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Metabolism aerobic

One of the important consequences of neuronal stimulation is increased neuronal aerobic metabolism which produces reactive oxygen species (ROS). ROS can oxidize several biomoiecules (carbohydrates, DNA, lipids, and proteins). Thus, even oxygen, which is essential for aerobic life, may be potentially toxic to cells. Addition of one electron to molecular oxygen (O,) generates a free radical [O2)) the superoxide anion. This is converted through activation of an enzyme, superoxide dismurase, to hydrogen peroxide (H-iO,), which is, in turn, the source of the hydroxyl radical (OH). Usually catalase... [Pg.280]

Pyruvate produced by glycolysis is a significant source of acetyl-CoA for the TCA cycle. Because, in eukaryotic ceils, glycolysis occurs in the cytoplasm, whereas the TCA cycle reactions and ail subsequent steps of aerobic metabolism take place in the mitochondria, pyruvate must first enter the mitochondria to enter the TCA cycle. The oxidative decarboxylation of pyruvate to acetyl-CoA,... [Pg.644]

Organisms also evolved powerful detoxifying mechanisms that remove toxic materials or convert them to non-toxic forms or nutrients. Examples of alterations to non-toxic forms are the conversions of hydrogen sulfide to sulfate and nitrite to nitrate. The prime example of development of the ability to use a toxic substance is the evolution of aerobic metabolism, which converted a serious and widespread toxin, oxygen, into a major resource. This development, as we have seen, greatly increased the productivity of the biosphere and generated the oxygen-rich atmosphere of today s Earth. [Pg.506]

Eairley DJ, DR Boyd, ND Sharma, CCR Allen, P Morgan, MJ Larkin (2002) Aerobic metabolism of 4-hydroxybenzoic acid in Archaea via an unusual pathway involving an intramolecular migration (NIH shift). Appl Environ Microbiol 68 6246-6255. [Pg.138]

A number of factors complicate the aerobic metabolism of amino acids—different enzymes may be used even for the same amino acid the enzymes may be inducible or constitutive depending on their function a-ketoacids may be produced by deamination or amines by decarboxylation. [Pg.312]

Whereas the anaerobic degradation of pyrimidines and pnrines has been extensively examined in a range of organisms, particnlarly in species of Clostridia, aerobic degradation has been stndied less often. The aerobic metabolism of nric acid (2,6,8-trihydroxypnrine) has been examined in pseudomonads and degradation has been shown to occnr by alternative pathways ... [Pg.542]

The simple porphyrin category includes macrocycles that are accessible synthetically in one or few steps and are often available commercially. In such metallopor-phyrins, one or both axial coordinahon sites of the metal are occupied by ligands whose identity is often unknown and cannot be controlled, which complicates mechanistic interpretation of the electrocatalytic results. Metal complexes of simple porphyrins and porphyrinoids (phthalocyanines, corroles, etc.) have been studied extensively as electrocatalysts for the ORR since the inihal report by Jasinsky on catalysis of O2 reduction in 25% KOH by Co phthalocyanine [Jasinsky, 1964]. Complexes of all hrst-row transition metals and many from the second and third rows have been examined for ORR catalysis. Of aU simple metalloporphyrins, Ir(OEP) (OEP = octaethylporphyrin Fig. 18.9) appears to be the best catalyst, but it has been little studied and its catalytic behavior appears to be quite distinct from that other metaUoporphyrins [CoUman et al., 1994]. Among the first-row transition metals, Fe and Co porphyrins appear to be most active, followed by Mn [Deronzier and Moutet, 2003] and Cr. Because of the importance of hemes in aerobic metabolism, the mechanism of ORR catalysis by Fe porphyrins is probably understood best among all metalloporphyrin catalysts. [Pg.655]

More energy is derived by microorganisms from the aerobic metabolism of MTBE and other fuel oxygenates consequently, MTBE degrading cultures grow more quickly under aerobic conditions. [Pg.1017]

However, the many pathways by which MTBE and other oxygenates may be biodegraded anaerobically have been the subject of recent research and ongoing studies. Table 24.12 highlights the various electron acceptors that are used in anaerobic bioremediation studies and contrasts the products of complete anaerobic degradation with those for aerobic metabolism. [Pg.1018]

The cells of the body require a continuous supply of oxygen to produce energy and carry out their metabolic functions. Furthermore, these aerobic metabolic processes produce carbon dioxide, which must be continuously eliminated. The primary functions of the respiratory system include ... [Pg.240]

Adenosine triphosphate (ATP) The principal chemical energy source for cellular processes. It is largely produced during aerobic metabolism. In the neuron most ATP is used in the maintenance of the electrochemical gradient required to generate an action potential. [Pg.235]


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Acetone, aerobic metabolism

Aerobic metabolic activities

Aerobic metabolic pathways

Aerobic metabolism biosynthesis

Aerobic metabolism chains

Aerobic metabolism citric acid cycle

Aerobic metabolism glycolysis

Aerobic metabolism growth conditions

Aerobic metabolism pathways

Aerobic metabolism phosphorylation

Aerobic metabolism production

Aerobic metabolism prolonged exercise

Aerobic metabolism properties

Aerobic metabolism respiration

Aerobic metabolism temperature

Aerobic oxidative metabolism

Affecting aerobic metabolism

Carbohydrate metabolism aerobic

Energy metabolism aerobic

Fermentative and Aerobic Energy Metabolism

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