Five Malaysian isolates of the protozoan Plasmodium falciparum Welch were cultured in vitro following the method of Träger and Jensen (1976, 1977) and subsequently cloned using the limiting dilution method of Rosario (1981). Thirty clones were obtained and were later characterized against schizontocidal drugs, chloroquinc, mefloquine and quinine, using the modified in vitro microtechnique. Results showed that these local isolates were heterogenous and most of the clones exhibited similar pattern of susceptibility as their parent isolate except for ST 168 clone and two ST 195 clones that were sensitive but two ST 165 clones, two ST 168 clones and five ST 195 clones were resistant against quinine, respectively. Results also indicated that they were pure clones compared to their parent isolate because their drug susceptibility studies were significantly different (p < 0.05).
Photosynthetic and respirátory electron transfers in cyanobacteria not only serve the bioenergetic needs of these prokaryotes during day and night time. The common use of the plastoquinone pool and the cytochrome (cyt) complex also establishes possibilities for sharing photosystem (PS) 2 plus dehydrogenases at the donor side and cyt c oxidase plus PSI at the acceptor side. Given metabolic conditions and radiant energy supply, the available choices may give rise to unusual combinations of connected electron transfer activities, for example PS2 and cyt c oxidase. In vivo measurements of energy storage in PSI cyclic photophosphorylation via photoacoustic spectroscopy, and of the P700 redox statě via absorbance changes at 820 nm detected with the pulse amplitudě modulation technique (PAM), as well as of PS2 fluorescence yield, all in the absence or presence of the cyt c oxidase inhibitor KCN were combined to demonstrate that the two pathways at the acceptor side communicate in vivo. This type of regulation serves proper poising of electron flow through and around PSI. The impaired cyt c oxidase activity (in this study achieved by addition of KCN) prevents a truly oxidized statě of P700 to be reached, which hampers electron passage from PS2. The relative overreduction of PS 1 in the KCN intoxicated samples reduces the electron flow directed to biosynthesis. The results illustrate the versatility of the P700 redox statě measurements at 820 nm as a means to study in vivo electron fluxes in cyanobacteria.
Prolonged storage of isolated photosystem 2 (PS2)-enriched subchloroplast particles in the frozen statě leads to a decrease of the PS2 activity and to an increase of the energy transfer between chlorophyll (Chl)-proteins of the light-harvesting chlorophyll a/b (LHC)-PS2 complex. The energy transfer was less influenced than the PS2-mediated electron transport at freeze-thaw treatment of PS2 particles. The change of these parameters was not affected by the rate of freezing. The addition of cryoprotectants such as glycerol, trehalose or saccharose in the suspension medium prior to freezing preserved fo a different extent the PS2-mediated electron transport and the energy transfer between the Chl molecules of the LHC-PS2 complex.
Chloroplasts isolated from Vigna sinensis L, seedlings grown under cool íluorescent (control chloroplasts) and ultraviolet-B (UV-B)-enhanced íluorescent (UV chloroplasts) radiation, when incubated at 10, 20, 30 and 40 °C, showed large variations in the photosynthetic electron transport reactions. The overall electron transport activity in both control and UV chloroplasts incubated at 40 decreased rapidly. In contrast to this, at 30 the control chloroplasts got inactivated very rapidly during the 30 min of incubation while the UV chloroplasts showed high stability. A similar trend was also noticed at 20 “C. At 10 °C, although the rate of inactivation was slow, UV chloroplasts were more stable than control chloroplasts. A similar trend was noticed in photosystern (PS) 2 activity. In contrast to overall electron transport and PS2 reactions, PS 1 activity showed only marginal changes at all temperatures. The polypeptide profiles of chloroplasts exposed to UV-B iixadiation for 60 min at different temperatures revealed marked decreases in the level of the 23 and 33 kDa polypeptides in control chloroplasts while in UV chloroplasts these polypeptides were highly stable. In addition, UV chloroplasts contained several new polypeptides of both high and low molecular masses. The polypeptide partem indicated that higher photochemical activity of UV chloroplasts over the control chloroplasts could be due to stabilization of PS 2 core complexes by the new polypeptides induced under UV-B enhanced radiation.