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酪氨酸代谢产物对人和羊肝脏二氢蝶啶还原酶的强效抑制作用。

Potent inhibitory effects of tyrosine metabolites on dihydropteridine reductase from human and sheep liver.

作者信息

Shen R S

出版信息

Biochim Biophys Acta. 1984 Mar 29;785(3):181-5. doi: 10.1016/0167-4838(84)90142-0.

DOI:10.1016/0167-4838(84)90142-0
PMID:6422988
Abstract

L-Phenylalanine and its metabolites, such as phenylpyruvate, phenylacetate and L-phenyllactate, do not significantly inhibit dihydropteridine reductase purified from human and sheep liver (I50 greater than or equal to 5 mM). However, L-tyrosine and its metabolites, such as L-DOPA, tyramine, p-hydroxyphenylpyruvate, p-hydroxyphenylacetate, and p-hydroxyphenylacetate, are potent noncompetitive inhibitors of this enzyme, with Ki values in the range 4-260 microM. These results suggest that tyrosine metabolites can potentially regulate levels of tetrahydrobiopterin, the required cofactor for the hydroxylation of aromatic amino acids.

摘要

L-苯丙氨酸及其代谢产物,如苯丙酮酸、苯乙酸和L-苯乳酸,不会显著抑制从人和羊肝脏中纯化的二氢蝶啶还原酶(半数抑制浓度大于或等于5 mM)。然而,L-酪氨酸及其代谢产物,如L-多巴、酪胺、对羟基苯丙酮酸、对羟基苯乙酸和对羟基苯乳酸,是该酶的强效非竞争性抑制剂,其抑制常数(Ki)值在4-260微摩尔范围内。这些结果表明,酪氨酸代谢产物可能潜在地调节四氢生物蝶呤的水平,而四氢生物蝶呤是芳香族氨基酸羟基化所需的辅助因子。

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Potent inhibitory effects of tyrosine metabolites on dihydropteridine reductase from human and sheep liver.酪氨酸代谢产物对人和羊肝脏二氢蝶啶还原酶的强效抑制作用。
Biochim Biophys Acta. 1984 Mar 29;785(3):181-5. doi: 10.1016/0167-4838(84)90142-0.
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Rat striatal synaptosomes as a model system for studying the inhibition of dihydropteridine reductase activity.大鼠纹状体突触体作为研究二氢蝶啶还原酶活性抑制作用的模型系统。
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New pteridine substrates for dihydropteridine reductase and horseradish peroxidase.用于二氢蝶啶还原酶和辣根过氧化物酶的新型蝶啶底物。
Biochem J. 1986 Mar 1;234(2):335-42. doi: 10.1042/bj2340335.