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  • 1
    ISSN: 1432-0886
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract Telomeres at the ends of linear chromosomes of eukaryotes protect the chromosome termini from degradation and fusion. While telomeric replication/elongation mechanisms have been studied extensively, the functions of subterminal sequences are less well understood. In general, subterminal regions can be quite polymorphic, varying in size from organism to organism, and differing among chromosomes within an organism. The subterminal regions of Drosophila melanogaster are not well characterized today, and it is not known which and how many different components they contain. Here we present the molecular characterization of DNA components and their organization in the subterminal region of the left arm of chromosome 2 of the Oregon RC wildtype strain of D. melanogaster, including a minisatellite with a 457 bp repeat length. Two distinct polymorphic arrangements at 2L were found and analyzed, supporting the Drosophila telomere elongation model by retrotransposition. The high incidence of terminal chromosome deficiencies occurring in natural Drosophila populations is discussed in view of the telomere structure at 2L.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Archives of microbiology 118 (1978), S. 99-108 
    ISSN: 1432-072X
    Keywords: Chromatium vinosum ; Membrane differentiation ; Subchromatophore fractions ; Protein patterns ; Reaction center and light harvesting bacteriochlorophyll complexes ; Photophosphorylation ; Sulfide oxidation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Chromatium vinosum, strain D, exhibits two extreme modifications of near infra-red absorption spectra when growing heterotrophically at temperatures either above or below 36.5° C. Chromatophores isolated from cells grown either at 33° C (33° C chromatophores) or 39° C (39° C chromatophores) were analyzed for structural and functional parameters. For this the following chromatophore subunits were solubilized and characterized; (i) a fraction absorbing maximally at 800 nm with shoulders at 820 and 850 nm when derived from 33° C chromatophores or absorbing at 800 nm and 850 nm when derived from 39° C chromatophores; (ii) reaction center-light harvesting bacteriochlorophyll complexes with identical spectra and ratios of reaction center to light harvesting bacteriochlorophyll (1:45); (iii) complexes containing cytochromes, (IV) reaction center bacteriochlorophyll complexes. Irrespective of their origins the fractions exhibited qualitatively identical protein patterns as analyzed by sodium dodecyl sulfate polyacrylamide gel electrophoresis. Protein patterns of 33° C and 39° C chromatophores revealed an identical ratio of proteins of reaction centers to proteins of cytochrome preparations. But the ratio of proteins of reaction centers to proteins of light harvesting moieties was 1.9 times higher in 39° C chromatophores than in 33° C chromatophores. Correspondingly, the ratio of reaction center per total bacteriochlorophyll was 1.7 times higher in 39° C chromatophores (1:110) then in 33° C chromatophores (1:190). Activities of photophosphorylation were 0.73 and 0.56 μmoles of ATP per μmoles of total bacteriochlorophyll per min for 33° C and 39° C chromatophores, respectively. Activities of sulfide oxidation in the light by whole cells were 2.37 and 1.96 μmoles of sulfide per μmole of total bacteriochlorophyll per min for 33° C and 39° C cells. Accordingly, on a reaction center basis activities are significantly lower after growth of the organisms at 39° C than at 33° C. The data indicate that spectral changes in Chromatium vinosum represent changes in the ratio of reaction center to light harvesting bacteriochlorophyll accompanied by a variation of the absorption spectra of the latter bacteriochlorophyll moiety. Concomitantly, activities coupled to the photochemical apparatus were subjected to variations.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Archives of microbiology 118 (1978), S. 91-97 
    ISSN: 1432-072X
    Keywords: Chromatium vinosum ; Near infra-red absorption spectra ; Photoheterotrophy ; Photoautotrophy ; Growth rates ; Bacteriochlorophyll-synthesis ; Specific bacteriochlorophyll contents
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The influence of light intensity and temperature on photoheterotrophically or photoautotrophically growing cultures of Chromatium vinosum, strain D, was investigated using the following parameters: growth, bacteriochlorophyll synthesis, cellular bacteriochlorophyll contents and near infra-red absorption spectra. Without regard of the respective light intensity cultures growing heterotrophically below 36.5°C exhibited an absorption spectrum characterized by a maximum at 800 nm with shoulders at 820, 850 and 880 nm. Also, without regard of light intensity cultures growing heterotrophically above 36.5°C exhibited an absorption spectrum characterized by a maximum at 850 nm with a shoulder at 880 nm and second peak at 800 nm. Under high light intensity (15000 Lux) and at 33°C autotrophic cultures formed a bacteriochlorophyll a spectrum resembling that of heterotrophic cultures growing above 36.5°C; in contrast at low light intensity (3000 Lux) and 33°C autotrophic cultures formed a spectral type resembling that of heterotrophic cultures growing below 36.5°C. Independent of temperature, heterotrophic cultures adjusted to identical specific bacteriochlorophyll contents at a given light intensity. Increasing light intensities increased the growth rate and, consequently, also the rate of bacteriochlorophyll synthesis as temperature increased. The data suggest a correlation between the growth rate and the rate of ATP regeneration. There is no conclusive evidence, however, that the growth rate is inevitably correlated with specific bacteriochlorophyll contents of cells or the fine structure of the near infra-red absorption spectra.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Archives of microbiology 118 (1978), S. 109-114 
    ISSN: 1432-072X
    Keywords: Chromatium ; Near infrared absorption spectra ; Physiological and artificial spectral changes ; Triton X-100 ; Subchromatophore fractions ; Fluorescence emission spectra
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Spectral changes in the near infrared absorption region of chromatophores of Chromatium vinosum, strain D, were analyzed. Spectral changes dependent in growing cultures on temperature (33° C and 39° C, respectively) were compared to artificial changes which take place under the influence of the detergent Triton X-100. Like addition of Triton X-100 to chromatophores, transfer of cells from 39° C to 33° C leads to the reversible formation of an absorption band at 820 nm at the expense of a band at 850 nm. But in contrast to the influence of Triton X-100, chromatophores isolated from cells grown at 39° C (39° C chromatophores), contain on an identical bacteriochlorophyll basis, higher amounts of pigment absorbing at 880 nm and lower amounts of pigment absorbing at 800 nm than found in 33° C chromatophores. Triton X-100 treatment does not influence the production of light induced absorbance changes characteristic of photochemical reaction centers; it does, however, change absorption spectra of a subchromatophore fraction which does not exhibit the known light dependent reaction center responses. The spectral properties of this fraction are altered with Triton X-100 in a manner comparable to whole chromatophores, i.e. translocation of the 850 nm band to 820 nm. Subchromatophore fractions isolated from 33° C chromatophores, which display an absorption band at 820 nm show in the presence of menadione a light induced absorbance change at 835 nm. Subchromatophore fractions from 39° C chromatophores, which display no absorbance at 820 nm show a light induced adsorbance change at 835 nm only after addition of Triton X-100. Spectral changes in growing cultures are accompanied by changes in the fluorescence emission spectra of isolated chromatophores. While 33° C chromatophores exhibit a major fluorescence emission band at 929 nm plus a minor band at 890 nm 39° C chromatophores exhibit only one band at 937 nm.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Biochemical and Biophysical Research Communications 116 (1983), S. 822-829 
    ISSN: 0006-291X
    Keywords: [abr] SDS; sodium dodecyl sulfate
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Biochemical and Biophysical Research Communications 107 (1982), S. 770-778 
    ISSN: 0006-291X
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Biochemical and Biophysical Research Communications 116 (1983), S. 822-829 
    ISSN: 0006-291X
    Keywords: [abr] SDS; sodium dodecyl sulfate
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 1432-0886
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract. Telomeres at the ends of linear chromosomes of eukaryotes protect the chromosome termini from degradation and fusion. While telomeric replication/elongation mechanisms have been studied extensively, the functions of subterminal sequences are less well understood. In general, subterminal regions can be quite polymorphic, varying in size from organism to organism, and differing among chromosomes within an organism. The subterminal regions of Drosophila melanogaster are not well characterized today, and it is not known which and how many different components they contain. Here we present the molecular characterization of DNA components and their organization in the subterminal region of the left arm of chromosome 2 of the Oregon RC wild-type strain of D. melanogaster, including a minisatellite with a 457 bp repeat length. Two distinct polymorphic arrangements at 2L were found and analyzed, supporting the Drosophila telomere elongation model by retrotransposition. The high incidence of terminal chromosome deficiencies occurring in natural Drosophila populations is discussed in view of the telomere structure at 2L.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Journal of cancer research and clinical oncology 115 (1989), S. 498-499 
    ISSN: 1432-1335
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 1617-4623
    Keywords: Drosophila recessive oncogene ; Mutations ; Molecular cloning ; Mobile elements ; Transcription
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary The Drosophila recessive oncogene lethal(2)giant larvae is located at the extreme left end of the second chromosome close to telomeric repetitive sequences. Of the 20 l(2)gl mutant alleles isolated from wild flies in widespread populations of the Soviet Union and California, all but two appear to represent large deletions which have removed the telomeric repetitive sequences and l(2)gl single copy sequences (Mechler et al. 1985). We have analyzed the structure of the two exceptions: the l(2)glGB52 mutation results from the insertion of a single transposable element of the B104 or roo family, whereas the more complex rearrangements of the l(2)glDV275 mutation consists of an 8 kb interstitial deletion whose breakpoints have become associated with a large transposed DNA fragment. Characterization of this fragment shows that it consists of B104 sequences flanked on one side by sequences originating from the chromosomal region 24D. Furthermore, we show that in both mutants normal transcription of the l(2)gl gene is abolished.
    Type of Medium: Electronic Resource
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