نتایج جستجو برای: concanamycin

تعداد نتایج: 178  

Journal: :The Journal of experimental biology 2008
Bettina Schewe Elmar Schmälzlin Bernd Walz

Blowfly salivary gland cells have a vacuolar-type H(+)-ATPase (V-ATPase) in their apical membrane that energizes secretion of a KCl-rich saliva upon stimulation with serotonin (5-hydroxytryptamine, 5-HT). We have used BCECF to study microfluometrically whether V-ATPase and carbonic anhydrase (CA) are involved in intracellular pH (pH(i)) regulation, and we have localized CA activity by histochem...

Journal: :Bioscience, biotechnology, and biochemistry 2010
Tomoko Iwaki Takayuki Sekito Yoshimi Kakinuma

The fission yeast Schizosaccharomyces pombe was sensitive to salinity; cell growth was stopped by 0.5 M NaCl and by 10 mM LiCl. The avt5+ gene encodes a vacuolar transporter with a broad specificity for amino acids. We found that the avt5Delta mutant became highly tolerant of Li+ and Na+ in growth. Concanamycin A-sensitive Li+ uptake as well as cellular Li+ content was lower in the avt5 mutant,...

Journal: :The Journal of antibiotics 1984
H Kinashi K Someno K Sakaguchi

Concanamycins A, B and C were isolated from the mycelium of Streptomyces diastatochromogenes S-45 as effective inhibitors of the proliferation of mouse splenic lymphocytes stimulated by concanavalin A. They represent a new class of 18-membered macrolide antibiotics, and are biologically active in vitro against several fungi and yeasts, but not against bacteria. Concanamycin A, the main componen...

Journal: :The Journal of Cell Biology 2007
David Halter Sylvia Neumann Suzanne M. van Dijk Jasja Wolthoorn Ann M. de Mazière Otilia V. Vieira Peter Mattjus Judith Klumperman Gerrit van Meer Hein Sprong

Glycosphingolipids are controlled by the spatial organization of their metabolism and by transport specificity. Using immunoelectron microscopy, we localize to the Golgi stack the glycosyltransferases that produce glucosylceramide (GlcCer), lactosylceramide (LacCer), and GM3. GlcCer is synthesized on the cytosolic side and must translocate across to the Golgi lumen for LacCer synthesis. However...

Journal: :The Biochemical journal 1995
F J Sharom X Yu J W Chu C A Doige

P-Glycoprotein (Pgp) was isolated from CHRC5 membranes by selective detergent extraction and further purified by lentil lectin affinity chromatography. The purified product displayed a very high basal ATPase activity (1.65 mumol/min per mg protein in the absence of added drugs or lipids) with an apparent Km for ATP of 0.4 mM. There was no evidence of cooperativity, suggesting that the two ATP s...

Journal: :Journal of immunology 2001
H Zhou T B Stuge N W Miller E Bengten J P Naftel J M Bernanke V G Chinchar L W Clem M Wilson

Two types of catfish alloantigen-dependent cytotoxic T cells were cloned from PBL from a fish immunized in vivo and stimulated in vitro with the allogeneic B cell line 3B11. Because these are the first clonal cytotoxic T cell lines derived from an ectothermic vertebrate, studies were undertaken to characterize their recognition and cytotoxic mechanisms. The first type of CTL (group I) shows str...

2000
Carola Förster Patricia M. Kane

The vacuole is the major site of intracellular Ca storage in yeast and functions to maintain cytosolic Ca levels within a narrow physiological range via a Ca pump (Pmc1p) and a H/Ca antiporter (Vcx1p) driven by the vacuolar H-ATPase (V-ATPase). We examined the function of the V-ATPase in cytosolic Ca homeostasis by comparing responses to a brief Ca challenge of a V-ATPase mutant (vma2D) and wil...

Journal: :Journal of cell science 2009
Jacqueline A Sobota Nils Bäck Betty A Eipper Richard E Mains

The vacuolar H(+)-ATPase (V-ATPase) establishes pH gradients along secretory and endocytic pathways. Progressive acidification is essential for proteolytic processing of prohormones and aggregation of soluble content proteins. The V-ATPase V(0) subunit is thought to have a separate role in budding and fusion events. Prolonged treatment of professional secretory cells with selective V-ATPase inh...

Journal: :The Journal of experimental biology 2009
Markus Huss Helmut Wieczorek

V-ATPases constitute a ubiquitous family of heteromultimeric, proton translocating proteins. According to their localization in a multitude of eukaryotic endomembranes and plasma membranes, they energize many different transport processes. Currently, a handful of specific inhibitors of the V-ATPase are known, which represent valuable tools for the characterization of transport processes on the ...

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