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161.
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Limin Yang Danqun Huo Kun He Suyi Zhang Changjun Hou 《Applied biochemistry and biotechnology》2013,170(4):909-924
Plant esterase extracted from wheat flour play key roles in the spectrophotometric detection of organophosphorus compounds (OPs) for food safety and human health. The purpose of the present study was to investigate the role of tryptophan residues in the activity and structure of plant esterase by chemical modification and fluorometric studies. Active site characterization of purified plant esterase showed the involvement of tryptophan in the catalytic activity. Only one was essential for the enzyme activity by the Tsou’s analysis. Substrate protection experiments further confirmed that the tryptophan residue was located at the substrate-binding site. Fluorescence quenching studies elucidated that the tryptophan residues were largely exposed to the solvent, and a smaller fraction of the surface tryptophan residues had electropositively charged amino acids around them. Experimental results obtained here are expected to promote the applications of plant esterase in OPs detection. Further confirmation of the existence of other critical residues and detailed explanation of their functions were also required for the elucidation of the mechanism involved in the detection of OPs. 相似文献
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Hou Yu-Ting Wu Fan Yao Jian-Hua Zhu Zhou-Hai Mi Qi-Li Gao Qian Zhou Min Ye Yan-Qing Wang Wei-Guang Yang Guang-Yu Hu Qiu-Fen Guan Ying 《Chemistry of Natural Compounds》2021,57(5):864-868
Chemistry of Natural Compounds - Two new isobenzofuranone derivatives (1 and 2) together with six known compounds (3–8) were isolated from the roots of Phlomis betonicoides, a highly sweet... 相似文献
166.
Jiancong Du Suhui Deng Shangguo Hou Lingling Qiao Jianfang Chen Qing Huang Chunhai Fan Ya Cheng Yun Zhao 《中国光学快报(英文版)》2014,12(4):41101-38
DNA tetrahedral nanostructures are considered to be uew nanocarriers because they can be precisely controlled and hold excellent penetration ability to the cellular membrane. Although the DNA tetrahedral nanostructure is extensively studied in biology and medicine, its behavior in the cells with nanoscale resolution is not understood clearly. In this letter, we demonstrate superrcsolution fluorescence imaging of the distribution of DNA tetrahedral nanostructures in the cell with a simulated emission depletion (STED) microscope, which is built based on a conventional eonfocal microscope and can t)rovide a resolution of 70 nm. 相似文献
167.
Yuying Qu Yingchun Li Xiaoli Tan Weixiang Zhai Dr. Guifang Han Dr. Jingli Hou Prof. Guoquan Liu Prof. Yuguang Song Prof. Yangping Liu 《Chemistry (Weinheim an der Bergstrasse, Germany)》2019,25(33):7888-7895
Tetrathiatriarylmethyl (TAM, trityl) radicals have found wide applications as spin probes/labels for EPR spectroscopy and imaging, and as polarizing agents for dynamic nuclear polarization. The high hydrophilicity of TAM radicals is essential for their biomedical applications. However, the synthesis of hydrophilic TAM radicals (e.g., OX063) is extremely challenging and has only been reported in the patent literature, to date. Herein, an efficient synthesis of a highly water-soluble TAM radical bis(8-carboxyl-2,2,6,6-tetramethylbenzo[1,2-d:4,5-d′]bis([1,3]dithiol-4-yl)-mono-(8-carboxyl-2,2,6,6-tetrakis(2-hydroxyethyl)benzo[1,2-d:4,5-d′]bis([1,3]dithiol-4-yl)methyl (TFO), which contains four additional hydroxylethyl groups, relative to the Finland trityl radical CT-03, is reported. Similar to OX063, TFO exhibits excellent properties, including high water solubility in phosphate buffer, low log P, low pKa, long relaxation times, and negligible binding with bovine serum albumin. On the other hand, TFO has a sharper EPR line and higher O2 sensitivity than those of OX063. Therefore, in combination with its facile synthesis, TFO should find wide applications in magnetic resonance related fields and this synthetic approach would shed new light on the synthesis of other hydrophilic TAM radicals. 相似文献
168.
Dr. Xisen Hou Prof. Chenfeng Ke Dr. Yu Zhou Dr. Zhuang Xie Dr. Ahmed Alngadh Dr. Denis T. Keane Dr. Majed S. Nassar Dr. Youssry Y. Botros Prof. Chad A. Mirkin Prof. J. Fraser Stoddart 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(35):12301-12306
Covalent and supramolecular polymerizations, both of which offer their own unique advantages, have emerged as popular strategies for making artificial materials. Herein, we describe a concurrent covalent and supramolecular polymerization strategy—namely, one which utilizes 1) a bis‐azide‐functionalized diazaperopyrenium dication that undergoes polymeriation covalently with a bis‐alkyne‐functionalized biphenyl derivative in one dimension as a result of a rapid and efficient β‐cyclodextrin(CD)‐accelerated, cucurbit[6]uril(CB)‐templated azide–alkyne cycloaddition, while 2) the aromatic core of the dication is able to dimerize in a criss‐cross fashion by dint of π–π interactions, enabling simultaneous supramolecular assembly, resulting in an extended polymer network in an orthogonal dimension. 相似文献
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170.
A theoretical scheme for preserving the entanglement in a two-qubit-spin coupled system in the presence of Dzyaloshinskii–Moriya (DM) anisotropic antisymmetric interaction is proposed. On the basis of a sequence of operations performed periodically on the system, the scheme can preserve the entanglement of the system starting from any initial state with any desired high precision for any desired long duration. 相似文献