| Name | catalase |
|---|---|
| Synonyms | CAT; Catalase; Erythrocyte derived growth promoting factor; Carnitine O acetyltransferase; Carnitine acetylase; Carnitine acetyltransferase; CAT; Catalases… |
| Name | nonanol |
|---|---|
| CAS | 3,5,5-trimethyl-1-hexanol |
| PubMed | Abstract | RScore(About this table) | |
|---|---|---|---|
| 10767287 | Matsumura T, Otera H, Fujiki Y: Disruption of the interaction of the longer isoform of Pex5p, Pex5pL, with Pex7p abolishes peroxisome targeting signal type 2 protein import in mammals. J Biol Chem. 2000 Jul 14;275(28):21715-21. We isolated peroxisome biogenesis-defective Chinese hamster ovary cell mutants from TKaG2 cells, wild-type CHO-K1 cells transformed with two cDNAs encoding rat Pex2p and peroxisome targeting signal (PTS) type 2-tagged green fluorescent protein, by the 9-(1'-pyrene) nonanol/UV selection method. One PEX5-deficient mutant, ZPG231, showed a novel phenotype: PTS2 proteins in the cytosol, but PTS1 proteins and catalase in peroxisomes. |
2(0,0,0,2) | Details |
| 9727033 | Kinoshita N, Ghaedi K, Shimozawa N, Wanders RJ, Matsuzono Y, Imanaka T, Okumoto K, Suzuki Y, Kondo N, Fujiki Y: Newly identified Chinese hamster ovary cell mutants are defective in biogenesis of peroxisomal membrane vesicles (Peroxisomal ghosts), representing a novel complementation group in mammals. J Biol Chem. 1998 Sep 11;273(37):24122-30. We isolated peroxisome biogenesis-defective mutants from Chinese hamster ovary cells by the 9-(1'-pyrene) nonanol/ultraviolet (P9OH/UV) method. Seven cell mutants, ZP116, ZP119, ZP160, ZP161, ZP162, ZP164, and ZP165, of 11 P9OH/UV-resistant cell clones showed cytosolic localization of catalase, a peroxisomal matrix enzyme, apparently indicating a defect of peroxisome biogenesis. |
1(0,0,0,1) | Details |
| 11825583 | Apel CL, Deamer DW, Mautner MN: Self-assembled vesicles of monocarboxylic acids and conditions for stability and for the encapsulation of biopolymers. Biochim Biophys Acta. 2002 Feb 10;1559(1):1-9. When catalase was encapsulated in vesicles of decanoic acid and decanol, the enzyme was protected from degradation by protease, and could act as a catalyst for its substrate, peroxide, which readily diffused across the membrane. However, addition of small amounts of an (nonanol) markedly stabilized the bilayers, and vesicles were present at significantly lower concentrations (approximately 20 mM) at pH ranges up to 11. |
1(0,0,0,1) | Details |
| 7814397 | Sakuraba H, Noguchi T: Alcohol:NAD+ oxidoreductase is present in rat liver peroxisomes. . J Biol Chem. 1995 Jan 6;270(1):37-40. The distribution of alcohol:NAD+ oxidoreductase activity with nonanol as substrate in the light mitochondrial fraction (peroxisome-enriched fraction) of rat liver was examined by centrifugation in a density gradient. |
0(0,0,0,0) | Details |
| 12054689 | Akiyama N, Ghaedi K, Fujiki Y: A novel pex2 mutant: catalase-deficient but temperature-sensitive PTS1 and PTS2 import. Biochem Biophys Res Commun. 2002 May 24;293(5):1523-9. From mutagenized wild-type CHO-K1 cells stably expressing rat Pex2p and Pex3p (1-40)-EGFP, cell colonies resistant to the 9-(1 (')-pyrene) nonanol/ultraviolet treatment were examined for intracellular location of peroxisomal proteins, including EGFP chimera, catalase, and matrix proteins with PTS types 1 and 2. |
9(0,0,1,4) | Details |
| 9270878 | Tateishi K, Okumoto K, Shimozawa N, Tsukamoto T, Osumi T, Suzuki Y, Kondo N, Okano I, Fujiki Y: Newly identified Chinese hamster ovary cell mutants defective in peroxisome biogenesis represent two novel complementation groups in mammals. Eur J Cell Biol. 1997 Aug;73(4):352-9. We isolated peroxisome biogenesis mutants from Chinese hamster ovary (CHO) cells, using the 9-(1'-pyrene) nonanol/ultraviolet (P9OH/ UV) method and wild-type CHO-K1 cells that had been stably transfected with cDNA encoding Pex2p (formerly peroxisome assembly factor-1, PAF-1). Three mutant cell clones, ZP110, ZP111, and ZP114, showed cytosolic localization of catalase, thereby indicating a defect in peroxisome biogenesis, whereas ZP112 and ZP113 contained fewer but larger catalase-positive particles. |
3(0,0,0,3) | Details |
| 11330054 | Ito M, Ito R, Miura S, Huang Y: Isolation of peroxisome-defective CHO mutant cells using green fluorescent protein. Cell Biochem Biophys. 2000;32 Spring:253-7. Each expressed PTS-GFP appeared to be localized in peroxisomes, because the GFP was observed in cellular structures, as was catalase. Following an enrichment of mutant cells by use of 9-(1'-pyrene) nonanol/ultraviolet irradiation (P9OH/UV) method, five peroxisome-defective mutants were isolated by pursuing the fluorescent signals from GFP. |
3(0,0,0,3) | Details |
| 10222139 | Ghaedi K, Itagaki A, Toyama R, Tamura S, Matsumura T, Kawai A, Shimozawa N, Suzuki Y, Kondo N, Fujiki Y: Newly identified Chinese hamster ovary cell mutants defective in peroxisome assembly represent complementation group A of human peroxisome biogenesis disorders and one novel group in mammals. Exp Cell Res. 1999 May 1;248(2):482-8. We isolated peroxisome biogenesis-defective mutants from rat PEX2-transformed Chinese hamster ovary (CHO) cells, using the 9-(1'-pyrene) nonanol/ultraviolet method. A total of 18 mutant cell clones showing cytosolic localization of catalase were isolated. |
2(0,0,0,2) | Details |
| 9184070 | Okumoto K, Bogaki A, Tateishi K, Tsukamoto T, Osumi T, Shimozawa N, Suzuki Y, Orii T, Fujiki Y: Isolation and characterization of peroxisome-deficient Chinese hamster ovary cell mutants representing human complementation group III. Exp Cell Res. 1997 May 25;233(1):11-20. We made use of the 9-(1'-pyrene) nonanol/ultraviolet (P9OH/UV) method and isolated peroxisome-deficient mutant cells. P9OH/UV-resistant cell colonies were examined for the intracellular location of catalase, a peroxisomal matrix enzyme, by immunofluorescence microscopy and using anti-catalase antibody. |
2(0,0,0,2) | Details |