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41.
42.
Prof. Dr. Heinz Langhals Dr. Bernd Böck M. Sc. Tanja Schmid Alexey Marchuk 《Chemistry (Weinheim an der Bergstrasse, Germany)》2012,18(41):13188-13194
Benzoperylene derivatives with two angularly attached dicarboxylic imide rings, which were prepared by the Diels–Alder‐Reaction, exhibit strong fluorescence and their free peri positions allow either control of the UV/Vis spectra through their substituents or form anchor positions for the attachment of functional units. The angular chromophore 3 may be used both for fluorescent labeling such as for primary amines or enzymes or as building blocks for more complex assemblies where they may act as energy donors for FRET or electron acceptors in PET such as for photovoltaic solar cells. 相似文献
43.
Dr. Tana Koudelakova Dr. Radka Chaloupkova Dr. Jan Brezovsky Dr. Zbynek Prokop Dr. Eva Sebestova Dr. Martin Hesseler Dr. Morteza Khabiri Maryia Plevaka Daryna Kulik Dr. Ivana Kuta Smatanova Dr. Pavlina Rezacova Dr. Rudiger Ettrich Prof. Uwe T. Bornscheuer Prof. Jiri Damborsky 《Angewandte Chemie (International ed. in English)》2013,52(7):1959-1963
44.
Dr. Ruth Matesanz Dr. José Fernando Diaz Dr. Francisco Corzana Andrés G. Santana Dr. Agatha Bastida Dr. Juan Luis Asensio 《Chemistry (Weinheim an der Bergstrasse, Germany)》2012,18(10):2875-2889
The most common mode of bacterial resistance to aminoglycoside antibiotics is the enzyme‐catalysed chemical modification of the drug. Over the last two decades, significant efforts in medicinal chemistry have been focused on the design of non‐ inactivable antibiotics. Unfortunately, this strategy has met with limited success on account of the remarkably wide substrate specificity of aminoglycoside‐modifying enzymes. To understand the mechanisms behind substrate promiscuity, we have performed a comprehensive experimental and theoretical analysis of the molecular‐recognition processes that lead to antibiotic inactivation by Staphylococcus aureus nucleotidyltransferase 4′(ANT(4′)), a clinically relevant protein. According to our results, the ability of this enzyme to inactivate structurally diverse polycationic molecules relies on three specific features of the catalytic region. First, the dominant role of electrostatics in aminoglycoside recognition, in combination with the significant extension of the enzyme anionic regions, confers to the protein/antibiotic complex a highly dynamic character. The motion deduced for the bound antibiotic seem to be essential for the enzyme action and probably provide a mechanism to explore alternative drug inactivation modes. Second, the nucleotide recognition is exclusively mediated by the inorganic fragment. In fact, even inorganic triphosphate can be employed as a substrate. Third, ANT(4′) seems to be equipped with a duplicated basic catalyst that is able to promote drug inactivation through different reactive geometries. This particular combination of features explains the enzyme versatility and renders the design of non‐inactivable derivatives a challenging task. 相似文献
45.
《Analytical letters》2012,45(9):1691-1699
Abstract Four kinds of mercury species (inorganic mercury (Hginorg), methylmercury (MeHg), total organic mercury (ΣHgorg), and insoluble mercury, deemed to be mercuric selenide (HgSe), were determined in the livers of dolphins from the Brazilian coast. The MeHg was identified and quantified in the toluene layer on a Gas Chromatograph with an Electron Capture Detector (GC-ECD). The ΣHgorg was isolated by acid leaching (H2SO4-KBr-CuSO4) and then extracted into CH2Cl2. The ΣHgorg and Hginorg were determined by Cold-Vapor Atomic Absorption Spectroscopy (CV-AAS). The MeHg was the smallest fraction of Hgtot, with a median of 9%, whereas the highest fraction of the Hgtot was as HgSe, corresponding to 53%. The fractions of Hginorg and ΣHgorg corresponded to 30% and 39%, respectively. The lowest fraction of MeHg and the highest fraction of HgSe in the liver of all animals are related to different capacities or strategies of detoxification of methylmercury in this organ. 相似文献
46.
Valery Kukhar Vladimir Solodenko Vadim Soloshonok Tamara Kasheva 《Phosphorus, sulfur, and silicon and the related elements》2013,188(1-4):529-532
Abstract Synthesis of enantiomeric amino phosphonic acids APA is described by using chiral auxiliary reagent or enzymatic resolution of racemic mixtures of APA phenacyl derivatives. Peptides with APA residue were obtained by application of trimethylsilyl derivatives or condensation in the presence of enzyme-papain 相似文献
47.
Langang Niu Ramaswamy Nagarajan Dingsong Feng Lynne A. Samuelson 《高分子科学杂志,A辑:纯化学与应用化学》2013,50(12):1983-1990
Main‐chain thermotropic liquid‐crystalline polyesters containing rigid biphenyl mesogens and flexible spacers were synthesized by chemo‐enzymatic route. The enzyme‐catalyzed polymerization showed high regio‐ and chemo‐ selectivity, and is environmentally friendly. The resulting polyesters were characterized with 1H‐NMR, 13C‐NMR, gel permeation chromatography (GPC), differential scanning calorimetry (DSC), and polarized light optical microscopy (POM). 相似文献
48.
Walter Torres 《高分子科学杂志,A辑:纯化学与应用化学》2013,50(12):1923-1928
Highly hydrated bioactive hydrogels containing immobilized oxidoreductase enzymes and immobilized redox mediators were simulated as the biorecognition layer of amperometric biosensors. The linear dynamic range of the amperometric response of mediated biosensors increases and moves to higher concentration brackets with an increase in the concentration of mediator. This informs the design of biosensors that target the same analyte but possesses several independently addressable electrodes modified with hydrogels that contain different concentrations of mediator. Increases in enzyme concentration increase the linear dynamic range but does not alter the sensitivity of amperometric biosensors. Both sensitivity and linear dynamic range of mediated amperometric enzyme biosensors may be “tuned” by varying the concentrations of the enzyme and the mediator. Simulations effectively guide the initial domains of study of complex systems such as implantable biosensors. 相似文献
49.
Mirosław Giurg Katarzyna Piekielska Magdalena Gębala Bartosz Ditkowski Marcin Wolański Wanda Peczyńska‐Czoch 《合成通讯》2013,43(11):1779-1789
The catalytic oxidative cyclocondensation of the o‐aminophenols 1a–f was investigated. The oxidants used were air/laccase, H2O2/horseradish peroxidase, H2O2/ebselen (3), and TBHP/diphenyl diselenide 4. The products obtained were 2‐amino‐3H‐phenoxazin‐3‐one—questiomycin A, its derivative 2b, and cinnabarinic acid and actinocin (2c,d). Substrates with methyl groups at 4 and 5 positions of benzene ring were converted to different dihydrophenoxazinones 2g,h. Compounds having chlorine atoms at the same positions underwent oxidation to planar phenoxa-zinones 2e,f with elimination of one hydrochloride molecule. 相似文献
50.
Kinetic features of the photo- and thermo-chromic behaviour of new cholesteric triple copolymers with photosensitive spiropyran-containing side groups are considered. The kinetics of the back thermal process at different temperatures have been studied; activation energies for this process for the copolymers with different contents of the dye units have been obtained. The photochromic homopolymer and copolymers with a low content of dye units are shown to possess maximum values of the activation energy. 相似文献