Biomedical subjects

R Struzinský

Publications and source records attributed to R Struzinský.

5 recordsLinked to original sources

PubMed1988

Sterol composition of a delta 5,7-sterol-rich strain of Saccharomyces cerevisiae during batch growth.

Sterol composition was examined during batch growth on complex media containing ethanol, molasses or glucose as the carbon source. The molasses-grown cells exhibited a balanced sterol composition throughout growth, maintaining the proportion of ergosterol to 24:28-dehydroergosterol equal to 1.4. The negative effect of glucose on sterol synthesis manifested itself by decreasing the accumulation of 24:28-dehydroergosterol and total sterols but not of ergosterol. Using ethanol as the sole carbon source, a large amount of 24:28-dehydroergosterol accumulated, partly at the expense of other sterols. The gradual addition of nitrogen source during growth significantly decreased the accumulation of ergosterol, 24:28-dehydroergosterol and of total sterols. A general scheme of regulation of sterol synthesis in baker's yeast is presented.

Ammonia↗

PubMed1985

Absence of glucose-stimulated transport in yeast protoplasts.

Protoplasts of Saccharomyces cerevisiae prepared by snail-gut juice treatment were compared in their transport properties with intact cells. 1. Constitutive monosaccharide transport (D-xylose, 6-deoxy-D-glucose), as well as inducible transport of D-galactose, were unaltered. 2. Phosphorylation-associated transport of 2-deoxy-D-glucose was enhanced in protoplasts, possibly as a consequence of removal of the unstirred layer of the cell wall. 3. Proton-driven transports of trehalose, L-leucine, L-proline and monophosphate could not be activated by preincubation with D-glucose, apparently owing to lack of proton-solute coupling in transport. Utilization of glucose was not depressed but respiration was reduced by about 50% while acidification of the external medium after glucose addition was inhibited by more than 90%. This may be related to the inability of protoplast plasma membrane H-ATPase to be activated by glucose and hence to impaired proton-translocating capacity. Uranyl ions inhibited generally much less in protoplasts than in intact cells although their binding to protoplasts was greater (maximum 0.68 fmol per cell but 3.2 fmol per protoplast).

Biological Transport↗

PubMed1983

Interaction of nystatin with nystatin-resistant Candida tropicalis.

Nystatin-resistant yeast Candida tropicalis was obtained after UV illumination and plating on nystatin-containing media. The mutant contained no ergosterol in the plasma membrane but bound nystatin to a degree similar to that of the wild strain (1.2 vs. 1.5 nmol per mg dry solid). Respiration of the mutant on glucose was reduced by 36% in the presence of 25 microM nystatin. This corresponded to a 25-43% decrease of the uptake of monosaccharides. Transport of amino acids was reduced by nystatin in the mutant by 44-86%, as compared with a 84-95% reduction in the wild strain. The intracellular ATP content was reduced by nystatin equally in the wild strain and in the mutant (by 43 and 47%). Nystatin appears to affect specifically membrane transport processes of nonelectrolytes while both the H+-extruding ATPase and the membrane potential are unaffected.

Biological Transport, Active↗

PubMed1981

A model system for bacteriorhodopsin chromophore.

The absorption characteristics of bacteriorhodopsin chromophore cannot be understand on the basis of a simple protonated Schiff-base linkage. A possible hypothetical explanation may be an interaction of the aromatic amino acid residues also with retinal. Mixtures of retinal and tryptophan analogues were reacted in organic solvents. Many similarities were found in the absorption spectra of the different products of these reactions and in those of the main forms of bacteriorhodopsin photocycle. Such products are suggested to model the purple complex of bacteriorhodopsin as well as the chromophores of the photointermediates.

Bacteriorhodopsins↗

PubMed1977

Effect of high substrate concentrations on active transport parameters.

A general model is described to account for the observation that steady-state accumulation ratios (mainly of non-electrolytes) decrease with increasing solute concentration, frequently reaching values of less than unity. Three variants of the model are treated, all of them including the assumption that the immediate supply of the source of energy is limited and its local concentration is appreciably reduced by its interaction with the transport system. Consequences of this assumption for the kinetic parameters of the initial rate of transport are analyzed and compared with experimental data.

Biological Transport, Active↗