» Articles » PMID: 34065948

The Pentose Phosphate Pathway in Yeasts-More Than a Poor Cousin of Glycolysis

Overview
Journal Biomolecules
Publisher MDPI
Date 2021 Jun 2
PMID 34065948
Citations 21
Authors
Affiliations
Soon will be listed here.
Abstract

The pentose phosphate pathway (PPP) is a route that can work in parallel to glycolysis in glucose degradation in most living cells. It has a unidirectional oxidative part with glucose-6-phosphate dehydrogenase as a key enzyme generating NADPH, and a non-oxidative part involving the reversible transketolase and transaldolase reactions, which interchange PPP metabolites with glycolysis. While the oxidative branch is vital to cope with oxidative stress, the non-oxidative branch provides precursors for the synthesis of nucleic, fatty and aromatic amino acids. For glucose catabolism in the baker's yeast , where its components were first discovered and extensively studied, the PPP plays only a minor role. In contrast, PPP and glycolysis contribute almost equally to glucose degradation in other yeasts. We here summarize the data available for the PPP enzymes focusing on and , and describe the phenotypes of gene deletions and the benefits of their overproduction and modification. Reference to other yeasts and to the importance of the PPP in their biotechnological and medical applications is briefly being included. We propose future studies on the PPP in to be of special interest for basic science and as a host for the expression of human disease genes.

Citing Articles

Genetic and Physiological Characterization of the Pentose Phosphate Pathway in the Yeast .

Bertels L, Walter S, Heinisch J Int J Mol Sci. 2025; 26(3).

PMID: 39940707 PMC: 11817168. DOI: 10.3390/ijms26030938.


Comparative Proteomics of Two Flor Yeasts in Sparkling Wine Fermentation: First Approach.

Garcia-Garcia J, Garcia-Martinez T, Roman-Camacho J, Moreno J, Mauricio J Foods. 2025; 14(2).

PMID: 39856948 PMC: 11764631. DOI: 10.3390/foods14020282.


tRNA regulation and amino acid usage bias reflect a coordinated metabolic adaptation in .

Li Q, Vetter L, Veith Y, Christ E, Vegvari A, Sahin C iScience. 2024; 27(11):111167.

PMID: 39524331 PMC: 11544085. DOI: 10.1016/j.isci.2024.111167.


A fungal metabolic regulator underlies infectious synergism during Candida albicans-Staphylococcus aureus intra-abdominal co-infection.

Paul S, Todd O, Eichelberger K, Tkaczyk C, Sellman B, Noverr M Nat Commun. 2024; 15(1):5746.

PMID: 38982056 PMC: 11233573. DOI: 10.1038/s41467-024-50058-w.


Reversing the directionality of reactions between non-oxidative pentose phosphate pathway and glycolytic pathway boosts mycosporine-like amino acid production in Saccharomyces cerevisiae.

Hengardi M, Liang C, Madivannan K, Yang L, Koduru L, Kanagasundaram Y Microb Cell Fact. 2024; 23(1):121.

PMID: 38725068 PMC: 11080194. DOI: 10.1186/s12934-024-02365-6.


References
1.
Heinisch J . Construction and physiological characterization of mutants disrupted in the phosphofructokinase genes of Saccharomyces cerevisiae. Curr Genet. 1986; 11(3):227-34. DOI: 10.1007/BF00420611. View

2.
Sundstrom M, Lindqvist Y, Schneider G . Three-dimensional structure of apotransketolase. Flexible loops at the active site enable cofactor binding. FEBS Lett. 1992; 313(3):229-31. DOI: 10.1016/0014-5793(92)81197-t. View

3.
He W, Wang Y, Liu W, Zhou C . Crystal structure of Saccharomyces cerevisiae 6-phosphogluconate dehydrogenase Gnd1. BMC Struct Biol. 2007; 7:38. PMC: 1919378. DOI: 10.1186/1472-6807-7-38. View

4.
Samland A, Sprenger G . Transaldolase: from biochemistry to human disease. Int J Biochem Cell Biol. 2009; 41(7):1482-94. DOI: 10.1016/j.biocel.2009.02.001. View

5.
Pfeiffer T, Morley A . An evolutionary perspective on the Crabtree effect. Front Mol Biosci. 2015; 1:17. PMC: 4429655. DOI: 10.3389/fmolb.2014.00017. View