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11.
Danielle G. Marty 《Biotechnology letters》1985,7(12):900-904
Summary Study of CMC fermentation by a marine syntrophic association of an anaerobic cellulose-degrader, a carbohydrate-fermenter, and a methanogen. Altered fermentation pattern in general agreement with the concept of interspecies hydrogen transfer was obtained only with pregrowth of methanogen followed by inoculation of the two fermentative bacteria. 相似文献
12.
Summary We have used response surface methodology to study the interactions between various parameters (pH, temperature, enzyme concentration) controlling the immobilization of ribonuclease A on to glutaraldehyde activated-amine Spherosil beads. The optimum activity of immobilized ribonuclease A was observed at pH=9.1. The specific activity of the immobilized enzyme was affected by the pH and by the enzyme concentration. 相似文献
13.
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15.
M. Rosa Pinol Urs Kägi Claus W. Heizmann Brigitte Vogel Jean-Marc Séquier Werner Haas Willi Hunziker 《Journal of neurochemistry》1990,54(6):1827-1833
Many processes in the CNS depend on calcium. The calcium signal is transduced into an intracellular response via Ca2(+)-binding proteins, including calbindin D-28K. In many laboratories, polyclonal antibodies against chicken intestinal calbindin D-28K have been used to study its localization in the brain (normal and degenerated) of various species, including humans, but some of these antisera cross-reacted with other proteins, including calretinin. We purified recombinant rat brain calbindin D-28K to raise antisera in rabbits and purified a recombinant rat-chicken calbindin D-28K hybrid protein to immunize mice for the generation of monoclonal antibodies. These antisera were highly specific for calbindin D-28K, as demonstrated by two-dimensional Western blotting analysis. Immunohistochemical analyses combined with in situ hybridization studies demonstrated that calbindin D-28K in the Purkinje cells of the cerebellum is independent of vitamin D. The antibodies described here will be important tools for studying the regulation of expression of calbindin D-28K and its biological function in the brain and in the PNS. 相似文献
16.
The brain organization of butterflyfishes 总被引:2,自引:0,他引:2
Roland Bauchot Jean-Marc Ridet Marie-Louise Bauchot 《Environmental Biology of Fishes》1989,25(1-3):205-219
Synopsis The encephalization indices of angelfishes (Pomacanthidae) and butterflyfishes (Chaetodontidae) are typical of advanced perciform
fishes: both families lie in the upper part of the polygon of teleost indices. The chaetodontids seem to be a little more
encephalized than pomacanthids. The general morphology of the brains in both families is very similar: small olfactory bulbs,
large optic tectum and a cerebellum which covers the brain structures in front of it like a cap. This morphology is shared
by another family of the coral reef biotope, the Acanthuridae. The histological architecture is also typical of advanced teleosts,
with a cortex-like pallium, a laminated nucleus geniculatus (= pretectalis superficialis), a complex valvula cerebelli and
a corpus glomerulosum with a clear neuropile centre. The quantitative analysis of the main subdivisions of the brain, either
from relative volumes or from indices, shows small olfactory bulbs (microsmy) but important telencephalic and diencephalic
centres, large tectal centres (vision) and large cerebellum (precise locomotion). Many of these peculiarities are shared by
other fishes inhabiting coral reefs. The differences between the two families seem to be primarily correlated with food habits:
the angelfishes, which are sponge-feeders and may have an overweight due to the ballast of the sponge-skeleton in their digestive
tract, and which do not need either such good vision or such precise locomotion to pick up their prey, could be a little less
encephalized than the butterflyfishes. 相似文献
17.
Sophie Seigneurin-Venin Elaine Parrish Isabelle Marty François Rieger Georges Romey Michel Villaz Luis Garcia 《Experimental cell research》1996,223(2):301
The process of myoblast fusion during skeletal myogenesis is calcium regulated. Both dihydropyridine receptor and ryanodine receptor are already present on muscle precursors, at the prefusional stage, before they are required for excitation–contraction coupling. Previous pharmacological studies have shown the need for a special pool of Ca2+associated with the membrane for the fusion process to occur. We hypothesized that this pool of Ca2+is mobilized via a machinery similar to that involved in excitation–contraction coupling. The process of fusion in rat L6 muscle precursors was either totally or partially abolished in the presence of the L-type calcium channel inhibitors SR33557 and nifedipine (half inhibition towards 2 μM), respectively. The inhibition was reversible and dose-dependent. Drugs able to deplete internal calcium stores (caffeine, ryanodine, and thapsigargin) were also tested on the fusion. Both caffeine and thapsigargin drastically inhibited fusion whereas ryanodine had no effect. This suggests that fusion may be controlled by internal pools of Ca2+but that its regulation may be insensitive to ryanodine. We presumed that an early form of the ryanodine receptor may exist, with different pharmacological properties than the adult forms. Indeed, Western blot analysis of pre- and postfusional L6 cells demonstrated the presence, at the prefusional stage, of a transient form of the ryanodine receptor protein with an apparent molecular weight slightly different from those of the classical skeletal and cardiac forms. Taken together, these results support the hypothesis that the fusion process is driven by a mechanism involving both the dihydropyridine receptor (α1 subunit of the L-type Ca2+channel) and the internal stores of Ca2+. The machinery underlying this mechanism might consist of slightly different forms of the classic molecules that in adult muscle ensure excitation–contraction coupling. It remains to be seen, however, whether the mobilization of the internal pool of Ca2+is triggered by the type of mechanism already described in skeletal muscle. 相似文献
18.
Identification and expression of water stress- and abscisic acid-regulated genes in a drought-tolerant sunflower genotype 总被引:17,自引:0,他引:17
19.
Drosophila melanogaster acetylcholinesterase: Identification and expression of two mutations responsible for cold- and heat-sensitive phenotypes 总被引:2,自引:0,他引:2
Annick Mutero Jean-Marc Bride Madeleine Pralavorio Didier Fournier 《Molecular & general genetics : MGG》1994,243(6):699-705
Ace
IJ29 and Ac
IJ40 are cold- and heat-sensitive variants of the gene coding for acetylcholinesterase in Drosophila melanogaster. In the homozygous condition, these mutations are lethal when animals are raised at restrictive temperatures, i.e., below 23° C for Ace
IJ29 or above 25° C for Ace
IJ40. The coding regions of the gene in these mutants were sequenced and mutations changing Ser374 to Phe in Ace
IJ29 and Pro75 to Leu in Ace
IJ40 were found. Acetylcholinesterases bearing these mutations were expressed in Xenopus oocytes and we found that these mutations decrease the secretion rate of the protein most probably by affecting its folding. This phenomenon is exacerbated at restrictive temperatures decreasing the amount of secreted acetylcholinesterase below the lethality threshold. In parallel, the substitution of the conserved Asp248 by an Asn residue completely inhibits the activity of the enzyme and its secretion, preventing the correct folding of the protein in a non-conditional manner. 相似文献
20.
Simon Lovestone C. Hugh Reynolds Donna Latimer Daniel R. Davis Brian H. Anderton Jean-Marc Gallo Diane Hanger Sandrine Mulot Betina Marquardt Silvia Stabel James R. Woodgett Christopher C. J. Miller 《Current biology : CB》1994,4(12)
Background: Paired helical filaments (PHFs) are a characteristic pathological feature of Alzheimer's disease; their principal component is the microtubule-associated protein tau. The tau in PHFs (PHF-tau) is hyperphosphorylated, but the cellular mechanisms responsible for this hyperphosphorylation have yet to be elucidated. A number of kinases, including mitogen-activated protein (MAP) kinase, glycogen synthase kinase (GSK)-3α, GSK-3β and cyclin-dependent kinase-5, phosphorylate recombinant tau in vitro so that it resembles PHF-tau as judged by its reactivity with a panel of antibodies capable of discriminating between normal tau and PHF-tau, and by a reduced electrophoretic mobility that is characteristic of PHF-tau. To determine whether MAP kinase, GSK-3α and GSK-3β can also induce Alzheimer's disease-like phosphorylation of tau in mammalian cells, we studied the phosphorylation status of tau in primary neuronal cultures and transfected COS cells following changes in the activities of MAP kinase and GSK-3.Results Activating MAP kinase in cultures of primary neurons or transfected COS cells expressing tau isoforms did not increase the level of phosphorylation for any PHF-tau epitope investigated. But elevating GSK-3 activity in the COS cells by co-transfection with GSK-3α or GSK-3β decreased the electrophoretic mobility of tau so that it resembled that of PHF-tau, and induced reactivity with eight PHF-tau-selective monoclonal antibodies.Conclusion Our data indicate that GSK-3α and/or GSK-3β, but not MAP kinase, are good candidates for generating PHF-type phosphorylation of tau in Alzheimer's disease. The involvement of other kinases in the generation of PHFs cannot, however, be eliminated. Our results suggest that aberrant regulation of GSK-3 may be a pathogenic mechanism in Alzheimer's disease. 相似文献