Effect of labuctril 25 and three other herbicides on wild soil isolates and mutant strains of streptomycetes

Labuctril 25 (3,5-dibromo-4-hydroxybenzonitrile, LAB) at concentrations up to 100μg/mL inhibits effectively growth, morphology, and pigmentation of most soil streptomycete isolates grown under laboratory conditions. Oxytril CM (OXT), Basagran (BAS) and Faneron 50 WP (FAN) applied at the same concentrations had no detectable effect on growth of substrate mycelium but suppressed both aerial mycelium and pigment formation, the effectivity decreasing in the order OXT—BAS—FAN. The LAB-sensitivity of mutant strains was markedly higher as compared with that of the soil isolates. A wild strain resistant to 100–400μg of LAB per mL (depending on the medium composition) was isolated. It was capable of supporting the growth and development of sensitive strains on the LAB-containing medium. A stimulatory effect of low doses of LAB (10–20μg/mL) on the antibiotic activity of streptomycetes was observed.     

Passage of foreign proteins across the intestinal wall of newborn rabbits

Foreign proteins penetrate across the wall of rabbit jejunum takes place within the first eight hours after birth. Sensitization by foreign protein (cow's milk protein) during early postnatal ontogeny is the cause of death of artificially fed germfree rabbits at the age of 21-23 d.     

Genetic Analysis of Murine Arylsulfatase C and Steroid Sulfatase

SWR/J mice possess two- to threefold higher 4-methylumbelliferyl sulfate (4MUS), dehydroepiandrosterone sulfate (DHEAS) and estrone sulfate (E1S) sulfatase activities in liver and kidney extracts than do A/J mice. These interstrain activity differences are maintained throughout the 6- to 45-day postnatal period. Characteristics of the hepatic activities of SWR/J mice suggest that all three activities reside in the same enzyme. Biochemical properties of the SWR/J and A/J enzyme were not significantly different. Expression of hepatic enzyme activity is subject to regulation by an autosomal locus possessing two alleles with additive effects. Postnuclear E1S- and DHEAS-sulfatase activities are primarily microsomal. Although postnuclear hepatic 4MUS-sulfatase activity is predominantly microsomal, renal activity is primarily nonmicrosomal. Only that portion of 4MUS-sulfatase occurring in cell membranes appears capable of hydrolyzing E1S and DHEAS. The hepatic- and renal-specific subcellular distributions of 4MUS-sulfatase activity may reflect tissue differences in enzyme processing. Renal 4MUS-sulfatase activity is also controlled by an autosomal gene with two alleles having additive effects. Positive correlation between hepatic and renal 4MUS-sulfatase activities indicates that both activities are most likely influenced by the same gene.     

Variability of quantitative markers of irradiated and non-irradiated fish from experimental populations. II. Changes in the values of some quantitative markers in relation to body length

The influences of a single rtg irradiation dose (14 mGy) on some quantitative signs in dependence on the body length was studied in the experimental fishes Barbus conchonius and B. tetrazona. The values of all followed signs increased positively due to the body length growth. The irradiation with the abovementioned dose in the given conditions had relative small influence on the growth course of the chosen quantitative sign values in the control and irradiated fishes of both species is the same (the regression lines are in good agreement, resp. they are parallel). The statistically significant difference was stated only between the irradiated the non-irradiated groups of B. tetrazona due to the head height (the regression lines are divergent).     

Cholinesterase activity in some species of theAllium genus

In partly purified protein complexes obtained from 22 species of theAllium genus and 6 cultivars ofAllium cepa the activity of cholinesterases was detected and measured using the method of Ellman et al. The degree of its inhibition with 10^-4 M neostigmine was also tested. It was found that the activity of cholinesterase differed in individual species up to two hundred times, while the differences in the inhibitory activity of 10^-4 M neostigmine occurred only in a few cases. Individual sections and cultivars could not be characterized on the basis of the differences in the activities of the cholinesterases. Of all the sections that ofPhyllodolon shows the highest average activity. In the case of the tested cultivars distinctly the lowest activity was observed in cv. Kastická. The values of the enzymatic activity measured by Ellman’s method in this plant material include the activity of specific and unspecific cholinesterases and the part uninhibitable by neostigmine.     

Developmental changes in gene expression during pollen differentiation and maturation inNicotiana tabacum L

Total and polysome-bound ribosomes and the uptake and incorporation of³H-uridine and¹⁴C-leucine were examined in dividing microspores and in pollen grains isolated from anthers of 6 different developmental stages. Direct evidence was obtained that the formation of cytoplasm of the vegetative cell following microspore division is related to a rapid activation of RNA and protein synthesis and of ribosomes in differentiating pollen. Total ribosomes associated with gametophytic programme rose about 10times and the process of differentiation was accompanied by a rapid increase in uptake capacity of pollen grains for both uridine and leucine. Pollen development after cytoplasm synthesis and starch deposition continued by pollen maturation, which was characterized by a decline in RNA synthesis, dissociation of polysomes and by a further rise of transport activity of pollen grain wall for exogenous substrates, indicating probable pollen adaptation for utilization of metabolites from the degenerating tapetal cytoplasm.     

Comparison of malate dehydrogenase isoenzymes in someAllium species by isoelectric focusing

Malate dehydrogenase isoenzymes were studied in tenAllium species and in six cultivars ofA. cepa by isoelectric focusing in polyacrylamide gel with Ampholine pH 3.5–10.0. Using this method better resolution was obtained than by polyacrylamide gel electrophoresis. The number of MDH isoenzymes obtained by isoelectric focusing is from five to ten in the range of pH 3.65 to 6.75. MDH isoenzymes can be used for characterization on the level of species and cultivars (inA. cepa), but its use on the level of sections and subgenera is questionable.     

The comparison of seed protein patterns within the genusArachis by polyacrylamide gel electrophoresis

The seed protein patterns of 12Arachis species were compared by polyacrylamide gel electrophoresis (PAGE), similarities between patterns were measured by the Jaccard index. Results obtained confirm the close relationships established between members of the genus on morphological grounds and support the more recent classification schemes.A. villosa andA. correntina could well be regarded as distinct species on grounds of protein differences whileA. macedoi andA. villosulicarpa (although members of the same section, Extranervosae) show considerable differentiation of their protein patterns. Surprisingly, the formA. ×batizogaea showed less similarity in protein pattern to those of its parental species than might have been expected. The principle value of seed protein pattern data appears to be in distinguishing species within sections.