共查询到20条相似文献,搜索用时 31 毫秒
1.
该文建立了一种可对莲子中多种代谢物进行高覆盖分析的基质辅助激光解吸附质谱成像(MALDI-MSI)方法,实现了莲子中生物碱类、黄酮类、氨基酸类、脂肪酸类、有机酸类、胆碱类、磷脂类等多种代谢物的组织原位可视化表征。结果表明,生物碱类代谢物主要分布在莲子胚芽中;黄酮类代谢物主要分布在莲子胚芽和种皮中;氨基酸类代谢物在莲子子叶中的含量显著高于莲子胚中;脂肪酸类代谢物在莲子不同组织中的分布差异很小;胆碱类代谢物在莲子胚芽和莲子子叶底部的含量更高,甘油磷酸胆碱在莲子子叶顶部的含量更高;有机酸类代谢物以及绝大多数磷脂类化合物在莲子子叶中的含量高于莲子胚。该研究为评价莲子药物质量、探究莲子中化合物的时-空代谢网络提供了新的技术支持。 相似文献
2.
Conclusions A model has been suggested to explain the observed relationship between the measured heats of dissolution of uranyl nitrate in aqueous nitrate solutions and the concentration of the salting-out agent. The model describes the change in the structure of water in the solution with change in its concentration. On the one hand, a destruction of the water structure by ions occurs, which is weakened with increase in the distance from the ion, and leads to such irregularity in the distribution of water molecules in the solution that the mean number of molecules of water in unit volume is increased with increase in the distance from the ions. In experiments on the heat of dissolution this increase leads to increased hydration of the uranyl cation and reduction in the endothermicity of the dissolution with increase in the concentration of the solution. On the other hand, an interaction occurs between the ions of the salting-out agent and the water molecules in the solution, leading to the opposite result: There is an increase in the mean number of water molecules of the solution in unit volume in the direction of these ions. In experiments on the heat of dissolution this is revealed in the dehydration of the uranyl cation, and correspondingly in an increase in the endothermicity of the dissolution with increase in the concentration of the solution. The proposed model is in harmony with data on vapor pressure above the solutions (the relationship between the activity coefficient of the water and the concentration of the solution).Translated from Zhurnal Strukturnoi Khimii. Vol. 3, No. 2, pp. 143–150, March–April. 1962 相似文献
3.
Grand canonical ensemble molecular dynamics simulation is employed to calculate the solubility of water in polyamide-6,6. It is shown that performing two separate simulations, one in the polymeric phase and one in the gaseous phase, is sufficient to find the phase coexistence point. In this method, the chemical potential of water in the polymer phase is expanded as a first-order Taylor series in terms of pressure. Knowing the chemical potential of water in the polymer phase in terms of pressure, another simulation for water in the gaseous phase, in the grand canonical ensemble, is done in which the target chemical potential is set in terms of pressure in the gas phase. The phase coexistence point can easily be calculated from the results of these two independent simulations. Our calculated sorption isotherms and solubility coefficients of water in polyamide-6,6, over a wide range of temperatures and pressures, agree with experimental data. 相似文献
4.
Masanao Oya Keikichi Uno Yoshio Iwakura 《Journal of polymer science. Part A, Polymer chemistry》1972,10(2):613-623
Copolymerization of NCA's was undertaken in a heterogeneous system in acetonitrile, which is not a solvent of the polypeptides. The reactivity ratio was calculated by using the Lewis-Mayo equation. Further, the conversion rate in the copolymerization and the configuration of the copolymer produced were compared with those of the copolymerization in the homogeneous system in nitrobenzene, in which the copolypeptides are swollen. The rate of copolymerization in acetonitrile was between the rates of polymerization of the individual monomers. It has been reported that the configuration of the copolymer obtained in dimethylformamide, in which the copolypeptides are swollen, is of the block type. On the other hand, many polypeptides obtained in acetonitrile, which is not a solvent of the copolypeptides, had a random configuration near to an alternating configuration. 相似文献
5.
The accelerated growth of aquaculture has resulted in a series of harmful effects to human health. The widespread and unrestricted use of antibiotics in this industry, to prevent bacterial infections, leads to remaining amounts in the aquatic environment. This has resulted in the emergence of antibiotic-resistant bacteria in aquaculture environments, in the increase in antibiotic resistance in fish pathogens as well as in the transfer of these resistance determinants to human pathogens. Moreover, the use of large amounts of antibiotics may lead to the presence of residual antibiotics in fish tissue and fish products. Fluoroquinolones, tetracyclines, penicillins, sulphonamides and other antibiotics, exhibiting activity against both Gram-positive and Gram-negative bacteria, are widely used for the treatment and prevention of diseases in fish. An extended and comprehensive review on the recent analytical methodologies concerning antibiotic residues in fish reported in the literature is provided in the present article. Emphasis is given on sample preparation regarding isolation and purification, chromatographic conditions and method validation according to legislation. Results of published assays are comparatively presented and criticised. 相似文献
6.
A. V. Ponomarev P. K. Metreveli V. N. Chulkov A. V. Bludenko 《High Energy Chemistry》2017,51(5):369-374
In the process of the electron-beam distillation of lignin, its conversion into benzenediols increases in the presence of alkanes in the irradiated sample. An increase in the yield of benzenediols is accompanied by a decrease in the fractions of guaiacol, creosol, ethylguaiacol, and vinylguaiacol in the tar distilled off. It has been noted that alkanes serve as an additional source of atomic hydrogen and alkyl radicals, which, in turn, play a key role in the formation of benzenediols. In the presence of alkanes in the irradiated sample, guaiacol can be the main precursor of catechols; the proportion of guaiacol in the tar is almost three times below that in the case of distillation of individual lignin. It has been hypothesized that the chain decomposition of lignin can occur with the participation of ?H and ?CH3 radicals. 相似文献
7.
Gianazza E Sirtori CR Castiglioni S Eberini I Chrambach A Rondanini A Vecchio G 《Electrophoresis》2000,21(8):1435-1445
Structural properties, and especially the differential stability, of complexes between carbonic anhydrase (CA) and three sulfonamide inhibitors, acetazolamide, dorzolamide and methazolamide, were investigated by spectroscopic and electrophoretic techniques. These included denaturant gradient gel electrophoresis either across a urea or a steady-state transverse sodium dodecyl sulfate (SDS) gradient. Acetazolamide, the smallest and most hydrophilic of the sulfonamides, forms the most stable complex in the presence of urea, whereas dorzolamide, with a bulky and hydrophobic structure, is most stable against the effects of SDS. At pH 7.4, complexes with dorzolamide show minimal changes in mobility across the SDS gradient, as if unaffected by the detergent, both in the presence and in the absence of excess ligand in the gel. When bound to both acetazolamide and methazolamide, on the other hand, CA displays an increase in mobility above 0.05% SDS, lower in the presence than in the absence of excess ligand. The finding of a distinct pattern for the unliganded enzyme, however, suggests the complexes can still retain the ligand, although binding of the surfactant changes their charge density. Under saturating conditions and in the presence of SDS, the surface charge of all complexes is much lower than for unliganded, denatured CA. Circular dichroism (CD) spectra clearly indicate that the increase in secondary structure and the decrease in tertiary structure brought about in CA by the presence of low concentrations of SDS are largely prevented by complexing with the inhibitors. These observations point out peculiar properties of each CA inhibitor, of potential value in the definition of their biological activities and also in the potential development of novel antagonist molecules. 相似文献
8.
George Khelashvili Xiaolu Cheng Maria E. Falzone Milka Doktorova Alessio Accardi Harel Weinstein 《Journal of computational chemistry》2020,41(6):538-551
Recent discoveries about functional mechanisms of proteins in the TMEM16 family of phospholipid scramblases have illuminated the dual role of the membrane as both the substrate and a mechanistically responsive environment in the wide range of physiological processes and genetic disorders in which they are implicated. This is highlighted in the review of recent findings from our collaborative investigations of molecular mechanisms of TMEM16 scramblases that emerged from iterative functional, structural, and computational experimentation. In the context of this review, we present new MD simulations and trajectory analyses motivated by the fact that new structural information about the TMEM16 scramblases is emerging from cryo-EM determinations in lipid nanodiscs. Because the functional environment of these proteins in in vivo and in in vitro is closer to flat membranes, we studied comparatively the responses of the membrane to the TMEM16 proteins in flat membranes and nanodiscs. We find that bilayer shapes in the nanodiscs are very different from those observed in the flat membrane systems, but the function-related slanting of the membrane observed at the nhTMEM16 boundary with the protein is similar in the nanodiscs and in the flat bilayers. This changes, however, in the bilayer composed of longer-tail lipids, which is thicker near the phospholipid translocation pathway, which may reflect an enhanced tendency of the long tails to penetrate the pathway and create, as shown previously, a nonconductive environment. These findings support the correspondence between the mechanistic involvement of the lipid environment in the flat membranes, and the nanodiscs. © 2019 Wiley Periodicals, Inc. 相似文献
9.
Sol-gel Transition of Methylcellulose Solution in the Coexistence of Hexadecyltrimethylammonium Bromide and Sodium Chloride
下载免费PDF全文
![点击此处可从《化学物理学报(中文版)》网站下载免费的PDF全文](/ch/ext_images/free.gif)
The sol-gel transition of methylcellulose (MC) solution in the presence of NaCl and hexade-cyltrimethylammonium bromide (HTAB), together with MC/NaCl solution in the presence of HTAB and MC/HATB solution in the presence of NaCl, was investigated by the rheolog-ical measurements. It has been found that the sol-gel transition temperature of MC solution decreases linearly with the concentration of NaCl in solution but increases linearly with the concentration of HTAB in solution, respectively. However, the sol-gel transition temperature of MC/NaCl solution in the presence of HTAB keeps the same value, independent of theconcentration of HTAB in solution. On the other hand, the sol-gel transition temperature of MC/HTAB solution decreases linearly with the concentration of NaCl in solution. The experimental results suggest that, for MC/NaCl solution in the presence of HTAB, the salt-induced spherical micelles of HTAB should have formed in bulk solution. For MC solution in the absence of NaCl, no spherical micelles have been formed in bulk solution, though the concentration of HTAB in our experiment is almost one order of magnitude higher than the critical micelle concentration of HTAB in polymer-free solution. In fact, due to adsorption of HTAB on MC chains, the realconcentration of HTAB in bulk solution, is much less than the apparent concentration of HTAB dissolved in MC solution. 相似文献
10.
Rodríguez A Muñoz M del Mar Graciani M Fernández Chacón S Moyá ML 《Langmuir : the ACS journal of surfaces and colloids》2004,20(23):9945-9952
The spontaneous hydrolysis of phenyl chloroformate was studied in water-ethylene glycol, EG, cationic, zwitterionic, nonionic, and anionic micellar solutions, the surfactants being tetradecyltrimethylammonium bromide, tetradecyl-N,N-dimethyl-3-ammonio-1-propanesulfonate, tricosaoxyethylene glycol ether, and sodium dodecyl sulfate. The dependence of the observed rate constant on surfactant concentration as well as on the percentage by weight of EG, varying from 0 to 50 wt %, was investigated. Information about changes in the critical micelle concentrations, in the micellar ionization degrees (for ionic surfactants), in the aggregation numbers, and in the polarity of the interfacial region of the micelles upon changing the weight percent of EG was obtained through conductivity, surface tension, spectroscopic, and fluorescence measurements. A simple pseudophase model was adequate to rationalize the kinetic data. Micellar medium effects were explained by considering charge-charge interactions and polarity, ionic strength, and water content in the micellar interfacial region. The acceleration of the reaction produced by an increase in the amount of EG present in the mixture was explained on the basis of the substantial decrease in the equilibrium binding constant of phenyl chloroformate molecules to the micelles, resulting in the contribution of the reaction taking place in the bulk water-EG phase being more important. The weight percent of EG did not substantially influence the rate constant in the micellar pseudophase. 相似文献
11.
Ya. V. Rashkes A. M. Rashkes M. M. Kiktev N. K. Khidyrova Kh. M. Shakhidoyatov A. A. Abdullaev 《Chemistry of Natural Compounds》1990,25(6):676-683
The amount of free and bound sterols and triterpenoids in the leaf blades and petioles of the variety Tashkent-1 and the deciduous lines L-275 and L-470 in the budding-flowering, maturing, and leaf-fall phases have been compared. In the leaf blades, the maximum accumulation of free sterols in the deciduous lines is observed in an earlier phase than in the variety Tashkent-1, and this is most characteristic for sterols saturated in the C-17 side chain. The dynamics of the change in the content of unsaturated sterols is individual for each line. The nature of the change in the amount of free sterols in the petioles is typical for each line and does not depend on the nature of the sterol for the variety Tashkent-1 this index falls sharply in the leaf-fall phase while for L-275 the process is retarded between the second and third phases, and for L-470 in the same period the amount of these substances rises sharply. In the leaf blades, as a rule, the level of sterol esters changes in parallel with the levels of free sterols, and in the petioles in the antiparallel direction between the first and second phases. In all the samples free and bound amyrin was detected. The dynamics of the change in the amounts of these substances in the three lines were different.Institute of the Chemistry of Plant Substances, Uzbek SSR Academy of Sciences, Tashkent. Institute of Experimental Plant Biology, Uzbek SSR Academy of Sciences, Tashkent. Translated from Khimiya Prirodnykh Soedinenii, Vol. 6, pp. 796–805, November–December, 1989. 相似文献
12.
Ya. V. Rashkes A. M. Rashkes M. M. Kiktev N. K. Khidyrova Kh. M. Shakhidoyatov A. A. Abdullaev 《Chemistry of Natural Compounds》1989,25(6):676-683
The amount of free and bound sterols and triterpenoids in the leaf blades and petioles of the variety Tashkent-1 and the deciduous
lines L-275 and L-470 in the budding-flowering, maturing, and leaf-fall phases have been compared. In the leaf blades, the
maximum accumulation of free sterols in the deciduous lines is observed in an earlier phase than in the variety Tashkent-1,
and this is most characteristic for sterols saturated in the C-17 side chain. The dynamics of the change in the content of
unsaturated sterols is individual for each line. The nature of the change in the amount of free sterols in the petioles is
typical for each line and does not depend on the nature of the sterol for the variety Tashkent-1 this index falls sharply
in the leaf-fall phase while for L-275 the process is retarded between the second and third phases, and for L-470 in the same
period the amount of these substances rises sharply. In the leaf blades, as a rule, the level of sterol esters changes in
parallel with the levels of free sterols, and in the petioles in the antiparallel direction between the first and second phases.
In all the samples free and bound amyrin was detected. The dynamics of the change in the amounts of these substances in the
three lines were different.
Institute of the Chemistry of Plant Substances, Uzbek SSR Academy of Sciences, Tashkent. Institute of Experimental Plant Biology,
Uzbek SSR Academy of Sciences, Tashkent. Translated from Khimiya Prirodnykh Soedinenii, Vol. 6, pp. 796–805, November–December,
1989. 相似文献
13.
Bengt Kronberg Miguel Castas Rebecca Silvestonti 《Journal of Dispersion Science and Technology》2013,34(3):333-351
The hydrophobic effect is the common expression for processes where nonpolar groups in molecules are spontaneously removed from water. Thermodynamic analysis of hydrocarbon solubility in water, micellization and adsorption of surfactants show that the hydrophobic effect can be understood in terms of two contributions. The first contribution is attributed to the structuring, or rearrangement, of water molecules in the vicinity of a hydrophobe. This contribution is favorable, and hence increases the solubility of hydrocarbons in water, increases the cmc, and decreases the adsorption of surfactants. The second contribution is attributed to the formation of a cavity in the water in order to accomodate the hydrophobe. This contribution dominates over the first one and is unfavorable, i.e. it decreases the solubility of hydrocarbons in water, decreases the cmc, and increases the adsorption of surfactants. Thus, the cause of the hydrophobic effect is to be found in the large energy required to form a cavity in the water. On the other hand the temperature dependence of the hydrophobic effect is entirely determined by the water structuring, or rearrangement, in the vicinity of a hydrophobe. 相似文献
14.
Wahadoszamen M Hamada T Iimori T Nakabayashi T Ohta N 《The journal of physical chemistry. A》2007,111(38):9544-9552
External electric field effects on absorption, fluorescence, and phosphorescence spectra of a series of unsubstituted diphenylpolyynes have been examined in a PMMA film. The analysis of the electroabsorption spectra indicates that the shorter diphenylpolyynes exhibit only the change in molecular polarizability, whereas the longer ones exhibit the change both in dipole moment and in molecular polarizability following absorption. The finding of the change in dipole moment following absorption of centrosymmetric diphenylpolyynes is interpreted in terms of the symmetry distortion upon doping a polymer film. When the external electric field is applied, the fluorescence yield is reduced and enhanced, respectively, in diphenylacetylene and diphenyloctatetrayne, indicating that the rate of the nonradiative process from the fluorescence state is accelerated in diphenylacetylene and decelerated in diphenyloctatetrayne by an external electric field. All of the diphenylpolyynes used in the present study exhibit the change in molecular polarizability following the phosphorescence process. 相似文献
15.
E. Kuzmann V. K. Garg P. A. de Souza Júnior L. A. Schuch A.C. de Oliveira Z. Homonnay A. Vértes 《Journal of Radioanalytical and Nuclear Chemistry》2000,246(1):61-68
Sediments from the Admiralty Bay, King George Island, Antarctica, were investigated by 57Fe Mössbauer spectroscopy, X-ray diffractometry, and radiometry. Quartz, feldspar, chlorite, calcite, dolomite, mica, kaolinite, hematite and magnetite were identified as constituent minerals in the sediment samples. The phase composition and the iron distribution among the crystallographic sites of iron-bearing minerals (silicates, magnetite and hematite) of samples from different location have been derived from the complex Mössbauer spectra. At different locations sediments had significant characteristic differences in the mineral composition, in the iron distribution among the crystallographic site of silicates, and in the specific radioactivity of Cs radionuclides. These results indicate differences in the rock formation and alteration by the sediments in this maritime part of Antarctica. There is a much higher amount of iron oxides in the sediments from south part of the geological fault across the Admiralty Bay than in the north part. This can be associated with much more alteration in the rocks in the south part compared to the northern one. This finding can contribute to the question of the history of the formation and alteration of volcanic rocks in the border of Antarctica. 相似文献
16.
The problem of the limits of validity of the Langevin equation is considered in detail in the case of (microscopic) test-particles in very dilute gases. It is shown that, in this case, the current Langevin equation follows from the Newton’s law in an exact way only in the Maxwell test-particle–gas-particle interaction model, and in an approximate way only in the Rayleigh-gas limit and in the low-velocity limit, while in any other interaction model, or limit, only a Langevin-like equation with speed-dependent friction coefficient and speed-dependent fluctuating force can be written. Such a circumstance, although probably limited to the particular physical situation considered in this paper, suggests that, in general, some preliminary, specific check of the validity of the Langevin equation should be performed before using the said equation to interpret laboratory experiments. 相似文献
17.
Knecht V Risselada HJ Mark AE Marrink SJ 《Journal of colloid and interface science》2008,318(2):477-486
Electrophoresis is widely used to determine the electrostatic potential of colloidal particles. Oil droplets in pure water show negative or positive electrophoretic mobilities depending on the pH. This is commonly attributed to the adsorption of hydroxyl or hydronium ions, resulting in a negative or positive surface charge, respectively. This explanation, however, is not in agreement with the difference in isoelectric point and point of zero charge observed in experiment. Here we present molecular dynamics simulations of oil droplets in water in the presence of an external electric field but in the absence of any ions. The simulations reproduce the negative sign and the order of magnitude of the oil droplet mobilities at the point of zero charge in experiment. The electrostatic potential in the oil with respect to the water phase, induced by anisotropic dipole orientation in the interface, is positive. Our results suggest that electrophoretic mobility does not always reflect the net charge or electrostatic potential of a suspended liquid droplet and, thus, the interpretation of electrophoresis in terms of purely continuum effects may need to be reevaluated. 相似文献
18.
T. T. Efremova S. P. Efremov K. P. Koutzenogii V. F. Peresedov 《Journal of Radioanalytical and Nuclear Chemistry》1999,241(2):355-360
An accumulation of Cu and As is found in the peat deposit of an eutrophic marsh together with anomalously high concentrations
of Ga in some layers. The element dispersed in the peatbog depth in the greatest extent in Zn, and in equally small portions
there is dispersed In and Au. The main factors of the biogeochemical migration of Cu, Zn, In, Au, As, Ga in peathog formation
are: the lithological peculiarities of the territory, the oxidation-reduction zonality of the deposit depth within the limits
of oxidation and the reduction background, the quality of the humus sorbing barriers, the carbonate equilibrium of marsh waters,
and anthropogenic factors. A tendency to accumulate Zn migration streams in the bedding of marsh forests in South West Siberian
taiga is observed. 相似文献
19.
M. B. A. Vasconcellos M. Saiki 《Journal of Radioanalytical and Nuclear Chemistry》2006,270(1):263-267
Summary Much concern has been expressed lately about the decline of teaching and research activities in radiochemistry in many countries,
as was discussed in an IAEA Technical Meeting in Antalya, Turkey, in 2002, and also at MTAA-11 in Guildford, UK. In the IAEA
meeting, a survey was presented about the current situation in different regions of the world (Eastern Europe, East and West
Asia, Africa, North America and Latin America) by experts of each region. In the case of Brazil, which has nuclear research
reactors and also cyclotrons in operation, the teaching and research activities in radiochemistry are concentrated in the
three main institutes of the Brazilian Nuclear Energy Commission, in the University of S?o Paulo and in other universities,
in different regions of the country. In the present paper, a closer look is given to the radiochemistry teaching and research
activities that are being conducted nowadays in Brazil, comprising: number of radiochemistry courses and students being formed,
main research areas being conducted, as well as research and production of radioisotopes for nuclear medicine, using nuclear
reactors and cyclotrons. 相似文献