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February 14 Chapter 26 Amino Acid Metabolism
Biochemistry 432/832 February 14 Chapter 26 Amino Acid Metabolism
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Announcements: -
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Outline 26.1 The Two Major Pathways of N Acquisition
26.2 The Fate of Ammonium 26.3 Glutamine Synthetase 26.4 Amino Acid Biosynthesis 26.5 Metabolic Degradation of Amino Acids
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The nitrogen cycle
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The glutamate dehydrogenase reaction
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The glutamine synthetase reaction
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The glutamate dehydrogenase/glutamine synthase pathway
Two N fixing steps - one inefficient One each
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The glutamate synthase reaction
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The glutamine synthase/GOGAT pathway
One N fixing step - inefficient but expensive One NADPH Two ATP
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Glutamine Synthetase A Case Study in Regulation
GS in E. coli is regulated in three ways: Feedback inhibition Covalent modification (interconverts between inactive and active forms) Regulation of gene expression and protein synthesis - - control the amount of GS in cells
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Allosteric regulation of glutamine synthase activity by feedback inhibition
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Covalent Modification of Glutamine Synthetase
Each subunit is adenylylated at Tyr-397 Adenylylation inactivates GS Adenylyl transferase catalyzes both the adenylylation and deadenylylation PII (regulatory protein) controls both activities AT:PIIA catalyzes adenylylation AT:PIID catalyzes deadenylylation -ketoglutarate and Gln regulate PII
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Covalent modification of glutamine synthase - adenylylation of Tyr397
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The cyclic cascade system that regulates the covalent modification of GS
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Gene Expression regulates GS
Gene GlnA is actively transcribed only if transcriptional enhancer NRI is in its phosphorylated form, NRI-P NRI is phosphorylated by NRII, a protein kinase If NRII is complexed with PIIA (inactivator) it acts as a phosphatase, not a kinase
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Transcriptional regulation of GlnA expression through the reversible phosphorylation of NR1
Activated by glutamine, inactivated by a-ketoglutarate
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Amino Acid Biosynthesis
Plants and microorganisms can make all 20 amino acids and all other organisms need N metabolites In these organisms, glutamate is the source of N, via transamination (aminotransferase) reactions Mammals can make only 10 of the 20 amino acids The others are classed as "essential" amino acids and must be obtained in the diet All amino acids are grouped into families according to the intermediates that they are made from
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Glutamate-dependent transamination - primary mechanism for amino acid synthesis
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The -Ketoglutarate Family
Glu, Gln, Pro, Arg, and sometimes Lys
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Proline biosynthesis from glutamate
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Synthesis of ornithine from glutamate - a step in arginine biosynthesis
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The Urea Cycle N and C in the guanidino group of Arg come from NH4+, HCO3- (carbamoyl-P), and the -NH2 of Glu and Asp Breakdown of Arg in the urea cycle releases two N and one C as urea Important N excretion mechanism in livers of terrestrial vertebrates Urea cycle is linked to TCA by fumarate
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The urea cycle
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The Aspartate Family Asp, Asn, Lys, Met, Thr, Ile
Transamination of oxaloacetate gives Asp Amidation of Asp gives Asn Thr, Met, and Lys are made from Asp
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Transamination of oxaloacetate yields aspartate
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Asp + Gln --> Asn + Glu
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The Pyruvate Family Ala, Val, Leu
Transamination of pyruvate gives Ala Val is derived from pyruvate Leu synthesis, like that of Ile and Val, begins with an -keto acid Transaminations from Glu complete each of these pathways
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3-Phosphoglycerate Family Ser, Gly, Cys
3-Phosphoglycerate dehydrogenase diverts 3-PG from glycolysis to amino acid paths Transamination by Glu gives 3-P-serine Phosphatase yields serine A PLP-dependent enzyme makes Cys
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Biosynthesis of serine from 3-phosphoglycerate
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Glycine biosynthesis from serine
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Cysteine biosynthesis
Sulfhydration of serine by sulfide Sulfhydration of O-acetylserine
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Sulfate assimilation
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Degradation of Amino Acids
The 20 amino acids are degraded to produce TCA and glycolytic intermediates
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Degradation of amino acids
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Degradation of Ala, Ser, Cys, Gly and Trp and Thr to pyruvate
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