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Biosynthetic regulation

R. R. Schmidt (1966). Intracellular control of enzyme synthesis and activity during synchronous growth of Chlorella. In I. L. Cameron and G. M. Padilla (Eds), Cell Synchrony Studies in Biosynthetic Regulation, Academic Press, New York, pp. 189-198. [Pg.254]

Atkinson, D. E. and Fall, L. 1967. Adenine triphosphate conservation in biosynthetic regulation Escherichia coli phosphori-bosylpyrophosphate synthetase. J. Biol. Chem. 242 3241-3242. [Pg.86]

Many careful studies with recombinant SATs as well as other GLTs will be needed to understand structure-function relationships of these enzymes and their roles in the biosynthetic regulation of cell surface glycoconjugates. [Pg.86]

Testosterone promotes muscle growth deepening of the voice the growth of body hair and other male secondary sex characteristics Testosterone is formed from cholesterol and IS the biosynthetic precursor of estradiol the principal female sex hormone or estrogen Estradiol is a key substance m the regulation of the menstrual cycle and the reproductive process It is the hormone most responsible for the development of female secondary sex characteristics... [Pg.1100]

It may seem surprising that isocitrate dehydrogenase is strongly regulated, because it is not an apparent branch point within the TCA cycle. However, the citrate/isocitrate ratio controls the rate of production of cytosolic acetyl-CoA, because acetyl-CoA in the cytosol is derived from citrate exported from the mitochondrion. (Breakdown of cytosolic citrate produces oxaloacetate and acetyl-CoA, which can be used in a variety of biosynthetic processes.) Thus, isocitrate dehydrogenase activity in the mitochondrion favors catabolic TCA cycle activity over anabolic utilization of acetyl-CoA in the cytosol. [Pg.668]

GPCR function has been shown to be regulated by several different mechanisms. The number of receptors on the plasma membrane may be regulated by transcription, mRNA stability, biosynthetic processing, and protein stability. In addition, the function of receptors in the plasma membrane can be influenced by regulatory phosphorylation and by association with other proteins that determine the subcellular location of receptors relative to other signaling molecules. [Pg.562]

Figure 9-5. Multiple feedback inhibition in a branched biosynthetic pathway. Superimposed on simple feedback loops (dashed, curved arrows) are multiple feedback loops (solid, curved arrows) that regulate enzymes common to biosynthesis of several end products. Figure 9-5. Multiple feedback inhibition in a branched biosynthetic pathway. Superimposed on simple feedback loops (dashed, curved arrows) are multiple feedback loops (solid, curved arrows) that regulate enzymes common to biosynthesis of several end products.
Use of biochemical and biological information for bioprocesses is also significant to the advancement of BRE. Here, the information on the signal transduction from external Ca was utilized for regulation of ginsenoside biosynthetic pathway of cultured cells of P. notoginseng. A quantitative study on the effects of external calcium and calcium sensors was conducted to... [Pg.92]

Abstract Pheromones are utilized by many insects in a complex chemical communication system. This review will look at the biosynthesis of sex and aggregation pheromones in the model insects, moths, flies, cockroaches, and beetles. The biosynthetic pathways involve altered pathways of normal metabolism of fatty acids and isoprenoids. Endocrine regulation of the biosynthetic pathways will also be reviewed for the model insects. A neuropeptide named pheromone biosynthesis activating neuropeptide regulates sex pheromone biosynthesis in moths. Juvenile hormone regulates pheromone production in the beetles and cockroaches, while 20-hydroxyecdysone regulates pheromone production in the flies. [Pg.101]


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See also in sourсe #XX -- [ Pg.636 ]




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