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The shikimate pathway: gateway to metabolic diversity.
- Source :
- Natural Product Reports; Apr2024, Vol. 41 Issue 4, p604-648, 45p
- Publication Year :
- 2024
-
Abstract
- Covering: 1997 to 2023 The shikimate pathway is the metabolic process responsible for the biosynthesis of the aromatic amino acids phenylalanine, tyrosine, and tryptophan. Seven metabolic steps convert phosphoenolpyruvate (PEP) and erythrose 4-phosphate (E4P) into shikimate and ultimately chorismate, which serves as the branch point for dedicated aromatic amino acid biosynthesis. Bacteria, fungi, algae, and plants (yet not animals) biosynthesize chorismate and exploit its intermediates in their specialized metabolism. This review highlights the metabolic diversity derived from intermediates of the shikimate pathway along the seven steps from PEP and E4P to chorismate, as well as additional sections on compounds derived from prephenate, anthranilate and the synonymous aminoshikimate pathway. We discuss the genomic basis and biochemical support leading to shikimate-derived antibiotics, lipids, pigments, cofactors, and other metabolites across the tree of life. [ABSTRACT FROM AUTHOR]
- Subjects :
- AMINO acids
PHENYLALANINE
TYROSINE
TRYPTOPHAN
BIOSYNTHESIS
PIGMENTS
Subjects
Details
- Language :
- English
- ISSN :
- 02650568
- Volume :
- 41
- Issue :
- 4
- Database :
- Complementary Index
- Journal :
- Natural Product Reports
- Publication Type :
- Academic Journal
- Accession number :
- 176812012
- Full Text :
- https://doi.org/10.1039/d3np00037k