Mitochondria, fee

Bernardi, P. and Pietrobon, D., 1982, On the nature of Pi-induced, Mg2+-prevented Ca2+ release in rat liver mitochondria, FEES Lett. 139, pp. 9-12... 

Atlante, A., Calissano, P, Bobba, A., Giannattasio, S., Marra, E., and Passarella, S. (2001). Glutamate neurotoxicity, oxidative stress and mitochondria. FEES Lett. 497, 1-5. 

Neve EPA, Ingelman-Sundbeig M (1999) A soluble NH2-terminally truncated catalytically active form of rat cytochrome P450 2E1 targeted to fiver mitochondria. FEES Lett 460 309-314... 

Ohyama Y, Hayashi S, Okuda K (1989) Purification of 25-hydroxyvitamin D3 24-hydroxylase from rat kidney mitochondria. FEES Lett 255 405 08... 

Korshunov, S.S., V.P. Skulachev, and A.A. Starkov, 1997. High protonic potential actuates a mechanism of production of reactive oxygen species in mitochondria FEES Lett. 416, 15-18. 

Zhai, D., Huang, X, Han, X., and Yang, R, 2000, Characterization of tBid-induced cytochrome c release from mitochondria and liposomes, FEES Lett. 472 293-296. 

Nor is a member of the superfamily of heme-copper oxidases that also include the cytochrome oxidases (found e.g. in mitochondria ). Although no crystal structure of Nor is known at present, the number of transmembrane a-helices and the location and structure of their cofactors (heme c, heme b, heme bs and Fee) are highly similar to those of the cytochrome oxidases. 

Halestrap initially concluded that the increases in mitochondrial pyruvate transport and carboxylation were due to an increase in A pH secondary to stimulation of the electron transport chain in the cytochrome fee, region [255]. The conclusion was based largely on spectral measurements of the redox state of these cytochromes in the control and stimulated states. The spectral measurements were later found to be artifactual due to low amplitude Ca swelling of the mitochondria. Halestrap then suggested that the stable changes in the mitochondria might reside in the lipid components of the membrane due to phospholipase A 2 activity [261,262], but he has been unable to confirm this with lysophospholipid measurements [263]. On the other hand, using an EPR spin label probe of the lipid environment of the isolated mitochondria, Hoek has found differences between control and treated mitochondria [264]. 

Cytochromes of this group are widely distributed. Examples are listed in Table 17. Cytochrome i> is a component of the respiratory chain in many aerobic organisms, but only as a complex bci in mitochondria (and fee/ in chloroplasts). The separation of he, may involve a modification of cytochrome b. Amino add sequences of a number of mitochondrial cytochromes b are available. ... 

Coleman, J.O.D., Hill, H.A.O., Walton, N.J. and Whatley, F.R. (1983) "Electrochemically-driven Respiration in Mitochondria and Paracoccus denitrificans , FEES Lett., 154, 319-322... 

Barile, M., Valenti, D., Brizio, C., Quagliariello, E., and Passarella, S., 1998. Rat liver mitochondria can hydrolyse thiamine pyrophosphate to thiamine monophosphate which can cross the mitochondrial membrane in a carrier-mediated process. FEES Letters. 435 6-10. 

Court, D.A., Kleene, R., Neupert, W. UU, R. (1996) FEES Lett., 390, 73-77. Role of the N- and C-termini of porin in import into the outer membrane of Neurospora mitochondria. 

Mujahid A., Y. Akiba, C.H. Warden and M. Toyomizu, 2007. Sequential changes in superoxide production, anion carriers and substrate oxidation in skeletal muscle mitochondria of heat-stressed chickens. FEES Lett. 581, 3461-3467. Mujahid A., Y. Akiba and M. Toyomizu, 2009. Olive oil-supplemented diet alleviates acute heat stress-induced mitochondrial ROS production in chicken skeletal muscle. Am. J. Physiol. Regul. Comp. Physiol. 297, R690-698. 

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