Evidence map›Paper›PMID 40781189›Full record

ArticleWorld journal of microbiology & biotechnology2025

Genome-Wide Screen using Escherichia coli Keio knockout mutant line reveals genes related to the antimicrobial properties of trans-Cinnamic Acid.

Merve Sezer Kürkçü, Kadriye Aslıhan Onat Taşdelen, Hatice Öztürkel Kabakaş, Esra Dibek, Anara Babayeva, Emine Sonay Elgin, Bekir Çöl

Abstract read
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In one paragraph

Article in World journal of microbiology & biotechnology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

7 authors.

Merve Sezer KürkçüResearch and Application Center for Research Laboratories (ALM Research Building), Mugla Sitki Kocman University, Mugla, 48000, Türkiye. mervesezer@mu.edu.tr.ORCID http://orcid.org/0000-0003-0947-2912
Kadriye Aslıhan Onat TaşdelenGraduate School of Natural and Applied Science, Biology, Mugla Sıtkı Koçman University, Mugla, 48000, Türkiye.ORCID http://orcid.org/0000-0002-5893-5728
Hatice Öztürkel KabakaşGraduate School of Natural and Applied Science, Biology, Mugla Sıtkı Koçman University, Mugla, 48000, Türkiye.ORCID http://orcid.org/0000-0002-2882-0401
Esra DibekBiotechnology Research Center (ALM Research Building), Mugla Sıtkı Koçman University, Mugla, 48000, Türkiye.
Anara BabayevaGraduate School of Natural and Applied Science, Biology, Mugla Sıtkı Koçman University, Mugla, 48000, Türkiye.ORCID http://orcid.org/0000-0001-6797-3366
Emine Sonay ElginFaculty of Science, Chemistry Department, Mugla Sıtkı Koçman University, Mugla, 48000, Türkiye.ORCID http://orcid.org/0000-0002-1278-328X
Bekir ÇölBiotechnology Research Center (ALM Research Building), Mugla Sıtkı Koçman University, Mugla, 48000, Türkiye. bcol@mu.edu.tr.ORCID http://orcid.org/0000-0001-8997-4116

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Trans-cinnamic acid (tCA), a naturally occurring phenolic compound with antimicrobial activity, has poorly understood molecular mechanisms governing bacterial sensitivity and resistance. This study employed a genome-wide screen of Escherichia coli K-12 Keio single-gene knockout library (3,985 mutants) to identify genes modulating tCA response. Mutants were screened on LB medium supplemented with tCA (0-1.5 mg/mL). Phenotypic analysis identified 78 sensitive and 52 resistant mutants, validated through visual and quantitative assessments. Sequential spot assays under tCA stress confirmed classifications: sensitive mutants (e.g., ∆aaeX, ∆aaeA, ∆seqA, ∆vacJ, ∆dksA) displayed growth inhibition, while resistant mutants (e.g., ∆yhfK, ∆hofQ, ∆ybaT, ∆groL) exhibited enhanced growth. Mutants were categorized into High, Moderate, or Low Sensitivity/Resistance groups using integrated data from SGA Tools, genome-wide screening (GWS), and spot testing, yielding 18 High Sensitive (HS), 43 Moderate Sensitive (MS), 17 Low Sensitive (LS), 20 High Resistant (HR), 23 Moderate Resistant (MR), and 9 Low Resistant (LR) strains. Complementation of sensitive mutants (e.g., ∆dksA, ∆seqA, ∆aaeA, ∆vacJ) with wild-type alleles via plasmids restored growth and elevated minimum inhibitory concentrations (MICs), directly linking these genes to tCA sensitivity. Functional evaluation (EcoCyc, DAVID, STRING) revealed HS gene hits were associated with transcriptional regulation, metabolic activity, protein folding, DNA repair, transport, and membrane stability. Resistant gene hits were linked to stress response and detoxification pathways. This systems-level analysis elucidates the genetic basis of E. coli's response to tCA, identifying targets for antimicrobial strategies leveraging tCA or its derivatives.

Indexed as

Anti-Bacterial AgentsCinnamatesEscherichia coliEscherichia coli K12Drug Resistance, BacterialEscherichia coli ProteinsGene Expression Regulation, BacterialGene Knockout TechniquesGenome, BacterialMicrobial Sensitivity TestsMutationPhenotypeAnti-Bacterial AgentsCinnamatescinnamic acidEscherichia coli ProteinsAntimicrobial agentsBacteriaFunctional genomicGenePhenolic acidTrans-cinnamic acid

Identifiers

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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.