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Chlorophylls reactions

In Photosystem II, chlorophyll absorbs a photon of fight, with maximum absorption occurring at 680 nm. The photon excites an electron in the chlorophyll, and this excited electron moves through the chlorophyll to chlorophylls reaction center. Here the photons energy is used by electron-transfer proteins to pump protons (hydrogen ions, H+) into the thylakoid. [Pg.79]

The photosynthetic process in green plants occurs in subcellular organelles called chloroplasts. These organelles resemble mitochondria they have two outer membranes and a folded inner membrane called the thy-lakoid. The apparatus for photosynthesis, including the chlorophyll reaction centers and electron carriers, is in the thylakoid membrane. The chemical reactions of the Calvin cycle take place in the stroma, the region around the thylakoid membrane. [Pg.347]

This reaction can be simplified by the following three major processes (Eqs. (19.2) to (19.4)), where water is an electron donor which provides electrons to the whole system obtained at the Mn protein complex (Eq. (19.2)), the electrons from water are excited by solar photons at the chlorophyl reaction center (two ... [Pg.162]

See also , Photosystem Summary, Cyclic Electron Flow, Chlorophyll, Reaction Center, FNR, Figure 17.16... [Pg.982]

Livingstone and Owens have shown that the triplet state is an essential intermediate in chlorophyll-sensitized photochemical reactions occurring in homogeneous solutions (17). It has not yet been satisfactorily proven whether or not the triple state participates in in viw chlorophyll reactions, but nevertheless there is considerable evidence that the sequence of biochemical reactions in photosynthesis is initiated by a chlorophyll molecule in its triplet state (5). [Pg.126]

Possible Mechanism of Water Photooxidation Sensitized by Chlorophyll Reaction Thermodynamics... [Pg.170]

JONAH - 1 would hope so. The development of pulsed neutron sources at Argonne (INPS) and elsewhere make such measurements possible. These types of studies might be particularly desirable for understanding the changes in configuration that can occur in chlorophyll reaction centers. At present the discussions of such techniques are most often catalyzed by alcohol. [Pg.14]

Woodward s synthesis, 4, 416-419 Chlorophyll b, 4, 382 Chlorophyll c, 4, 382 Chlorophyll d, 4, 382 Chlorophylls, 4, 378 biosynthesis reviews, 1, 99 structure, 4, 370 substituents reactions, 4, 402 Chloroporphyrin e, 4, 404 Chloroprothixene pharmacology, 3, 942 Chloropyramine as antihistamine, 1, 177 Chloropyrifos synthesis, 2, 201 Chloropyrifos-ethyl as insecticide, 2, 516 Chloropyrifos-methyl as insecticide, 2, 516 Chloroquine, 1, 145 adsorption on nucleic acids, 1, 179 as antimalarial, 1, 173, 2, 517 Chloroquine, hydroxy-as antimalarial, 2, 517 Chlorosulfonyl isocyanate cycloaddition reactions... [Pg.577]

A method of detecting herbicides is proposed the photosynthetic herbicides act by binding to Photosystem II (PS II), a multiunit chlorophyll-protein complex which plays a vital role in photosynthesis. The inhibition of PS II causes a reduced photoinduced production of hydrogen peroxide, which can be measured by a chemiluminescence reaction with luminol and the enzyme horseradish peroxidase (HRP). The sensing device proposed combines the production and detection of hydrogen peroxide in a single flow assay by combining all the individual steps in a compact, portable device that utilises micro-fluidic components. [Pg.332]

The interiors of rhodopseudomonad bacteria are filled with photosynthetic vesicles, which are hollow, membrane-enveloped spheres. The photosynthetic reaction centers are embedded in the membrane of these vesicles. One end of the protein complex faces the Inside of the vesicle, which is known as the periplasmic side the other end faces the cytoplasm of the cell. Around each reaction center there are about 100 small membrane proteins, the antenna pigment protein molecules, which will be described later in this chapter. Each of these contains several bound chlorophyll molecules that catch photons over a wide area and funnel them to the reaction center. By this arrangement the reaction center can utilize about 300 times more photons than those that directly strike the special pair of chlorophyll molecules at the heart of the reaction center. [Pg.235]

Figure 12.16 View of the reaction center perpendicular to the membrane illustrating that the pigments are bound between the transmembrane helices. The five transmembrane-spanning a helices of the L (yellow) and the M (red) subunits are shown as well as the chlorophyll (green) and pheophytin (blue) molecules. Figure 12.16 View of the reaction center perpendicular to the membrane illustrating that the pigments are bound between the transmembrane helices. The five transmembrane-spanning a helices of the L (yellow) and the M (red) subunits are shown as well as the chlorophyll (green) and pheophytin (blue) molecules.
In the bacterial reaction center the photons are absorbed by the special pair of chlorophyll molecules on the periplasmic side of the membrane (see Figure 12.14). Spectroscopic measurements have shown that when a photon is absorbed by the special pair of chlorophylls, an electron is moved from the special pair to one of the pheophytin molecules. The close association and the parallel orientation of the chlorophyll ring systems in the special pair facilitates the excitation of an electron so that it is easily released. This process is very fast it occurs within 2 picoseconds. From the pheophytin the electron moves to a molecule of quinone, Qa, in a slower process that takes about 200 picoseconds. The electron then passes through the protein, to the second quinone molecule, Qb. This is a comparatively slow process, taking about 100 microseconds. [Pg.239]

The light-harvesting complex LHl is directly associated with the reaction center in purple bacteria and is therefore referred to as the core or inner antenna, whereas LH2 is known as the peripheral antenna. Both are huilt up from hydrophohic a and p polypeptides of similar size and with low hut significant sequence similarity. The two histidines that hind to chlorophyll with absorption maxima at 850 nm in the periplasmic ring of LH2 are also present in LHl, but the sequence involved in binding the third chlorophyll in LH2 is quite different in LHl. Not surprisingly, the chlorophyll molecules of the periplasmic ring are present in LHl but the chlorophyll molecules with the 800 nm absorption maximum are absent. [Pg.242]

Figure 12.22 Schematic diagram showing the flow of excitation energy in the bacterial photosynthetic apparatus. The energy of a photon absorbed by LH2 spreads rapidly through the periplasmic ring of bacterio-chlorophyll molecules (green). Where two complexes touch in the membrane, the energy can be transmitted to an adjacent LH2 ring. From there it passes by the same mechanism to LHl and is finally transmitted to the special chlorophyll pair in the reaction center. (Adapted from W. Kiihlbrandf, Structure 3 521-525, 1995.)... Figure 12.22 Schematic diagram showing the flow of excitation energy in the bacterial photosynthetic apparatus. The energy of a photon absorbed by LH2 spreads rapidly through the periplasmic ring of bacterio-chlorophyll molecules (green). Where two complexes touch in the membrane, the energy can be transmitted to an adjacent LH2 ring. From there it passes by the same mechanism to LHl and is finally transmitted to the special chlorophyll pair in the reaction center. (Adapted from W. Kiihlbrandf, Structure 3 521-525, 1995.)...
Modeling of the reaction center inside the hole of LHl shows that the primary photon acceptor—the special pair of chlorophyll molecules—is located at the same level in the membrane, about 10 A from the periplasmic side, as the 850-nm chlorophyll molecules in LH2, and by analogy the 875-nm chlorophyll molecules of LHl. Furthermore, the orientation of these chlorophyll molecules is such that very rapid energy transfer can take place within a plane parallel to the membrane surface. The position and orientation of the chlorophyll molecules in these rings are thus optimal for efficient energy transfer to the reaction center. [Pg.244]

In the post-World War II years, synthesis attained a different level of sophistication partly as a result of the confluence of five stimuli (1) the formulation of detailed electronic mechanisms for the fundamental organic reactions, (2) the introduction of conformational analysis of organic structures and transition states based on stereochemical principles, (3) the development of spectroscopic and other physical methods for structural analysis, (4) the use of chromatographic methods of analysis and separation, and (5) the discovery and application of new selective chemical reagents. As a result, the period 1945 to 1960 encompassed the synthesis of such complex molecules as vitamin A (O. Isler, 1949), cortisone (R. Woodward, R. Robinson, 1951), strychnine (R. Woodward, 1954), cedrol (G. Stork, 1955), morphine (M. Gates, 1956), reserpine (R. Woodward, 1956), penicillin V (J. Sheehan, 1957), colchicine (A. Eschenmoser, 1959), and chlorophyll (R. Woodward, 1960) (page 5). ... [Pg.3]

Fungus. simple organism that contains no chlorophyll, which may consist of one cell or of many cellular filaments called hyphae. If allowed to grow in HVAC equipment it may cause allergic reactions. [Pg.1444]


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See also in sourсe #XX -- [ Pg.667 , Pg.668 ]




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