Results 181 to 190 of about 25,031 (244)
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Microbody proliferation and segregation cycle in the single-microbody alga Cyanidioschyzon merolae
Planta, 1999The proliferation cycle of the microbody was studied in the primitive red alga Cyanidioschyzon merolae, which contains one microbody per cell. Cells were synchronized with a dark/light cycle, and the morphology of the microbody and its interaction with other organelles were observed three-dimensionally by fluorescence microscopy, transmission electron ...
S. Miyagishima +5 more
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Microbody of n-alkane-grown yeast
Archives of Microbiology, 1977Microbodies appearing abundantly in n-alkane-grown cells of Candida tropicalis pK 233 were isolated by means of sucrose density gradient centrifugation. Electron microscopical observation showed that the microbodies isolated were intact. Localization of catalase and D-amino acid oxidase in the isolated microbodies was confirmed.
S. Kawamoto +4 more
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Immobilization of yeast microbodies and the properties of immobilized microbody enzymes
European Journal of Applied Microbiology and Biotechnology, 1978Yeast microbodies isolated from methanol-grown cells of Kloeckera sp. No. 2201 were immobilized by two types of entrapping techniques: photocrosslinking of liquid oligomers of suitable photosensitive resins and crosslinking of albumin molecules with glutaraldehyde.
Atsuo Tanaka +4 more
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Microbodies of the pig liver [PDF]
Cells Tissues Organs, 1978 The ultrastructure of hepatic microbodies of pigs was studied in liver samples fixed in phosphate-buffered 2% glutaraldehyde (pH 7.4) and postfixed in 2% osmium tetroxide. The microbodies were rounded or ovoid in shape and contained a granular matrix enclosed with a single limiting membrane. The matrix, in many of the organelles, contained an amorphous
Amreek Singh +3 more
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Microbodies inCrithidia fasciculata
Protoplasma, 1973Electron microscopy of thin sections ofCrithidia fasciculata showed cytoplasmic organelles 0.2–0.8 μm in diameter containing a finely granular matrix limited by a single membrane. Utilization of cytochemical techniques (DAB) for endogenous catalase revealed pronounced deposition of a highly electron-opaque material in these organelles.
Kenneth E. Muse, John F. Roberts
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2009
Microbodies are novel pharmacophoric entities which are derived from naturally occurring cystine-knot microproteins. They provide extremely stable scaffolds that can be engineered to high-affinity binding proteins. A peptide-grafting approach yielded specific ligands for human thrombopoietin receptor (TPO-R).
Hans-Ulrich, Schmoldt +3 more
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Microbodies are novel pharmacophoric entities which are derived from naturally occurring cystine-knot microproteins. They provide extremely stable scaffolds that can be engineered to high-affinity binding proteins. A peptide-grafting approach yielded specific ligands for human thrombopoietin receptor (TPO-R).
Hans-Ulrich, Schmoldt +3 more
openaire +2 more sources
The ultrastructure and cytochemistry of microbodies inPorphyridium
Protoplasma, 1974This work establishes the presence of a microbody-like organelle in a unicellular red alga,Porphyridium purpureum (Bory) Drew et Ross. There are several of these per cell. They are spherical or slightly ovoid in shape and 0.2–0.4 microns in diameter.
John D. Dodge, Berl R. Oakley
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FURTHER OBSERVATIONS ON INTRANUCLEAR MICROBODIES
British Journal of Dermatology, 1968SUMMARY.— The authors have observed the presence of intranuclear micro-bodies, 0·4—2·5 μ in size, containing osmiophilic particles 200 A. in size, in 1 of 2 cases of oral leukoplakia and in 1 of 7 cases of bullous erythema multiforme. The different types of intranuclear microbodies so far reported in various dermotoses are classified and their ...
A. G. Bellone, Ruggero Caputo
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