Synchronization of Division in Vitamin B12-Starved Euglena gracilis

SYNOPSIS Vitamin B₁₂ deficiency arrests cell division in Euglena gracilis. B₁₂ starvation for short periods made it possible to induce synchronous growth by addition of the vitamin. Culture conditions were established to optimize replenishment synchrony. The DNA content of E. gracilis in steady state culture and vitamin B₁₂ deficiency culture was measured by flow cytofluorometry and was consistent with colorimetric determinations. The cell volume and DNA distributions of E. gracilis in synchronous culture were analyzed and the sequential changes during the division cycle were computed. Synchronous culture permits more definitive studies of shifts in cell volume and DNA distributions, in which the biochemical events required for cell division are presumably synchronized.     

Culturing chelifers (Pseudoscorpions) that consume Varroa mites

Chelifers (Pseudoscorpions) are generalist predators of small prey such as mites. Their occasional presence in honeybee hives suggests potential to exploit them as part of a management programme against Varroa mites (Varroa destructor), a significant pest of honeybees. Two species of native New Zealand chelifers Nesochernes gracilis and Heterochernes novaezealandiae, shown to consume Varroa mites, were collected from commercial nucleus hives or in litter surrounding the hives. Methods for mass‐rearing the chelifers were developed to provide specimens for research and introduction into beehives for biological control of Varroa. Cultures were fed aphids and fruit fly larvae in vented containers containing sand and bark. N. gracilis was maintained at 14°C, 18°C, and 22°C. At 18°C, 1423 nymphs were reared from 140 N. gracilis adults, with 84.8% of all nymphs produced at this temperature. H. novaezealandiae was maintained at 18°C and 22°C, with 5 nymphs raised from 12 adults at 18°C and none at the higher temperature.     

Phénomènes Périodiques, Métaboliques et Structuraux Chez un Protiste, Euglena gracilis

RESUME. Des divisions synchrones chez Euglena gracilis Z peuvent ětre obtenues par différentes méthodes. Lorsque les cellules sont cultivées sur milieu contenant du lactate comme seule source de carbone, des divisions synchrones sont observables, indépen-damment des conditions d'éclairement. Toutefois, il existe une relation entre la phase des divisions cellulaires et les périodes lumière-obscurité appliquée à la culture. Pendant le cycle cellulaire, nous montrons que les synthèses des macromolécules sont discontinues: c'est le cas pour les ADN nucléaire et mitochondrial, les ARN ribosomaux et non-ribosomaux, ainsi que pour certaines protéines (cytochrome c 558). Des variations cycliques touchant la morphologie des mitochondries et des chloroplastes sont observées. Au cours du cycle cellulaire, les processus métaboliques séquentiels accompagnent les modifications de structure des organites. C'est ainsi qu'en début du cycle, au commencement de la phase G₁, sont synthétisés les ribosomes cytoplasmiques et qu'ensuite, chez les euglènes vertes, les ARN non-ribosomaux sont formés. Ces synthèses d'ARN précèdent l'accroissement du chondriome et du plastidome dans la cellule. En milieu de phase G₁, une nouvelle synthèse d'ARN non-ribosomal commence et est observée avant la synthèse des ADN nucléaire et mitochondrial. En fin de phase G₁, démarre la division des organites à partir du chondriome et du plastidome en réseau. SYNOPSIS. Synchronous divisions of Euglena gracilis strain Z can be obtained by various methods. When the cells are cultivated in a medium containing lactate as the sole carbon source, synchronous divisions are observed, independent of the conditions of illumination. Nevertheless, there exists a relationship between the phase of cell division and the periods of light and darkness applied to the culture. During the cell cycle, the synthesis of macromolecules is discontinuous—this is true of nuclear and mitochondrial DNA, ribosomal and nonribosomal RNA, and certain proteins (cytochrome c 558). Cyclic variations in the structure of mitochondria and chloroplasts are also observed. In the course of the cell cycle, sequential metabolic processes accompany structural modifications of the organelles. Also, at the beginning of the cycle, at the start of phase G₁, the cytoplasmic ribosomes are synthesized, and then, in green euglenids, nonribosomal RNAs are formed. These syntheses of RNA precede enlargement of the chondriome and plastids. In mid-G₁ phase, a new synthesis of RNA begins, which precedes synthesis of nuclear and mitochondrial DNA. At the end of G₁ phase, division of organelles starts, beginning with the chondriome and plastids, arranged in a network.     

Ecophysiological studies on Sonoran Desert plants,VI. Seasonal photosynthesis and production of Machaeranthera gracilis,a winter ephemeral*

Abstract. A comparative study of two chromosomal races of the winter-active ephemeral Machaeranthera gracilis showed that the seasonal magnitudes of photosynthesis were only slightly greater for a progeny desert race than for an ancestral foothills race. Maximum observed photosynthetic capacity and the seasonal reduction in foliar photosynthesis occurred earlier in the year for the desert race. The relative growth rate was higher in this race up until the time of its peak seasonal biomass. A ratio of harvested net production to estimated gross primary production decreased until anthesis. Photosynthesis contributing to net growth continued into periods with moderate environmental stress. The continuation of growth by the desert race was enhanced by maintenance of a higher root-shoot ratio, as well as greater relative stem growth. During reproduction, foliar CO₂ assimilation could not solely provide the measured dry matter accumulation, suggesting the importance of assimilate contribution by photosynthetic stems. Seasonal increases in the enthalpy content of whole plants and plant organs occurred for both races, indicating the absence of significant translocation during reproduction and the potential for stem photosynthesis.     

Production of paramylon,a β‐1,3‐glucan,by heterotrophic cultivation of Euglena gracilis on a synthetic medium

Euglena gracilis was cultivated on a synthetic medium of well‐defined components. Biomass and paramylon (β‐1,3‐glucan) concentrations were the most important variables monitored. Mass production in the bioreactor was carried out following studies of operating conditions in shaken flasks. E. gracilis grew best at about 30°C and at a low pH of 3. A pH control was not necessary, although the pH increased considerably at the end of the cultivation processes. Aeration could be performed at low stirrer frequency. Biomass concentrations of about 13–14 g/L were obtained with paramylon mass fractions of 50–60%, by starting with a synthetic medium containing 15 g/L of glucose as the main carbon source.     

Identification and characterization of 10 microsatellite primers for the calanoid freshwater copepods Eudiaptomus gracilis and E. graciloides using enriched genomic libraries

The calanoid copepods Eudiaptomus gracilis and Eudiaptomus graciloides are widespread among European lakes. We constructed enriched genomic libraries for both species in order to isolate and characterise microsatellite markers. The obtained 7 polymorphic microsatellite‐loci for E. gracilis and 3 for E. graciloides are the first for any freshwater copepod. They display an expected heterozygosity ranging from 0.60 to 0.96 and 0.63 to 0.94 and observed heterozygosity ranging from 0.53 to 0.87 and 0.57 to 0.87, respectively. We were not able to cross‐amplify the isolated loci across species, indicating long divergence among both congeneric species despite morphological similarity.