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. 1990 Aug;93(4):1273–1279. doi: 10.1104/pp.93.4.1273

Biosynthesis of the Tetrapyrrole Pigment Precursor, δ-Aminolevulinic Acid, from Glutamate 1

Samuel I Beale 1
PMCID: PMC1062668  PMID: 16667613

Abstract

δ-Aminolevulinic acid (ALA), the common biosynthetic precursor of hemes, chlorophylls, and bilins, is synthesized by two distinct routes. Among phototrophic species, purple nonsulfur bacteria form ALA by condensation of glycine with succinyl-CoA, catalyzed by ALA synthase, in a reaction identical to that occurring in the mitochondria of animals, yeast, and fungi. Most or all other phototrophic species form ALA exclusively from the intact carbon skeleton of glutamic acid in a reaction sequence that begins with activation of the α-carboxyl group of glutamate by an ATP-dependent ligation to tRNAGlu, catalyzed by glutamyl-tRNA synthetase. Glutamyl-tRNA is the substrate for a pyridine nucleotide-dependent dehydrogenase reaction whose product is glutamate-1-semialdehyde or a similar reduced compound. Glutamate-1-semialdehyde is then transaminated to form ALA. Regulation of ALA formation from glutamate is exerted at the dehydrogenase step through end product feedback inhibition and induction/repression. In some species, end product inhibition of the glutamyl-tRNA synthetase step and developmental regulation of tRNAGlu level may also occur.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

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