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Enzymes feedback regulators

In this scheme, F symbolizes an essential metabolite, such as an amino acid or a nucleotide. In such systems, F, the essential end product, inhibits enzyme 1, xAie first step in the pathway. Therefore, when sufficient F is synthesized, it blocks further synthesis of itself. This phenomenon is called feedback inhibition or feedback regulation. [Pg.468]

Enzymes such as enzyme 1, which are subject to feedback regulation, represent a distinct class of enzymes, the regulatory enzymes. As a class, these enzymes have certain exceptional properties ... [Pg.469]

Production of phenylalanine starts after depletion of tyrosine at about 6 hours. This is logical since the micro-oiganism needs a certain amount of tyrosine, for example to synthesise key enzymes, but synthesis of L-phenylalanine is feedback regulated if tyrosine is present. [Pg.255]

To provide a mechanism for the feedback inhibition of these enzymes, the allosteric model was put forward in 1963. It was proposed that the enzyme that regulates the flux through a pathway has two distinct binding sites, the active site and a separate site to which the regulator binds. This was termed the allosteric site. The word allosteric means different shape , which in the context of this mechanism means a different shape from the substrate. The theory further proposed that when the regnlator binds to the allosteric site, it canses a conformational change in... [Pg.49]

Figure 6-3. The pentose phosphate pathway. In the oxidative phase of the pentose phosphate pathway, NADP is reduced to NADPH H, with feedback regulation by NADPH at the step catalyzed by glucose 6-phosphate dehydrogenase. In the nonoxidative phase, multiple sugar interconversions catalyzed by three different enzymes occur. Figure 6-3. The pentose phosphate pathway. In the oxidative phase of the pentose phosphate pathway, NADP is reduced to NADPH H, with feedback regulation by NADPH at the step catalyzed by glucose 6-phosphate dehydrogenase. In the nonoxidative phase, multiple sugar interconversions catalyzed by three different enzymes occur.
Both bacteria and plants have separate enzymes that catalyze the individual steps in the biosynthetic sequence (Fig. 17-12). The fatty acyl group grows while attached to the small acyl carrier protein (ACP).54 58 Control of the process is provided, in part, by the existence of isoenzyme forms. For example, in E. coli there are three different P-oxoacyl-ACP synthases. They carry out the transfer of any acyl primer from ACP to the enzyme, decarboxylate malonyl-ACP, and carry out the Claisen condensation (steps b, e, and/in Eq. 17-12)58a e One of the isoenzymes is specialized for the initial elongation of acetyl-ACP and also provides feedback regulation.58c The other two function specifically in synthesis of unsaturated fatty acids. [Pg.1185]

Ribonucleotide reductases are discussed in Chapter 16. Some are iron-tyrosinate enzymes while others depend upon vitamin B12, and reduction is at the nucleoside triphosphate level. Mammalian ribonucleotide reductase, which may be similar to that of E. coli, is regarded as an appropriate target for anticancer drugs. The enzyme is regulated by a complex set of feedback mechanisms, which apparently ensure that DNA precursors are synthesized only in amounts needed for DNA synthesis.273 Because an excess of one deoxyribonucleotide can inhibit reduction of all... [Pg.1452]

Carbamyl-L-aspartate is the key precursor in the biosynthesis of pyrimidines. The enzyme aspartate transcarbamylase is inhibited by several pyrimidine nucleotides, notably cytidine triphosphate, and is activated by ATP, a purine nucleotide. Thus the enzyme is under feedback regulation, and controls the relative concentration of pyrimidine and purine nucleotides. [Pg.607]

Pyocyanin (160) is derived from the shikimate pathway, and one protein, PhzC, is equivalent to enzymes that catalyze the first step in this pathway, converting erythrose 4-phosphate (162) and phosphoenolpyruvic acid (163) to 3-deoxy-D-arabinoheptulosonate 7-phosphate (164) (Fig. 28). The equivalent enzyme in the shikimate pathway is thought to be feedback regulated, and PhzC is likely to shunt intermediates toward the shikimate pathway in preparation for pyocyanin (160)... [Pg.183]

Allosteric control involves the reversible binding of a compound to an allosteric site referred to as a regulatory site on the enzyme. These compounds may be either one of the compounds involved in the metabolic pathway (feedback regulators) or a compound that is not a product of the metabolic pathway. In both cases, the binding usually results in conformational changes, which either activate or deactivate the enzyme. Proenzymes also act as a form of enzyme control. [Pg.254]

Aromatase inhibitors serve to eliminate ex-traovarian synthesis of estrogens in breast cancer patients. This can be achieved effectively only in postmenopause because, as an FSH-dependent enzyme, ovarian aromatase is subject to feedback regulation of female Luellmann, Color Atlas of Pharmacology 2005 Thieme All rights reserved. Usage subject to terms and conditions of license. [Pg.256]

Gain ratio 17 r can be calculated at a reference force ratio, such as xopt, which is a natural steady-state force ratio of oxidative phosphorylation. This is seen as a result of the adaptation of oxidative phosphorylation to various metabolic conditions and also as a result of the thermodynamic buffering of reactions catalyzed by enzymes. The experimentally observed linearity of several energy converters operating far from equilibrium may be due to enzymatic feedback regulations with an evolutionary drive towards higher efficiency. [Pg.588]

In cell cultures, the expression of the reductase mRNA, like the tdc and stric-tosidine synthase sts) genes, was found to be induced by elicitors and down-regulated by auxins. GlOH was found to be localized in provacuolar membranes and not in the endoplasmic reticulum like many other cytochrome P450 enzymes. Interestingly, this enzyme is inhibited by the end product, alkaloid catharanthine, but not by vindoline and vinblastine. Therefore, feedback regulation may also operate in vivo, provided that the catharanthine and GlOH are within the same cellular compartment (Facchini and De Luca, 2008). [Pg.48]


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See also in sourсe #XX -- [ Pg.257 ]




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