Protein cost minimization promotes the emergence of coenzyme redundancy

Author:

Goldford Joshua E.123ORCID,George Ashish B.456ORCID,Flamholz Avi I.7ORCID,Segrè Daniel3489ORCID

Affiliation:

1. Physics of Living Systems, Massachusetts Institute of Technology, Cambridge, MA 02139

2. Blue Marble Space Institute of Science, Seattle, WA, 98154

3. Bioinformatics Program, Biological Design Center, Boston University, Boston, MA, 02215

4. Department of Physics, Boston University, Boston, MA, 02215

5. Carl R. Woese Institute for Genomic Biology, University of Illinois at Urbana–Champaign, Urbana, IL 61801

6. Department of Plant Biology, University of Illinois at Urbana–Champaign, Urbana, IL 61801

7. Division of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA

8. Department of Biomedical Engineering, Boston University, Boston, MA, 02215

9. Department of Biology, Boston University, Boston, MA, 02215

Abstract

SignificanceMetabolism relies on a small class of molecules (coenzymes) that serve as universal donors and acceptors of key chemical groups and electrons. Although metabolic networks crucially depend on structurally redundant coenzymes [e.g., NAD(H) and NADP(H)] associated with different enzymes, the criteria that led to the emergence of this redundancy remain poorly understood. Our combination of modeling and structural and sequence analysis indicates that coenzyme redundancy may not be essential for metabolism but could rather constitute an evolved strategy promoting efficient usage of enzymes when biochemical reactions are near equilibrium. Our work suggests that early metabolism may have operated with fewer coenzymes and that adaptation for metabolic efficiency may have driven the rise of coenzyme diversity in living systems.

Funder

Gordon and Betty Moore Foundation

National Aeronautics and Space Administration

NSF | BIO | Division of Emerging Frontiers

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

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