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  • Synechococcus 6301  (2)
  • Coleoptiles (physiological tip)  (1)
  • 1
    ISSN: 1432-2048
    Keywords: Auxin (immunoassay) ; Avena ; Coleoptiles (physiological tip) ; Enzyme immunoassay ; Zea
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract A specific solid-phase enzyme immunoassay for the detection of as little as 3–4 pg of indole-3-acetic acid (IAA) is described. The assay involves minimal procedural efforts and requires only standard laboratory equipment. Up to 50 samples in triplicate, processed simultaneously, can be assayed and evaluated in 2.5 h. As little as 1 mg oat coleoptile tissue is sufficient for a quantitative IAA analysis and little or no extract purification is necessary. Using this assay, levels of IAA have been determined in coleoptiles of maize and oat. The distribution of IAA within single coleoptiles was quantitated and the production of IAA during the regeneration of the physiological tip in Avena coleoptiles was investigated. The changes in levels of IAA and other major phytohormones were quantitated during the growth of oat coleoptiles.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1573-5079
    Keywords: State transitions ; excitation energy transfer ; photosystem stoichiometry ; chromatic acclimation ; non-photochemical quenching ; cyanobacteria ; Synechococcus 6301
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Cells of the cyanobacterium Synechococcus 6301 were grown in yellow light absorbed primarily by the phycobilisome (PBS) light-harvesting antenna of photosystem II (PS II), and in red light absorbed primarily by chlorophyll and, therefore, by photosystem I (PS I). Chromatic acclimation of the cells produced a higher phycocyanin/chlorophyll ratio and higher PBS-PS II/PS I ratio in cells grown under PS I-light. State 1-state 2 transitions were demonstrated as changes in the yield of chlorophyll fluorescence in both cell types. The amplitude of state transitions was substantially lower in the PS II-light grown cells, suggesting a specific attenuation of fluorescence yield by a superimposed non-photochemical quenching of excitation. 77 K fluorescence emission spectra of each cell type in state 1 and in state 2 suggested that state transitions regulate excitation energy transfer from the phycobilisome antenna to the reaction centre of PS II and are distinct from photosystem stoichiometry adjustments. The kinetics of photosystem stoichiometry adjustment and the kinetics of the appearance of the non-photochemical quenching process were measured upon switching PS I-light grown cells to PS II-light, and vice versa. Photosystem stoichiometry adjustment was complete within about 48 h, while the non-photochemical quenching occurred within about 25 h. It is proposed that there are at least three distinct phenomena exerting specific effects on the rate of light absorption and light utilization by the two photoreactions: state transitions; photosystem stoichiometry adjustment; and non-photochemical excitation quenching. The relationship between these three distinct processes is discussed.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Photosynthesis research 38 (1993), S. 135-140 
    ISSN: 1573-5079
    Keywords: photosynthesis ; light-harvesting ; light-state transition ; signal transduction ; cyanobacteria ; Synechococcus 6301 ; Synechococcus sp.
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Light-state transitions in cyanobacteria are a rapid physiological adaptation mechanism which changes the distribution of excitation energy absorbed by the light-harvesting complexes between Photosystem II and Photosystem I. State transitions in two cyanobacterial species are shown to be inhibited by buffers containing 0.2–0.4 M phosphate. Both the state 1 and the state 2 transition are inhibited, so that cells may be locked in the state to which they were adapted before the addition of phosphate. The inhibition of the state 1 transition is due to inhibition of photosynthetic electron transport. However, the inhibition of the state 2 transition is probably due to a direct effect on the biochemical signal transduction pathway. The implications for the biochemical mechanism of state transitions are discussed.
    Type of Medium: Electronic Resource
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