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The shikimate pathway: gateway to metabolic diversity.

Authors :
Shende, Vikram V.
Bauman, Katherine D.
Moore, Bradley S.
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]

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