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Direct pathway

If areas identified as likely to receive significant atmospheric contaminant concentrations include areas supporting edible biota, the biouptake of contaminants must be considered as a possible environmental fate pathway. Direct biouptake from the atmosphere is a potential fate mechanism for lipophilic contaminants. Biouptake from soil or water following transfer of contaminants to these media must also be considered as part of the screening assessments of these media. [Pg.235]

Fructose-6-phosphate generated in this way enters the glycolytic pathway directly in step 3, the second priming reaction. This is the principal means for channeling fructose into glycolysis in adipose tissue, which contains high levels of fructose. [Pg.634]

As described in Section II,A, gram-positive bacteria have only one membrane (the cytoplasmic membrane). Therefore, the translocation through the Sec pathway directly leads proteins to be secreted (Simonen and Palva, 1993 Nagarajan, 1993). The issue of protein sorting into the cell wall is described in a separate section. [Pg.299]

Soil - Human Health Pathway Direct Contact) ... [Pg.248]

Plant. In plants, mevinphos is hydrolyzed to phosphoric acid dimethyl ester, phosphoric acid, and other less toxic compounds (Hartley and Kidd, 1987). In one day, the compound is almost completely degraded in plants (Cremlyn, 1991). Casida et al. (1956) proposed two degradative pathways of mevinphos in bean plants and cabbage. In the first degradative pathway, cleavage of the vinyl phosphate bond affords methylacetoacetate and acetoacetic acid, which may be precursors to the formation of the end products dimethyl phosphoric acid, methanol, acetone, and carbon dioxide. In the other degradative pathway, direct hydrolysis of the carboxylic ester would yield vinyl phosphates as intermediates. The half-life of mevinphos in bean plants was 0.5 d (Casida et ah, 1956). In alfalfa, the half-life was 17 h (Huddelston and Gyrisco, 1961). [Pg.814]

Five pathways were assessed during the project Groundwater, Surface water. Air pathway. Direct contact, and Stream sediments. [Pg.549]

It was recently discovered that 5. cerevisiae Ubrlp and Ufd4p, the E3 components of two distinct Ub-dependent proteolytic pathways, directly interact with specific proteins of the 26S proteasome (1). These results stemmed from the initial finding that overexpression of some subunits of the 19S particle inhibited ubiquitin-dependent degradation of engineered N-end rule substrates. To determine whether this effect could be caused by interaction of these subunits with a component(s) of the N-end rule pathway, glutathione transferase (GST)-pulldown assays with Ubrlp (also called... [Pg.17]

Methyldopa (l -adrenergic nerve vesicles, where it stoichiometrically replaces norepinephrine, and is released by nerve stimulation to interact with postsynaptic adrenoceptors. Flowever, this replacement of norepinephrine by a false transmitter in peripheral neurons is not responsible for methyldopa s antihypertensive effect, because the a-methylnorepinephrine released is an effective agonist at the cx adrenoceptors that mediate peripheral sympathetic constriction of arterioles and venules. In fact, methyldopa s antihypertensive action appears to be due to stimulation of central a adrenoceptors by a-methylnorepinephrine or a-methyldopamine. [Pg.228]

Figure 6 Diagram illustrating qualitative energetics for back ET via two pathways direct transfer from the bottom of the conduction band and transfer mediated by interfacial surface states (trap states). Note that the rate constants for the two processes may differ. Figure 6 Diagram illustrating qualitative energetics for back ET via two pathways direct transfer from the bottom of the conduction band and transfer mediated by interfacial surface states (trap states). Note that the rate constants for the two processes may differ.
Similar studies have been carried out in the 1,4-dihydropyridine series. Nevertheless, the detailed mechanism remains questionable and evidence in support of both possible reaction pathways, direct hydride transfer and electron-proton-electron transfer, were presented. [Pg.241]

Normally, under acidic conditions (pH < 4) the direct pathway dominates, above pH = 10 it changes to the indirect. In ground and surface waters (pH = 7) both pathways - direct and indirect - can be of importance (Staehelin and Hoigne, 1983 a). In special waste waters even at pH = 2 the indirect oxidation can be of importance, depending much on the contaminants present (Beltran et al., 1994). Both pathways should always be considered when developing a treatment scheme. [Pg.15]

Organic micropollutants are found in surface and ground waters, always in conjunction with more or less NOM, but at relatively low concentrations in the range of 0.1 pg L I to 100 pg L-1 (in water sources of sufficient quality for a water supply). Their degradation by ozone to oxidized metabolites or even to mineral products is a complex process, due to the influences of various water quality parameters (pH, inorganic and organic carbon etc.) on the two known major reaction pathways direct electrophilic ozone reaction and the oxidation via the nonselective, fast reacting OH-radicals. [Pg.25]

Reactions that replenish the intermediates in the TCA fcle are termed anaplerotic, from a Greek root that means [filling up. It is not necessary to replenish the intermedi-that is used in a biosynthetic pathway directly, because ly intermediate can be replenished by a feeding-in process om any point in the cycle. [Pg.295]

The phenomenon of such bimodal lifetime distribution proposed for reaction 1 on the basis of direct quasiclassical trajectory calculations were tested experimentally with the reaction of diaza-[2.2.1]bicycloheptane to [2.1. Ojbicyclopentane [Equation (2)].6 8 Experimental study on reaction 2 showed that the exo isomer 5x is formed favorably over the endo isomer 5n by about 3 1 in the gas phase. One explanation for the preferential formation of 5x invokes a competitive concerted and stepwise mechanism the concerted pathway directly from 4 to 5 gives 5x with the inversion of configuration at the carbon from which N2 is departing, whereas the stepwise pathway goes through the radical intermediate and leads to both 5x and 5n in equal amount. Alternatively, the product stereochemistry can be rationalized by dynamic matching between the entrance channel to the cyclopentane-1,3-diyl radical intermediate and the exit channel to bicyclo[2.1. Ojpentane as was assumed for reaction 2. [Pg.179]

It is worth noting that in one pathway toward ternary complex formation, the equilibrium constant Aa represents the receptor affinity for ligand and Aga represents the affinity of ligand-bound receptor for G protein. In this soluble receptor system, there is an opportunity to visualize the alternate pathway directly, where Ag is the receptor affinity for G protein in the absence of ligand, and Aag is the affinity of precoupled receptor (RG) for ligand. [Pg.109]

Three approaches leading to 8 were considered (Figure 3.6.9) Following the biosynthetic pathway directly, polymer-supported thiamine 9 was constructed (path A) and could lead via crossed acyloin couplings to the target structure. Polymer-supported hydrazones 10 were reported to add directly to aldehydes in a non-catalyzed Umpolung reaction (path B) with results reported in due course. Finally, phosphine ylides 11 were investigated as polymer-supported acyl anion equivalents (path C). [Pg.287]

Although in principle the metabolic clearance of plasma T3 may occur via several pathways, direct deiodination of the inner ring of T3 by the type I enzyme seems of minor importance (Section 2.2). Also, glucuronidation in the liver does not represent an irreversible pathway of T3 elimination since enzymatic hydrolysis of the conjugate in the intestine allows for the reabsorption of free T3 (enterohepatic cycle). Further, the finding that plasma T3 clearance is not affected in patients with liver cirrhosis [115] suggests that hepatic metabolism of T3 by sulfation and subsequent deiodination is less important than in rats. It appears, therefore, that the type III deiodinase of extrahepatic tissues is a major site for the clearance of plasma T3 as it is also for the production of plasma rT3. [Pg.99]

The activation barriers for these two steps have been computed as +14.0 and + 21.9 kcal/mol. The alternative pathways, direct addition of an oxygen to the ethylene and the [2 + 2]-addition both have a higher activation energy of + 30.0 and... [Pg.154]

These neuropeptides are coexpressed with GABA in subpopulations of striatal medium-sized spiny neurons, and therefore in subsets of the fibers which target the SN. As will be mentioned further (see Section 4.3), the striatal output reaches the SN through two main circuits distinct from the anatomical and functional points of view, defined as direct and indirect pathways. Direct pathway striatal neurons express the neuropeptide substance P and dynorphin, whereas indirect pathway striatal neurons express enkephalin (see Section 6.1). [Pg.33]

Figure 22.20. Models of two damage tolerance mechanisms. At the lesion site, template switching (the left pathway) uses the newly synthesized daughter strand as the template for DNA synthesis, thus, bypassing the lesion in an error-free manner. In contrast, translesion synthesis (the right pathway) directly copies the damaged site on the template. Consequently, mutations, shown as a square, are often generated opposite the lesion. Figure 22.20. Models of two damage tolerance mechanisms. At the lesion site, template switching (the left pathway) uses the newly synthesized daughter strand as the template for DNA synthesis, thus, bypassing the lesion in an error-free manner. In contrast, translesion synthesis (the right pathway) directly copies the damaged site on the template. Consequently, mutations, shown as a square, are often generated opposite the lesion.

See other pages where Direct pathway is mentioned: [Pg.1016]    [Pg.1249]    [Pg.480]    [Pg.700]    [Pg.260]    [Pg.265]    [Pg.214]    [Pg.22]    [Pg.201]    [Pg.456]    [Pg.247]    [Pg.389]    [Pg.500]    [Pg.583]    [Pg.1141]    [Pg.4]    [Pg.108]    [Pg.566]    [Pg.129]    [Pg.498]    [Pg.87]    [Pg.81]    [Pg.188]    [Pg.1285]    [Pg.39]    [Pg.79]    [Pg.251]    [Pg.254]    [Pg.1016]    [Pg.1249]   
See also in sourсe #XX -- [ Pg.14 , Pg.117 , Pg.128 ]




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Direct dehydration pathway

Direct dehydrogenation pathway

Direct four-electron pathway, oxygen

Direct four-electron pathway, oxygen reduction

Direct methanol fuel cell pathway

Direct percolation pathway

The direct, indirect and hyperdirect pathways of basal ganglia information processing

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