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  • ...ransfer from beta-oxidation and TCA cycle and impact of OXPHOS coupling on NADH and coenzyme Q redox states. ...o analyze the relationships between the N- and Q-redox states and electron transfer rates. <br>
    4 KB (495 words) - 16:44, 12 July 2023
  • ...e the reduction level of NADP and NAD, which, in turn, affects respiratory electron flow through succinate dehydrogenase.
    2 KB (315 words) - 09:36, 20 April 2021
  • ...aila VR, WikstrΓΆm M, Hummer G (2014) Electrostatics, hydration, and proton transfer dynamics in the membrane domain of respiratory Complex I. Proc Natl Acad Sc ...lecules establishing enhanced lateral connectivity and pathways for proton transfer between conserved ionizable residues along the center of the membrane domai
    2 KB (327 words) - 19:56, 27 January 2024
  • ...and glycerophosphate-pathways to the Q-junction regulate reversed electron transfer to Complex I and H<sub>2</sub>O<sub>2</sub> production. ...pressure generated by the linear S- and Gp-pathways or the convergent SGp-pathway on the Q-junction drives RET into CI and thus regulates H<sub>2</sub>O<sub>
    5 KB (694 words) - 18:54, 10 January 2022
  • ...are designed to measure simultaneously O<sub>2</sub> flux and the Q-redox state in isolated mitochondria and permeabilized cells. ...t D072]] simultaneous determination of O<sub>2</sub> flux and the Q-redox state in isolated mitochondria and cells permeabilized previously to addition to
    4 KB (623 words) - 17:57, 13 December 2023
  • ...support NADH-linked respiration. Oligomycin (Omy) is used to induce a LEAK state of respiration via the inhibition of the ATP synthase. Since higher concent :::* Comparison of GM- with PM-capacity yields important information on N-pathway respiratory control upstream of CI.
    5 KB (697 words) - 15:58, 8 June 2020
  • ...r W (2016) Adapting high-resolution respirometry to glucose-limited steady state mycelium of the filamentous fungus ''Penicillium ochrochloron'': method dev ...y does not depend on a complete saturation or inhibition of the cytochrome pathway.
    3 KB (386 words) - 15:46, 14 October 2023
  • ...f the ATP synthase. Since higher concentrations of Omy can decrease the ET state induced upon addition of uncoupler, the required concentration of Omy has t :::* Comparison of GM- with PM-capacity yields important information on N-pathway respiratory control upstream of CI.
    5 KB (756 words) - 15:03, 17 September 2020
  • |abbr=''ET-pathway state'' ...[[Categories of SUIT protocols]] are defined according to mitochondrial ET-pathway states.
    15 KB (1,913 words) - 19:27, 25 August 2023
  • ...ain components. These interactions would regulate mitochondrial CoQ steady-state levels and function. This article is part of a Special Issue entitled 'EBEC
    2 KB (234 words) - 16:11, 3 November 2021
  • |abbr=NADH ...dition of NADH may indicate an alteration of the mtIM integrity. Cytosolic NADH is effectively made available for mitochondrial respiration through the [[m
    4 KB (477 words) - 10:41, 4 April 2024
  • ...-[[ET capacity| ''E'']]) with NADH-linked substrates ([[PM-pathway control state|PM]] and PGM)''' ...may be relevant in the presence of [[glutamate-anaplerotic pathway control state]]. SUIT-012 can be extended with the CIV assay module.
    4 KB (505 words) - 23:57, 12 April 2021
  • ...den Bergen CW, Wagner AM, Krab K, Moore AL (1994) The relationship between electron flux and the redox poise of the quinone pool in plant mitochondria. Interpl ...oplasmic NADH ''in vivo'' uses the cyanide-resistant pathway more than the pathway involving the oxidation of succinate. A model is used to predict the kineti
    7 KB (1,023 words) - 09:03, 16 July 2021
  • ...f the ATP synthase. Since higher concentrations of Omy can decrease the ET state induced upon addition of uncoupler, the required concentration of Omy has t :::* Comparison of GM- with PM-capacity yields important information on N-pathway respiratory control upstream of CI.
    6 KB (834 words) - 14:07, 6 September 2021
  • ...Rich PR, Gnaiger E (2021) Coupling and pathway control of coenzyme Q redox state and respiration in isolated mitochondria. https://doi.org/10.26124/mitofit: ...omlodi_2021_MitoFit_Q.pdf Coupling and pathway control of coenzyme Q redox state and respiration in isolated mitochondria]
    5 KB (767 words) - 08:41, 8 January 2023
  • :::* Comparison of GM- with PM-capacity yields important information on N-pathway respiratory control upstream of CI. ...tate| S]] and [[NADH Electron transfer-pathway state| N-]] pathway control state.
    3 KB (420 words) - 09:20, 18 September 2020
  • ...rdoso LHD, Donnelly C, KomlΓ³di T, Gnaiger E (2022) Characterizing electron transfer through the mitochondrial Q-junction from fatty acid oxidation and TCA cycl ...posite directions. Therefore, our aim was to characterize the influence of pathway and coupling control on these two bioenergetic parameters.
    4 KB (519 words) - 14:25, 23 August 2022
  • |info='''A''' Linear coupling control with NADH-linked substrates for isolated mitochondria, tissue homogenate and permeabi ...he involvement of the [[complex II]] ([[Succinate pathway control state| S-pathway]]). It can be useful to understand the contribution and the activity of the
    3 KB (397 words) - 00:12, 13 April 2021
  • ...nitoring of respiration together with NAD(P)H autofluorescence and Q-redox state [1] provides unique analytical and diagnostic power in the study of mitocho ...Rich PR, Gnaiger E (2021) Coupling and pathway control of coenzyme Q redox state and respiration in isolated mitochondria. https://doi.org/10.26124/bec:2021
    3 KB (463 words) - 08:34, 28 July 2022
  • ...K state. Pyruvate (P) supports [[NADH Electron transfer-pathway state|NADH-pathway (N)]], and usually in the presence of ADP it does not increase further the :::: 1. the S- and NS-pathway-linked respiration and H<sub>2</sub>O<sub>2</sub> flux.
    5 KB (681 words) - 00:11, 13 April 2021
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