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Catabolic processes

Until now we have viewed the TCA cycle as a catabolic process because it oxidizes acetate units to COg and converts the liberated energy to ATP and reduced coenzymes. The TCA cycle is, after all, the end point for breakdown of food materials, at least in terms of carbon turnover. However, as shown in Figure 20.22, four-, five-, and six-carbon species produced in the TCA cycle also fuel avariety of biosynthetic processes. a-Ketoglutarate, succinyl-CoA, fumarate, and oxaloacetate are all precursors of important cellular species. (In order to par-... [Pg.661]

The regulation of NCR-sensitive amino acid transporters in Saccharomyces cerevisiae has many points in common with that of catabolic enzymes. Amino acid permeases, as well as some other transporters of nitrogenous nutrients, are integrated into the regulatory circuits, both general and specific, which control catabolic processes. [Pg.242]

The catabolic processes provide the energy needed for production of new cell biomass as well as for the maintenance of the fundamental functions in the existing biomass. [Pg.12]

The microbial catabolic processes, which proceed in wastewater, provide the biomass with energy. These processes include two process steps oxidation of organic matter and reduction of an electron acceptor. The entire oxidation-reduction process, or redox process, consists basically of transfer of electrons from the electron donor (the organic matter) to the relevant electron acceptor, i.e., from the oxidation step to the reduction step. [Pg.14]

The metabolism of microorganisms is complex. However, the metabolic pathways followed by anabolic and catabolic processes need to be described in simple terms to be applied for design and operation of urban wastewater systems. [Pg.25]

The flavin-based coenzymes flavin adenine dinucleotide (FAD) and flavin mononucleotide (FMN) are associated with a wide variety of enzymes that catalyze reactions in critical biosynthetic and catabolic processes (Fig. 16). Unlike other coenzymes, the reactions catalyzed do not conserve specific mechanistic pathways. In each case the apoenzyme serves to steer the course of the reaction through specific interactions with substrate and coenzyme [55]. Nonetheless, there are common features of the interactions of the apoenzymes with the flavin which can be exploited in the design of functional peptides and proteins. [Pg.23]

General catabolic process Amino acid Nitrogen end product... [Pg.160]

Although demethylation, which occurs in the liver, is normally considered to be a catabolic process, it may result in conversion of an inactive form of a drug to the active form. Thus 6-(methylthio)purine (XXXIX) is demethylated by the rat to 6-mercaptopurine [205]. This demethylation occurs in the liver micro-somes and is an oxidative process which converts the methyl group to formaldehyde [204, 207]. The 1-methyl derivative of 4-aminopyrazolo[3,4-d] pyrimidine (XLI) is demethylated slowly, but 6-mercapto-9-methylpurine (XLII) not at all [208]. The A -demethylation of puromycin (XLlIl) [209, 210], its aminonucleoside (XLIV) [211], and a number of related compounds, including V-methyladenine and V,V-dimethyladenine, occurs in the liver microsomes of rodents [212]. In the guinea-pig the rate-limiting step in the metabolism of the aminonucleoside appears to be the demethylation of the monomethyl compound, which is the major urinary metabolite [213]. The relationship of lipid solubility to microsomal metabolism [214], and the induction of these demethylases in rats by pre-treatment with various drugs have been studied [215]. [Pg.84]

Mecfianism of Action A skeletal muscle relaxant that reduces muscle contraction by interfering with release of calcium ion. Reduces calcium ion concenfrafion. Therapeutic Effect Dissociafes excitation-conf racf ion coupling. Interferes wifh catabolic process associated with malignant hyperthermic crisis. [Pg.324]

The term metabolism comprises the entire physical and chemical processes involved in the maintenance and reproduction of life in which nutrients are broken down to generate energy and to give simpler molecules (catabolism) which by themselves may be used to form more complex molecules (anabolism). In case of heterotrophic organisms, the energy evolving from catabolic processes is made available for use by the organism (IUPAC). [Pg.586]

The oxidation of pyruvate is an important catabolic process, but pyruvate has anabolic fates as well. It can, for example, provide the carbon skeleton for the synthesis of the amino acid alanine. We return to these anabolic reactions of pyruvate in later chapters. [Pg.523]

This pathway is the hub of intermediary metabolism. Four- and five-carbon end products of many catabolic processes feed into the cycle to serve as fuels. Oxaloac-etate and a-ketoglutarate, for example, are produced from aspartate and glutamate, respectively, when proteins are degraded. Under some metabolic circumstances, intermediates are drawn out of the cycle to be used as precursors in a variety of biosynthetic pathways. [Pg.616]


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See also in sourсe #XX -- [ Pg.12 , Pg.14 ]

See also in sourсe #XX -- [ Pg.107 , Pg.370 , Pg.437 , Pg.481 ]




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