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Volume 113,
Issue 1,
1979
Volume 113, Issue 1, 1979
- Short Communications
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Changes in Activities of Three RNAases During the Heat-synchronized Cell Cycle of Tetrahymena pyriformis ST
More LessAcid RNAases of Tetrahymena pyriformis ST were resolved into one minor and two major peaks by Sulphopropyl Sephadex chromatography. The same three peaks were obtained from exponentially growing cells and from heat-synchronized cells. The two major RNAases (peaks 2 and 3) were also separated by polyacrylamide gel electrophoresis at pH 4·5 and 8·3. The stepwise increase in total RNAase activity during synchronous growth was primarily caused by a large and preferential increase in the activity of the peak 3 RNAase during the first hour after the heat shock.
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Denaturation Map of the ColE1-Km Plasmid pCR11
More LessThe denaturation map of Eco RI-digested pCR11, a ColE1-Km plasmid, is described. The 2·0 kilobase ColE1-derived segment contains an adenine + thymine rich site in the colicin immunity gene region. In the 7·2 kilobase kanamycin resistance region, the transposon Tn903 consists of an adenine + thymine rich 0·98 kilobase kan gene region flanked by a guanine + cytosine rich 1·09 kilobase inverted duplication.
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Changes in Glucose 6-Phosphate and Storage Carbohydrates during Catabolite Derepression in Saccharomyces cerevisiae
More LessChanges in the cellular content of glucose 6-phosphate and storage carbohydrates during catabolite derepression were measured during the diauxic growth of Saccharomyces cerevisiae on glucose (1 %, w/v) medium. After the exhaustion of glucose there were transient increases in glucose 6-phosphate, alkali-soluble glycogen and trehalose, reflecting enhanced gluconeogenesis, followed by an increase in acid-soluble glycogen. During the subsequent adaptation to growth on ethanol the amounts of glucose 6-phosphate, trehalose and glycogen returned to basal levels. Thus storage carbohydrates, of which glycogen is quantitatively the most important, appear to act as the energy source for catabolite derepression.
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Changes in the Lipid Composition of Candida utilis during the Cell Cycle
More LessAlthough contents of triacylglycerols, free sterols and esterified sterols did not alter during the 3·5 h cell cycle of Candida utilis NRRL Y-900 growing synchronously under glucose limitation, changes were detected in the phospholipid content. Phospholipid:sterol molar ratios were lowest in organisms sampled after 2·5 h and highest in those analysed after 0·5 h of the cycle.
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- Taxonomy
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Taxonomy of Clostridium tetani and Related Species
More LessClostridium tetani and its related species C. tetanomorphum, C. cochlearium and C. lentoputrescens were examined for DNA-DNA homology and biochemical properties. Two distinctly different groups were included under the name of C. tetanomorphum: one was identical with C. cochlearium and the name C. tetanomorphum was applied to the other group with some amendment of biochemical properties. Comparison of the type strain of C. lentoputrescens with wild strains obtained from horse faeces indicated that the name C. lentoputrescens should be abolished as a later synonym of C. cochlearium. Liquefaction of gelatin and spore shape, which have been used as the important criteria for differentiation of C. tetani-related species, were genetically insignificant.
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Taxonomic Significance of Yeast Sphaeroplast Release after Enzymic Treatment of Intact Cells
More LessTreatment of whole yeast cells with a mixture of a reducing agent and 1,3-β-glucanase isolated from Basidiomycete QM806 led to the production of sphaeroplasts from ascomycetes, from some fungi imperfecti, but not from basidiomycetes. Association of 1,3-β-glucanase with a second enzyme, 1,4-α-glucanase, from Trichoderma viride, was required for sphaeroplast release from some, but not all, basidiomycetes and fungi imperfecti. The ability of yeast cells to liberate sphaeroplasts following appropriate enzymic treatment is proposed as a taxonomic criterion for differentiating basidiomycetous from ascomycetous yeasts and for classifying fungi imperfecti yeasts.
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