Spontaneous Reaction Silencing in Metabolic Optimization
Takashi Nishikawa, Natali Gulbahce, Adilson E. Motter

TL;DR
This paper demonstrates that organisms evolving for optimal growth tend to spontaneously silence many metabolic reactions, a phenomenon driven by reaction irreversibility, with implications for understanding microbial behavior and metabolic engineering.
Contribution
It provides a computational and analytical explanation for spontaneous reaction silencing in metabolism, highlighting the role of reaction irreversibility and its impact on microbial evolution and robustness.
Findings
Optimal growth leads to significant reduction in active reactions.
Reaction irreversibility triggers cascade silencing.
Silencing pattern is consistent across microbial species.
Abstract
Metabolic reactions of single-cell organisms are routinely observed to become dispensable or even incapable of carrying activity under certain circumstances. Yet, the mechanisms as well as the range of conditions and phenotypes associated with this behavior remain very poorly understood. Here we predict computationally and analytically that any organism evolving to maximize growth rate, ATP production, or any other linear function of metabolic fluxes tends to significantly reduce the number of active metabolic reactions compared to typical non-optimal states. The reduced number appears to be constant across the microbial species studied and just slightly larger than the minimum number required for the organism to grow at all. We show that this massive spontaneous reaction silencing is triggered by the irreversibility of a large fraction of the metabolic reactions and propagates through…
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