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941.
Designs, Codes and Cryptography - Recently, Horlemann-Trautmann and Weger (Adv Math Commun, https://doi.org/10.3934/amc.2020089 , 2020) proposed a general framework for a Quaternary McEliece... 相似文献
942.
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944.
Rebecca R. Chao Ian C.-K. Lau Dr. Tom Coleman Luke R. Churchman Dr. Stella A. Child Joel H. Z. Lee Dr. John B. Bruning Prof. James J. De Voss Dr. Stephen G. Bell 《Chemistry (Weinheim an der Bergstrasse, Germany)》2021,27(59):14765-14777
The serine 244 to aspartate (S244D) variant of the cytochrome P450 enzyme CYP199A4 was used to expand its substrate range beyond benzoic acids. Substrates, in which the carboxylate group of the benzoic acid moiety is replaced were oxidised with high activity by the S244D mutant (product formation rates >60 nmol.(nmol-CYP)−1.min−1) and with total turnover numbers of up to 20,000. Ethyl α-hydroxylation was more rapid than methyl oxidation, styrene epoxidation and S-oxidation. The S244D mutant catalysed the ethyl hydroxylation, epoxidation and sulfoxidation reactions with an excess of one stereoisomer (in some instances up to >98 %). The crystal structure of 4-methoxybenzoic acid-bound CYP199A4 S244D showed that the active site architecture and the substrate orientation were similar to that of the WT enzyme. Overall, this work demonstrates that CYP199A4 can catalyse the stereoselective hydroxylation, epoxidation or sulfoxidation of substituted benzene substrates under mild conditions resulting in more sustainable transformations using this heme monooxygenase enzyme. 相似文献
945.
Qasem Ramadan Ting Ting Lau Shihan Bryan Ho 《Analytical and bioanalytical chemistry》2010,396(2):707-714
Simultaneous washing and concentration of magnetic microparticles was demonstrated using a rotational magnetic system under a continuous-flow condition. The rotation of periodically arranged permanent magnets close to a fluidic channel carrying a suspension of magnetic particles allows the trapping and releasing of particles along the fluidic channel in a periodic manner. Each trapping and releasing event resembles one washing cycle in conventional biological assays. Concentration efficiencies of 99.75?±?0.083% at a flow rate of 200 µl/min and 88.10?±?3.17% at a flow rate of 1,000 µl/min and a purification efficiency of 99.10?±?4.3% at a flow rate of 900 µl/min were achieved. 相似文献
946.
Maggie P. Y. Lam S. O. Siu Edward Lau Xiuli Mao H. Z. Sun Philip C. N. Chiu William S. B. Yeung David M. Cox Ivan K. Chu 《Analytical and bioanalytical chemistry》2010,398(2):791-804
We have developed a novel system for coupling reverse-phase (RP) and hydrophilic interaction liquid chromatography (HILIC) online in a micro-flow scheme. In this approach, the inherent solvent incompatibility between RP and HILIC is overcome through the use of constant-pressure online solvent mixing, which allows our system to perform efficient separations of both hydrophilic and hydrophobic compounds for mass spectrometry-based proteomics applications. When analyzing the tryptic digests of bovine serum albumin, ribonuclease B, and horseradish peroxidase, we observed near-identical coverage of peptides and glycopeptides when using online RP-HILIC—with only a single sample injection event—as we did from two separate RP and HILIC analyses. The coupled system was also capable of concurrently characterizing the peptide and glycan portions of deglycosylated glycoproteins from one injection event, as confirmed, for example, through our detection of 23 novel glycans from turkey ovalbumin. Finally, we validated the applicability of using RP-HILIC for the analysis of highly complex biological samples (mouse chondrocyte lysate, deglycosylated human serum). The enhanced coverage and efficiency of online RP-HILIC makes it a viable technique for the comprehensive separation of components displaying dramatically different hydrophobicities, such as peptides, glycopeptides, and glycans. 相似文献
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948.
Tatjana Trtić-Petrović Jelena Ðorđević Nikolina Dujaković Ksenija Kumrić Tatjana Vasiljević Mila Laušević 《Analytical and bioanalytical chemistry》2010,397(6):2233-2243
An optimised extraction and cleanup method for the analysis of pesticide in natural water samples is presented. Sixteen pesticides
of different polarity and from the different chemical classes (organophosphates, triazines, benzimidazoles, carbamates, carbamides,
neonicotinoides, methylureas, phenylureas and benzohydrazides), most frequently used in Serbia, were selected for the analysis.
Liquid-phase microextraction in a single hollow fibre (HF-LPME) has been applied for sample preparation. The concentrations
of pesticides were determined using HPLC-MS/MS method with electrospray ionisation. The extraction behaviour and selection
of the experimental conditions was predicted based on log D and pK
a values of targeted pesticides, which were calculated applying the computer software ACD/Labs PhysChem Suite v12. The influence
of the donor pH and concentration of pesticides, organic phase composition as well as the extraction time on the extraction
efficiency was investigated. Optimum extraction conditions were evaluated with respect to the investigated parameters of the
extraction. The extraction method was validated for 10 out of 16 studied pesticides. Linear range of the pesticides was 0.1–5 μg L−1 with the correlation coefficient from 0.991 to 0.9998, and the relative standard deviation for three standard measurements
was between 0.2 and 11.8%. The limits of detections ranged from 0.026 to 0.237 μg L−1 and the limits of quantifications from 0.094 to 0.793 μg L−1. The optimised two-phase HF-LPME method was successfully applied for determination of moderately polar as well low-polar
pesticides in the environmental water samples. 相似文献
949.
Quan-Bin Han Ting Yu Yan Zhou Wei-Na Wang Clara Bik-San Lau Hong-Xi Xu Kwok-Pui Fung 《Talanta》2010,82(4):1521-162
Analytical high-speed counter-current chromatography (HSCCC), a unique liquid-to-liquid separation technology, has an inherent capability to provide perfect fractionation for tracking active ingredients of medicinal herbs, in a quick, efficient, and high-recovery manner. A high throughput screening (HTS) method which utilizes a novel biosensor that selectively detects apoptosis based on the fluorescence resonance energy transfer (FRET) technique, was newly established and proved to be very sensitive in detecting apoptosis induced by various known anticancer drugs. The first combination of both advanced techniques formed an efficient platform for drug discovery and succeeded in quickly identifying the most potent apoptotic constituent of a Chinese herb namely Isodon eriocalyx. The system of n-hexane/ethyl acetate/methanol/water was used as the separation solvent. The solvent ratio was first set at 3:5:3:5 to check the water-soluble part of the crude extract, and then 1:1:1:1 was used to isolate the target compounds. The active fraction was tracked and purified continuously using HSCCC which was guided by the apoptosis detection at gradually decreased drug concentrations. As a result, the most potent apoptosis inducer in this herb was discovered by analytical HSCCC equipped with a 16 ml mini-coil column, using less than 50 ml diphase solvent, from about 50 mg active fraction. It was identified as eriocalyxin B, a well-known antitumor natural product, by NMR analysis of the HSCCC purified fraction. 相似文献
950.
Chemical state X-ray photoelectron spectroscopic analysis of first row transition metals and their oxides and hydroxides is challenging due to the complexity of the 2p spectra resulting from peak asymmetries, complex multiplet splitting, shake-up and plasmon loss structure, and uncertain, overlapping binding energies. A review of current literature shows that all values necessary for reproducible, quantitative chemical state analysis are usually not provided. This paper reports a more consistent, practical and effective approach to curve-fitting the various chemical states in a variety of Sc, Ti, V, Cu and Zn metals, oxides and hydroxides. The curve-fitting procedures proposed are based on a combination of (1) standard spectra from quality reference samples, (2) a survey of appropriate literature databases and/or a compilation of the literature references, and (3) specific literature references where fitting procedures are available. Binding energies, full-width at half maximum (FWHM) values, spin-orbit splitting values, asymmetric peak-shape fitting parameters, and, for Cu and Zn, Auger parameters values are presented. The quantification procedure for Cu species details the use of the shake-up satellites for Cu(II)-containing compounds and the exact binding energies of the Cu(0) and Cu(I) peaks. The use of the modified Auger parameter for Cu and Zn species allows for corroborating evidence when there is uncertainty in the binding energy assignment. These procedures can remove uncertainties in analysis of surface states in nano-particles, corrosion, catalysis and surface-engineered materials. 相似文献