RESUMEN
The performance of p-Anisaldehyde (PAA) for preserving pitaya fruit quality and the underpinning regulatory mechanism were investigated in this study. Results showed that PAA treatment significantly reduced fruit decay, weight loss and loss of firmness, and maintained higher content of total soluble solids, betacyanins, betaxanthins, total phenolics and flavonoids in postharvest pitaya fruits. Compared with control, the increase in hydrogen peroxide (H2O2) content and superoxide anion (O2â¢-) production was inhibited in fruit treated with PAA. Meanwhile, PAA significantly improved the activity of antioxidant enzymes superoxide dismutase (SOD), peroxidase (POD) and catalase (CAT). Moreover, PAA-treated pitaya fruit maintained higher ascorbic acid (AsA) and reduced-glutathione (GSH) content but lower dehydroascorbate (DHA) and oxidized glutathione (GSSG) content, thus sustaining higher ratio of AsA/DHA and GSH/GSSG. In addition, activities of ascorbate peroxidase (APX), glutathione reductase (GR), monodehydroascorbate reductase (MDHAR) and dehydrogenation ascorbic acid reductase (DHAR), as well as the expression of HpSOD, HpPOD, HpCAT, HpAPX, HpGR, HpDHAR and HpMDHAR, were enhanced after PAA treatment. The findings suggest that postharvest application of PAA may be a reliable method to control postharvest decay and preserve quality of harvested pitaya fruit by enhancing the antioxidant potential of the AsA-GSH cycle and activating an antioxidant defense system to alleviate reactive oxygen species (ROS) accumulation.
RESUMEN
Tea (Camellia sinensis) cultivars with green leaves are the most widely used for making tea. Recently, tea mutants with white or yellow young shoots have attracted increasing interest as raw materials for making "high-quality" tea products. Albino teas are generallycharacterized as having metabolites of relatively high amino acid content and lower catechin content. However, little is known about aroma compounds in albino tea leaves. Herein, we compared original normal leaves (green) and light-sensitive albino leaves (yellow) of cv. Yinghong No. 9. GC-MS was employed to analyze endogenous tea aroma compounds and related precursors. Quantitative real time PCR was used to measure expression levels of genes involved in biosyntheses of tea aromas.The total contents of most endogenous free tea aromas, including aroma fatty acid derivatives, aroma terpenes, and aroma phenylpropanoids/benzenoids, and their glycosidically bound aroma compounds, were lower in yellow leaves than in green leaves. The content of the key precursor geranyl diphosphate (GDP) and expression levels of key synthetic genes involved in the formation of linalool, a major aroma compound in cv. Yinghong No. 9, were investigated. Linalool content was lower in albino-induced yellow leaves, which was due to the lower GDP content compared with normal green leaves.
Asunto(s)
Camellia sinensis/química , Hojas de la Planta/química , Brotes de la Planta/química , Compuestos Orgánicos Volátiles/química , Aminoácidos/química , Camellia sinensis/genética , Catequina/química , Color , Cromatografía de Gases y Espectrometría de Masas , Humanos , Mutación , Hojas de la Planta/genética , Brotes de la Planta/genética , Té/químicaRESUMEN
1-Phenylethanol (1PE) can be used as a fragrance in food flavoring and cosmetic industries and as an intermediate in the pharmaceutical industry. 1PE can be synthesized from acetophenone, and the cost of 1PE is higher than the cost of acetophenone. Therefore, it is important to establish an effective and low-cost approach for producing 1PE. Our previous studies found that tea (Camellia sinensis) flowers, which are an abundant and waste resource, contained enzymes that could transform acetophenone to 1PE. In the present study, we extracted crude enzymes from tea flowers and optimized the production conditions of 1PE using response surface methodology. The optimized conditions were an extraction pH of 7.0, a reaction pH of 5.3, a reaction temperature of 55 °C, a reaction time of 100 min, a coenzyme NADPH concentration of 3.75 µmol/mL in the reaction assay, and a substrate acetophenone concentration of 1.25 µmol/mL in the reaction assay. The results provide essential information for future industrial 1PE production using plant-derived enzymes.
Asunto(s)
Acetofenonas/química , Alcoholes Bencílicos/química , Camellia sinensis/química , Flores/química , Aditivos Alimentarios/química , Proteínas de Plantas/química , Biocatálisis , Camellia sinensis/enzimología , Cosméticos/química , Análisis Factorial , Flores/enzimología , Concentración de Iones de Hidrógeno , Cinética , NADP/química , Proteínas de Plantas/aislamiento & purificación , TemperaturaRESUMEN
1-Phenylethanol (1PE) is a major aromatic volatile in tea (Camellia sinensis) flowers, whereas it occurs in a much smaller amounts in leaves. Enzymes involved in the formation of 1PE in plants and the reason why 1PE differentially accumulates in plants is unknown. In the present study, enzymes in the last step leading from acetophenone to 1PE were isolated from tea flowers by traditional biochemical chromatography. The two types of partially purified enzymes were proposed to be responsible for formations of (R)-1PE and (S)-1PE, respectively. Tea leaves also contained such enzymes having equivalent activities with flowers. Stable isotope labeling experiments indicated that weak transformation from l-phenylalanine to acetophenone in leaves mainly resulted in little occurrence of 1PE in leaves. This study provided an example that differential distribution of some metabolites in plant tissues was not only determined by enzyme(s) in the last step of metabolite formation, but also can be due to substrate availability.
Asunto(s)
Alcoholes Bencílicos/metabolismo , Camellia sinensis/metabolismo , Flores/metabolismo , Hojas de la Planta/metabolismo , Acetofenonas/metabolismo , Fenilalanina/metabolismoRESUMEN
The effect of 3.0kJ/m(2) ultraviolet-C (UV-C) treatment on respiratory activity and mitochondrial membrane associated with fruit senescence in peach fruit stored at 20°C for 8days was investigated. UV-C treatment could reduce senescence development, as evidenced by higher fruit firmness due to inhibition of respiration rate via reducing succinic dehydrogenase and cytochrome C oxidase activity. Meanwhile, the activities of superoxide dismutase, catalase and ascorbate peroxidase in the UV-C-treated fruit were much higher than those in control fruit, resulting in lower levels of superoxide radicals (O2(-)) and hydrogen peroxide (H2O2). In addition, this treatment maintained a higher level of mitochondrial membrane fluidity and inhibited opening of mitochondrial permeability transition pore. Our results suggest that the induction of antioxidant enzymes to scavenge O2(-) and H2O2 by UV-C treatment was associated with the maintenance of mitochondrial membrane integrity, which also played an important role in senescence retardation in peach fruit.