A parallel glycolysis provides a selective advantage through rapid growth acceleration
Open accessAbstract
Glycolysis is a universal metabolic process that breaks down glucose to produce adenosine triphosphate (ATP) and biomass precursors. The Entner-Doudoroff (ED) pathway is a glycolytic pathway that parallels textbook glycolysis but yields half as much ATP. Accordingly, in organisms that possess both glycolytic pathways (for example, Escherichia coli), its raison d'être remains a mystery. In this study, we found that the ED pathway provides a selective advantage during growth acceleration. Upon carbon and nitrogen upshifts, E. coli accelerates growth faster with than without the ED pathway. Concurrent isotope tracing reveals that the ED pathway flux increases faster than that of textbook glycolysis. We attribute the fast response time of the ED pathway to its strong thermodynamic driving force and streamlining of glucose import. Intermittent nutrient supply manifests the evolutionary advantage of the parallel glycolysis; thus, the dynamic nature of an ostensibly redundant pathway's role in promoting rapid adaptation constitutes a metabolic design principle.
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Enhanced aerobic glycolysis supports rapid ATP production and provides metabolic intermediates required for biosynthetic processes, thereby conferring a selective growth advantage to cancer cells.
“Enhanced aerobic glycolysis supports rapid ATP production and provides metabolic intermediates required for biosynthetic processes, thereby conferring a selective growth advantage to cancer cells (24–26).”
From Bioinformatics-based identification of glycolysis-related signatures associated with drug resistance and prognosis in lung adenocarcinoma (2026) · cites this paper as [25]
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References 57 · Cited by 30
- Authors
- Law, R. C., Nurwono, G., & Park, J. O.
- Affiliations
- University of California, Los Angeles (US)
- Corresponding author
- Park, Junyoung O.
- Venue
- Nature Chemical Biology
- Published
- 2023-08-03
- Volume
- 20
- Issue
- 3
- Pages
- 314-322
- ISSN
- 1552-4450 (ISSN-L)
- 1552-4469
- PMC
- PMC10987256
- OpenAlex
- W4385555863
- Cited by
- 30
- References
- 57
- Citations by year
- 2026: 12 · 2025: 10 · 2024: 8
- FWCI
- 2.67
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- Locations
- Nature Chemical Biology (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- eScholarship (California Digital Library) (submittedVersion)
- Funders
- National Science Foundation (1933487, 1735325)
- National Institutes of Health (1s10od016387-01)
- National Institute of General Medical Sciences (1S10OD016387, R35GM143127)
- Division of Materials Research (. DMR-1933487, 1933487)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Microbial Metabolic Engineering and Bioproduction
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Bacterial Genetics and Biotechnology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Microbial metabolism and enzyme function
- Keywords
- Entner-Doudoroff pathway, Escherichia coli, growth acceleration, isotope tracing, thermodynamic driving force, metabolic flux, metabolic adaptation
- MeSH terms
- Acceleration, Adenosine Triphosphate, Escherichia coli, Glucose, Glycolysis
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