Role of Photosynthetic Electron Transfer in Light Activation of Calvin Cycle Enzymes

The effect of light in activating fructose-1,6 biphosphate phosphatase (E.C. 3.1.3.11), sedoheptulose-1,7, biphosphate phosphatase (E.C. 3.1.3.11), ribulose-5 phosphate kinase (E.C. 2.7.1.19), ribulose-1,5 biphosphate carboxylase (E.C. 4.1.1.39) and (NADPH) glyceraldehyde-3 phosphate dehydrogenase (E.C. 1.2.1.13) in intact spinach chloroplasts in the presence of antimycin A, tetramethylethylenediamine (TMEDA) or chlorophenyl-1,1-dimethylurea (CMU) was examined. Antimycin A and TMEDA were added as stimulating agents for photosynthetic electron transfer in intact chloroplasts while CMU was added for its inhibitory characteristics. Light exerted its control through the mediation of the photosynthetic electron transfer. Antimycin A and TMEDA promoted the light activation. CMU nullified the light activation as well as the stimulatory effect of antimycin A and TMEDA. Thus the control by light of the activities of the Calvin cycle enzymes involves a reduced agent formed by the photosynthetic electron transport chain. From the presently available evidence, it seems appropriate to hypothesize that the light activation of the enzymes is not a single mechanism. In fact three types of enzymes can be distinguished: Ru-5 P kinase and (NADPH) G-3 P dehydrogenase, maximal activation of which appears within the first minute of illumination and is promoted by antimycin A and by TMEDA; F-1,6 P2 phosphatase and S-1,7 P2 phosphatase, ferredoxin-dependent enzymes, activation of which is slightly slower but is also promoted by antimycin A and by TMEDA; finally Ru-1,5 P2 carboxylase, activation of which is still slower and characterized by the absence of any response to antimycin A as well as to TMEDA.     

Ex Vivo Reconstruction of the Epidermis With Melanocytes and the Influence of UVB

To study pigmentation, we have reconstructed an epidermis ex vivo with keratinocytes and melanocytes. Keratinocytes and melanocytes were grown first in primary cocultures and separately in secondary cultures, then seeded on a dead deepidermized dermis (Pruniéras type) at a 1:20 melanocyte/keratinocyte ratio. Reconstructed epidermis were grown in a special medium enriched with calcium and fetal bovine serum lifted for 15 days at the air-liquid interface. Using histology, immunohistochemistry and electron microscopy we have shown an excellent level of differentiation of the reconstructed epidermis and a physiologic distribution of dendritic melanocytes in the basal layer capable of melanosome transfer to keratinocytes. UVB irradiation 0.15 J/cm²× 5 consecutive days increased melanocyte numbers and stimulated pigmentation as evidenced macroscopically and microscopically and at the biochemical level. Following UVB irradiation melanosome transfer was markedly increased and isolated or clumps of melanosomes were seen in the basal layers as well as in the stratum corneum. This model allows the study of the physiology of pigmentation ex vivo.     

Purification of Immunosuppressive Factors Extracted From Bovine Spleen (Lymphoid Chalone)

A low molecular weight immunosuppressive factor FA which is able to reduce the blastic transformation capacity of lymphoid cells from treated mice has been characterized. It was prepared from a bovine spleen acetone powder and found to be associated partly with high molecular weight carriers in the form of an active complex characterized previously as part of a ‘lymphoid chalone’ fraction. FA may be obtained by selective ultrafiltration of F followed by P-2 Biogel chromatography of the ultrafiltrate. Thymidine, deoxyinosine and deoxycytidine have been identified as the major constituents of FA by mass spectrometry, ultraviolet absorption data and thin layer chromatography. However, none of these nucleotides has the biological activity of FA.     

Trophic positioning and microphytobenthic carbon uptake of biofilm‐dwelling meiofauna in a temperate river

1. δ¹³C and δ¹⁵N stable isotope signatures combined with an in situ microphytobenthic ¹³C labelling experiment were performed on epilithic biofilms of a large temperate river (the Garonne, France) to infer the trophic positioning of biofilm‐dwelling meiofauna and their uptake of microphytobenthic carbon. 2. Chironomidae larvae and Chromadorina spp. nematodes rapidly incorporated freshly produced microphytobenthic carbon in contrast to Rhyacophilidae larvae and Naididae oligochaetes. Quantitatively, macrofaunal Chironomidae incorporated more microphytobenthic carbon per day than did meiofauna. Moreover, Chironomidae seemed more involved in the spatial export of microphytobenthic carbon than nematodes. 3. Rhyacophilidae larvae were predators feeding on large meiofauna (Naididae and Chironomidae) but not on nematodes. Naididae oligochaetes primarily gained their carbon from allochthonous and/or microbial‐loop recycled sources. 4. A rapid and significant loss of labelled microphytobenthic carbon was observed. Feeding activity of biofilm‐dwelling invertebrates seemed not to be primarily involved in this loss.     

EXPRESSION OF PNA,WGA, SBA,AND Con A LECTIN RECEPTORS IN THE ADULT AND DEVELOPING HONEYBEE ANTENNAL LOBE

Glycoproteins are thought to play a crucial role in cell—cell interactions during nervous system ontogeny both in vertebrates and invertebrates. In order to investigate the putative involvement of such molecules during bee brain ontogeny we used lectins for their ability to bind specifically carbohydrate moieties. The expression of four lectin receptors, i.e. Arachis hypogea (PNA), Triticum vulgaris (WGA), Glycine max(SBA), and Concanavalin A (Con A) has been studied during pupal development and in the adult. The antennal lobe shows a complementary pattern of expression of Con A which stains both neuron somata and glomerular contours, and PNA, which stains the glomerular neuropile. SBA strongly stained the perineurium, trachea and mushroom body neuropile, while other neuropiles were not stained. WGA stained neuronal somata and the core of the glomeruli.     

FUNCTIONAL APPROACH FOR THE ANALYSIS OF TIME INTENSITY CURVES USING B-SPLINES

This article deals with a functional approach based on the projection upon a B‐spline basis in order to analyze Time Intensity curves. The modelization is followed, on the one hand, by the assessment of the repeatability and the discrimination ability of the panelists, and on the other hand, by the determination of a good compromise over repetitions. Finally, a multidimensional analysis enables the comparison of the shapes of the curves associated with the assessors (assessors’ signature) and the characterization of the products. The properties of this functional approach are illustrated with TI curves describing sweetness variations of drinks.