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Compartmentalization

The succeeding material is broadly organized according to the types of experimental quantities measured because much of the literature is so grouped. In the next chapter spread monolayers are discussed, and in later chapters the topics of adsorption from solution and of gas adsorption are considered. Irrespective of the experimental compartmentation, the conclusions as to the nature of mobile adsorbed films, that is, their structure and equations of state, will tend to be of a general validity. Thus, only a limited discussion of Gibbs monolayers has been given here, and none of such related aspects as the contact potentials of solutions or of adsorption at liquid-liquid interfaces, as it is more efficient to treat these topics later. [Pg.92]

It has become fashionable to prefix the names of disciplines with bio , as in biophysics, bioinfonnatics and so on, giving the impression that in order to deal with biological systems, a different kind of physics, or infonnation science, is needed. But there is no imperative for this necessity. Biological systems are often very complex and compartmentalized, and their scaling laws may be different from those familiar in inanimate systems, but this merely means that different emphases from those useful in dealing with large unifonn systems are required, not that a separate branch of knowledge should necessarily be developed. [Pg.2846]

EBHP is mixed with a catalyst solution and fed to a horizontal compartmentalized reactor where propylene is introduced into each compartment. The reactor operates at 95—130°C and 2500—4000 kPa (360—580 psi) for 1—2 h, and 5—7 mol propylene/1 mol EBHP are used for a 95—99% conversion of EBHP and a 92—96% selectivity to propylene oxide. The homogeneous catalyst is made from molybdenum, tungsten, or titanium and an organic acid, such as acetate, naphthenate, stearate, etc (170,173). Heterogeneous catalysts consist of titanium oxides on a siUca support (174—176). [Pg.140]

Electrodialysis. Electro dialysis processes transfer ions of dissolved salts across membranes, leaving purified water behind. Ion movement is induced by direct current electrical fields. A negative electrode (cathode) attracts cations, and a positive electrode (anode) attracts anions. Systems are compartmentalized in stacks by alternating cation and anion transfer membranes. Alternating compartments carry concentrated brine and purified permeate. Typically, 40—60% of dissolved ions are removed or rejected. Further improvement in water quaUty is obtained by staging (operation of stacks in series). ED processes do not remove particulate contaminants or weakly ionized contaminants, such as siUca. [Pg.262]

Figure 13.3 A typical cubicle-type fully compartmentalized power distribution board (Courtesy EC-3)... Figure 13.3 A typical cubicle-type fully compartmentalized power distribution board (Courtesy EC-3)...
Non-compartmentalized type In this type a group of feeders are housed in one enclosure, and attending one would mean an exposure to the others (Figure 13.4). [Pg.341]

Compartmentalized type In this type each feeder is housed in a separate compartment (module) of its own and attending one would limit the exposure only to that unit (Figures 13.1 and 13.3). In this construction a fault, particularly of the nature of a short-circuit. [Pg.341]

Figure 13.28 A typical compartmentalized outdoor-type panel (Courtesy ECS)... Figure 13.28 A typical compartmentalized outdoor-type panel (Courtesy ECS)...
In what follows, both macromixing and micromixing models will be introduced and a compartmental mixing model, the segregated feed model (SFM), will be discussed in detail. It will be used in Chapter 8 to model the influence of the hydrodynamics on a meso- and microscale on continuous and semibatch precipitation where using CFD, diffusive and convective mixing parameters in the reactor are determined. [Pg.49]

The model is able to predict the influence of mixing on particle properties and kinetic rates on different scales for a continuously operated reactor and a semibatch reactor with different types of impellers and under a wide range of operational conditions. From laboratory-scale experiments, the precipitation kinetics for nucleation, growth, agglomeration and disruption have to be determined (Zauner and Jones, 2000a). The fluid dynamic parameters, i.e. the local specific energy dissipation around the feed point, can be obtained either from CFD or from FDA measurements. In the compartmental SFM, the population balance is solved and the particle properties of the final product are predicted. As the model contains only physical and no phenomenological parameters, it can be used for scale-up. [Pg.228]

H. J. M. Kramer, J. W. Dijkstra, A. M. Neumann, R. O Meadhra, G. M. van Rosmalen. Modelling of industrial crystalhzers, a compartmental approach using a dynamic flow-sheeting tool. J Cryst Growth 755 1084, 1996. [Pg.932]

FIGURE 18.16 Compartmentalization of glycolysis, the citric acid cycle, and oxidative phosphorylation. [Pg.584]

What are the advantages of compartmentalizing particular metabolic pathways within specific organelles ... [Pg.608]

Lowen.stein, J. M., ed., 1969. Citric Acid Cycle Control and Compartmentation. New York Marcel Dekker. [Pg.672]

Compartmentation of these reactions to prevent photorespiration involves the interaction of two cell types, mescrphyll cells and bundle sheath cells. The meso-phyll cells take up COg at the leaf surface, where Og is abundant, and use it to carboxylate phosphoenolpyruvate to yield OAA in a reaction catalyzed by PEP carboxylase (Figure 22.30). This four-carbon dicarboxylic acid is then either reduced to malate by an NADPH-specific malate dehydrogenase or transaminated to give aspartate in the mesophyll cells. The 4-C COg carrier (malate or aspartate) then is transported to the bundle sheath cells, where it is decarboxylated to yield COg and a 3-C product. The COg is then fixed into organic carbon by the Calvin cycle localized within the bundle sheath cells, and the 3-C product is returned to the mesophyll cells, where it is reconverted to PEP in preparation to accept another COg (Figure 22.30). Plants that use the C-4 pathway are termed C4 plants, in contrast to those plants with the conventional pathway of COg uptake (C3 plants). [Pg.738]

Two particularly interesting aspects of the pyruvate carboxylase reaction are (a) allosteric activation of the enzyme by acyl-coenzyme A derivatives and (b) compartmentation of the reaction in the mitochondrial matrix. The carboxy-lation of biotin requires the presence (at an allosteric site) of acetyl-coenzyme A or other acylated coenzyme A derivatives. The second half of the carboxylase reaction—the attack by pyruvate to form oxaloacetate—is not affected by CoA derivatives. [Pg.745]

COMPARTMENTALIZED PYRUVATE CARBOXYLASE DEPENDS ON METABOLITE CONVERSION AND TRANSPORT The second interesting feature of pyruvate carboxylase is that it is found only in the matrix of the mitochondria. By contrast, the next enzyme in the gluconeogenic pathway, PEP carboxykinase, may be localized in the cytosol or in the mitochondria or both. For example, rabbit liver PEP carboxykinase is predominantly mitochondrial, whereas the rat liver enzyme is strictly cytosolic. In human liver, PEP carboxykinase is found both in the cytosol and in the mitochondria. Pyruvate is transported into the mitochondrial matrix, where it can be converted to acetyl-CoA (for use in the TCA cycle) and then to citrate (for fatty acid synthesis see Figure 25.1). /Uternatively, it may be converted directly to 0/ A by pyruvate carboxylase and used in glu-... [Pg.746]

FIGURE 23.5 Pyruvate carboxyl compartmentalized reaction. Pyruva verted to oxaloacetate in the mitoci Because oxaloacetate cannot be trai across the mitochondrial membrant reduced to malate, transported to tl and then oxidized back to oxaloace gluconeogenesis can continue. [Pg.747]

Sies, H., ed., 1982. Metabolic Compartmentation. London Academic Press. [Pg.774]

Li.scnm, L., and Underwood, K. W., 1995. Intracellular chole.sterol tran.s-port and compartmentation. Journal of Biological Chemistry 270 15443-15446. [Pg.850]

Oppenheimer. Like the Chicago-based scientists before him, Oppenheimer and his researchers often clashed with Groves and the project engineers, who preferred to compartmentalize and control information about the project rather than exchange it freely among the scientists. At Los Alamos, Oppenheimer s approach prevailed. [Pg.851]

Compartmentalization of the structure (and maintenance of such compartmentalization) may contain or minimize fire spread ... [Pg.52]

It is essential to discuss the requirements for stmc-tural protection, compartmentalization, emergency lighting, detection, alarms, call points, suppression, means of escape and signage with the applicable local authority, fire brigade or insurance company personnel before finalizing designs. [Pg.52]

Western science has traditionally emphasized reductionism as the road to understanding. Reductionism, of course, is a process that involves the systematic labeling, categorizing and compartmentalizing of objects. Unfortunately, the western world has also somewhere along the line lost sight of the fact that the universe is ojjc, essentially unlmgmented, whole. [Pg.700]


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Activation barriers, compartmentalized

Adenine nucleotides, compartmentation

Advanced compartmental absorption

Advanced compartmental absorption and

Advanced compartmental absorption and transit

Advanced compartmental absorption and transit model

Advantages of Compartmentalization

Approach compartmental

Berberine enzyme compartmentalization

Berberines compartmentation

Biological models compartmentalization

Biosynthesis enzyme compartmentalization

Boundary conditions, compartmentalized

Building compartmentation

Cell compartmentation

Cellular compartmentalization

Cellular compartmentation

Chemical compartmentation

Closed compartmental system

Closed generalized compartmental

Column compartmentalization

Compartment models versus non-compartmental analysis

Compartment, compartmentation

Compartmental

Compartmental Models and Heterogeneity

Compartmental absorption and transit

Compartmental absorption and transit model

Compartmental analysis

Compartmental barriers

Compartmental dynamic systems

Compartmental ecokinetics

Compartmental folate

Compartmental identifiability

Compartmental ligands

Compartmental ligands, functions

Compartmental membrane transport

Compartmental model mass transfer

Compartmental model, discussion

Compartmental modeling

Compartmental modeling 3-carotene

Compartmental modeling dynamic systems

Compartmental modeling identifiability

Compartmental modeling membrane transport

Compartmental modeling parameters

Compartmental modeling population kinetics

Compartmental modeling techniques

Compartmental modeling, 3-caroten

Compartmental models

Compartmental models, definition

Compartmental parameters

Compartmental pharmacokinetic

Compartmental pharmacokinetic models

Compartmental pharmacokinetics

Compartmental population kinetics

Compartmental specificity, description

Compartmental structure

Compartmental system

Compartmental vitamin

Compartmentalization analysis

Compartmentalization chloroplasts

Compartmentalization mitochondria

Compartmentalization of radicals

Compartmentalization of tissue

Compartmentalization, basic principles

Compartmentalization, functional groups

Compartmentalized deposition fraction

Compartmentalized shell

Compartmentalized system

Compartmentalized systems, chemical reaction clays

Compartmentalized water

Compartmentation

Compartmentation breaches

Compartmentation fire resistance

Compartmentation horizontal

Compartmentation of metabolites

Compartmentation of proteins

Compartmentation openings

Compartmentation services

Compartmentation, of enzymes

Compositional compartmentalization

Concentration effect, compartmentalized

Conditional probability, compartmentalized

Deterministic Compartmental Models

Dimensionality, compartmentalized systems

Dimensionality, compartmentalized systems chemical reaction efficiency

Dimensionality, compartmentalized systems reduction

Emulsion polymerization compartmentalization

Enzyme compartmentalization

Enzyme compartmentation solubility

Enzyme regulation compartmentalization

Enzymes compartmentation

Eukaryotic cells compartmentation

Extracellular space compartmental

Flow, fluid compartmentalization

Folate metabolism compartmentation

Fractal sets compartmentalized systems

Generalised compartmental system

Genome compartmentalization

Geometrical effects, compartmentalized

Gluconeogenesis compartmentation

Glutathione compartmentation

Heterometallic Complexes Derived from Bridging and Multi-compartmental Ligands

In vitro compartmentalization

Intracellular Compartmentation and Metabolism

Intracellular compartmentation

Isoprenoids compartmentation

Linear Compartmental Models

Lipid bilayer compartmentalization

Liposomes compartmentalized reactions

Liver compartmental modeling

Metabolic compartmentation

Metabolism compartmentation

Metabolism compartmentation and

Metabolites compartmentation

Miniemulsion polymerization compartmentalization effects

Model Advanced Compartmental

Model modeling compartmental

Modeling/simulation compartmental models

Multi-compartmental ligands

Multienzyme compartmentalization

Multimedia compartmental models

Non-compartmental analysis

Non-compartmental model

Nonlinear Compartmental Models

On the inverse problem of generalised compartmental systems

Oxidative phosphorylation compartmentation

Parasagittal zonation in the cerebellar cortex Antigenic compartmentation for Zebrin and other markers

Pharmacokinetic profile compartmental pharmacokinetics

Pharmacokinetics compartmental analysis

Pharmacokinetics parameters from compartmental

Physiology, question compartmentation

Potential effects, compartmentalized systems

Radical compartmentalization

Radical compartmentalization effect

Radical compartmentalization effect emulsion polymerization

Radical polymerization reactions, compartmentalized

Reactive processes, compartmentalized

Reservoir compartmentalization

Ribosomes compartmentalization

Rotaxanes compartmental

Secondary compartmentalization

Species Differences in Compartmentation

Stochastic Compartmental Models

Subcellular Compartmentation of NAD and Its Metabolism

Subcellular compartmentalization

Suberization as a Means of Compartmentalization

Substrate cycles compartmentation

Surface-compartmentalized nanoparticl

The Compartmentation of CAM Enzymes and Metabolites

Trace compartmental modeling

Transport processes, compartmentalized

Vacuole compartmentation, 187

Vitamin compartmental analysis

Vitamin compartmental modeling

Ways in which Synthetic Polymers Cross Compartmental Barriers

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