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Fusao Tomita

Other affiliations: Ajinomoto
Bio: Fusao Tomita is an academic researcher from Hokkaido University. The author has contributed to research in topics: Fermentation & Magnaporthe grisea. The author has an hindex of 46, co-authored 176 publications receiving 7692 citations. Previous affiliations of Fusao Tomita include Ajinomoto.


Papers
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Journal ArticleDOI
TL;DR: Staurosporine, microbial alkaloid which has been known to have antifungal activity was found to inhibit markedly phospholipid/Ca++dependent protein kinase (protein kinase C) from rat brain, with an IC50 value of 2.7 nM.

2,408 citations

Journal ArticleDOI
TL;DR: In Hypocrea jecorina and Penicillium purpurogenum, the respective inducers are sophorose and gentiobiose, which do not have beta-1,4 linkages though cellobiose , which has this linkage, is an inducer in other fungi.

248 citations

Journal ArticleDOI
TL;DR: Two kinds of glycolipids were produced in the culture media by several strains of Pseudomonas aeruginosa when grown on n paraffin and demonstrated mycoplasmacidal and antiviral activities in vitro.
Abstract: Two kinds of glycolipids (R-l and R-2) were produced in the culture media by several strains of Pseudomonas aeruginosa when grown on n paraffin (mixture of C12, C13. and C14 fractions). These compounds were isolated through the extraction of the culture broth with ethylacetate and the chromatography on silicic acid column. On the basis of chemical analysis, these lipids were characterized as 2-O-α-L-rhamnopyranosyl-α-L-rhamnopyranosyl-β- hydroxydecanoyl-β-hydroxydecanoate (R-l) and L-α-rhamnopyranosyl-β- hydroxydecanoyl-β-hydroxydecanoate (R-2). Bactericidal activity of R-2 which is postulated to be a precursor of R-1 was remarked against grampositive bacteria. Further, these compounds also demonstrated mycoplasmacidal and antiviral activities in vitro.

199 citations

Journal ArticleDOI
TL;DR: It is concluded that the three indigestible saccharides directly affect the epithelial tissue and activate the passage of tight junctions, thereby promoting Ca absorption in the small and large intestine in vitro.
Abstract: An Ussing chamber technique was used to determine the effects of three indigestible disaccharides on net Ca transport from the luminal side to the basolateral side of isolated preparations of jejunal, ileal, cecal and colonic epithelium in rats. Permeability of Lucifer Yellow (LY) and transepithelial electrical resistance (TEER), which are indicators of intercellular passage of the intestinal mucosa, were also determined. The concentrations of Ca in the serosal and mucosal media were 1.25 mmol/L and 10 mmol/L, respectively. After a 30-min incubation, the net Ca transport, LY passage and TEER were determined. In the control experiment, LY permeability was lowest, and TEER value was highest in the colon. The addition of 1-100 mmol/L melibiose, difructose anhydride (DFA)III, or DFAIV to the mucosal medium increased the net Ca absorption and LY permeability dose-dependently in the jejunum, ileum, cecum and colon preparations. Melibiose decreased TEER dose-dependently in the jejunum and cecum, but not in the ileum and colon. DFAIII decreased TEER dose-dependently in the jejunum, cecum and colon, but not in the ileum. DFAIV decreased TEER dose-dependently in all four intestinal portions. Positive linear relationships were found between net Ca transport and LY passage in all portions of the intestine, whereas negative linear relationships were found between net Ca absorption and TEER. We concluded that the three indigestible saccharides directly affect the epithelial tissue and activate the passage of tight junctions, thereby promoting Ca absorption in the small and large intestine in vitro.

105 citations


Cited by
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Journal ArticleDOI
TL;DR: This review covers the literature published in 2014 for marine natural products, with 1116 citations referring to compounds isolated from marine microorganisms and phytoplankton, green, brown and red algae, sponges, cnidarians, bryozoans, molluscs, tunicates, echinoderms, mangroves and other intertidal plants and microorganisms.

4,649 citations

Journal ArticleDOI
TL;DR: GF 109203X was a competitive inhibitor with respect to ATP and displayed high selectivity for PKC as compared to five different protein kinases, illustrating the potential of this compound as a tool for studying the involvement of PKC in signal transduction pathways.

2,486 citations

Journal ArticleDOI
TL;DR: Staurosporine, microbial alkaloid which has been known to have antifungal activity was found to inhibit markedly phospholipid/Ca++dependent protein kinase (protein kinase C) from rat brain, with an IC50 value of 2.7 nM.

2,408 citations

Journal ArticleDOI
TL;DR: The potential exists for altering the bile acid pool by targeting key enzymes in the 7α/β-dehydroxylation pathway through the development of pharmaceuticals or sequestering bile acids biologically in probiotic bacteria, which may result in their effective removal from the host after excretion.

2,144 citations

Journal ArticleDOI
TL;DR: A personal view of some of the most important advances that have shaped this field of protein kinases, after G-protein-coupled receptors.
Abstract: Protein phosphorylation regulates most aspects of cell life, whereas abnormal phosphorylation is a cause or consequence of disease. A growing interest in developing orally active protein-kinase inhibitors has recently culminated in the approval of the first of these drugs for clinical use. Protein kinases have now become the second most important group of drug targets, after G-protein-coupled receptors. Here, I give a personal view of some of the most important advances that have shaped this field.

2,113 citations