[Antimycoplasmal effect of HI-78 (author's transl)].
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Biomedical subjects
Publications and source records attributed to K Hara.
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Two bovine growth hormone peptides containing residues 96 to 133 in one and a larger peptide corresponding to residues 1 to 95 and 151 to 191 linked by a disulfide bond have been recombined. Recombination was performed in 1.0 N acetic acid without and with 8 M urea and the recombined peptides were purified by gel filtration. Evidence of recombination of the peptides has been established by gel filtration, polyacrylamide gel disc electrophoresis, amino acid composition, ultraviolet absorption, circular dichroism, and intrinsic fluorescence. The molar growth promoting activity of the recombined peptides measured by tibial width assay in hypophysectomized rats was 10% that of the native hormone and greater than the sum (1%) of the growth promoting activities of the individual peptides. These studies suggest that some contribution of the larger peptide is necessary for more complete expression of the growth promoting activity of the bovine growth peptide corresponding to residues 96 to 133.
A 19-year-old Japanese man in good health was found on a routine chest X-ray to have considerable lung abnormalities. An open lung biopsy was performed and 30 third-instar larvae of Megaselia spiracularis Schmitz were found in the suction tube postoperatively. This appears to be the first recorded case of lung myiasis.
Studies were made to determine the effect of UV-irradiation of herpes simplex virus (HSV) on Concanavalin A (Con-A)-mediated agglutination of 3T3 cells. There were three different phases of agglutination by Con-A of cells infected with HSV. The agglutinability began to increase from 3 or 4 hr, or 72 hr after exposure of cells to HSV. The early-appearing agglutinability was further divided into two phases, based on its sensitivity to metabolic inhibitors. These were tentatively called "Early 1 or inhibitor sensitive", "Early 2 or inhibitor insensitive" and "Late" agglutinability. "Early 1" agglutination, detected from 3 hr post infection (pi), was induced by treating cells with HSV, either active or UV-irradiated for less than 5 min and was inhibited when actinomycin D (1 microgram/ml) or cycloheximide (50 microgram/ml) was added to the cultures. "Early 2" agglutination began to increase from 4 hr pi when cells were inoculated with HSV irradiated for 7 to 20 min and was not affected by either inhibitor. HSV irradiated for 6 min failed to induce either agglutinability. "Late" agglutination, observed 72 hr pi, was detected in cultures which had been treated with HSV irradiated for 4 to 15 min. Among those, virus irradiated for 6 to 8 min was most efficient. HSV-transformed cells were also agglutinated without exception by low concentrations of Con-A.
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