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1.
F. Servat D. Montet M. Pina N. Bernet A. Arnaud P. Galzy H. Ledon L. Marcou J. Graille 《Biotechnology letters》1990,12(9):689-692
Summary Oleylhydroxamic acid (Oleyl HA) was produced by acylation of neutralized hydroxylamine with oleic acid in buffered or in solvent media using the broad-spectrum amidase activity ofBrevibacterium (BB) sp 19 cells. 相似文献
2.
Margot Tertrais Claire Bigot Emmanuel Martin Renaud Poincloux Arnaud Labrousse Isabelle Maridonneau-Parini 《European journal of cell biology》2021,100(4):151161
Phagocytosis consists in ingestion and digestion of large particles, a process strictly dependent on actin re-organization. Using synchronized phagocytosis of IgG-coated latex beads (IgG-LB), zymosan or serum opsonized-zymosan, we report the formation of actin structures on both phagocytic cups and closed phagosomes in human macrophages. Their lifespan, size, protein composition and organization are similar to podosomes. Thus, we called these actin structures phagosome-associated podosomes (PAPs). Concomitantly to the formation of PAPs, a transient disruption of podosomes occurred at the ventral face of macrophages. Similarly to podosomes, which are targeted by vesicles containing proteases, the presence of PAPs correlated with the maturation of phagosomes into phagolysosomes. The ingestion of LB without IgG did not trigger PAPs formation, did not lead to podosome disruption and maturation to phagolysosomes, suggesting that these events are linked together. Although similar to podosomes, we found that PAPs differed by being resistant to the Arp2/3 inhibitor CK666. Thus, we describe a podosome subtype which forms on phagosomes where it probably serves several tasks of this multifunctional structure. 相似文献
3.
Effect of adrenocorticotrophic hormone on the activity of sterol ester hydrolase from rat brain 总被引:1,自引:0,他引:1
J Arnaud O Nobili J Boyer 《Biochemical and biophysical research communications》1981,100(3):1167-1172
Adrenocorticotrophic hormone (ACTH) stimulates in vitro the hydrolysis of oleoylcholesterol by a sterol ester hydrolase from rat brain synaptosomes. The stimulatory effect involves an alkaline shift of the pH optimum of catalysis and culminates at pH 6 with a 15 to 20-fold increase in lipolytic rates. The effect requires trace amount of organic solvent in the substrate emulsion and is dependent on the NH2-terminal sequence extending through the basic amino acid residues at positions 15–18. The hormonal stimulation is decreased when a lipid-depleted preparation is used as enzyme source, and fully restored upon addition of lecithin. The results raise the possibility that ACTH may have a neuro-hormonal role in brain via modulation of local lipolytic processes. 相似文献
4.
A rapid and easy method based on proton magnetic resonance spectrometry is proposed for the determination of nitrilase and amidase activities. The technique is applicable to many substrates of different chemical types: aliphatic, α-ethylenic, α-hydroxy, and α-amino nitriles and amides. The rate of hydrolysis of the above substrates may be monitored in a continuous fashion by using proton magnetic resonance. A good correlation has been achieved between the results obtained by proton magnetic resonance and those found by gas-liquid chromatography. 相似文献
5.
We studied the interaction of alpha 2-HS-glycoprotein with immobilized Cibacron blue F3-GA (Blue A) and Procion red HE-3B (Red A). When whole plasma was applied on the Blue A, alpha 2-HS-glycoprotein remained unbound, together with other plasma proteins. In contrast, when this fraction was applied on the Red A, alpha 2-HS-glycoprotein was shown to bind tightly and was eluted with a linear sodium chloride gradient between 0.5 and 0.8 M. This proved to be a useful two-step technique for the purification of alpha 2-HS-glycoprotein. Further characterization revealed that the protein appeared homogeneous by immunoelectrophoresis and SDS-polyacrylamide gel electrophoresis with yields greater than 30%. A small (less than 5%) but significant fraction of alpha 2-HS-glycoprotein with a same molecular weight as the native protein was consistently found in the wash of the Red A column, and may correspond to alpha 2-HS-glycoprotein bound to a yet unidentified ligand. 相似文献
6.
Abstract A mutant strain of Candida molischiana was selected. Analysis of the exocellular activity of Candida molischiana 35M5N grown on different carbon sources revealed that the biosynthesis of β-glucosidase is derepressed in this yeast strain. The strain is not a hyper-producer mutant. There were no observed differences in the endocellular and parietal activities of the wild and mutant strains. However, the mutant strain produced 35-fold more enzyme than the wild-type in the culture medium with glucose as carbon source. When glucose was used as carbon source, the mutant strain produced 90% more exocellular enzyme than when cellobiose was used as the carbon source. 相似文献
7.
Stephan Francke Karine Clement Christian Dina Hiroshi Inoue Philip Behn Vincent Vatin Arnaud Basdevant Bernard Guy-Grand M. Alan Permutt Philippe Froguel J. Hager 《Human genetics》1997,100(5-6):491-496
Family studies have shown that in some populations up to 75% of the variation of body mass index can be explained by genetic
factors. However, in humans, no major obesity gene has been identified to date. In contrast, there are a number of genetically
well defined animal models for obesity. In two of those models (ob/ob and db/db), defects in the same pathway are responsible
for obesity. Recently, some evidence has been found for the OB gene also being involved in human obesity. In this study we
investigated the potential role of the OB receptor (OBR) in the etiology of massive obesity in humans using familial linkage
analyses and case-control association studies. The typing of two microsatellite markers (D1S198 and D1S209), flanking the
OBR gene, in 256 sib pairs showed no evidence for linkage with obesity. In order to be able to detect small gene effects,
association studies with a 3′-UTR insertion/deletion polymorphism were carried out. The results of these analyses remained
non-significant (χ2 = 3.442, P = 0.18). However, subjects heterozygous for the insertion/deletion polymorphism showed a slight trend towards lower insulin
values 30 min after an oral glucose load compared to homozygous individuals (P = 0.02). In summary, our results do not support a major role of the human OBR gene in the development of morbid obesity in
our population.
Received: 4 December 1996 / Accepted: 25 June 1997 相似文献
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10.
Purification and properties of the endocellular β-glucosidase of Candida cacaoi Buckley and Van Uden CBS 2020 总被引:1,自引:1,他引:0
D. Drider P. Pommares P. Chemardin A. Arnaud P. Galzy 《Journal of applied microbiology》1993,74(4):473-479
D. DRIDER, P. POMMARES, P. CHEMARDIN, A. ARNAUD AND P. GALZY. 1993. The endocellular enzyme β-glucosidase of Candida cacaoi was purified by ion-exchange chromatography and gel filtration. The molecular weight was 220 ± 10 kDa; its optimum pH was between 4 and 5.5 and its optimum temperature was 60C. This enzyme was active against soluble glucosides tested with β(1–2), β(1–3), β(1–4) and even α(1–4) and α(1–6) and was inhibited by D-glucono-δ-lactone. The enzyme was constitutive but its synthesis was repressed by glucose. 相似文献