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An oxidase for reduced diphosphopyridine nucleotide.

作者信息

HUENNEKENS F M, BASFORD R E, GABRIO B W

出版信息

J Biol Chem. 1955 Apr;213(2):951-67.

PMID:14367356
Abstract
摘要

相似文献

1
An oxidase for reduced diphosphopyridine nucleotide.一种用于还原二磷酸吡啶核苷酸的氧化酶。
J Biol Chem. 1955 Apr;213(2):951-67.
2
Oxidation of reduced diphosphopyridine nucleotide by Clostridium perfringens. II. Purification of the oxidase: relation to cytochrome c reductase.产气荚膜梭菌对还原型二磷酸吡啶核苷酸的氧化作用。II. 氧化酶的纯化：与细胞色素c还原酶的关系。
J Bacteriol. 1959 Apr;77(4):393-402. doi: 10.1128/jb.77.4.393-402.1959.
3
The requirement of diphosphopyridine nucleotide for choline dehydrogenase activity.二磷酸吡啶核苷酸对胆碱脱氢酶活性的需求。
J Biol Chem. 1953 Jul;203(1):63-7.
4
alpha-Ketoglutaric dehydrogenase. VI. Reversible oxidation of dihydrothioctamide by diphosphopyridine nucleotide.α-酮戊二酸脱氢酶。VI. 二磷酸吡啶核苷酸对二氢硫辛酰胺的可逆氧化作用。
J Biol Chem. 1959 Jan;234(1):178-82.
5
[On the oxidation of reduced diphosphopyridine nucleotide in the presence of polyphenoloxidase: number of molecules of substrate oxidized by a mole of enzyme per minute].[关于在多酚氧化酶存在下还原型二磷酸吡啶核苷酸的氧化：每分钟每摩尔酶氧化的底物分子数]
C R Seances Soc Biol Fil. 1960;154:270-2.
6
Kinetic studies on the rôle of zinc and diphosphopyridine nucleotide in the activity of yeast alcohol dehydrogenase.锌和二磷酸吡啶核苷酸在酵母醇脱氢酶活性中作用的动力学研究。
J Biol Chem. 1956 Jul;221(1):491-500.
7
Studies on alpha-ketoglutaric oxidase. III. Role of coenzyme A and diphosphopyridine nucleotide.α-酮戊二酸氧化酶的研究。III. 辅酶A和二磷酸吡啶核苷酸的作用。
J Biol Chem. 1953 Mar;201(1):103-15.
8
Isolation of an ascorbic acid dependent reduced diphosphopyridine nucleotide oxidase.
Biochim Biophys Acta. 1957 Apr;24(1):222. doi: 10.1016/0006-3002(57)90180-4.
9
The role of plant phenolic compounds in the oxidation of reduced diphosphopyridine nucleotide by peroxidase.植物酚类化合物在过氧化物酶催化还原型二磷酸吡啶核苷酸氧化反应中的作用。
Can J Biochem Physiol. 1961 Jul;39:1113-24. doi: 10.1139/o61-115.
10
The cytochemical localization of oxidative enzymes. I. Diphosphopyridine nucleotide diaphorase and triphosphopyridine nucleotide diaphorase.氧化酶的细胞化学定位。I. 二磷酸吡啶核苷酸黄递酶和三磷酸吡啶核苷酸黄递酶。
J Biophys Biochem Cytol. 1958 Nov 25;4(6):747-52. doi: 10.1083/jcb.4.6.747.

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Selective NADH communication from α-ketoglutarate dehydrogenase to mitochondrial transhydrogenase prevents reactive oxygen species formation under reducing conditions in the heart.在心脏的还原条件下，从α-酮戊二酸脱氢酶到线粒体转氢酶的选择性NADH通讯可防止活性氧的形成。
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Bio-Fenton reaction involved in the cleavage of the ethoxylate chain of nonionic surfactants by dihydrolipoamide dehydrogenase from Pseudomonas nitroreducens TX1.生物 Fenton 反应涉及假单胞菌 TX1 中的二氢硫辛酸脱氢酶对非离子表面活性剂乙氧基链的断裂。
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An Updated View on the Molecular Pathomechanisms of Human Dihydrolipoamide Dehydrogenase Deficiency in Light of Novel Crystallographic Evidence.
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Neurochem Res. 2019 Oct;44(10):2307-2313. doi: 10.1007/s11064-019-02766-9. Epub 2019 Mar 7.
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Formation of reactive oxygen species by human and bacterial pyruvate and 2-oxoglutarate dehydrogenase multienzyme complexes reconstituted from recombinant components.由重组成分重构的人源和细菌丙酮酸脱氢酶及2-酮戊二酸脱氢酶多酶复合物产生活性氧物种。
Free Radic Biol Med. 2015 Dec;89:642-50. doi: 10.1016/j.freeradbiomed.2015.10.001. Epub 2015 Oct 9.
5
Inhibitors of succinate: quinone reductase/Complex II regulate production of mitochondrial reactive oxygen species and protect normal cells from ischemic damage but induce specific cancer cell death.琥珀酸：醌还原酶/复合物 II 抑制剂可调节线粒体活性氧的产生，保护正常细胞免受缺血损伤，但诱导特定的癌细胞死亡。
Pharm Res. 2011 Nov;28(11):2695-730. doi: 10.1007/s11095-011-0566-7. Epub 2011 Aug 24.
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Alpha-ketoglutarate dehydrogenase: a target and generator of oxidative stress.α-酮戊二酸脱氢酶：氧化应激的靶点与产生源
Philos Trans R Soc Lond B Biol Sci. 2005 Dec 29;360(1464):2335-45. doi: 10.1098/rstb.2005.1764.
7
Generation of reactive oxygen species in the reaction catalyzed by alpha-ketoglutarate dehydrogenase.在α-酮戊二酸脱氢酶催化的反应中活性氧的生成。
J Neurosci. 2004 Sep 8;24(36):7771-8. doi: 10.1523/JNEUROSCI.1842-04.2004.
8
The lactic dehydrogenase of Propionibacterium pentosaceum.戊糖丙酸杆菌的乳酸脱氢酶。
Biochem J. 1960 Apr;75(1):57-65. doi: 10.1042/bj0750057.
9
[Amount of mercury given off by Hg203-silver amalgam dental fillings].
Klin Wochenschr. 1957 Jun 1;35(11):591. doi: 10.1007/BF01480814.