نتایج جستجو برای: nadh dehydrogenase i nd1 gene

تعداد نتایج: 2127823  

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1999
D T Lucas L I Szweda

We previously reported that cardiac reperfusion results in declines in mitochondrial NADH-linked respiration. The degree of inactivation increased with age and was paralleled by modification of protein by the lipid peroxidation product 4-hydroxy-2-nonenal. To gain insight into potential sites of oxidative damage, the present study was undertaken to identify specific mitochondrial protein(s) ina...

Journal: :The Journal of biological chemistry 1975
H Yanagawa F Egami

1. Lipoyl dehydrogenase (NADH: lipoamide oxidoreductase, ED 1.6.4.3) and two asparagusate dehydrogenases from asparagus mitochondria were purified by a series of steps, freezing and thawing, sodium dodecylsulfate extraction, and chromatography on Sephadex G-200 and DEAE-cellulose. 2. Lipoyl dehydrogenase was highly specific for alpha-lipoic acid, which could not be replaced at all by asparagus...

Journal: :Biochemical Society transactions 1988
R N Perham A Berry N S Scrutton

Reduced glutathione (GSH) plays a crucial role in ensuring that other thiol groups remain reduced within the cell and is particularly important in the biosynthesis of DNA [for ;I review, see Holmgren ( 1985)l. Dihydrolipoamide dehydrogenase is an essential component of the 2-ox0 acid dehydrogenase multi-enzyme complexes (Reed, 1974; Perham, 1983) in which it acts to oxidize the dihydrolipoic ac...

2015
María Isabel González-Siso Alba Touriño Ángel Vizoso Ángel Pereira-Rodríguez Esther Rodríguez-Belmonte Manuel Becerra María Esperanza Cerdán

In this paper, we report the metabolic engineering of the respiratory yeast Kluyveromyces lactis by construction and characterization of a null mutant (Δklndi1) in the single gene encoding a mitochondrial alternative internal dehydrogenase. Isolated mitochondria of the Δklndi1 mutant show unaffected rate of oxidation of exogenous NADH, but no oxidation of matrix NADH; this confirms that KlNdi1p...

Journal: :Applied and environmental microbiology 2010
Víctor Guadalupe Medina Marinka J H Almering Antonius J A van Maris Jack T Pronk

In anaerobic cultures of wild-type Saccharomyces cerevisiae, glycerol production is essential to reoxidize NADH produced in biosynthetic processes. Consequently, glycerol is a major by-product during anaerobic production of ethanol by S. cerevisiae, the single largest fermentation process in industrial biotechnology. The present study investigates the possibility of completely eliminating glyce...

Journal: :The Biochemical journal 1989
O Marcillat Y Zhang K J Davies

The quinonoid anthracycline, doxorubicin (Adriamycin) is a potent anti-neoplastic agent whose clinical use is limited by severe cardiotoxicity. Mitochondrial damage is a major component of this cardiotoxicity, and rival oxidative and non-oxidative mechanisms for inactivation of the electron transport chain have been proposed. Using bovine heart submitochondrial preparations (SMP) we have now fo...

Journal: :Indian journal of biochemistry & biophysics 1999
V H Obungu J K Kiaira N K Olembo M R Njogu

Studies of respiration on glucose in procyclic Trypanosoma congolense in the presence of rotenone, antimycin, cyanide, salicylhydroxamic acid and malonate have indicated the presence of NADH dehydrogenase, cytochrome b-c1, cytochrome aa3, trypanosome alternate oxidase and NADH fumarate reductase/succinate dehydrogenase pathway that contributes electrons to coenzyme Q of the respiratory chain. T...

2014
Jonathon L. Burman Leslie S. Itsara Ernst-Bernhard Kayser Wichit Suthammarak Adrienne M. Wang Matt Kaeberlein Margaret M. Sedensky Philip G. Morgan Leo J. Pallanck

Mutations affecting mitochondrial complex I, a multi-subunit assembly that couples electron transfer to proton pumping, are the most frequent cause of heritable mitochondrial diseases. However, the mechanisms by which complex I dysfunction results in disease remain unclear. Here, we describe a Drosophila model of complex I deficiency caused by a homoplasmic mutation in the mitochondrial-DNA-enc...

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