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81.
82.
A new, improved sensor for the electrocatalytic determination of ascorbate has been developed that has both a low applied operating potential and a low detection limit. The sensor was constructed by depositing copper hexacyanoferrate film either electrochemically or chemically onto carbon film electrode, and it was then characterised by cyclic voltammetry and electrochemical impedance spectroscopy. Chemically deposited films were shown to be the best for ascorbate determination and were used as an amperometric sensor at +0.05 V versus SCE to determine ascorbate in wines and juice. The linear range extended to 5 mM with a limit of detection of 2.1 M, the sensor was stable for more than four months, and it could be used continuously for at least 20 days. 相似文献
83.
Oxidation of alcohols to corresponding carbonyl compounds by coenzyme PQQ-trimethyl ester was performed in the presence of aluminum t-butoxide or aluminum chloride under anaerobic conditions. Reduced PQQTME (PQQTMEH2) was obtained by acidification of an aluminum complex of reduced PQQTME which was isolated in the reaction. 相似文献
84.
85.
Manol Ognyanov Petko Denev Desislava Teneva Yordan Georgiev Sabina Taneva Iskra Totseva Mariana Kamenova-Nacheva Yana Nikolova Svetlana Momchilova 《Molecules (Basel, Switzerland)》2022,27(6)
Gamma irradiation is efficiently applied to many foods, but nevertheless there is a distinct lack of information about the changes of macro- and micronutrients (e.g., carbohydrates, lipids, organic acids, and phenolics) in dried rose hip (RH) fruits. Therefore, in this study, for the first time, the effect of gamma irradiation (10 and 25 kGy) on RH constituents is investigated. Different analytical techniques (GC-FID, HPLC-UV, HPSEC-RID, IR-FT, and SEM) are employed to examine this effect. The irradiation treatment (10 kGy) increased the glucose content by 30% and released cellobiose from RH fruits, thus revealing cellulose destruction. The extractability of total uronic acids increased from 51% (control) to 70.5% (25 kGy-irradiated), resulting in a higher pectin yield (10.8% < 12.8% < 13.4%) and molecular heterogeneity. Moreover, de-esterification was not a major effect of the irradiation-induced degradation of pectin. The sample exposure to the highest dose did not change the content of total carotenoids, β-carotene, and (un)saturated fatty acids, but it affected the tocopherols levels. Gamma rays had a negligible effect on the phenolic constituents and did not affect ORAC and HORAC antioxidant activity. In conclusion, it can be compromised that the exposition of dried RH is safe and can be successfully applied to decontaminate fruits without affecting their nutritional value and biological activity. 相似文献
86.
Peralta Cecilia Mariana Acosta Gimena Henestrosa Cecilia Gil Raúl Andrés Fernández Liliana Patricia 《Journal of Analytical Chemistry》2022,77(3):308-317
Journal of Analytical Chemistry - The present development involved a flow injection strategy using a mini-column of multiwalled carbon nanotubes and fluorescent detection (λex of 283 nm,... 相似文献
87.
Rodrigues Ana Luísa Marques Rosa Dias Maria Isabel Prudêncio Maria Isabel Russo Dulce Diniz Mariana Martins Andrea Neves César Kasztovszky Zsolt Harsányi Ildiko Szilágyi Veronika Kovács Imre Szőkefalvi-Nagy Zoltán 《Journal of Radioanalytical and Nuclear Chemistry》2022,331(9):3887-3903
Journal of Radioanalytical and Nuclear Chemistry - A contribution to the discussion about Vila Nova de São Pedro (VNSP) as a production centre of symbolic lithic artefacts, the origin of raw... 相似文献
88.
Mariana Dennehy Oscar V. Quinzani Robert A. Burrow 《Acta Crystallographica. Section C, Structural Chemistry》2007,63(9):m395-m397
The centrosymmetric title compound, [Ag(C7H4NO2S2)]n, consists of dinuclear units in which two thiosaccharinate anions each bridge two Ag atoms via an endocyclic N atom and an exocyclic S atom across a crystallographic centre of inversion midway between the Ag atoms. The dimeric units are connected via Ag—Sexo interactions to create two‐dimensional networks. The thiosaccharinate anions bridge in a μ3‐S:S:N manner. The Ag...Ag distance can be considered a strong argentophilic interaction. 相似文献
89.
Moore RH Spies MA Culpepper MB Murakawa T Hirota S Okajima T Tanizawa K Mure M 《Journal of the American Chemical Society》2007,129(37):11524-11534
The biogenesis of the topaquinone (TPQ) cofactor of copper amine oxidase (CAO) is self-catalyzed and requires copper and molecular oxygen. A dopaquinone intermediate has been proposed to undergo 1,4-addition of a copper-associated water molecule to form the reduced form of TPQ (TPQ(red)), followed by facile oxidation by O(2) to yield the mature TPQ (TPQ(ox)). In this study, we have incorporated a lysine residue in the active site of Arthrobacter globiformis CAO (AGAO) by site-directed mutagenesis to produce D298K-AGAO. The X-ray crystal structure of D298K-AGAO at 1.7-A resolution revealed that a covalent linkage formed between the epsilon-amino side chain of Lys298 and the C2 position of a dopaquinone derived from Tyr382, a precursor to TPQ(ox). We assigned the species as an iminoquinone tautomer (LTI) of lysine tyrosylquinone (LTQ), the organic cofactor of lysyl oxidase (LOX). The time course of the formation of LTI at pH 6.8 was followed by UV/vis and resonance Raman spectroscopies. In the early phase of the reaction, an LTQ-like intermediate was observed. This intermediate then slowly converted to LTI in an isosbestic manner. Not only is the presence of a dopaquinone intermediate in the TPQ biogenesis confirmed, but it also provides strong support for the proposed intermediacy of a dopaquinone in the biogenesis of LTQ in LOX. Further, this study indicates that the dopaquinone intermediate in AGAO is mobile and can swing from the copper site into the active-site wedge to react with Lys298. 相似文献
90.
Zorica M. Bugar?i? Vera M. Divac Mariana P. Gavrilovi? 《Monatshefte für Chemie / Chemical Monthly》2007,40(9):985-988
An efficient protocol for the preparation of phenylselenoethers from unsaturated alcohols using phenylselenenyl halides at
room temperature was developed. The procedure employs phenylselenenyl chloride and bromide, some Δ 4- and Δ 5-alkenols and Ag2O, as an additive, to generate the tetrahydropyrans or tetrahydrofurans. This method permits the preparation of cyclic phenylselenoethers
in high yields and under extremely mild conditions. 相似文献