Factors Affecting Ethanol Induced Luminescence in Dark-Treated Chloroplasts

Dark-treated chloroplasts emit light when treated with a high ethanol concentration. The ethanol treatment causes chlorophyll solvation. The light is red and emanates from a singlet excited molecule, probably a chlorophyll peroxide. It is quenched by acetone, sodium dodecyl sulfate treatment of the chloroplasts before the addition of ethanol, boiling, reducing substances and low pH. It is enhanced by ferricyanide and high pH. This is interpreted as a requirement for an organized structure and for an energy transfer system for light emission to occur.     

Dependence of fluorescence spectra of chloroplasts from the activity of photosystem 2]

By means of high sensitive spectrofluorometer the fluorescence spectra have been measured of normal chloroplasts and those with blocked photosystem 2 activity due to photoinhibition or treatment with 0.6 M tris-buffer. At room temperature fluorescence spectra of inactivated chloroplasts are similar to the spectrum of normal chloroplasts measured at low light intensity. Under excitation by intense light a decrease of intensity at 685 nm is appeared (about 3-4 times) in the fluorescence spectra of inactivated chloroplasts as compared to the spectrum of normal chloroplasts. The sharp intensity decrease of maxima at 685 and 695 nm (3-4 times) and small decrease at 680 and 730 nm (by 30-50%) are observed in low temperature fluorescence spectra of inactivated chloroplasts. Thus, the damage of photosystem 2 reaction centres is not accompanied by the preferential decrease of the only fluorescence band. The similarity of fluorescence difference spectra of chloroplasts distinguished by the state of photosystem 2 reaction centre, and the complex structure of difference spectra indicate that the variable fluorescence of chloroplasts during the induction is due to the emission of bulk chlorophyll alpha of the photosystem 2.     

THE INTRINSIC MECHANISM OF CHROMATIN DECONDENSATION AND ITS ACTIVATION IN HUMAN SPERMATOZOA*

In vitro decondensation of human sperm chromatin induced by the activation of an intrinsic mechanism was studied by light microscopy, scanning and transmission electron microscopy. Morphological evidence was provided to support the concept that this mechanism is essential for the chromatin decondensation occurring in vivo. Prostatic zinc is hypothesized to preserve this potential decondensation ability from oxidative destruction, by reversibly binding to free thiol-groups. The unique occurrence of disulphide-stabilized structures in eutherian spermatozoa may serve to protect the spermatozoon from structural degradation by its own proteolytic activity during the relatively slow passage through the eutherian egg investments.     

SEDIMENTARY STRUCTURES IN CAMBRIAN LIMESTONES STUDIED BY RADIOGRAPHY

The paper deals with radiographic studies of Middle Cambrian 'fragment limestone', and Upper Cambrian anthraconite concretions from Bornholm (Denmark). A very simple method provides good insight into the sedimentary structures of the rocks and hence a good foundation for interpretation of the lithogenesis.