Glycolysis mitochondrial

In contrast to substrate level phosphorylation in glycolysis, mitochondrial oxidative phosphorylation is an efficient process in that it generates in excess of 30 ATP per mole of glucose. In essence, the movement of electrons along the respiratory chain or electron transport chain is coupled with phosphorylation of ADP. 

Fig. 3. Primary carbon metabolism in a photosynthetic C3 leaf. An abbreviated depiction of foliar C02 uptake, chloroplastic light-reactions, chloroplastic carbon fixation (Calvin cycle), chloroplastic starch synthesis, cytosolic sucrose synthesis, cytosolic glycolysis, mitochondrial citric acid cycle, and mitochondrial electron transport. The photorespiration cycle spans reactions localized in the chloroplast, the peroxisome, and the mitochondria. Stacked green ovals (chloroplast) represent thylakoid membranes. Dashed arrows near figure top represent the C02 diffusion path from the atmosphere (Ca), into the leaf intercellular airspace (Ci), and into the stroma of the chloroplast (Cc).SoHd black arrows represent biochemical reactions. Enzyme names and some substrates and biochemical steps have been omitted for simplicity. The dotted line in the mitochondria represents the electron transport pathway. Energy equivalent intermediates (e.g., ADP, UTP, inorganic phosphate Pi) and reducing equivalents (e.g., NADPH, FADH2, NADH) are labeled in red. Membrane transporters Aqp (CO2 conducting aquaporins) and TPT (triose phosphate transporter) are labeled in italics. Mitochondrial irmer-membrane electron transport and proton transport proteins are labeled in small case italics.

Keywords Hepatocarcinogenesis iNOS Glycolysis Mitochondrial activity Prostaglandins Signal transduction S-adenosylmethionine DNA methylation... 

Most of the NADH used in electron transport is produced in the mitochondrial matrix space, an appropriate site because NADH is oxidized by Complex I on the matrix side of the inner membrane. Furthermore, the inner mitochondrial membrane is impermeable to NADH. Recall, however, that NADH is produced in glycolysis by glyceraldehyde-3-P dehydrogenase in the cytosol. If this NADH were not oxidized to regenerate NAD, the glycolytic pathway would cease to function due to NAD limitation. Eukaryotic cells have a number of shuttle systems that harvest the electrons of cytosolic NADH for delivery to mitochondria without actually transporting NADH across the inner membrane (Figures 21.33 and 21.34). 

Figure 12-14. The creatine phosphate shuttle of heart and skeletal muscle. The shuttle allows rapid transport of high-energy phosphate from the mitochondrial matrix into the cytosol. CKg, creatine kinase concerned with large requirements for ATP, eg, muscular contraction CIC, creatine kinase for maintaining equilibrium between creatine and creatine phosphate and ATP/ADP CKg, creatine kinase coupling glycolysis to creatine phosphate synthesis CK, , mitochondrial creatine kinase mediating creatine phosphate production from ATP formed in oxidative phosphorylation P, pore protein in outer mitochondrial membrane.

This is true of skeletal muscle, particularly the white fibers, where the rate of work output—and therefore the need for ATP formation—may exceed the rate at which oxygen can be taken up and utilized. Glycolysis in erythrocytes, even under aerobic conditions, always terminates in lactate, because the subsequent reactions of pymvate are mitochondrial, and erythrocytes lack mitochondria. Other tissues that normally derive much of their energy from glycolysis and produce lactate include brain, gastrointestinal tract, renal medulla, retina, and skin. The liver, kidneys, and heart usually take up... 

It is well known that the selective transport of ions through a mitochondrial inner membrane is attained when the oxygen supplied by the respiration oxidizes glycolysis products in mitochondria with the aid of such substances as flavin mononucleotide (FMN), fi-nicotinamide adenine dinucleotide (NADH), and quinone (Q) derivatives [1-3]. The energy that enables ion transport has been attributed to that supplied by electron transport through the membrane due to a redox reaction occurring at the aqueous-membrane interface accompanied by respiration [1-5],... 

The electron transport chain gets its substrates from the NADH and FADH2 supplied by the TCA cycle. Since the TCA cycle and electron transport are both mitochondrial, the NADH generated by the TCA cycle can feed directly into oxidative phosphorylation. NADH that is generated outside the mitochondria (for example, in aerobic glycolysis) is not transported directly into the mitochondria and oxidized—that would be too easy. 

However in the absence of O2, anaerobic glycolysis—fermentation—produces only 2 mol of ATP per mol of glucose consumed. In the absence of O2 the mitochondrial cytochrome chain ceases to operate and as a resnlt NADH2 accumnlates... 

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