Evidence map›Paper›PMID 42465806›Full record

ArticleArXiv2026

Rethinking the Choice Behavior of Sugar Metabolism in Bacteria.

Jeffrey D Varner

Abstract readPreprint
In one paragraph

Article in ArXiv, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

1 author.

Jeffrey D VarnerR.F. Smith School of Chemical and Biomolecular Engineering, Cornell University, Ithaca, NY 14853.

Funding

Project 3: Physical and Metabolic Constraints of Cancer Cell InvasionU54CA210184 · NCI · CORNELL UNIVERSITY · PI SCHAFFER, CHRIS B · 2016 to 2020
$10.2M
NCI NIH HHS U54 CA210184
6 · The paper itself

Abstract

Ramkrishna, Kompala, and Tsao proposed the cybernetic model of microbial growth, in which cells allocate enzyme synthesis resources according to a matching rule that mimics rational decision-making. The matching rule was later shown to be optimal under general assumptions about the underlying return-on-investment structure, yet the specific objective the cell maximizes and the constraints bounding that choice were never written down as an explicit economic decision. Here we supply that missing decision, recasting cybernetic enzyme-synthesis control as a consumer choice problem from microeconomic theory: the cell allocates a limited proteome budget among competing catabolic enzymes as a linear program (LP), maximizing a linear growth utility subject to a linear proteome budget constraint. Because the utility is linear, the LP's solution is geometric: whenever the iso-utility line's slope differs from the budget constraint's, the optimum is a corner, and the entire proteome budget is allocated to the enzyme for the single most profitable substrate. Corner solutions correspond to diauxic growth, and sequential substrate consumption follows from the choice of corner rather than a distinct regulatory mechanism. Only when the two slopes coincide does the optimum spread across the entire budget line instead of concentrating at a single corner; this degenerate case is where simultaneous substrate use becomes admissible. Using kinetic parameters from single-substrate experiments together with a small set of model-level parameters set in this study, the LP-derived cybernetic variables reproduced the diauxic and triauxic batch growth of

Identifiers

PMID42465806
PMCPMC13370590

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.