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  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    The @journal of eukaryotic microbiology 7 (1960), S. 0 
    ISSN: 1550-7408
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Ergosterol was isolated from the non-saponifiable lipids of Euglena. For this, after saponification of the cells, the petroleum-ether extract was chromatographed on deactivated alumina. Development was achieved by pet. ether and 10% (v/v) benzene in pet. ether, and the sterol fraction was subsequently eluted with 10% (v/v) ethyl acetate in pet. ether. This sterol was identified as ergosterol by a) precipitation with digitonin, b) The Liebermann-Burchard reaction, c) co-chromatography with known ergosterol, d) ultraviolet absorption spectrum, e) conversion to the acetate with determination of the melting and mixed melting points and !” infra-red absorption spectrum of the acetate derivative. By these techniques, ergosterol content was measured in the-following strains of Euglena gracilis under various conditions of nutrition and illumination: bacillaris and Z strains, and several albino and pigment mutants derived from them. A. functional chloroplast seems unnecessary for ergosterol synthesis; the ergosterol content of cells (dry weight basis) was constant regardless of strain and growth conditions.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of bioenergetics and biomembranes 23 (1991), S. 393-408 
    ISSN: 1573-6881
    Keywords: Signal transduction ; photosynthesis ; blue light ; plasma membrane redox ; light-induced absorbance change ; flavin ; cytochromeb ; sphingoid bases
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Physics
    Notes: Abstract Stimulations by light of electron transport at the plasma membrane make it possible that redox activity is involved in light-induced signal transduction chains. This is especially true in cases where component(s) of the chain are also located at the plasma membrane. Photosynthetic reactions stimulate transplasma membrane redox activity of mesophyll cells. Activity is measured as a reduction of the nonpermeating redox probe, ferricyanide. The stimulation is due to production of a cytosolic electron donor from a substance(s) transported from the chloroplast. It is unknown whether the stimulation of redox activity is a requirement for other photosynthetically stimulated processes at the plasma membrane, but a reduced intermediate may regulate proton excretion by guard cells. Blue light induces an absorbance change (LIAC) at the plasma membrane whose difference spectrum resembles certainb-type cytochromes. This transport of electrons may be due to absorption of light by a flavoprotein. The LIAC has been implicated as an early step in certain blue light-mediated morphogenic events. Unrelated to photosynthesis, blue light also stimulates electron transport at the plasma membrane to ferricyanide. The relationship between LIAC and transmembrane electron flow has not yet been determined, but blue light-regulated proton excretion and/or growth may depend on this electron flow. No conclusions can be drawn regarding any role for phytochrome because of a paucity of information concerning the effects of red light on redox activity at the plasma membrane.
    Type of Medium: Electronic Resource
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