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Compartment theory

It is obvious why the spectroscopist wants to investigate the structure of integral membrane proteins or enzymes, whose biological action is linked to the presence of phospholipids such as phospholipase, in a membrane-mimicking environment Why such an environment should also be used for other peptides like hormones becomes more clear when we take into account the membrane compartment theory [10-12] as postulated by R. Schwyzer. This theory states that peptides that target membrane-embedded receptors... [Pg.95]

Fig. 4.—Compartment Theory of Starch Synthesis. (Key MM, membrane permeable to D-gluoose and maltosacoharides of DP 4 (1), D-enzyme (2) hexokinase-adenosine 5-triphosphate (3), phosphoglucomutase (4), P-enzyme with maltotetraose primer (5), Q-enzyme.)... Fig. 4.—Compartment Theory of Starch Synthesis. (Key MM, membrane permeable to D-gluoose and maltosacoharides of DP 4 (1), D-enzyme (2) hexokinase-adenosine 5-triphosphate (3), phosphoglucomutase (4), P-enzyme with maltotetraose primer (5), Q-enzyme.)...
BIOPATH (Befrgstrom et al., 1982) computes the contaminant transport in geo- and biosphere based on compartment theory, and the subsequent radiological doses to critical groups. It apphes first order differential equations for kinetics. [Pg.88]

The expression for the nucleation rate 5 in the compartment / is derived from the theory of primary nucleation and found to be (Mullin, 2001)... [Pg.219]

Eriksson, E. (1971). Compartment models and reservoir theory. Ann. Rev. Ecol. Syst. 2, 67-84. [Pg.83]

In Chapter 11 it was shown that control volume theory for the bulk compartment smoke properties could be expressed in dimensionless solutions. The characteristic length scale involves the geometric components of wall vents as 1 = f/f0 (//0 )1 /2]2/ 5. Hence, the MQH correlation [18] leads to... [Pg.398]

In SSP, the boundaries for the mass balances are defined by the particle instead of the reactor or the reactor compartment dimensions and the process conditions are accounted for by a boundary condition. The mass transfer at the particle/gas interface is mostly described according to the film theory by using a mass-transfer coefficient. [Pg.85]

The simplest practicable approach considers the membrane as a continuous, nonporous phase in which water of hydration is dissolved.In such a scenario, which is based on concentrated solution theory, the sole thermodynamic variable for specifying the local state of the membrane is the water activity the relevant mechanism of water back-transport is diffusion in an activity gradient. However, pure diffusion models provide an incomplete description of the membrane response to changing external operation conditions, as explained in Section 6.6.2. They cannot predict the net water flux across a saturated membrane that results from applying a difference in total gas pressures between cathodic and anodic gas compartments. [Pg.398]

In the present study, EXAMS was used to calculate volatilization rate constants from water, wet soil, and a water-soil mixture. EXAMS uses the two-film theory to calculate volatilization rates from the 10 cm wind speed as discussed above. EXAMS requires as a minimum environment at least one littoral (water) and one benthic (sediment) compartment. A very small benthic compartment for the water system and a very small littoral compartment for the wet soil system (7.09 x 10 m3 volume and 1 x 10 8 m depth in both cases) was used, so that these compartments and their input parameters had a negligible effect on the calculated rates. For the water-soil system, the same proportions were used as in the laboratory experiment. Transfer rates between soil and water were assumed to be rapid relative to volatilization rates, and were set as recommended in the EXAMS manual (24). The input data needed by EXAMS in order to calculate volatilization rates from a water-soil system, using parathlon as an example, are shown in Table IV. [Pg.290]

Figure 3 summarizes the principal environmental compartments that can in theory be affected by coal mining, as well as the principal potential environmental stresses that can arise from active and abandoned mine voids on the one hand, and from mine waste management facilities (i.e., spoil heaps and washery finings ponds) on the other. Further details on the mechanisms and impacts of these environmental stresses are given in Table 4 (for coal mine voids) and Table 5 (for coal mine wastes). [Pg.180]

In this theory, calcium enters the cell down the enormous electrochemical gradient that normally exists between the extracellular and intracellular fluid compartments. In doing so, it actually reverses the calcium pump and synthesizes ATP in a similar way as the reversal of the sarcoplasmic calcium pumps617 (Fig. 7). There is however, no evidence to support this theory and it has a number of unlikely features. It stresses the need for relevant data rather than circumstantial evidence, and this is particularly necessary in considering intracellular theories. [Pg.101]

The last term in equation 5.245 represents the dilution of active component /, by the expansion of the biomass. Esener et al.m also present a two-compartment model which takes this effect into account and they emphasise the need to devise the theory so that it can be tested by experiment. In their model they identify a K compartment of the biomass which comprised the RNA and other small cellular molecules. The other compartment contained the larger genetic material, enzymes, and structural material. The model assumes that the substrate is absorbed by the cell to produce, in the first instance, K material, and thence it is transformed into G material. Additionally, the G material can be reconverted to K material, a feature intended to account for the maintenance requirement of the micro-organism. A series of material balances for the cellular components during growth in a CSTF produced the following differential equations ... [Pg.401]

The common ancestor of life was probably a chemoautotrophic hyperthermophilic anaerobe. This metabolism first theory assumes that life started with catalytic metal sulfide surface/compartments in a hydro thermal-vent setting in the Hadean... [Pg.49]

The uptake of tetrachloroethene in pine needles is reported to be more complex than the published model [45]. In that study, pine needles in a chamber were exposed to elevated levels of tetrachloroethene, and its concentration in the needles were predicted via its Koa and lipid content. When the needles had been exposed to the much lower environmental levels, the concentration of tetrachlorethene was much greater than predicted. It was suggested that an additional compartment in the needles bioconcentrated the tetrachlorethene in excess of theory but had a limited capacity to absorb tetrachlorethene. [Pg.223]

S. Claudel, C. Fonteix, J.P. Leclerc, and H.G. Lintz. Application of the possibility theory to the compartment modelling of flow pattern in industrial processes. Chemical Engineering Science, 58 4005-4016, 2003. [Pg.170]

To understand any extraction technique it is first necessary to discuss some underlying principles that govern all extraction procedures. The chemical properties of the analyte are important to an extraction, as are the properties of the liquid medium in which it is dissolved and the gaseous, liquid, supercritical fluid, or solid extractant used to effect a separation. Of all the relevant solute properties, five chemical properties are fundamental to understanding extraction theory vapor pressure, solubility, molecular weight, hydrophobicity, and acid dissociation. These essential properties determine the transport of chemicals in the human body, the transport of chemicals in the air water-soil environmental compartments, and the transport between immiscible phases during analytical extraction. [Pg.37]


See other pages where Compartment theory is mentioned: [Pg.25]    [Pg.25]    [Pg.104]    [Pg.51]    [Pg.147]    [Pg.435]    [Pg.306]    [Pg.209]    [Pg.422]    [Pg.57]    [Pg.957]    [Pg.339]    [Pg.23]    [Pg.192]    [Pg.293]    [Pg.482]    [Pg.177]    [Pg.317]    [Pg.223]    [Pg.524]    [Pg.139]    [Pg.98]    [Pg.98]    [Pg.24]    [Pg.7]    [Pg.224]    [Pg.101]    [Pg.134]    [Pg.16]   
See also in sourсe #XX -- [ Pg.25 , Pg.26 ]




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Membrane compartment theory

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