ABSTRACT
AIM: To clarify the effects of selenium (Se), parameters related to oxidative issues, as well as the antioxidant response were investigated on an autochthonous wine yeast strain. METHODS AND RESULTS: Antioxidant enzyme activity, gel electrophoresis, Western blot and MDA level were used to investigate the effects of different concentration of Se in wine yeast. We found that Se is able to affect the enzymatic activities of catalase (CAT), glutathione peroxidase (GPx) and superoxide dismutase (SOD). An increase in lipid peroxidation was observed in a dose-dependent manner of (Se), thus, indicating the occurrence of cell membrane damage. Additionally, Se induced post-translational oxidative modifications of proteins, especially oxidation of thiol groups (both reversible and irreversible) and protein carbonylation (irreversible oxidation). CONCLUSION: These results obtained could further the understanding the effect of different concentration of Se in wine yeast strain with which Se affect the enzymatic activities and induces some post-translational modifications of proteins. SIGNIFICANCE AND IMPACT OF THE STUDY: The understanding of mechanisms regulating the response of wine yeast to Se is important for future work using selenized yeast as enriched Se supplements in human nutrition.
Subject(s)
Oxidative Stress , Saccharomyces cerevisiae/drug effects , Selenium/toxicity , Antioxidants/metabolism , Catalase/metabolism , Glutathione Peroxidase/metabolism , Lipid Peroxidation , Oxidation-Reduction , Protein Processing, Post-Translational , Saccharomyces cerevisiae/enzymology , Saccharomyces cerevisiae/metabolism , Saccharomyces cerevisiae Proteins/metabolism , Superoxide Dismutase/metabolism , Wine/microbiologyABSTRACT
Tebuconazole (Tbz) and diniconazole (Dnz) were deposited as thin film on quartz plaques. They were submitted to OH-radicals and ozone and their kinetic was measured. OH-radical oxidation was performed relative to a reference whose rate constant is well known. Terbuthylazine (Tbt) and Chlorpyriphos Ethyl (Clp) were chosen as reference for Tbz and Dnz kinetics determination, respectively. OH-radical rate constants of Tbz and Dnz were found to be: kOH+Tbzâ¯=â¯(1.7⯱â¯0.2) 10-13â¯cm3â¯molecule-1â¯s-1 and k OH+Dnzâ¯=â¯(1.74⯱â¯1.21) 10-12â¯cm3â¯molecule-1â¯s-1, respectively. Ozone heterogeneous oxidation rate constants were determined in an absolute way: kO3+Tbzâ¯=â¯(0.5⯱â¯0.2) 10-20â¯cm3â¯molecule-1â¯s-1; kO3+Dnzâ¯=â¯(1.4⯱â¯0.2) 10-19â¯cm3â¯molecule-1â¯s-1. Dnz is ten times more reactive toward OH-radicals than Tbz and 27 times more reactive than Tbz toward ozone maybe because of the presence of a double bond in Dnz. Lifetimes of Tbz and Dnz on quartz like surfaces are against OH-radicals are of 68â¯days and 8â¯days, respectively and 4â¯months and several years against ozone, respectively.
ABSTRACT
Pome trees, apple, pear, and quince, are classified into the subfamily Pomoideae, belonging to the Rosaceae family. Their autumnal fruits are consumed worldwide in different forms, that is, fresh or transformed into jams, jelly, juices, etc. Their well-established beneficial properties to human health were found mainly related to their phenolic content. Pulp and peel aqueous acetone extracts obtained from Tunisian fruits at commercial maturity were comparatively evaluated for their phenolic profiles and antioxidant and antimicrobial potentials. The phenolic compounds present in the extracts were identified and quantified using RP-HPLC-DAD and ESI-MS techniques. Significant differences in the chromatographic profiles among these fruits, as well as between pulp and peel extracts of each fruit, were observed. Quince, followed by 'Red Delicious', peel extracts showed the highest phenolic content (160.33 and 110.90 mg/100 g of fresh weight). The stronger inhibitory effect on DPPH radicals corresponded to those obtained from peel materials. A comparative analysis of the antimicrobial potential against a range of microorganism strains was also carried out. Staphylococcus aureus, Pseudomonas aeruginosa, and Bacillus cereus were the most sensitive to the active extracts. Among the examined phenolic extracts, 'Red Delicious' and quince peels showed the highest effects for inhibiting bacteria growth. Minimum inhibitory and bactericide concentrations ranged from 10(2) to 10(4) microg of polyphenol/mL. Red skin apple and quince peels could be of great interest as important antioxidant and antimicrobial polyphenol sources.
Subject(s)
Anti-Infective Agents/pharmacology , Antioxidants/pharmacology , Flavonoids/analysis , Fruit/chemistry , Phenols/analysis , Plant Extracts/chemistry , Acetone , Chromatography, High Pressure Liquid , Malus/chemistry , Polyphenols , Pyrus/chemistry , Rosaceae/chemistry , Spectrometry, Mass, Electrospray Ionization , TunisiaABSTRACT
Tunisian grapevine culture is affected by many viruses caused by some phytovirus belonging to nepovirus, closterovirus and trichovirus groups. The present work deal with the economically important viroses identified in tunisian grapevines. We present here the development methods to detect these viruses in propagating material. The important viruses biologically, biochemically, serologically and using molecular techniques, characterised are: GFLV, GLRaV3 and GVB. The genetic polymorphism analysis was also carried and tunisian isolates were compared to previously described ones in literature.
Subject(s)
Closterovirus/genetics , Nepovirus/genetics , Plant Diseases/virology , Plant Viruses/genetics , Virology/methods , Vitis/virology , Closterovirus/chemistry , Closterovirus/classification , Closterovirus/isolation & purification , DNA, Viral/analysis , DNA, Viral/genetics , Enzyme-Linked Immunosorbent Assay/methods , Molecular Sequence Data , Nepovirus/chemistry , Nepovirus/classification , Nepovirus/isolation & purification , Plant Viruses/chemistry , Plant Viruses/classification , Plant Viruses/isolation & purification , Polymorphism, Genetic/genetics , Reverse Transcriptase Polymerase Chain Reaction/methods , TunisiaABSTRACT
A recent advance in the study of plant lipases involving immunological techniques is presented. In an attempt to characterize lipases of cotyledons from germinating rapeseed seedlings and to investigate an eventual cross-reactivity with animal lipases, we have prepared anti-porcine pancreatic lipase antibodies raised in rabbit. It is shown by enzyme-linked immunosorbent assay and dot-blotting that these antibodies react with lipases in the rapeseed crude extract and in the different cellular fractions obtained by differential centrifugation. Preincubation of the antiserum with the rapeseed crude extract affects the amount of antibodies binding to the porcine pancreatic lipase. We demonstrate immunochemical cross-reactivity between rapeseed and porcine pancreatic lipase. Using the immunoblotting procedure, it is found that antibodies bind specifically to a single polypeptide with a molecular mass of about 55 kDa. Rapeseed lipase activity decreased after immunoprecipitation suggesting that antibodies were bound to some catalytic site residues. We conclude from the data obtained in this study that the two different lipase species present close similarities in amino acid sequence and antigen characteristics.