Evidence map›Paper›PMID 41423610›Full record

ArticleNature communications2025

Exploring single-cell biosynthetic noise and dynamics for enhanced betaxanthin production in Escherichia coli.

Xinyue Mu, Alexander C Schmitz, Zhenya Ding, Wei Li, Abhyudai Singh, Fuzhong Zhang

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

6 authors.

Xinyue Mu *Department of Energy, Environmental and Chemical Engineering, Washington University in St. Louis, Saint Louis, MO, USA.
Alexander C Schmitz *Department of Energy, Environmental and Chemical Engineering, Washington University in St. Louis, Saint Louis, MO, USA.
Zhenya DingDepartment of Chemical Engineering, Texas Tech University, Lubbock, TX, USA.
Wei LiDepartment of Chemical Engineering, Texas Tech University, Lubbock, TX, USA.ORCID http://orcid.org/0000-0002-4738-1475
Abhyudai SinghDepartment of Electrical & Computer Engineering, University of Delaware, Newark, DE, USA.ORCID http://orcid.org/0000-0002-1451-2838
Fuzhong ZhangDepartment of Energy, Environmental and Chemical Engineering, Washington University in St. Louis, Saint Louis, MO, USA. fzhang@seas.wustl.edu.ORCID http://orcid.org/0000-0001-6979-7909

Funding

Supplement for Purchase of a Cell Sorter for R35GM133797R35GM133797 · NIGMS · WASHINGTON UNIVERSITY · PI ZHANG, FUZHONG · 2019 to 2023
$2.2M
Generalized fluctuation test for deciphering phenotypic switching within cell populationsR35GM148351 · NIGMS · UNIVERSITY OF DELAWARE · PI Abhyudai Singh · 2023 to 2026
$1.6M
NIGMS NIH HHS R35 GM133797NIGMS NIH HHS R35 GM148351United States Department of Defense | Defense Advanced Research Projects Agency (DARPA) HR0011-25-9-0055U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences (NIGMS) R35GM133797
6 · The paper itself

Abstract

Cell-to-cell variability often limits the efficiency of microbial bioproduction, yet how individual cells fluctuate over time and how these fluctuations shape population-level output remain unclear. To address this issue, we tracked a heterologous betaxanthin pathway in Escherichia coli using microfluidics-assisted time-lapse microscopy, allowing simultaneous measurement of fluctuations in betaxanthin, its biosynthetic enzyme DOD and growth across generations. Here we show that over 50% of high betaxanthin producers become medium or low producers after two divisions. Betaxanthin variation primarily originates from DOD noise, with a smaller contribution from growth rate fluctuations. We further develop a stochastic model to explore various control circuits and find that pathway enzyme or metabolite-based growth selection strategies are most effective in enhancing production. We experimentally validate the model by coupling enzyme expression to nutrient availability, which enriches high producers and boosts titer by 4.4-fold. Our results highlight key sources of metabolic heterogeneity and provide a framework for designing robust microbial processes.

Indexed as

Escherichia coliBiosynthetic PathwaysEscherichia coli ProteinsModels, BiologicalSingle-Cell AnalysisEscherichia coli Proteins

Identifiers

PMID41423610
PMCPMC12848102

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.