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Published bySilvester Reed Modified over 9 years ago
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Chorismate is an important precursor for aromatic amino acids Derived from PEP and erythrose 4- phosphate First branch point of pathways, one leading to tryptophan, another to phenylalanine and tyrosine
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Tryptophan biosynthesis requires PRPP, glutamine and serine
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Tryptophan synthase has separable activities Has an 2 2 structure These distinct subunits ( and ) catalyze different portions of overall reaction First reaction ( subunit) generates glyceraldehyde 3-phosphate Second reaction ( subunit) involves PLP Presents another example of substrate channeling (p. 540)
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Tryptophan synthase reaction
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Phenylalanine and tyrosine share prephenate as a common intermediate
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Animals produce tyrosine from phenylalanine Use an enzyme phenylalanine hydroxylase, which also participates in phenylalanine catabolism, lack of this enzyme causes phenylketonuria…more on that later
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Lastly - Histidine biosynthesis Histidine is derived from three precursors –PRPP contributes five carbons –Purine ring of ATP contributes nitrogen and a carbon –Glutamine supplies the second nitrogen This pathway produces AICAR, a precursor in purine biosynthesis
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Orchestrating the regulation of amino acid biosynthesis No surprise – Feedback inhibition For example:
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However, remember it can be more complex Concerted inhibition of glutamine synthetase Also, do not observe a equal frequency of amino acids in proteins – must make proportional amounts to be efficient Pathways can be organized into hierarchical clusters
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Add parallelism through Isozymes Can modulate flux Sequential feedback inhibition
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Intermediary metabolism Amino acids more biomolecules Glycine and succinyl-CoA Are precursors for porphyrins
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Glutathione, a redox buffer
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Aromatic amino acids are precursors for several biologically significant compounds Lignin – abundant plant polymer derived from tyrosine and phenyl- alanine Plant growth hormone – auxin
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Including neurotransmitters All require PLP decarboxylation Know the origin of compounds in fig 22-29
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Another neurotransmitter, NO And finally, back to nucleotides (in the book that is)
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Amino acid catabolism Account for 10-15% of human body energy production (primary pathways are glycolysis and fatty acid oxidation) The twenty catabolic cycles converge to form five products, all entering the citric acid cycle Chapter 18
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Cofactors of amino acid catabolism Know importance of H4folate, be able to recognize SAM (adoMet) and know its importance
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Tetrahydrofolate Intracellular carrier of methyl groups (can also can carry a methylene, or a formimino, formyl or methenyl; different oxidative states (fig 18-16) Major source of these one carbon units is serine Although versatile, most methyl group transfers are performed by adoMet
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AdoMet Synthesized from ATP and methionine Displacement of triphosphates only observed in one other known reaction involved in coenzyme B 12 synthesis
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Acetyl-CoA is derived from several (ten) amino acids Pyruvate can be a common intermediate
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Glycine has an alternative fate In addition to being converted to serine, and then acetyl-CoA, Glycine can be oxidized to form ammonia, carbon dioxide and a methylene group, which is transferred to tetrahydrofolate Primarily an animal pathway Also can form oxalate
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Acetyl CoA is also a product of other amino acid catabolism Portions of tryptophan, lysine, phenylalanine, tyrosine, leucine and isoleucine generate acetyl-CoA or Acetoacetyl CoA or both.
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Disease from deficiencies in phenylalanine and tyrosine metabolism
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Loss of phenylalanine hydroxylase leads to another pathway
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