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Collapsed membranes

Macri R, Vianello A, Pennazio S. 1986. Salicylate-collapsed membrane potential in pea stem mitochondria. Physiol Plantarum 67 136-140. [Pg.548]

Recently there has been considerable interest in the phase transition of polymerized (tethered) membranes with attractive interactions [1-4]. In a pioneer work [1], Abraham and Nelson found by molecular dynamics simulations that the introduction of attractive interactions between monomers leads to a collapsed membrane with fractal dimension 3 at a sufficiently low temperature. Subsequently, Abraham and Kardar [2] showed that for open membranes with attractive interactions, as the temperature decreases, there exists a well-defined sequence of folding transitions and then the membrane ends up in the collapsed phase. They also presented a Landau theory of the transition. Grest and Petsche [4] extensively carried out molecular dynamics simulations of closed membranes. They considered flexible membranes the nodes of the membrane are connected by a linear chain of n monomers. For short monomer chains, n = 4, there occurs a first-order transition from the high-temperature flat phase to... [Pg.288]

Fouling Industrial streams may contain condensable or reactive components which may coat, solvate, fill the free volume, or react with the membrane. Gases compressed by an oil-lubricated compressor may contain oil, or may be at the water dew point. Materials that will coat or harm the membrane must be removed before the gas is treated. Most membranes require removal of compressor oil. The extremely permeable poly(trimethylsilylpropyne) may not become a practical membrane because it loses its permeability rapidly. Part of the problem is pore collapse, but it seems extremely sensitive to contamination even by diffusion pump oil and gaskets [Robeson, op. cit., (1994)]. [Pg.2050]

Figure 12-8. Principles of the chemiosmotic theory of oxidative phosphorylation. The main proton circuit is created by the coupling of oxidation in the respiratory chain to proton translocation from the inside to the outside of the membrane, driven by the respiratory chain complexes I, III, and IV, each of which acts as a protonpump. Q, ubiquinone C, cytochrome c F Fq, protein subunits which utilize energy from the proton gradient to promote phosphorylation. Uncoupling agents such as dinitrophenol allow leakage of H" across the membrane, thus collapsing the electrochemical proton gradient. Oligomycin specifically blocks conduction of H" through Fq. Figure 12-8. Principles of the chemiosmotic theory of oxidative phosphorylation. The main proton circuit is created by the coupling of oxidation in the respiratory chain to proton translocation from the inside to the outside of the membrane, driven by the respiratory chain complexes I, III, and IV, each of which acts as a protonpump. Q, ubiquinone C, cytochrome c F Fq, protein subunits which utilize energy from the proton gradient to promote phosphorylation. Uncoupling agents such as dinitrophenol allow leakage of H" across the membrane, thus collapsing the electrochemical proton gradient. Oligomycin specifically blocks conduction of H" through Fq.
Compression of the PS II membrane monolayer shows that the monolayer collapses at a relatively low surface pressure, at around 20mN/m. This can be attributed to the formation of a multilayered structure [8] and some of PS II membrane fragments diffuse into the subphase. This observation further indicates that PS II membranes can only marginally stay at the air-water interface and one must be very careful in choosing the experimental parameters. [Pg.643]

Most slabstock foams are open-celled, that is, the walls around each cell are incomplete. Towards the end of the foaming process, the polymer migrates from the membranes between cells to the cell struts, which results in a porous structure. In some cases, cells near the surface of the foam collapse to form a continuous skin, which may be trimmed off later. [Pg.389]


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