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61.
We report the use of a novel pulsed ESR technique for distance measurement, based on the detection of double quantum coherence (DQC), which yields high quality dipolar spectra, to significantly extend the range of measurable distances in proteins using nitroxide spin-labels. Eight T4 lysozyme (T4L) mutants, doubly labeled with methanethiosulfonate spin-label (MTSSL), have been studied using DQC-ESR at 9 and 17 GHz. The distances span the range from 20 A for the 65/76 mutant to 47 A for the 61/135 mutant. The high quality of the dipolar spectra also allows the determination of the distance distributions, the width of which can be used to set upper and lower bounds in future computational strategy. It is also demonstrated that the shape of these distributions can reveal the presence of multiple conformations of the spin-label, an issue of critical relevance to the structural interpretation of the distances. The distances and distributions found in this study are readily rationalized in terms of the known crystal structure, the characteristic conformers of the nitroxide side chains, and molecular modeling. This study sets the stage for the use of DQC-ESR for determining the tertiary structure of large proteins with just a small number of long-distance constraints. 相似文献
62.
63.
Donners JJ Heywood BR Meijer EW Nolte RJ Sommerdijk NA 《Chemistry (Weinheim an der Bergstrasse, Germany)》2002,8(11):2561-2567
Poly(propylene imine) dendrimers that are modified with long alkyl chains self-assemble to form well-defined aggregates. The geometry and surface chemistry of the dendrimer assemblies can be varied through the addition of surfactants. These dendrimer/surfactant aggregates can be tuned to template the formation of the different phases of calcium carbonate. The use of octadecylamine results in the formation of polyhedral aggregates that become embedded within an amorphous calcium carbonate phase that persists in competition with the thermodynamic product, calcite. In combination with hexadecyltrimethylammonium bromide, small spherical aggregates are formed that induce the formation of vaterite. The use of the negatively charged surfactant SDS results in growth retardation by the Ca(2+)-induced agglomeration of dendrimer/surfactant aggregates into giant spherical particles. Eventually these particles become overgrown by rhombohedral calcite. 相似文献
64.
[Reaction: see text] We report a one-step, racemization-free method for the diversification of peptide thiazoles via direct lithiation of the thiazole ring. The method is compatible with N-Boc, N-trityl, carboxylic ester, and carboxamide protecting groups and has been used to directly functionalize the thiazole ring of cyclopeptide natural products. 相似文献
65.
N. P. Krut'ko L. V. Dikhtievskaya A. D. Markin V. V. Shevchuk A. S. Gorbachev M. M. Varava V. M. Kirienko 《Russian Journal of Applied Chemistry》2005,78(8):1213-1217
The surface activity of higher aliphatic amines and their salts at the interface between their solutions and air, oil, and KCl grains and their influence on the strength characteristics, moisture absorption, and caking of the grains were studied. 相似文献
66.
Summary The rhodium(I) carboxylates,trans-RhO2CR(CO)(PPh3)2 (R = C6F5, C6Cl5,p-HC6F4,m-HC6F4,o-HC6F4,p-McOC6F4, 4,5-H2C6F3, 3,5-H2C6F3, or 2,6-F2C6H3, have been prepared by reaction of RhH(CO)(PPh3)3 with the appropriate polyhalogenobenzoic acids in ethanol and/or by reaction oftrans-RhCl(CO)(PPh3)2 with the appropriate thallous carboxylates in benzene. Decarboxylations with formation of polyhalogenoarylrhodium(I) compounds,trans-RhR(CO)(PPh3)2 (R = C6F5, C6Cl5,p-HC6F4,m-HC6F4,p-MeOC6F4, 4,5-H2C6F3 or 3,5-H2C6F3), have been achieved either by decomposition of the corresponding rhodium(I) carboxylates in pyridine or by reaction oftrans-RhCl(CO)(PPh3)2 and the thallous carboxylates in pyridine, but the derivatives R =o-HC6F4 or 2,6-F2C6H3 could not be obtained by this method. The rate of decarboxylation decreased in the sequence R = C6F5 >p-MeOC6F4 >p-HC6F4 >m-HC6F4 > 4,5-H2C6F3 > 3,5-H2C6F3.Part 1, ref. 10.Preliminary communication, ref. 9. 相似文献
67.
68.
Xuejun Pan Dan Xie Neil Gilkes David J. Gregg Jack N. Saddler 《Applied biochemistry and biotechnology》2005,124(1-3):1069-1079
Pretreatment of Douglas-fir by steam explosion produces a substrate containing approx 43% lignin. Two strategies were investigated
for reducing the effect of this residual lignin on enzymatic hydrolysis of cellulose: mild alkali extraction and protein addition.
Extraction with cold 1% NaOH reduced the lignin content by only approx 7%, but cellulose to glucose conversion was enhanced
by about 30%. Before alkali extraction, addition of exogenous protein resulted in a significant improvement in cellulose hydrolysis,
but this protein effect was substantially diminished after alkali treatment. Lignin appears to reduce cellulose hydrolysis
by two distinct mechanisms: by forming a physical barrier that prevents enzyme access and by non-productively binding cellulolytic
enzymes. Cold alkali appears to selectively remove a fraction of lignin from steam-exploded Douglas-fir with high affinity
for protein. Corresponding data for mixed softwood pretreated by organosolv extraction indicates that the relative importance
of the two mechanisms by which residual lignin affects hydrolysis is different according to the pre- and post-treatment method
used. 相似文献
69.
70.
Jack C. Kim Sang-Duk Bae Ji-A Kim Soon-Kyu Choi 《Journal of heterocyclic chemistry》1998,35(3):531-533
A Regioselective synthesis of (R)-11-hydroxyaporphine 2 directly from (R)-10,11-dihydroxyaporphine ((R)-apomorphine, 1 ) is described for the first time. The isopropylidene ketal ring of 10,11-(isopropyl-idenyldioxy)aporphine 5 obtained by the isopropylidenation of apomorphine was regioselectively opened by ten equivalents of trimethylaluminum to give (R)-10-hydroxy-11-tert-butyloxyaporphine 6 . The free 10-hydioxyl position of 6 was triflated with N-pbenyltrifluoromethanesulfonimide and potassium carbonate under reflux to give (R)-10-[(trifluoromethyl)sulfonyloxy]-11-tert-butyloxyaporphine 7 . The reduced product, 11-tert-butyloxyaporphine 8 was prepared from 7 by a palladium-catalyzed hydrogenolysis. The ether cleavage of (R)-11-tert-butyloxyaporphine with 48% hydrobromic acid afforded the desired (R)-11-hydroxyaporphine 2 in good yield. 相似文献