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21.
Purification and some properties of three serine carboxypeptidases from Aspergillus niger 总被引:1,自引:0,他引:1
Three enzymes exhibiting peptidyl-L-amino acid hydrolase and esterase activities have been purified by immobilized metal-ion affinity chromatography and ion-exchange chromatography. The three enzymes were entirely free of the acid protease activity that normally exists along with them in the crude culture filtrates of Aspergillus niger. Although all three exo-peptidases possessed nearly identical molecular weights (ca. 140,000), isoelectric points (ca. 5.0) and other properties, their affinities for the two substrates tested, carbobenzoxy-L-Glu-L-Tyr and benzoyl L-arginine ethyl ester, differed. All three peptidases were inhibited by phenylmethanesulphonyl fluoride, indicating that they are serine carboxypeptidases. They were also inhibited by tosyl phenylalanine chloromethyl ketone, suggesting the presence of a histidyl residue in their active sites. The differences in the number of accessible histidyl residues on the enzyme surfaces could explain the differences in their retentions on Cu2+-iminodiacetate-Sepharose 6B. 相似文献
22.
Melt or cold crystallization kinetics has a strong bearing on morphology and the extent of crystallization, which significantly affects the physical properties of polymeric materials. Nonisothermal crystallization kinetics are often analyzed by the classical Johnson–Mehl–Avrami–Kolmogorov (JMAK) model or one of its variants, even though they are based on an isothermal assumption. As a result, during the nonisothermal (e.g. constant heating or cooling rate) crystallization of polymeric material, different sets of model parameters are required to describe crystallization at different rates, thereby increasing the total number of model parameters. In addition, due to the uncorrelated nature of these model parameters with the cooling or heating rate, accurate modeling at any intermediate condition is not possible. In the present work, these two limitations of the conventional approach have been eliminated by exhibiting the existence of a functional relationship between cooling or heating rate and effective activation energy during nonisothermal melt or cold crystallization in three linear aromatic polyesters. Furthermore, it has been shown that when the JMAK model is used in conjunction with this functional relationship, it is possible to precisely predict the experimental nonisothermal melt or cold crystallization kinetics at any linear cooling or heating rate with a single set of model parameters. 相似文献
23.
S. S. Krishnan M. T. Bayley A. J. W. Hitchman S. C. Lin K. G. McNeill J. E. Harrison 《Journal of Radioanalytical and Nuclear Chemistry》1987,114(1):173-180
This work describes an in vivo neutron activation analysis facility for small samples, such as rats or human hand, using two 100 g252Cf neutron sources. The irradiation area is a cylindrical space, of 12 cm diameter and about 15 cm length, with fairly uniform neutron flux distribution. Experimental data on the reproducibility, effects of volume and other conditions for in vivo measurements are given. Comparative atomic absorption data on calcium measurements on rats are reported. The facility is now used for animal experiments as well as human hand irradiations in clinical investigations involving calcium metabolism and bone diseases. 相似文献
24.
R. Krishnan 《European Polymer Journal》2004,40(10):2269-2276
Atom transfer radical polymerization (ATRP) of tert-butyl methacrylate (tBMA) was investigated using cuprous bromide with different ligands, solvents, deactivators, etc. The polymerization in bulk and diphenyl ether solvent system performed using Cu(I)Br complexed with N, N, N′, N″, N″-pentamethyldiethylenetriamine (PMDETA) catalyst in conjunction with 2-bromopropionitrile as an initiator at room temperature showed a curvature in the first-order kinetic plot. The controlled polymerization in methanol solution resulted in slower rate of polymerization and lower molecular weights. Well-defined diblock copolymers of PSt-b-PtBMA synthesized by polystyrene bromo macroinitiator (PSt-Br) with Cu(I)Cl/PMDETA catalyst system yielded predetermined molecular weights and lower polydispersities. Otherwise, the Cu(I)Br/PMDETA catalytic system showed an inefficient polymerization of tert-butyl methacrylate with lower molecular weights and higher polydispersities. Subsequent hydrolysis of the homopolymer refluxed in dioxane with addition of HCl afforded well-defined poly(methacrylic acid). 相似文献
25.
Thirunavukkarasu K Thirumoorthy K Libuda J Gopinath CS 《The journal of physical chemistry. B》2005,109(27):13272-13282
Nitric oxide (NO) reduction with carbon monoxide (CO) on the Pd(111) surface was studied under isothermal conditions by molecular beam techniques as a function of temperature, NO:CO beam composition, and beam flux. Systematic experiments were performed under transient and steady state conditions. Displacement of adsorbed CO by NO in the transient state of the reaction was observed at temperatures between 375 and 475 K for all the NO:CO compositions studied. NO accumulation occurs on Pd(111) surface under steady state conditions, below 475 K, due to stronger chemisorption of NO. The steady state reaction rates attain a maximum at about 475 K, nearly independent of beam composition. N2 was found to be the major product of the reduction, along with a minor production of N2O. The production of N2 and N2O indicates molecular and dissociative adsorption of NO on Pd(111) at temperatures up to 525 K. Postreaction TPD measurements were performed in order to determine the nitrogen coverage under steady-state conditions. Finally, the results are discussed with respect to the rate-controlling character of the different elementary steps of the reaction system. 相似文献
26.
Schiff-base (SB) derivatives of Ni(II) and Cu(II) porphyrins endowed with various amine functions (R−NH2),n-butylamine,p-anisidine andm-nitroaniline have been prepared from corresponding formyl porphyrins. Protonation studies of these SB derivatives reveal
a marked red shift of the optical absorption bands in the visible region relative to the unprotonated imines. The magnitude
of the observed red shifts in the protonated derivatives, (SBH+) are found to depend on the electron-withdrawing or electron-donating nature of the R group of the amines. The results of
the optical absorption,1H NMR, EPR, and cyclicovoltammetric studies are illustrative of the fact that protonation of the SB derivatives results in
a localized positive charge,
in the periphery of the porphyrin (p) system. The dibenzo-18-crown-6 interspersedbisporphyrin schiff bases have been prepared fromtrans 4,4′-diamino dibenzo-18-crown-6 and formyl porphyrins. The protonation of these SB derivatives is found to proceed in a concerted
fashion. The cation complexation studies by the crown ether entity in thebisporphyrin systems have been investigated using optical absorption, magnetic resonance and electrochemical methods. The redox
characteristics of the protonated dimeric SB porphyrins reveal that the first oxidation step involves a two-electron transfer
reaction. This is important in view of their possible usage in multielectron transfer reactions of biological and catalytic
interest. 相似文献
27.
Manojkumar TK Suh SB Oh KS Cho SJ Cui C Zhang X Kim KS 《The Journal of organic chemistry》2005,70(7):2651-2659
[reaction: see text] We present an ab initio study of the acid-promoted hydrolysis reaction mechanism of N-formylaziridine in comparison with formamide. Since the rate of amide hydrolysis reactions depends on the formation of the tetrahedral intermediate, we focused our attention mainly on the reactant complex, the tetrahedral intermediate, and the transition state connecting these two stationary points. Geometries were optimized using the density functional theory, and the energetics were refined using ab initio theory including electron correlation. Solvent effects were investigated by using polarizable continuum method calculations. The proton-transfer reaction between the O-protonated and N-protonated amides was investigated. In acidic media, despite that the N-protonated species is more stable than the O-protonated one, it is predicted that both N-protonated and O-protonated pathways compete in the hydrolysis reaction of N-formylaziridine. 相似文献
28.
Investigation of the use of B3LYP zero-point energies and geometries in the calculation of enthalpies of formation 总被引:1,自引:0,他引:1
Larry A. Curtiss Krishnan Raghavachari Paul C. Redfern John A. Pople 《Chemical physics letters》1997,270(5-6):419-426
The use of B3LYP/6–31G* zero-point energies and geometries in the calculation of enthalpies of formation has been investigated for the enlarged G2 test set of 148 molecules [J. Chem. Phys. 106 (1997) 1063]. A scale factor of 0.96 for the B3LYP zero-point energies gives an average absolute deviation nearly the same as scaled HF/6–31G* zero-point energies for G2, G2(MP2), and B3LYP/6–311 + G(3df,2p) enthalpies. A scale factor of 0.98, which has been recommended in some studies, increases the average absolute deviation by about 0.2 kcal/mol. Geometries from B3LYP/6–31G* are found to do as well as MP2/6–31G* geometries in the calculation of the enthalpies of formation. 相似文献
29.
K. D. Singh Mudher K. Krishnan N. C. Jayadevan 《Journal of Radioanalytical and Nuclear Chemistry》1993,176(2):175-184
Chemical characterization of rubidium uranium(IV) trisulfate, Rb2U(SO4)3, a new chemical assay standard for uranium requires accurate analysis of rubidium. A gravimetric and an X-ray fluorescence method (XRF) for the determination of rubidium in this compound are described. In the gravimetric method, rubidium is determined as Rb2Na[Co(NO2)6].H2O without separating uranium with a precision of the order of ±0.5%. In the XRF method, the concentration ratio of rubidium to uranium, CRb/CU, is determined in the solid samples by the binary ratio method using calibration between intensity ratios (IRb/IU) and concentration ratios (CRb/CU). The concentration of rubidium is derived using the uranium value which is known with a precision better than ±0.05%. The XRF method has a precision better than ±0.8% for rubidium determination. 相似文献
30.
Krishnan Raghavachari Michael J. Frisch John A. Pople Paul von R. Schleyer 《Chemical physics letters》1982,85(2):145-149
Calculations with an extended polarized basis set and Møller-Plesset perturbation theory including triple substitution correlation corrections in the fourth-order treatment indicate that singlet ethylidene (CH3CH:) is not a local minimum on the C2H4 potential energy surface. Rearrangement to ethylene occurs without actuation. Barriers for hydrogen scrambling and for 1,1-hydrogen elimination are estimated. 相似文献