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Parked reaction

Switching the system to zero potential for a fixed period of time within the time window bracketing the passage of the enzyme by the detector would allow for product accumulation. When the power is switched on again, the enzyme will be separated from the product and, if the product has suitable detection properties, it will appear as a peak on the enzyme plateau. This approach is sometimes referred to as parked reaction. A practical application featuring the activity assay of D-glucose-6-phosphate NADPH oxidore-ductase is shown in Figure 8.10. [Pg.189]

Figure 8.10 Electropherograms showing accumulated peaks resulting from the parked reaction at different running times. (A) NADPH accumulated at the beginning before electrophoresis. (fl) NADPH accumulated just before glucose-6-phosphate oxidore-ductase passed the detection window. (From Bao and Regnier 1992, with permission.)... Figure 8.10 Electropherograms showing accumulated peaks resulting from the parked reaction at different running times. (A) NADPH accumulated at the beginning before electrophoresis. (fl) NADPH accumulated just before glucose-6-phosphate oxidore-ductase passed the detection window. (From Bao and Regnier 1992, with permission.)...
J.W. Park, Reaction of S-nitrosoglutathione with sulfhydryl groups in proteins, Biochem. Biophys. Res. Commun. 152 (1988) 916-920. [Pg.99]

Park T J and Light J C 1989 Accurate quantum thermal rate constants for the three-dimensional H + H2 reaction J. Chem. Phys. 91 974... [Pg.2328]

RIchtsmeler S C, Parks E K, Liu K, Polo L G and Riley S J 1985 Gas phase reaction of Iron clusters with hydrogen. I. Kinetics J. Chem. Rhys. 82 3659... [Pg.2403]

Precipitation can also occur upon chemical reaction between the impurity and a precipitating agent to form a compound insoluble in the molten metal. The refining of cmde lead is an example of this process. Most copper is removed as a copper dross upon cooling of the molten metal, but the removal of the residual copper is achieved by adding sulfur to precipitate copper sulfide. The precious metals are separated by adding zinc to Hquid lead to form soHd intermetaHic compounds of zinc with gold and silver (Parkes process). The precious metals can then be recovered by further treatment (see Lead). [Pg.169]

Controlled Nuclear Chain Reaction The First 50 Years, American Nuclear Society, La Grange Park, lU., 1992. [Pg.226]

H. O. House, Modem Synthetic Reactions, W. A. Benjamin, Inc., Menlo Park, Calif., 1972. [Pg.385]

P. W. Lumiann, W. P. L. Carter, and L. A. Coyner, M Surrogate Species Chemical Reaction Mechanism for Urban-Scale Mir Quality Simulation Models, Report No. EPA/600/3-87-014, U.S. Environmental Protection Agency, Research Triangle Park, N.C., 1987. [Pg.388]

RB Yelle, N-S Park, T Ichiye. Molecular dynamics simulations of rubredoxm from Clostridium pasteurianum Changes m structure and electrostatic potential during redox reactions. Proteins 22 154-167, 1995. [Pg.412]

The in-out bicyclic amines prepared by Simmons and Park bear a remarkable semblance to the cryptands but lack the binding sites in the bridges. As a result, these molecules interact with electrophiles in a fashion similar to other tertiary amines and generally do not exhibit strong interactions with alkali or alkaline earth metal ions. The in-out bicyclic amines are prepared by reaction of the appropriate acid chlorides and amines in two stages to yield the macrobicyclic amine after reduction of the amidic linkages. A typical amine is shown above as compound 18. [Pg.355]

J. Zhuo, S. Redner, H. Park. Critical behavior of an interacting surface reaction model. J Phys A (Math Gen) 26 4197-4213, 1993. [Pg.436]

The addition of nucleophiles to cyclic fluoroolefins has been reviewed by Park et al. [2 ]. The reaction with alcohols proceeds by addition-elimination to yield the cyclic vinylic ether, as illustrated by tlie reaction of l,2-dichloro-3,3-di-fluorocyclopropene Further reaction results in cyclopropane ring opening at the bond opposite the difluoromethylene carbon to give preferentially the methyl and ortho esters of (Z)-3-chloro-2-fluoroacrylic acid and a small amount of dimethyl malonate [29] (equation 8). [Pg.731]

Unlike in the case of conventional organic solvents, most research groups prepare the ionic liquids themselves. This may be the reason why different results are sometimes obtained with the same ionic liquids. Park and Kazlauskas performed a washing procedure with aqueous sodium carbonate and found improved reaction rates, but this might also be related to a more precisely defined water content/water activity in the reaction system [22]. [Pg.338]

ILZRO, High Temperature Galvanizing, ILZRO Research Triangle Park, N.C. (1980) Horstmann, D., Reactions Between Iron and Molten Zinc, ZDA, London (1978)... [Pg.394]

H. 0. House, Modern Synthetic Reactions, p. 606, Benjamin, Menlo Park 1972. [Pg.999]

Locke, BR Arce, P Park, Y, Applications of Self-Adjoint Operators to Electrophoretic Transport, Enzyme Reactions, and Microwave Heating Problems in Composite Media—II. Electrophoretic Transport in Layered Membranes, Chemical Engineering Science 48, 4007, 1993. [Pg.615]

J. Kim, J.-K. Park and B.-S. Kwak Proceedings of the "4th Asia-Pacific Chemical Reaction Engineering Symposium, APCRE05", pp. 441 (12 -15 June 2005) Gyeongju, Korea. [Pg.42]

Typically the reaction was carried out as follows to a mixture of lipase in the IL were added this racemic alcohol and vinyl acetate as the acyl donor. The resulting mixture was stirred at 35°C and the reaction course was monitored by GC analysis. After the reaction, ether was added to the reaction mixture to form a biphasic layer, and product acetate and unreacted alcohol were extracted with ether quantitatively. The enzyme remained in the IL phase as expected (Fig. 2). Two months later, Kim and co-workers reported similar results and Lozano and Ibora " reported other examples of lipase-catalyzed reaction in June. Further Park and Kazlauskas reported full details of lipase-catalyzed reaction in an IL solvent... [Pg.4]


See other pages where Parked reaction is mentioned: [Pg.243]    [Pg.310]    [Pg.243]    [Pg.310]    [Pg.370]    [Pg.293]    [Pg.177]    [Pg.122]    [Pg.32]    [Pg.385]    [Pg.184]    [Pg.216]    [Pg.413]    [Pg.388]    [Pg.1117]    [Pg.82]    [Pg.629]    [Pg.152]    [Pg.965]    [Pg.133]    [Pg.154]    [Pg.196]    [Pg.80]    [Pg.617]    [Pg.323]    [Pg.511]    [Pg.965]    [Pg.427]   
See also in sourсe #XX -- [ Pg.189 ]




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