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Cell metabolism regulation

Figure 1.20). All of these reactions, many of which are at apparent crosspurposes in the cell, must be fine-tuned and integrated so that metabolism and life proceed harmoniously. The need for metabolic regulation is obvious. This metabolic regulation is achieved through controls on enzyme activity so that the rates of cellular reactions are appropriate to cellular requirements. [Pg.23]

The theoretical limits are 1.0 (all ATP) and 0 (all AMP) with a normal working range of 0.75 to 0.9. The involvement of energy charge in the integration and regulation of metabolism is considered further in die BIOTOL text entitled Biosynthesis and the Integration of Cell Metabolism. ... [Pg.123]

Girod, R-A. and Zryd, J.-R, Secondary metabolism in cultured red beet Beta vulgaris L.) cells Differential regulation of betaxanthin and betacyanin biosynthesis. Plant Cell Tiss. Org. Cult., 25, 1, 1991. [Pg.517]

From a genetical point of view, Saccharomyces cerevisiae is an ideal organism which may be considered the Escherichia coli of eukaryotic cells [4,5]. This is true in particular for the study of metabolic regulation and for that of membrane transport [6]. Finally, the astonishing resemblance between many yeast proteins and certain mammalian-cell proteins has seriously broadened the scope of interest. Although a few reports have appeared on amino acid transport in some other yeasts, most investigations in this field have used strains of Saccharomyces cerevisiae. [Pg.220]

Webb GC et al. Expression profiling of pancreatic (S cells glucose regulation of secretory and metabolic pathway genes. Proc Natl Acad Sci USA 2000 97 5773-5778. [Pg.118]

NO is recognized as a mediator of bone cell metabolism, where it regulates osteoblast and osteoclast activity [141-143]. Osteoporosis, which frequently occurs in postmenopausal women, is a systemic skeletal disease associated with abnormal bone resorption. Addition of NO or NO donors to osteoclasts in vitro results in a reduction in bone resorption, whereas NO synthase inhibitors increase bone resorption, both in vitro and in vivo. Further research has shown that NO reduces bone resorption, via inhibition of the cysteine protease cathepsin K, which is believed to be a key protease in bone resorption. Most of the NO donors, i.e., nitroglycerin, 3-... [Pg.23]

Based on the accessibility of high-quality experimental information, we now focus on aspects of model interrogation and analysis. The question how cells actually control and distribute their flux under different conditions requires a mathematical and formal approach to metabolic regulation. The knowledge obtained by quantitative experiments must be, in the sense of Section II.B, encoded into a mathematical system, scrutinized utilizing the tools of formal analysis, and eventually decoded back into predictions about the natural system. [Pg.164]

Glycolysis is the major route of carbohydrate metabolism in all cell types and the TCA is a focal point allowing the integration of carbohydrate, amino acid and lipid metabolism. The two pathways are illustrated in Figures 3.9 and 3.14. These two well-known pathways exemplify many of the general principles of metabolic regulation described above. [Pg.71]

Sixth, if the vast array of sites and site-important molecules is not enough, protein-protein interactions are part of most cellular processes including carbohydrate, lipid, protein, and nucleic acid metabolism, signal transduction, cellular architecture, and cell-cycle regulation. In fact, many of the major diseases are believed to involve a breakdown in such protein-protein interactions. These include some cancer, viral infections, and autoimmune disorders. [Pg.353]

Another evolving subdiscipline is interaction proteomics. Protein-protein interactions are a key element of almost all cellular processes. These interactions underlie the events of cell-cycle regulation, cellular architecture, intracellular signal transduction, nucleic acid metabolism, lipid metabolism, and carbohydrate metabolism. A rigorous... [Pg.126]


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