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L-pipecolic acid metabolism in human liver: detection of L-pipecolate oxidase and identification of its reaction product.

作者信息

Rao V V, Chang Y F

机构信息

Department of Biochemistry, University of Maryland Dental School, Baltimore 21201.

出版信息

Biochim Biophys Acta. 1990 May 8;1038(3):295-9. doi: 10.1016/0167-4838(90)90240-g.

DOI:10.1016/0167-4838(90)90240-g
PMID:2340290
Abstract

L-Pipecolate oxidase, an enzyme that oxidizes L-pipecolic acid in the human liver has been demonstrated in the peroxisomal preparation. This enzyme oxidizes L-pipecolic acid with concomitant production of H2O2 in the peroxisome of the normal human liver. The immediate product of L-pipecolic acid oxidation has been identified as L-alpha-aminoadipate delta-semialdehyde. This reaction product was directly, and also after conversion to pipecolic acid by NaBH4 reduction, characterized by use of an amino acid analyzer and thin-layer chromatography. The pit fall of an indirect assay of L-pipecolate oxidase by means of the assay of alpha-aminoadipic acid formation was discussed.

摘要

相似文献

1
L-pipecolic acid metabolism in human liver: detection of L-pipecolate oxidase and identification of its reaction product.
Biochim Biophys Acta. 1990 May 8;1038(3):295-9. doi: 10.1016/0167-4838(90)90240-g.
2
L-pipecolic acid metabolism in human liver: L-alpha-aminoadipate delta-semialdehyde oxidoreductase.
Biochim Biophys Acta. 1990 May 8;1038(3):300-5. doi: 10.1016/0167-4838(90)90241-7.
3
Assay for L-pipecolate oxidase activity in human liver: detection of enzyme deficiency in hyperpipecolic acidaemia.人肝脏中L-哌啶酸氧化酶活性的测定:高哌啶酸血症中酶缺乏的检测。
Biochim Biophys Acta. 1992 Jul 7;1139(3):189-95. doi: 10.1016/0925-4439(92)90133-8.
4
L-pipecolate oxidase: a distinct peroxisomal enzyme in man.L-哌啶酸氧化酶:人类一种独特的过氧化物酶体酶。
Biochem Biophys Res Commun. 1989 Oct 16;164(1):550-5. doi: 10.1016/0006-291x(89)91754-3.
5
Peroxisomal oxidation of pipecolic acid in the rat.
J Clin Chem Clin Biochem. 1989 May;27(5):319-21.
6
Peroxisomal L-pipecolic acid oxidation is deficient in liver from Zellweger syndrome patients.
Pediatr Res. 1989 May;25(5):548-52. doi: 10.1203/00006450-198905000-00024.
7
Purification and characterization of peroxisomal L-pipecolic acid oxidase from monkey liver.
J Biol Chem. 1991 Mar 15;266(8):4822-30.
8
Pipecolic acid is oxidized by renal and hepatic peroxisomes. Implications for Zellweger's cerebro-hepato-renal syndrome (CHRS).哌可酸被肾和肝过氧化物酶体氧化。对泽尔韦格脑肝肾综合征(CHRS)的影响。
Exp Cell Res. 1986 May;164(1):267-71. doi: 10.1016/0014-4827(86)90475-1.
9
L-Pipecolic acid oxidase, a human enzyme essential for the degradation of L-pipecolic acid, is most similar to the monomeric sarcosine oxidases.L-哌啶酸氧化酶是一种参与L-哌啶酸降解的人体必需酶,与单体肌氨酸氧化酶最为相似。
Biochem J. 2000 Feb 1;345 Pt 3(Pt 3):487-94.
10
Lysine metabolism in the human and the monkey: demonstration of pipecolic acid formation in the brain and other organs.人类和猴子体内的赖氨酸代谢:大脑及其他器官中哌啶酸形成的证明。
Neurochem Res. 1982 May;7(5):577-88. doi: 10.1007/BF00965124.

引用本文的文献

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3
Conversion of pipecolic acid into lysine in Penicillium chrysogenum requires pipecolate oxidase and saccharopine reductase: characterization of the lys7 gene encoding saccharopine reductase.
产黄青霉中哌啶酸转化为赖氨酸需要哌啶酸氧化酶和酵母氨酸还原酶:编码酵母氨酸还原酶的lys7基因的特性分析。
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