specific protein (RC1) isolated from Ricinus communis beans was found to give a precipitin reaction with concanavalin A. Its carbohydrate content amounted to 8–9% of the total protein and was found to be rich in mannose. The interaction of RC1 with galactose and lactose was measured in 0.05 M phosphate buffer containing 0.2 M NaCl (pH 6.8) by the method of conventional equilibrium dialysis. From the analysis of the binding data according to Scatchard method the association constant (Ka) at 5°C was calculated as 3.8 mM−1 and 1.2 mM−1 for lactose and galactose, respectively. In both cases the number of binding sites per molecule of RC1 with molecular weight of 120000 was found to be 2. From the temperature-dependent Ka values for the binding of lactose, the values of –5.7 kcal/mol and –4.3 cal × mol−1× K−1 were calculated for ΔH and ΔS, respectively. The addition of concanavalin A to RC1 or vice versa led to the formation of the insoluble complex RC1· ConA4 containing one molecule of RC1 and one molecule of tetrameric concanavalin A (ConA4) which could be dissociated upon addition of concanavalin A-specific sugars. The complex formation results in a time-dependent appearance of turbidity in the time range from 10s to 10 min. From the measurement of the time-dependent appearance and disappearance of the turbidity the formation (kf) and dissociation (kd) rate constants were calculated as 3 mM−1× s−1 and 0.07 ks−1 respectively. The ratio kf/kd (43μM −1), that corresponds to the association constant of complex RC1· ConA4, is higher than that of mannoside · ConA4 and thereby suggests that protein-protein interaction contributes significantly in stabilising glycoprotein · lectin complexes. The relevance of this finding to the understanding of the chemical specificities that are involved in a model cell-lectin interaction is discussed.

Maternal effect on salinity tolerance during germination of Ricinus communis

p.93-101

The determination of asialoglycoforms of serum glycoproteins by lectin blotting with Ricinus communis agglutinin

Serum proteins were fractionated by polyacrylamide gel electrophoresis under denaturing conditions and transferred to nitrocellulose membranes. The blotted polypeptides were probed with biotinylated Ricinus communis lectin (RCA120) followed by streptavidin/alkaline phosphatase. This procedure detected five asialoglycoproteins (a2-macroglobulin, transferrin, a1-antitrypsin, a1-antichymotrypsin and haptoglobin ß chain). The asialoform of the a1-trypsin inhibitor was found to be decreased in inflammation.