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  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    The @journal of eukaryotic microbiology 12 (1965), S. 0 
    ISSN: 1550-7408
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: SYNOPSIS. Antibodies to purified chloroplast preparations from Euglena gracilis var. bacillaris were prepared in rabbits. Success was achieved only after removal of lipids by forming acetone powders af chloroplasts. Ouchterlony agar-diffusion procedures showed that light-grown cells (containing chloroplasts) have at least 3 antigens reacting with these antibodies and not detectable in the dark-grown cells (which contained proplastids but no chloroplasts), The antigens uniquely associated with the chloroplast appear sequentially during the development of the proplastid into the chloroplast on light induction of the dark-grown cells. The first of these antigens appears at about 10 hr of development. Mutants of the parent strain showed varying numbers of antigens which were cor-related with their capacities to form plastid structures. Cells developing abnormal chloroplasts at low light intensities did not reveal any antigenic differences from cells developing normal chloroplasts. Various antigenic bands were also found which were common to all cell types studied. These can be ascribed either to non-chloroplast contaminants in the original preparation used to immunize the rabbits or to antigens which, although not in the chloroplasts, are cross-reacting with chloroplast materials. In the case of the dark-grown cells, it is likely that portions of the proplastids are cross-reacting with chloroplast materials.
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  • 2
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    The @journal of eukaryotic microbiology 11 (1964), S. 0 
    ISSN: 1550-7408
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: SYNOPSIS. Sulfate-S35 uptake by intact Euglena cells, as well as incorporation of sulfate-S35 into the insoluble fractions of the cells, was partially inhibited by adding iodoacetamide simultaneously or ten minutes before radioactive sulfate. The identification of S-cysteine acetamide and S-glutathione acetamide showed the presence of glutathione and cysteine in the soluble pool of Euglena but methionine, homocysteine, and S-adenosylmethionine were not found during these experiments. An unidentified radioactive peak was eluted by 2 n HCl during column chromatography of the soluble fraction of Euglena cells. The major compound in this peak was identified as L-cystine on the basis of its infra-red spectrum, paper and column chromatographic characteristics and optical rotation. The use of iodoacetamide permitted the independent demonstration of cysteine and cystine in the soluble pools by eliminating oxidation artifacts.
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  • 3
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Annals of the New York Academy of Sciences 175 (1970), S. 0 
    ISSN: 1749-6632
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Natural Sciences in General
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  • 4
    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.
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  • 5
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    The @journal of eukaryotic microbiology 8 (1961), S. 0 
    ISSN: 1550-7408
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Electron and fluorescence microscopy reveal a proplastid about 1 μ in diameter in dark-grown Euglena gracilis quite like those in higher plants. After the cells are placed in the light these structures lengthen, probably in part by coalescence of several proplastids. Full size is reached in some cells after about one day in light. Lamellae, growing as blebs off the inner proplastid membrane, develop in a roughly linear fashion with time, art average of one new lamella appearing after each 6 hours in the light. The maturation of the proplastid thus appears to differ appreciably from that in higher plants since the latter presumably create several lamellae simultaneously, and these appear able to replicate themselves in a geometrically parallel fashion. The question is raised whether the apparent differences in development may not be due to lesser discrimination in observing the sequence in the higher plants, for there are no observations necessarily inconsistent with the sequence found in Euglena.
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  • 6
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Physiologia plantarum 66 (1986), S. 0 
    ISSN: 1399-3054
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: The phototransformation of protochlorophyll(ide) (Pchl(ide)) to chlorophyll(ide) (Chl(ide)) can be demonstrated in a proplastid fraction from Euglena gracilis Klebs var. bacillaris Cori if appropriate conditions are employed. Pigments were measured fluorometrically in acetone extracts of cell or organelles. Pchl(ide) and the phototransformation to Chl(ide) are at their highest levels in cells grown in darkness on normal or low vitamin B12-containing medium (pH 3.5) to the late exponential phase (1.2–1.4 × 106 cells ml−1). Late exponential cells on low B12 medium yield a proplastid fraction that contains Pchl(ide) which is phototransformed to Chl(ide) when illuminated with red light (5.6 W m−2 for 4 min) in the presence of 10 mM Hepes, 20 mM TES, 0.5 mM potassium phosphate (pH 7.4), 70 mM sorbitol, 5 mM DTT, 5 mM ATP, 5 mM fructose-1, 6-bisphosphate, 10 mM malate and 2 mM MgCl2; intact organelles appear to be involved since deletion of osmoticum gives a lower activity, and addition of NAD(P)H is without effect. Phototransformation of Pchl(ide) to Chl(ide) in red light shows Bunsen-Roscoe reciprocity between fluence rate and duration of illumination. Although mitochondria are present, they do not appear to be involved since inhibitors of respiration and uncouplers of oxidative phosphorylation fail to block the phototransformation. The percentage phototransformation of Pchl(ide) to Chl(ide) in late exponential normal B12 cells is 61 ± 10, and is 52 ± 3 in low B12 cells. About 67% of the activity in low B12 cells is recovered in the proplastid fraction incubated with the complete incubation mixture in saturating light. In both types of cells and in the proplastid fraction, the stoichiometry of conversion of Pchl(ide) to Chl(ide) is about 1:1 (mol/mol).
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  • 7
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Physiologia plantarum 58 (1983), S. 0 
    ISSN: 1399-3054
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Dark-grown non-dividing cells of Euglena gracilis Klebs var. bacillaris Cori were exposed to light for up to 72 h and thylakoid membrane fractions were isolated by sedimentation in sucrose step gradients at various stages of development. The membrane-bound coupling factor (CF1)-ATPase activity of these prothylakoids (0 h of light) and developing thylakoid membranes (12 to 72 h of light) was characterized by its cation specificity and sensitivity to inhibitors. The enzyme at all stages of development was activated by Mg2+ and to a lesser extent by Ca2+; Mn2+ was found to activate, as well as or better than Mg2 + at comparable concentrations. The activity of the enzyme was almost completely inhibited by dicyclohexylcarbodiimide (DCCD; 0.3 mM), but was insensitive to oligomycin, valinomycin and carbonyl cyanide P-trifluoromethoxyphenylhydrazone (FCCP). Low concentrations of NH4CI gave a slight stimulation of enzyme activity, whereas high concentrations of the uncoupler were inhibitory. The specific activity of the membrane-bound CF,-ATPase was highest in prothylakoid membranes. Specific activity decreased on a thylakoid protein or chlorophyll basis during the first 12 h of development, and achieved a steady state level by 48 h following light induction. Estimates of total CF1-ATPase activity per cell indicate that the time for major synthesis of the enzyme is between 12 and 3d h ol development. These results suggest that following an initial lag period in membrane development lasting about 12 h, there is a formation of CF1-ATPase that accompanies further thylakoid membrane development.
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  • 8
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Annals of the New York Academy of Sciences 361 (1981), S. 0 
    ISSN: 1749-6632
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Natural Sciences in General
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Planta 146 (1979), S. 119-127 
    ISSN: 1432-2048
    Keywords: Blue light ; ζ-carotene (cis-trans isomerization) ; Euglena ; Isomerization (ζ-carotene) ; Light (blue) ; Phototaxis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract When treated with blue light, intact cells of Euglena gracilis Klebs var. bacillaris Cori, bleached strain W3BUL, show a series of positive peaks at 384, 411, and 440 nm in the blue-light-minus-dark difference spectrum; bleached strain 1224-5/24 shows a series of positive peaks at 386, 417, and 448 nm under the same conditions. The same changes are observed in a 27,000xg supernatant from darkgrown W3. The absorption change appears to be a consequence of shifts in the absorption of carotenoids; it is not seen in cells of W3BUL grown on SAN 9789 (4-chloro-5-(methylamino)-2-(α,α, α-trifluoro-m-tolyl)-3(2H)pyridazinone) to deplete the carotenoids or in cells of W10BSmL, a mutant lacking carotenoids. Inhibitors of flavin-mediated reactions, reductants and valinomycin had no effect on the activity of the system. The activity in the 27,000xg supernatant was associated with material of a molecular weight more than 2.5×106 and was insensitive to heating for 2 min at 100° C but was reduced or eliminated on longer heat treatment or addition of Triton X-100, indicating a possible association with membrane material. Photoactivity is enriched in the lower density fractions of a flotation gradient, and correlates with the ζ-carotene content in all fractions. Similar spectral changes can be obtained by comparing the iodine catalyzed cis-to-trans isomerization of ζ-carotene in a CS2-CHCl3 solvent. The action spectrum for the absorbance change shows effectiveness peaks in the 370–390 and 420–448-nm regions, with no marked effectiveness past 500 nm. Thus the photosensitizer may not be a carotenoid (at least not a normally-occurring C40 carotenoid). These blue-lightinduced absorption changes and their action spectra are discussed in relation to such blue-light-mediated responses as carotenogenesis, chloroplast development and phototaxis.
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  • 10
    ISSN: 1432-2048
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary The possibility that 32PO 4 3- (32Pi) labeling of both chloroplast and non-chloroplast RNAs during light-induced chloroplast development in Euglena is due, in part, to the break-down of existing RNAs and their resynthesis into labeled RNAs has been examined by comparing the RNA content of dark-grown, non-dividing cells after completion of light-induced chloroplast development with that of identical cells maintained in darkness for the same period of time. The involvement of the photo-conversion of protochlorophyll to chlorophyll and other photoreceptor systems in the labeling of RNA during chloroplast development has been considered by comparing the labeling pattern obtained with wild-type cells with the patterns obtained with mutants of Euglena which either lack detectable amounts of protochlorophyll and chlorophyll or form only rudimentary chloroplasts upon light induction. No significant difference in RNA content between dark-grown, non-dividing cells containing fully developed chloroplasts and the same cells maintained in darkness for the development period can be detected. This observation is interpreted to mean that in non-dividing cells precursors for chloroplast-associated RNAs are derived from pools and pre-existing RNAs, including non-chloroplast RNAs, and that the matebolic entrapment of 32Pi involves a light-dependent turnover and DNA-directed RNA synthesis in wild-type cells. The RNA profiles on sucrose gradients of mutants of Euglena show no remarkable deviation from the profile established for wild-type cells. The labeling patterns obtained after 24 hours of incubation in light and in darkness differ from that obtained for wild-type cells in that all mutants show less of a light-minus-dark difference than wild-type and that mutants lacking plastid-associated DNA and detectable amounts of chlorophyll incorporate considerably more 32Pi into RNA in darkness than wild-type. One such mutant shows no significant difference in its light-dark labeling pattern. These observations indicate that cells possessing normal proplastids capable of forming functional chloroplasts regulate metabolism of RNA in darkness in a different manner than with either rudimentary chloroplasts or containing no detectable plastids structures. The possible involvement of more than one photoreceptor system in metabolic control is discussed.
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