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Keywords: oxidative phosphorylation
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Biochem J (2024) 481 (23): 1831–1854.
Published: 04 December 2024
...Bernardo Gindri dos Santos; Niki F. Brisnovali; Leigh Goedeke Mild uncoupling of oxidative phosphorylation is an intrinsic property of all mitochondria, allowing for adjustments in cellular energy metabolism to maintain metabolic homeostasis. Small molecule uncouplers have been extensively studied...
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Biochem J (2020) 477 (21): 4085–4132.
Published: 05 November 2020
...Daniella H. Hock; David R. L. Robinson; David A. Stroud Mitochondria produce the bulk of the energy used by almost all eukaryotic cells through oxidative phosphorylation (OXPHOS) which occurs on the four complexes of the respiratory chain and the F 1 –F 0 ATPase. Mitochondrial diseases...
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Biochem J (2016) 473 (6): 797–804.
Published: 10 March 2016
... oxidative phosphorylation YME1L Mitochondria are essential cellular organelles containing their own DNA (mtDNA) of non-nuclear origin. They take part in a variety of fundamental cellular processes, including haem biosynthesis, programmed cell death (apoptosis), iron–sulfur complex assembly...
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Biochem J (2016) 473 (4): 487–496.
Published: 09 February 2016
... collected on ice. Supernatants were centrifuged at 10000  g to pellet any detached cells and were then assayed for insulin by ELISA. Secreted insulin was normalized to cell density determined from DAPI fluorescence [ 15 ]. glucolipotoxicity mitochondria obesity oxidative phosphorylation...
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Biochem J (2013) 456 (3): 417–426.
Published: 22 November 2013
...-sensitivity of mitochondrial respiration and lowers coupling efficiency of glucose-stimulated oxidative phosphorylation. These mitochondrial defects coincide with an increased level of ROS (reactive oxygen species), impaired GSIS (glucose-stimulated insulin secretion) and decreased cell viability. Palmitate...
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Biochem J (2010) 427 (1): 105–112.
Published: 15 March 2010
... 344 rats. OXPHOS (oxidative phosphorylation) of intact mitochondria and cytochrome c oxidase activity in permeabilized mitochondria were determined with polarographic assays. The activities of the ETC (electron transport chain) complexes and the cytochrome content in solubilized mitochondria were...
Includes: Supplementary data
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Biochem J (2010) 426 (3): 319–326.
Published: 24 February 2010
... Journal compilation © 2010 Biochemical Society 2010 cancer H + -ATP synthase mitochondrion oxidative phosphorylation regulation of gene expression translation Mitochondria play a central role in the physiology of eukaryotic cells. The biogenesis of mitochondria is a complex genetic...
Includes: Supplementary data
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Biochem J (2009) 423 (3): 421–428.
Published: 12 October 2009
...Bernard Korzeniewski; Véronique Deschodt-Arsac; Guillaume Calmettes; Gilles Gouspillou; Jean-Michel Franconi; Philippe Diolez Mitochondrial respiration/oxidative phosphorylation is the main source of energy, in the form of ATP, in the heart under physiological conditions. Different respiratory...
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Biochem J (2009) 420 (1): 67–72.
Published: 28 April 2009
... oxidative phosphorylation 31 P-MR (magnetic resonance) spectroscopy skeletal muscle As an effective oxygen sink, mitochondria house the ultimate step of the fate of the oxygen pathway from air through the cardiovascular and pulmonary systems. Oxygen is used for substrate oxidation by mitochondria...
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Biochem J (2009) 418 (3): 595–604.
Published: 25 February 2009
... © 2009 Biochemical Society 2009 apoptosis membrane attack complex (MAC) oxidative phosphorylation reactive oxygen species (ROS) Trypanosoma cruzi trypanosomatid Trypanosoma cruzi is a protozoan parasite of the order Kinetoplastida that causes Chagas' disease, an infection...
Includes: Supplementary data
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Biochem J (2008) 413 (2): 343–347.
Published: 26 June 2008
... of the regulation of oxidative phosphorylation in heart postulated previously in a theoretical way. 1 To whom correspondence should be addressed (email [email protected] ). 21 1 2008 26 3 2008 31 3 2008 31 3 2008 © The Authors Journal compilation © 2008 Biochemical...
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Biochem J (2007) 405 (1): 1–9.
Published: 13 June 2007
... different regulatory mechanism, suggesting that selection for O 2 -dependent homoeostatic regulation of mitochondrial respiration is ancient and likely to be shared by all eukaryotic organisms. The goal of oxidative phosphorylation is the transfer of electrons through a series of acceptor cytochromes...
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Biochem J (2006) 396 (3): 573–583.
Published: 29 May 2006
... coefficient and the threshold value of cytochrome oxidase are modified with respect to the uncoupled condition. The results obtained are consistent with a model based on changes in the assembly state of the oxidative phosphorylation enzyme complexes and possible implications in the understanding of exercise...
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Biochem J (2004) 383 (3): 537–542.
Published: 26 October 2004
... mitochondrial respiratory chain oxidative phosphorylation trypanosome Intriguingly, there is a small group of organisms within the phylum Euglenozoa that does not conform to the usual pattern of c -type cytochromes with a CXXCH haem-binding motif. The cytochromes c and c 1 from the mitochondria...
Includes: Supplementary data
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Biochem J (2004) 379 (3): 703–710.
Published: 01 May 2004
...Bernard KORZENIEWSKI; Jerzy A. ZOLADZ Using a computer model of oxidative phosphorylation developed previously [Korzeniewski and Mazat (1996) Biochem. J. 319 , 143–148; Korzeniewski and Zoladz (2001) Biophys. Chem. 92 , 17–34], we analyse the effect of several factors on the oxygen-uptake kinetics...
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Biochem J (2003) 375 (3): 799–804.
Published: 01 November 2003
...Bernard KORZENIEWSKI It has been shown previously that direct stimulation of oxidative-phosphorylation complexes in parallel with the stimulation of ATP usage is able to explain the stability of intermediate metabolite (ATP/ADP, phosphocreatine/creatine, NADH/NAD + , protonmotive force...
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Biochem J (2003) 370 (3): 751–762.
Published: 15 March 2003
... 1.10.2.2) IV (EC 1.9.3.1) V (EC 3.6.1.34) 38 0 10 10 14 7 4 1 3 2 FMN, [Fe S] centres, ubiquinones FAD, [Fe S] centres, cytochrome b560 Cytochromes b and c1, Rieske protein [Cua] centre, [Cub-haem a3] centre None Pyruvate H+ Q Figure 1 Oxidative phosphorylation network and composition of mito- chondrial...
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Biochem J (2002) 364 (1): 317–322.
Published: 08 May 2002
..., and the isogenic wild type. The results indicated that the importance of cardiolipin for energetic coupling strongly depends on the rate of oxidative phosphorylation, which was set by using NADH (maximal rate limited by coupling mechanism) or ethanol (moderate rate limited by electron supply) as a respiratory...
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Biochem J (2001) 357 (3): 835–842.
Published: 25 July 2001
...Bernard KORZENIEWSKI; Monique MALGAT; Thierry LETELLIER; Jean-Pierre MAZAT Respiratory-chain-complex subunits in mitochondria are encoded by nuclear or mitochondrial DNA. This property might have profound implications for the phenotypic expression of mutations affecting oxidative phosphorylation...
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Biochem J (2000) 351 (1): 251–256.
Published: 26 September 2000
... specific suppressor domains, inhibits cytochrome c 1 promoter activity when co-transfected into HeLa cells, indicating that the E2F proteins modulate the cytochrome c 1 promoter in mammalian cells. However, E2F is not a general regulator of oxidative phosphorylation genes since three additional nuclear...
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Biochem J (2000) 346 (3): 849–855.
Published: 07 March 2000
...José M. IZQUIERDO; José M. CUEZVA Translation in vitro of the mammalian nucleus-encoded mRNA for the β subunit of mitochondrial H + -ATP synthase (β-mRNA) of oxidative phosphorylation is promoted by a 150 nt translational enhancer sequence in the 3ʹ-untranslated region (3ʹ UTR). Titration...