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1.
Screening of 400 Streptomyces strains for biotransformation of the natural lignan matairesinol led to the identification of Streptomyces sp. LS136, capable of producing a single metabolite in moderate yields. Isolation and purification by preparative HPLC, followed by structural analyses by LC-MS and NMR, established the structure as matairesinol-4-O-rhamnoside. This bacterial strain was also used for rhamnosylation of the abundant natural lignans, hydroxymatairesinol and secoisolariciresinol. 相似文献
2.
An immobiline DryStrip application method enabling high-capacity two-dimensional gel electrophoresis 总被引:5,自引:0,他引:5
Sabounchi-Schütt F Aström J Olsson I Eklund A Grunewald J Bjellqvist B 《Electrophoresis》2000,21(17):3649-3656
In the field of proteomics the need to detect low-abundance cellular components, such as regulatory proteins, is of critical importance. Two-dimensional polyacrylamide gel electrophoresis (2-D PAGE) is one of the most commonly used separation tools for these biological investigations. In this paper we report an alternative micropreparative 2-D PAGE sample application method, called the "paper bridge loading" method. This method makes it possible to apply a larger sample volume to commercially available immobilized pH gradient (IPG) strips. The Vh products required for focusing are only marginally longer than those used in analytical experiments. The method was compared to traditional cup loading and in-gel rehydration. With 18 cm long narrow-range Immobiline DryStrip pH 4.5-5.5, the "paper bridge" method allowed the application of 10 mg human plasma proteins compared to 3 mg with traditional loading methods. The corresponding figures using Escherichia coli sample was found to be 6 mg and less than 2 mg, respectively. The paper bridge method also showed the best results in terms of spot resolution and separation of high molecular weight proteins. 相似文献
3.
4.
The neutral, cationic, and anionic structures of both prototropic tautomers oftrans- andcis-urocanic acid [(E)- and (Z)-3-(1H-imidazol-4(5)-yl)propenoic acid, respectively] were studied by using semiempirical andab initio gas-phase calculations. Potential energy surfaces of the structures were calculated by using the semiempirical AM1 method, and the geometries corresponding to global minima on these surfaces were optimized up to the MP2/6-31G* level of theory. The calculated protonation forms of each urocanic acid isomer have a planar molecular structure due to a delocalized -electron system, and all of them prefer thes-trans conformation with respect to the bond between the imidazole and the propenoic acid moieties. Thecis-urocanic acid structures are stabilized by an intramolecular hydrogen bond. The chargedcis-urocanic acid isomers have a lower molecular energy than the correspondingtrans-isomers, whereas the neutral molecules have, after inclusion of thermodynamic corrections, approximately the same energy. The cationic urocanic acid structures have about 2500 kJ mol–1 lower energy than the anionic ones and about 1000 kJ mol–1 lower energy than the neutral ones. The nonzwitterionic forms of the neutral urocanic acid isomers have about 200 kJ mol–1 lower energy than the zwitterionic ones. These energy differences are explained by the proton affinities of the imidazole and the propenoic acid moieties of the urocanic acid structures. 相似文献
5.
The origin of radiative background in GD-OES is discussed, in connection with the problem of multi-matrix measurements in depth profile analysis. Backed by some experimental evidence in the form of line scans, it is argued that line emission from sample material and the plasma gas (Ar) make up the dominating contributions to the radiative background. The contribution from Ar, in this work termed Matrix-independent Background (MIB), is investigated in more detail. It is shown that, at constant voltage and current, the Ar emission intensity is nearly constant and independent of the pressure, but somewhat matrix-dependent. It is suggested that the MIB can be expressed as a linear function of the intensity of an Ar reference line. This idea is tested experimentally by making intensity measurements on a large set of calibration standards of varying composition. The results are fitted to a calibration function which allows optional definitions of the MIB. It is shown that with a MIB defined as a linear function of the Ar intensity, the different contributions to the spectral background can be more accurately determined than with the MIB defined as a constant. 相似文献
6.
Simplistic modeling approach to heterogeneous dilute-acid hydrolysis of cellulose microcrystallites 总被引:9,自引:0,他引:9
Pär O. Pettersson Robert W. Torget Robert Eklund Qian Xiang Y. Y. Lee Guido Zacchi 《Applied biochemistry and biotechnology》2003,106(1-3):451-455
The classic kinetic model for cellulose hydrolysis is often referred to as pseudo-homogeneous, a term revealing the insight that the process is actually heterogeneous. During the past 10–15 yr, the shortcomings of this
model have been demonstrated in various studies and the interest in the heterogeneous aspects has increased. The present work
presents a simplistic model in which the intrinsic, heterogeneous hydrolysis and transport rates are coupled by the assumption
of a constant glucosidic surface concentration. The mechanisms affecting these two rates are largely unknown, but the model
serves as a guideline for further exploration of the process. 相似文献
7.
N. Ipek N. Lior F. Bark A. Eklund A. Alemany 《Russian Journal of Electrochemistry》2002,38(3):238-246
Electrolytic pickling of steel with neutral solutions, to remove the surface scale, reduces the need for the use of strong acids as needed in conventional pickling. This study is a step towards a more in-depth understanding of the factors affecting the former process. A theoretical model, sufficiently simplified to allow analytical solution, is developed and evaluated to provide a first approximation of the potential and current distributions in the electrolyte and steel band. To gain knowledge and validate the model, a small electrolytic pickling cell is constructed, and experiments, including bubble generation and motion observation, are conducted. The experimental work has shown the remarkable bubble production and adherence to the surfaces, and its effects on reducing pickling efficiency and uniformity. The pickling efficiency is about 30%, confirming other researchers" results. The analytical model shows trends very similar to those observed in the experiments, and provides very valuable guidance. It shows, for example, that the current efficiency decreases as the electrode–band distance increases, and it increases with the band thickness and the band-to-electrolyte conductivity ratio. The energy efficiency decreases by orders of magnitude faster than the current efficiency with all of the above-mentioned parameters, because of the correspondingly strong drop in the band–surface potential. A large amount of current is lost due to interelectrode short circuiting. 相似文献
8.
Chemical studies on antioxidant mechanisms and free radical scavenging properties of lignans 总被引:1,自引:0,他引:1
Eklund PC Långvik OK Wärnå JP Salmi TO Willför SM Sjöholm RE 《Organic & biomolecular chemistry》2005,3(18):3336-3347
The antioxidant activity, in terms of radical scavenging capacity, of altogether 15 different lignans was measured by monitoring the scavenging of the free radical 2,2-diphenyl-1-picrylhydrazyl (DPPH). The effect of differences in skeletal arrangement or the degree of oxidation of the lignans was investigated in a structure-activity relationship study. A large variety in the radical scavenging capacities of the different lignans was observed and related to some structural features. Lignans with catechol (3,4-dihydroxyphenyl) moieties exhibited the highest radical scavenging capacity, while the corresponding guaiacyl (3-methoxy-4-hydroxyphenyl) lignans showed a slightly weaker scavenging capacity. In addition, the butanediol structure was found to enhance the activity, whereas a higher degree of oxidation at the benzylic positions decreased the activity. Additionally, the readily available lignans (-)-secoisolariciresinol, a mixture of hydroxymatairesinol epimers and (-)-matairesinol were studied in more detail, including kinetic measurements and identification of oxidation products in the reactions with DPPH and ABAP (2,2-azobis(2-methylpropionamidine) dihydrochloride. The identification of reaction products, by GC-MS, HPLC-MS and NMR spectroscopy, showed that dimerisation of the two aromatic moieties was the major radical termination reaction. Also, the formation of adducts was a predominant reaction in the experiments with ABAP. The kinetic data obtained from the reactions between the lignans and DPPH indicated a complex reaction mechanism. 相似文献
9.
T. C. Awes C. Barlag F. Berger M. A. Bloomer C. Blume D. Bock R. Bock E. -M. Bohne D. Bucher A. Claussen G. Clewing L. Dragon A. Eklund S. Garpman R. Glasow H. Gustafsson H. H. Gutbrod G. Hölker J. Idh P. Jacobs K. H. Kampert B. W. Kolb H. Löhner I. Lund F. E. Obenshain A. Oskarsson I. Otterlund T. Peitzmann F. Plasil A. M. Poskanzer M. Purschke B. Roters S. Saini R. Santo H. R. Schmidt S. P. Sørensen K. Steffens P. Steinhaeuser E. Stenlund D. Stüken G. R. Young 《Zeitschrift fur Physik C Particles and Fields》1995,65(2):207-213
Correlations between protons are studied in the target fragmentation region of reactions of protons and16O with C, Cu, Ag, Au and of32S with Al and Au at 200A GeV. The emitted protons were measured with the Plastic Ball detector in the WA80 experiment at the CERN SPS. The comparison of the correlation function with calculations, assuming a spherical, gaussian shaped source with a lifetime τ=0 fm/c, allows the extraction of radius parameters. The values are very close to those expected from the geometry of the target nuclei and increase with the target mass as αA Target 1/3 . Even in proton induced reactions the whole target nucleus is involved. The dependence of the radii on centrality, polar angleθ lab, and energy, and their relation to measured proton yields are presented. 相似文献
10.