Gracilitheca astronauta n. sp. and Nephrotheca sophia n. sp. (Hyolitha,Orthothecida) from the Cambrian of Czech Republic

Two orthothecid hyoliths, Gracilitheca astronauta n. sp. and Nephrotheca sophia n. sp. are described from the “middle” Cambrian Buchava Formation of the Skryje-Tý?ovice Basin in the Czech Republic. The new forms are based on about thirty well-preserved external and internal moulds of both conchs and opercula. Gracilitheca astronauta n. sp. is classified under the family Gracilithecidae Sysoev, 1972 and may be distinguished by clearly triangular cross-section of the conch, whereas Nephrotheca sophia n. sp. is characterized by transversally elongated cardinal processes reaching the lateral opercular margin and is combined with the family Orthothecidae Sysoev, 1958 emended Malinky, 2009. Several specimens of G. astronauta show operculum preserved inside of the conch. Stratigraphic ranges and geographic distributions within the Skryje-Tý?ovice Basin are established for both taxa.     

Collagen/hyaluronan membrane as a scaffold for chondrocytes cultivation

Rabbit chondrocytes were cultivated in vitro using the collagen/hyaluronan membrane. The membrane did not show any adverse effects on chondrocyte viability during in vitro cultivation. The inoculated cells grew without any negative changes. According to the histochemical analyses: (i) hematoxylin and eosin; (ii) safranin O; and (iii) rabbit anti-human collagen type II staining, the rabbit chondrocytes maintained their morphology and phenotype during in vitro cultivation. The collagen/hyaluronan membrane became more stable and stiffer after long time cultivation. The proliferation of the chondrocytes stabilised the structure of the membrane. The collagen/hyaluronan membrane is suitable material for the chondrocyte growth and could provide functional tissue-engineered scaffold for cartilage repair.     

Incorporation of mannoproteins into the walls of aculeacin A-treated yeast cells

Inhibition of the synthesis of alkali-insoluble glucan by aculeacin A in Saccharomyces cerevisiae cells caused a decrease in the incorporation of a high molecular weight heterogeneous mannoprotein material and of a 33000 mannoprotein into the wall network. This was concomitant with the excretion of the latter molecule into the growth medium. Regenerating yeast protoplasts liberated considerable amounts of the heterogeneous material to the medium independently of the presence of aculeacin. The protoplast walls did lack this component and contained only minor amounts of the 33000 molecule, which was also completely absent from walls of aculeacin-treated protoplasts. Considerable levels of the 33000 species were immunodetected in the supernatants from treated and untreated protoplasts. These results point to the existence of specific interactions between the glucan network of the yeast cell surface and some of the wall mannoproteins. On the other hand, the presence of a population of SDS-solubilizable mannoproteins in the wall was independent of glucan levels.Abbreviations SDS sodium dodecyl sulphate - YNB Yeast nitrogen base