THE LABORATORY CULTIVATION OF STEMONITIS

Alexopoulos , Constantine J. (State U. Iowa, Iowa City.) The laboratory cultivation of Stemonitis. Amer. Jour. Bot. 46(2): 140-142. Illus. 1959.—The cultivation of a species of Stemonitis, probably S. flavogenita, in laboratory culture is reported here for the first time. The organism completed its entire life cycle on artificial media from spore to spore, in the presence of contaminating bacteria, in 36 days. The plasmodium, characteristically different from those of the Physarales, is described and illustrated.     

Discrete steps in dioxygen activation—The cytochrome oxidase/O2 reaction

The kinetic constraints that are imposed on cytochrome oxidase in its dual function as the terminal oxidant in the respiratory process and as a redox-linked proton pump provide a unique opportunity to investigate the molecular details of biological O₂ activation. By using flow/flash techniques, it is possible to visualize individual steps in the O₂-binding and reduction process, and results from a number of spectroscopic investigations on the oxidation of reduced cytochrome oxidase by O₂ are now available. In this article, we use these results to synthesize a reaction mechanism for O₂ activation in the enzyme and to simulate time-concentration profiles for a number of intemediates that have been observed experimentally. Kinetic manifestation of the consequences of coupling exergonic electron transfer to endergonic proton translocation emerge from this analysis. Energetic efficiency in this process apparently requires that potentially toxic intermediate oxidation states of dioxygen accumulate to substantial concentration during the reduction reaction.     

Long‐range movement by Hector's dolphins provides potential genetic enhancement for critically endangered Maui's dolphin

For endangered populations with low genetic diversity, low levels of immigration could lead to genetic rescue, reducing the risk of inbreeding depression and enhancing chances of long‐term species survival. Our genetic monitoring of Maui's dolphins revealed the first contemporary dispersal of their sister subspecies, Hector's dolphin, from New Zealand's South Island into the Maui's dolphin distribution along ~300 km of the North Island's northwest coast. From 2010 to 2012, 44 individuals were sampled within the Maui's dolphin distribution, four of which were genetically identified as Hector's dolphins (two living females, one dead female, one dead male). We also report two Hector's dolphins (one dead female neonate, one living male) sampled along the North Island's southwest coast, outside the presumed range of either subspecies. Together, these records demonstrate long‐distance dispersal by Hector's dolphins (≥400 km) and the possibility of an unsampled Hector's dolphin population along the southwest coast of the North Island. Although two living Hector's dolphins were found in association with Maui's dolphins, there is currently no evidence of interbreeding between the subspecies. These results highlight the value of genetic monitoring for subspecies lacking distinctive physical appearances as such discoveries are not detected by other means, but have important conservation implications.     

The expression of Galectin-3 in endometrial cancer: a systematic review of the literature

Molecular Biology Reports - Galectin-3 is part of a protein group called lectins and acts as a multifunctional glycoprotein due to its expression location. Galectin-3 is expressed by different...     

Photosynthetic activity in synchronized cultures of algae and its dependence on light intensity

Summary Photosynthetic capacity at several levels of illuminance was investigated in cells of the successive developmental stages of the high temperature strain, Chlorella 7-11-05. The saturating light intensity, rates of photosynthesis at light saturation and at half-saturation, and the slope of the light dependent portion of the light intensity curves were proved to be bound with the developmental status of cells. The effect of the choosing of the basis for calculations of photosynthetic activity — whether packed cell volume, dry weight, nitrogen, or chlorophyll content—was discussed. The fact was stressed that with the available synchronization technique the observable amplitude of changes in metabolic activity in the course of cell development is a minimal one and the actual fluctuations in photosynthetic rates in non-synchronized suspensions in the course of the life cycle of the individual cells are expected to be higher than those recorded for synchronized populations.