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11.
12.
Song Yinjie Zhang Hui Yang Qiaoling Zhao Aimin 《Journal of Radioanalytical and Nuclear Chemistry》1995,198(2):375-384
Two kinds of crystalline zirconium phosphate, - and -ZrP were prepared by direct method, and characterized by means of X-ray powder diffractometry, thermogravimetric analysis and pH titration. The total exchange capacity of -ZrP and -ZrP for Na+ ions determined by pH titration was 8.80 mmol/(g Zr(HPO4)2·6H2O) and 3.80 mmol/(g NH4ZrH(PO4)2·H2O), respectively. The thermodynamic equilibrium constant of exchange reactions on -ZrP and on -ZrP at 25.0°C is 2.5 and 1.1, respectively. Although UO
2
2+
in solution is more preferred by -ZrP than by -ZrP, the selectivity of -ZrP for UO
2
2+
decreases with decreasing pH value while less effect of pH on the amount of UO
2
2+
ions exchanged to -ZrP has been found. It is also interesting to find out that both H+ and NH
4
+
ions in -ZrP can be replaced by UO
2
2+
ions existed in concentrated solution. 相似文献
13.
Inchul Shin Ian Davis Karinel Nieves-Merced Yifan Wang Stanton McHardy Aimin Liu 《Chemical science》2021,12(11):3984
SfmD is a heme-dependent enzyme in the biosynthetic pathway of saframycin A. Here, we present a 1.78 Å resolution de novo crystal structure of SfmD, which unveils a novel heme cofactor attached to the protein with an unusual HxnHxxxC motif (n ∼ 38). This heme cofactor is unique in two respects. It contains a single thioether bond in a cysteine–vinyl link with Cys317, and the ferric heme has two axial protein ligands, i.e., His274 and His313. We demonstrated that SfmD heme is catalytically active and can utilize dioxygen and ascorbate for a single-oxygen insertion into 3-methyl-l-tyrosine. Catalytic assays using ascorbate derivatives revealed the functional groups of ascorbate essential to its function as a cosubstrate. Abolishing the thioether linkage through mutation of Cys317 resulted in catalytically inactive SfmD variants. EPR and optical data revealed that the heme center undergoes a substantial conformational change with one axial histidine ligand dissociating from the iron ion in response to substrate 3-methyl-l-tyrosine binding or chemical reduction by a reducing agent, such as the cosubstrate ascorbate. The labile axial ligand was identified as His274 through redox-linked structural determinations. Together, identifying an unusual heme cofactor with a previously unknown heme-binding motif for a monooxygenase activity and the structural similarity of SfmD to the members of the heme-based tryptophan dioxygenase superfamily will broaden understanding of heme chemistry.The de novo crystal structure of SfmD reveals a novel c-type heme cofactor for promoting a monooxygenation reaction in the biosynthetic pathway of saframycin A. 相似文献
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16.
A strain ofRhodococcus equi SHB-121 forming 3-cyanopyridine hydratase was screened from nitrile-polluted soil. The optimum conditions for the formation
of 3-cyanopyridine hydratase by the strain SHB-121 have been studied. Under the optimum conditions, the specific activity
of the enzyme reached 5.32 U/mg of dry cell, 95 times higher than that cultured in screening medium. In addition, the activity
of coexistent amidase was very low.
3-Cyanopyridine hydratase was purified from methylacrylamide-induced cells ofRh. equi SHB-121 by procedures including ultrasonic oscillation, ammonium sulfate precipitation, and column chromatographies on DEAE-cellulose
DE52, hydroxyapatite, and Sephadex G-25. The overall purification was 31-fold. The molecular weight of the enzyme was about
30 kDA by SDS-PAGE. The pI value was 4.1. The transition temperature and pH were 7.0°C and 6.0, respectively, resulting from
the differential spectra.
The optimum pH and temperature for the enzyme reaction were 8.0 and 30°C. The enzyme activity was strongly inhibited by Ag+, Hg2+, Cu2+, and NH4
+, whereas it was enhanced by Fe3+ slightly. The enzyme catalyzed the hydration of 3-cyanopyridine to nicotinamide, and itsKm value was 0.1 mol/L. Uncompetitive inhibitor sodium cyanide has a K, value of 5 mmol/L. 相似文献
17.
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19.
Guodong Feng Yanfu Huan Yanbo Cao Shuhua Wang Xinghua Wang Jie Jiang Aimin Yu Qinhan Jin Hongmei Yu 《Microchemical Journal》2004,76(1-2):17
An unique miniature simultaneous microwave plasma torch (MPT) atomic emission spectrometer employing linear UV intensified charge-coupled device (ICCD) array detector has been developed and studied preliminarily. The detection limits and precisions of the spectrometer for Ag, Al, Ba, Ca, Cr, Cu, Fe, Mg, Mn, Sr and V by using different CCD exposure times have been determined. An analysis of a practical sample has been carried out. The preliminary results demonstrate that such simultaneous spectrometer has advantages of saving sample and time, especially suitable for use as detector for chromatography and in combination with flow injection systems. Taking analytical figures of merit and portability into accounts, the miniature simultaneous MPT system will have extended application areas and greater competition potential as compared with commercialized scanning MPT spectrometers. 相似文献
20.
Gao D Tian Y Bi S Chen Y Yu A Zhang H 《Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy》2005,62(4-5):1203-1208
The interactions of colloidal gold and serum albumins, including bovine serum albumin (BSA) and human serum albumin (HSA), were studied by fluorescence and absorption spectrometry. Fluorescence quenching spectrometry was applied to study the interactions between colloidal gold and serum albumins. At pH 7.4 phosphate-buffered saline (PBS), the intensity of fluorescence emission spectrum of serum albumins decreased in the presence of colloidal gold, which indicated that colloidal gold quenched the fluorescence of serum albumins. Experimental results indicated that the combination reactions of colloidal gold and serum albumins were static quenching processes. Based on the effect of colloidal gold on fluorescence intensity, the binding constants, the numbers of binding sites and the acting forces between colloidal gold and serum albumins were found. 相似文献