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  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    The @journal of eukaryotic microbiology 34 (1987), S. 0 
    ISSN: 1550-7408
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Marine amoebae were isolated during a search for organisms which degrade cell walls of seaweed. One of the isolates, a multinucleated amoeba (referred to here as Amoeba-I-7 or Am-I-7) was isolated from live tissues of the brown seaweed Sargassum muticum. It digested a variety of brown and red seaweeds including their walls and cuticles. Axenic clone cultures were isolated from cells that migrated on agar. Cultures were grown on agar or in liquid media. Seaweeds, seaweed wall extracts, and unicellular algae were tested as food sources.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Applied microbiology and biotechnology 34 (1991), S. 814-817 
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary A marine amoeba, Trichosphaerium I-7, originally found feeding on macroalgae in a region of natural oil seepage, was maintained in the laboratory for prolonged periods on hexadecane, octadecane, 1-chlorooctadecane, or 1-bromooctadecane as a carbon source. The cells attached readily and eroded holes in thin layers of these compounds. Crystalline and clear spherical inclusions appeared in the cytoplasm of cells fed these xenobiotics followed by a marked cell darkening. Thin layer chromatographic analyses of acetone extracts from amoebae grown for 12 days on [1-14C]octadecane demonstrated the formation of labelled substances of higher polarity than the original alkane. Sodium dodecyl sulfate-polyacrylamide gel electrophoresis followed by autoradiography revealed that 14C derived from [1-14C]octadecane was incorporated into acetone-insoluble macromolecules.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1573-5176
    Keywords: protoplasts ; flow cytometry ; seaweed ; biotechnology
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The ability to rapidly distinguish viable sub-populations of cells within populations of macroalgal protoplast isolations was demonstrated using flow cytometry. Viable protoplasts from Ulva sp. and Porphyra perforata J. Ag. were distinguished from non-viable protoplasts based on differential fluorescein accumulation. The identities of cortical and epidermal protoplasts from Macrocystis pyrifera (L.) C. Ag. were inferred based on light-scattering and chlorophyll a autofluorescence. Three cell types could be distinguished among protoplasts released from thalli of P. perforata based on chlorophyll a and phycoerythrin autofluorescence. Mixed protoplast populations of Ulva sp. and P. perforata were also discernable based on relative chlorophyll a and phycoerythrin autofluorescence. The ability to screen heterogenous protoplast populations rapidly, combined with the cell sorting capabilities of many flow cytometers, should prove valuable for seaweed biotechnology.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1573-5176
    Keywords: compression ; LiCl ; Porphyra ; seaweed ; tension
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The mechanical properties of various differentiated regions of thePorphyra perforata thallus and the effect of LiCl were studied by performing compression and tension tests. Among the various differentiated tissues, the holdfast area was high in its ‘compressive modulus of elasticity’ and ‘tensile modulus of elasticity’, possibly related to its thick matrix. Vegetative non-dividing tissue and vegetative dividing tissue were the most flexible and strong, showing the highest ‘percentage elongation at break’ and ‘tensile strength’. The patch area, which is a transition zone leading to sexually mature tissue, had moderate values of tensile properties. Meanwhile, sexually differentiated male and female tissues had the highest ‘compressive modulus of elasticity’ and lowest tensile properties. Thes tisues tended to crumble easily. Treatments in LiCl, as used for DNA extraction, resulted in a decrease in both ‘compressive modulus of elasticity’ (87%) and ‘tensile modulus of elasticity’ (54%). After treatment of tissue for chromosome staining in a method using LiCl, there was a marked decrease in ‘tensile modulus of elasticity’ (49%), while the ‘compressive modulus of elasticity’ remained unchanged. Such mechanical changes verify the softening effect of LiCl on the seaweedP. perforata tissue.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Journal of applied phycology 7 (1995), S. 101-107 
    ISSN: 1573-5176
    Keywords: DNA extraction ; LiCl ; PCR ; Porphyra perforata ; seaweed
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract A rapid and economical method of DNA extraction from a red seaweedPorphyra perforata J. Agardh has been developed by the use of lithium chloride. This paper describes the optimization of extraction conditions. Heat treatment of tissues in a solution (0.8 M LiCl, 0.6% Sarkosyl, 10 mM EDTA, 0.2% PVPP, 5% ß-mercaptoethanol, pH 9.0) at 55 °C for 10 min extracts DNA that is of sufficient quality to be used as a template for PCR amplification. Total DNA yield was approximately 30 to 50μg g−1 t of partially dried tissue. Total RNA yield was approximately 400μg g−1 of partially dried tissue. Carbohydrate was contained as approximately 40 to 90 mM (expressed as glucose equivalents) from 1 g tissue, and protein contamination calculated as the O.D. 260/280 ratio was in the range of 1.4 to 1.7. The DNA was characterized by high molecular weight larger than 50 kb.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Hydrobiologia 151-152 (1987), S. 131-138 
    ISSN: 1573-5117
    Keywords: seaweed ; calluses ; induction ; culture ; differentiation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Hydrobiologia 151-152 (1987), S. 405-409 
    ISSN: 1573-5117
    Keywords: seaweed ; seaweed pathogens ; cell wall digestion ; seaweed-digesting amoeba
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Biotechnology and Bioengineering 49 (1996), S. 559-567 
    ISSN: 0006-3592
    Keywords: Acrosiphonia ; macroalgae ; tissue culture ; stirred-tank bioreactor ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: A semidifferentiated tissue culture consisting of linear filaments in liquid suspension was established from Acrosiphonia coalita, a cold-water green macroalga known to express pharmacologically active oxylipins deriving from lipoxygenase metabolism of linolenic acid. The tissue was vegatively propagated by blending the filaments down to 1 to 5 mm in length prior to subculture. The filamentous A. coalita tissue suspension was successfully cultivated in an illuminated, 3-L stirred-tank bioreactor at 12°C, 0.46-vvm aeration rate, 250-rpm mixing speed, and incident illumination intensity of 77 μE m-2s-1. The mean specific growth rate over the exponential phase was 0.185 day-1 and a final cell density of 1083 mg dry cell weight (DCW) L-1 was achieved within 15 days of cultivation from an initial cell density of 200 mg DCW L-1. The addition of 3500 ppm CO2 to the aeration gas provided a maximum CO2 transfer rate of six times the maximum CO2 consumption rate and stabilized the pH to 8.0 during the light phase of growth, but did not improve biomass productivity. © 1996 John Wiley & Sons, Inc.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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