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  • 1
    ISSN: 1432-2048
    Keywords: Cell cultures ; Chlorophyll protein ; Photosynthesis (light harvesting) ; Poly(A)RNA ; Thylakoid membranes
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract In thylakoid membranes isolated from green plants of parsley, pea, and barley, the light-harvesting chlorophyll a/b protein complex (LHCP, mol. weight: 25,000), is a major constituent. Poly(A)RNA isolated from these species was translated in a wheat germ, cell-free system. The in vitro translation products were treated with antibodies raised against the LHCP. This treatment resulted in the precipitation of a precursor protein (mol. weight: 29,000). Poly(A)RNA was also prepared from a cell culture ofPetroselinum that does not develop chloroplasts upon illumination. This poly(A)RNA is capable of stimulating amino acid incorporation in the in vitro translation system, however, it does not direct the synthesis of LHCP.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-2048
    Keywords: Chlorophyll protein ; Hordeum ; Photosynthesis (light harvesting) ; Poly(A)RNA ; Polysomes ; Thylakoid membranes
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Polysomes from dark-grown and illuminated barley seedlings were translated in cell-free systems. The translation products reacting with the antibody against the light-harvesting chlorophyll a/b protein (LHCP) were analyzed by polyacrylamide gel electrophoresis. It was found that, in addition to the precursor protein of LHCP, a product was obtained that co-migrated with the mature protein. Furthermore, the results show that the light-induced proly(A)RNA for LHCP is integrated into the polysomal complex without delay, indicating that the integration of LHCP into the membrane is controlled at a higher level of gene expression.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1432-2048
    Keywords: Chlorophyll protein ; Hordeum ; Photosynthesis (light harvesting) ; Poly(A)RNA ; Polysomes ; Thylakoid membranes
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Polysomes from dark-grown and illuminated barley seedlings were translated in cell-free systems. The translation products reacting with the antibody against the light-harvesting chlorophyll a/b protein (LHCP) were analyzed by polyacrylamide gel electrophoresis. It was found that, in addition to the precursor protein of LHCP, a product was obtained that co-migrated with the mature protein. Furthermore, the results show that the light-induced proly(A)RNA for LHCP is integrated into the polysomal complex without delay, indicating that the integration of LHCP into the membrane is controlled at a higher level of gene expression.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1432-2048
    Keywords: Cell cultures ; Chlorophyll protein ; Photosynthesis (light harvesting) ; Poly(A)RNA ; Thylakoid membranes
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract In thylakoid membranes isolated from green plants of parsley, pea, and barley, the light-harvesting chlorophyll a/b protein complex (LHCP, mol. weight: 25,000), is a major constituent. Poly(A)RNA isolated from these species was translated in a wheat germ, cell-free system. The in vitro translation products were treated with antibodies raised against the LHCP. This treatment resulted in the precipitation of a precursor protein (mol. weight: 29,000). Poly(A)RNA was also prepared from a cell culture ofPetroselinum that does not develop chloroplasts upon illumination. This poly(A)RNA is capable of stimulating amino acid incorporation in the in vitro translation system, however, it does not direct the synthesis of LHCP.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Mechanical creep and creep recovery in small shearing deformations have been studied in unligated clots formed with both thrombin and ancrod. In thrombin clots, both A binding sites (which interact with “a” sites to link monomer units within a protofibril) and B sites (which interact with “b” sites to form links between protofibrils) are exposed to enable formation of linkages; in ancrod clots, only the A sites are exposed. Fine clots (with minimal lateral aggregation of protofibrils), coarse clots (with substantial aggregation of fibril bundles), and clots of intermediate coarseness were compared. Fine thrombin clots showed less creep at short times but more creep at long times than coarse or intermediate clots and had more irrecoverable deformation relative to the initial elastic deformation. Ancrod clots had greater irrecoverable deformation than the corresponding thrombin clots, both fine and coarse. The permanent deformation in fine ancrod clots was enormous, corresponding almost to fluid character; the rate of permanent deformation was larger than that in fine thrombin clots by more than two orders of magnitude. For all types of clots, differential measurements of compliance (or its reciprocal, elastic modulus), as well as the applicability of the Boltzmann superposition principle to calculation of creep recovery, showed that the overall density of structure remained constant throughout the mechanical history; i.e., if structural elements were breaking, they were reforming at the same rate in different configurations. The possibility that the weakness of ancrod clots is attributable to partial degradation of α-chains rather than absence of Bb linkages was eliminated by comparisons of clots made with thrombin, ancrod, and ancrod plus thrombin; the last two showed identical partial degradation of α-chains (by gel electrophoresis), but the first and third had essentially identical initial elastic moduli and creep behavior. Two alternative mechanisms for irrecoverable deformation in fine clots are discussed, involving rupture of protofibrils and slippage of twisted segments, respectively.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 0009-2940
    Keywords: Bases, concave / Protonation, regioselective / Nef reaction / aci-Nitro compounds ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The intramolecular competition for C- or O-protonation of the nitronate anion 5a is determined by sterical factors and by the [EtOH⊕2] concentration. The product of the Nef reaction 6 is formed in buffered, non-acidic media when the proton donors are sterically hindered.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 123 (1990), S. 643-645 
    ISSN: 0009-2940
    Keywords: Concave base / Macrocycle / 1,10-Phenanthroline / Cyclophane / Aryl lithium compounds ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The addition of lithium aryls 3 to 1,10-phenanthroline (2), functionalization of the rearomatized bisadduct 8b to the tetraphenol 8d, and cyclization of 8d with two equivalents of an α,ω-ditosylate 9 led to a highly symmetrical, conformer-free bimacrocyclic 1,10-phenanthroline 10a in which the basic and coordinating region possesses a concave shielding.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 0009-2940
    Keywords: Isocyanide ; Rearrangement ; Sweetener ; Cycloalkanecarboxylic Acid ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Use of the Isonitrile-Nitrile Rearrangement for the Synthesis of 2,2,5,5-Tetramethylcyclopentanecarboxylic Acid, a Building Block for Sweeteners on the Basis of Amino Acids1)2,2,5,5-Tetramethylcyclopentanecarboxylic acid (7) was synthesized in four steps from 2,2,5,5-tetramethylcyclopentanone (3). The key step of the reaction is the gas-phase rearrangement of 2,2,5,5-tetramethylcyclopentyl isocyanide (5) to 2,2,5,5-tetra-methylcyclopentanecarbonitrile (6), which is hydrolyzed to 7.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 185 (1984), S. 1727-1737 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Poly(diacetylene)s dissolved in common organic solvents undergo random chain scission, if irradiated by UV-light. The pure polymers and their solutions are, however, stable, if they are photoirradiated within the main-absorption band of the polymer backbone. The usual triplet sensitizers, especially in the presence of oxygen, and radical donors such as 2,2′-azoisobutyronitrile (AIBN) enhance the rate of photodegradation. Suitable dyes are able to sensitize the chain-scission in the visible regions as well. Random chain scission occurs also in the dark, but only at temperatures above room temperature and is enhanced by the addition of radical-donors, e.g. AIBN. A mechanism of chain scission, induced by the attack of a radical to a multiple bond of the polyconjugated backbone of the polymer is proposed.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 189 (1988), S. 2823-2837 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The commercially available poly(1-octenylene) Vestenamer® formed by the metathetic polymerization of cyclooctene with a tungsten catalyst, is highly crystalline at room temperature; it shows specific properties as a blend component, thus favourably influencing the processing characteristics and the final product quality. Differential scanning calorimetry, infrared and torsion pendulum experiments indicate that the melting temperature and the degree of crystallinity depend on the concentration of trans double bonds, on their distribution along the polymer chain as well as on the sample history. The formation of crosslinks induced by very intensive UV irradiation of 100 μm thin films leads to a reduction of the melting temperature and the crystallinity. A correlation between stiffness (shear modulus G′) and crystallinity was found for samples with varying amounts of trans double bonds.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
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