Literature DB >> 1991137

D-aspartate oxidase, a peroxisomal enzyme in liver of rat and man.

P P Van Veldhoven1, C Brees, G P Mannaerts.   

Abstract

By means of subcellular fractionation D-aspartate oxidase was shown to be localized in peroxisomes in rat and human liver. The oxidase from both sources was most active on D-aspartate and N-methyl-D-aspartate. In different rat tissues, the highest enzyme activity was found in kidney, followed by liver and brain. In these tissues, oxidase activities became detectable 1-4 days after birth, reaching adult values after 4 weeks. Analysis of liver samples from patients with Zellweger syndrome, a generalized peroxisomal dysfunction, demonstrated no significant deficiency of this particular oxidase.

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Year:  1991        PMID： 1991137     DOI： 10.1016/0304-4165(91)90203-s

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN： 0006-3002


  27 in total

1.  Modeling DNA methylation by analyzing the individual configurations of single molecules.

Authors:  Ornella Affinito; Giovanni Scala; Domenico Palumbo; Ermanno Florio; Antonella Monticelli; Gennaro Miele; Vittorio Enrico Avvedimento; Alessandro Usiello; Lorenzo Chiariotti; Sergio Cocozza
Journal:  Epigenetics       Date:  2016-10-17       Impact factor: 4.528

Review 2.  D-Aspartate acts as a signaling molecule in nervous and neuroendocrine systems.

Authors:  Nobutoshi Ota; Ting Shi; Jonathan V Sweedler
Journal:  Amino Acids       Date:  2012-08-08       Impact factor: 3.520

3.  Further characterization of rat dihydroceramide desaturase: tissue distribution, subcellular localization, and substrate specificity.

Authors:  C Causeret; L Geeraert; G Van der Hoeven; G P Mannaerts; P P Van Veldhoven
Journal:  Lipids       Date:  2000-10       Impact factor: 1.880

4.  Spatiotemporal localization of D-amino acid oxidase and D-aspartate oxidases during development in Caenorhabditis elegans.

Authors:  Yasuaki Saitoh; Masumi Katane; Tomonori Kawata; Kazuhiro Maeda; Masae Sekine; Takemitsu Furuchi; Hiroyuki Kobuna; Taro Sakamoto; Takao Inoue; Hiroyuki Arai; Yasuhito Nakagawa; Hiroshi Homma
Journal:  Mol Cell Biol       Date:  2012-03-05       Impact factor: 4.272

5.  Mitochondrial short-chain acyl-CoA dehydrogenase of human liver and kidney can function as an oxidase.

Authors:  G Vanhove; P P Van Veldhoven; H J Eyssen; G P Mannaerts
Journal:  Biochem J       Date:  1993-05-15       Impact factor: 3.857

6.  The biogenesis protein PEX14 is an optimal marker for the identification and localization of peroxisomes in different cell types, tissues, and species in morphological studies.

Authors:  Phillip Grant; Barbara Ahlemeyer; Srikanth Karnati; Timm Berg; Ingra Stelzig; Anca Nenicu; Klaus Kuchelmeister; Denis I Crane; Eveline Baumgart-Vogt
Journal:  Histochem Cell Biol       Date:  2013-10       Impact factor: 4.304

7.  D-aspartate localizations imply neuronal and neuroendocrine roles.

Authors:  M J Schell; O B Cooper; S H Snyder
Journal:  Proc Natl Acad Sci U S A       Date:  1997-03-04       Impact factor: 11.205

Review 8.  In situ heterogeneity of peroxisomal oxidase activities: an update.

Authors:  R J Van den Munckhof
Journal:  Histochem J       Date:  1996-06

9.  C-terminal tripeptide Ser-Asn-Leu (SNL) of human D-aspartate oxidase is a functional peroxisome-targeting signal.

Authors:  L Amery; C Brees; M Baes; C Setoyama; R Miura; G P Mannaerts; P P Van Veldhoven
Journal:  Biochem J       Date:  1998-12-01       Impact factor: 3.857

10.  Identification and subcellular localization of sphinganine-phosphatases in rat liver.

Authors:  P De Ceuster; G P Mannaerts; P P Van Veldhoven
Journal:  Biochem J       Date:  1995-10-01       Impact factor: 3.857
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