ABSTRACT
A produção de gengibre no Paraná concentra-se no município de Morretes, ocupando uma área de plantio de aproximadamente 300 ha. O objetivo deste trabalho foi avaliar o teor e a composição do óleo essencial de rizomas de gengibre produzidos em Morretes e submetidos a diferentes períodos de secagem em temperatura ambiente. O delineamento experimental foi inteiramente casualizado, em esquema fatorial 5 x 5, com quatro repetições (quatro plantas por repetição), avaliando cinco procedências e cinco períodos de secagem a temperatura ambiente (0, 15, 30, 45 e 60 dias). As extrações de óleo essencial foram realizadas por hidrodestilação em aparelho graduado Clevenger durante três horas e a análise dos constituintes foi realizada por meio de cromatografia em fase gasosa acoplada à espectrometria de massas. A secagem de rizomas de gengibre em temperatura ambiente por até 60 dias resultou na diminuição de teores de óleo essencial na maioria das procedências. Os constituintes geranial e o neral apresentaram maior concentração em todas as procedências e tiveram teores superiores com o aumento nos períodos de secagem. Os teores de geraniol e acetato de geranila foram inferiores após a secagem em todas as procedências, assim como eucaliptol, canfeno, zingibereno e β-bisaboleno na maioria das procedências.
Ginger production in Paraná State, Brazil, has predominated in Morretes Municipality, with around 300 ha cultivated area. The aim of this work was to evaluate the essential oil yield and composition of ginger rhizomes produced in Morretes and subjected to different drying periods at room temperature. Experimental design was completely randomized, in a 5x5 factorial arrangement, with four replicates (four plants each), five origins and five drying periods at room temperature (0, 15, 30, 45 and 60 days). The essential oil was extracted by hydrodistillation in a Clevenger-type device for 3h and the constituents were analyzed by gas chromatography-mass spectrometry (GC/MS). The drying of ginger rhizomes at room temperature for up to 60 days decreased the essential oil yield in most origins. Geranial and neral levels were higher in all origins and as drying periods were longer. Geraniol and geranyl acetate levels decreased after drying in all origins, as well as eucalyptol, camphene, zingiberene and β-bisabolene in most origins.
Subject(s)
Food Preservation/statistics & numerical data , Zingiber officinale , Oils, Volatile/analysis , Rhizome/chemistry , Analysis of Variance , Brazil , Plants, Medicinal/enzymologyABSTRACT
High frequency plant regeneration in A. longifolia (L.) was achieved from leaf explant implanted on MS basal medium supplemented with NAA (0.5 mg/l) + BA (2.0 mg/l) through intervening callus phase. Well-developed shoots (>3cm) were successfully rooted on MS medium supplemented with NAA (0.1 mg/l). Protein and total soluble sugar contents were maximum during organogenesis and multiple shoot induction phase compared with non-organogenic callus and root induction phase. Esterase and catalase activities were maximum during organogenic differentiation, while activities were minimum at non-differentiated callus stages. Peroxidase activities were higher during rhizogenesis. Contradiction to peroxidase activity, acid phosphatase activities were high during organogenesis and declined during rhizogenesis. SDS-PAGE analysis of total soluble proteins revealed expression of non-organogenic callus (97.9 kDa), organogenic callus (77.2, 74.1, 21.9 kDa), multiple shoot induction phase (106.6, 26.9, 11.6 kDa) and root induction phase (15.9 kDa) specific polypeptides. Esterase zymogram revealed one band (Rm 0.204) appeared in both organogenic callus and multiple shoot induction phase. Peroxidase zymogram detected two stage specific bands, one band (Rm 0.42) was specific to root induction phase, while another (Rm 0.761) was specific to multiple shoot induction. Catalase and acid phosphatase zymogram resolved one band (Rm 0.752 and 0.435, respectively) in differentiated stages including both multiple shoot induction phase and root induction phase, but absent in undifferentiated phases.
Subject(s)
Acanthaceae/enzymology , Acid Phosphatase/metabolism , Catalase/metabolism , Esterases/metabolism , Peptides/metabolism , Peroxidases/metabolism , Plant Proteins/metabolism , Plants, Medicinal/enzymologyABSTRACT
Nigella is widely used in Egypt as a food additive as well as a drug for the treatment of some respiratory diseases. It was given orally to rats [20 g/kg body weight orally for ten days] and its effects were compared with the effect of phenobarbitone [microsomal enzymes inducer]. Nigella and phenobarbitone caused an increase in the level of microsomal cytochrome P450 from rat liver. Nigella produced a decrease in the activity of UDP-glucuronyl transferase [bilirubin and phenolphthalein as substrates] from rat liver microsomes. This indicated that Nigella is an inducer of cytochrome P450 which may produce toxic free radicals from other drugs not accompanied by glucuronidation of these metabolites. Serum enzymes commonly used as liver functions were not affected
Subject(s)
Animals, Laboratory , Plants, Medicinal/enzymology , Phenobarbital , Cytochrome P-450 Enzyme System , Free Radicals , Rats, WistarABSTRACT
Indole alkaloids in Catharanthus roseus have been in focus because of their medicinal value. These alkaloids consist of an indole moiety provided by tryptamine and a terpenoid portion provided by the secologanin. The most important catharanthus alkaloids are vinblastine (VLB), vincristine (VCR) and ajmalicine. VLB and VCR are clinically useful anticancer agents whereas ajmalicine is used for the treatment of circulatory diseases. VCR and VLB are the most expensive because of their low abundance in the plant, and are formed by the coupling of monomeric indole alkaloids vindoline and catharanthine, catalysed by peroxidases. The pathway that lead to monomeric indole alkaloids involves more than 20 enzymes of which 16 enzymes have been isolated and characterized biochemically, and only three at the molecular level. The present state of knowledge on enzymes and genes involved in indole alkaloid biosynthesis and various aspects of their regulation has been discussed.