Evidence map›Paper›PMID 40788026›Full record

ArticlemBio2025

The growth benefits and toxicity of quinone biosynthesis are balanced by a dual regulatory mechanism and substrate limitations.

Siliang Li, Jiangguo Zhang, Caroline M Ajo-Franklin, Oleg A Igoshin

Abstract read
In one paragraph

Article in mBio, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Menaquinone biosynthesis inEngineering microbiology · 2026
    Review
  2. Article
  3. Metabolic Engineering Strategy forFoods (Basel, Switzerland) · 2025
    Review
  4. 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

4 authors.

Siliang Li *Department of BioSciences, Rice University, Houston, Texas, USA.ORCID 0000-0002-8277-4792
Jiangguo Zhang *Department of Bioengineering, Rice University, Houston, Texas, USA.ORCID 0000-0001-6504-4360
Caroline M Ajo-Franklin *Department of BioSciences, Rice University, Houston, Texas, USA.ORCID 0000-0001-8909-6712
Oleg A Igoshin *Department of BioSciences, Rice University, Houston, Texas, USA.ORCID 0000-0002-1449-4772

Funding

Cancer Prevention and Research Institute of Texas RR190063National Science Foundation IOS 1856742Welch Foundation C-1995
6 · The paper itself

Abstract

Quinones play a central role in maintaining redox balance and conserving energy but can trigger oxidative stress at high levels. However, the mechanisms by which microbes regulate quinone levels remain poorly understood, hindering effective metabolic engineering to modulate microbes for quinone production. Here, we show that the biosynthesis of the menaquinone precursor 1,4-dihydroxy-2-naphthoic acid (DHNA) in the lactic acid bacterium IMPORTANCE: Quinones are crucial molecules in cellular respiration, helping cells produce energy and maintain balance in their redox state. However, excessive quinone levels can be toxic, making it vital for microbes to tightly regulate their production. Our study uncovers how

Indexed as

Gene Expression Regulation, BacterialLactococcus lactisNaphtholsQuinonesBacterial ProteinsMetabolic EngineeringOxidation-ReductionVitamin K 21,4-dihydroxy-2-naphthoic acidBacterial ProteinsNaphtholsQuinonesVitamin K 2biosensorLactococcus lactismathematical modelmetabolic engineeringquinone

Identifiers

PMID40788026
PMCPMC12421875

What OpenQuestion holds

Textmetadata
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.