Evidence map›Paper›PMID 39342090›Full record

ArticleBMC microbiology2024

Heterologous expression of the Oenococcus oeni two-component signal transduction response regulator in the Lactiplantibacillus plantarum WCFS1 strain enhances acid stress tolerance.

Yujuan Zheng, Yumiao Zhang, Yifan Zhao, Xiaoqiu Wu, Huan Wang, Hongyu Zhao, Junhua Liu, Bin Liu, Longxiang Liu, Weiyu Song

Abstract read
In one paragraph

Article in BMC microbiology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Gene manipulation inFrontiers in microbiology · 2025
    Article
  3. 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

10 authors.

Yujuan Zheng *Shandong Provincial Engineering and Technology Research Center for Wild Plant Resources Development and Application of Yellow River Delta, College of Biological and Environmental Engineering, Shandong University of Aeronautics, Binzhou, 256600, China.
Yumiao Zhang *Shandong Provincial Engineering and Technology Research Center for Wild Plant Resources Development and Application of Yellow River Delta, College of Biological and Environmental Engineering, Shandong University of Aeronautics, Binzhou, 256600, China.
Yifan ZhaoShandong Provincial Engineering and Technology Research Center for Wild Plant Resources Development and Application of Yellow River Delta, College of Biological and Environmental Engineering, Shandong University of Aeronautics, Binzhou, 256600, China.
Xiaoqiu WuShandong Provincial Engineering and Technology Research Center for Wild Plant Resources Development and Application of Yellow River Delta, College of Biological and Environmental Engineering, Shandong University of Aeronautics, Binzhou, 256600, China.
Huan WangShandong Provincial Engineering and Technology Research Center for Wild Plant Resources Development and Application of Yellow River Delta, College of Biological and Environmental Engineering, Shandong University of Aeronautics, Binzhou, 256600, China.
Hongyu ZhaoCollege of Enology, Northwest A&F University, Xinong Road 22, Yangling, Shaanxi, 712100, China.
Junhua LiuShandong Provincial Engineering and Technology Research Center for Wild Plant Resources Development and Application of Yellow River Delta, College of Biological and Environmental Engineering, Shandong University of Aeronautics, Binzhou, 256600, China.
Bin LiuShandong Provincial Engineering and Technology Research Center for Wild Plant Resources Development and Application of Yellow River Delta, College of Biological and Environmental Engineering, Shandong University of Aeronautics, Binzhou, 256600, China.
Longxiang LiuShandong Provincial Engineering and Technology Research Center for Wild Plant Resources Development and Application of Yellow River Delta, College of Biological and Environmental Engineering, Shandong University of Aeronautics, Binzhou, 256600, China. longxiang8802@163.com.
Weiyu SongShandong Provincial Engineering and Technology Research Center for Wild Plant Resources Development and Application of Yellow River Delta, College of Biological and Environmental Engineering, Shandong University of Aeronautics, Binzhou, 256600, China. songweiyu2007@126.com.

Funding

Binzhou University Scientific Research Fund Project BZXYLG2001National Natural Science Foundation of China 32001659National Natural Science Foundation of China 32102002Science and Technology Support Plan for Youth Innovation of Colleges and Universities in Shandong Province 2022KJD088Shandong Natural Science Foundation of Youth project ZR2022QC171Youth Science and Technology Rising Star Program Project of Binzhou City QMX2023002
6 · The paper itself

Abstract

backgroundOenococcus oeni is a commercial wine-fermenting bacterial strain, owing to its high efficiency of malolactic fermentation and stress tolerance. The present study explored the function of key genes in O. oeni to enhance stress resistance by heterologous expression of these genes in another species.

resultsThe orf00404 gene that encodes a two-component signal transduction response regulator in O. oeni was heterologously expressed in Lactiplantibacillus plantarum WCFS1. The expression of orf00404 significantly enhanced the growth rate of the recombinant strain under acid stress. At 60 h, 72 h, and 108 h of culture at pH 4.0, the recombinant strain had 1562, 641, and 748 differentially expressed genes compared to the control strain, respectively. At all three time points, 20 genes were upregulated in the recombinant strain, including the lamA-D operon-coding genes of the quorum-sensing two component signal transduction system and the spx5 RNA polymerase-binding protein coding gene, which may help adaptation to acid stress. In addition, 47 genes were downregulated in the recombinant strain at all three time points, including the hsp1 heat shock protein-coding gene, the trxA1 thioredoxin-coding gene, and the dinP, mutY, umuC, and uvrB DNA damage repair-related protein-coding genes, potentially indicating that the recombinant strain was less susceptible to stress and had less DNA damage than the control strain in acid stress conditions. The recombinant strain had higher membrane fluidity, permeability, and integrity at an early stage of logarithmic growth (72 h), suggesting that it had a more complete and active cell membrane state at this stage. The intracellular ATP content was significantly reduced in the recombinant strain at the beginning of logarithmic growth (60 h), implying that the recombinant strain consumed more energy at this stage to resist acid stress and growth.

conclusionsThese results indicated that the recombinant strain enhances acid stress tolerance by regulating a gene expression pattern, increasing ATP consumption, and enhancing cell membrane fluidity, membrane permeability, and membrane integrity at specific growth stages. Thus, the recombinant strain may have potential application in the microbial biotechnology industry.

Indexed as

Bacterial ProteinsGene Expression Regulation, BacterialOenococcusSignal TransductionStress, PhysiologicalAcidsFermentationHydrogen-Ion ConcentrationLactobacillaceaeQuorum SensingWineAcidsBacterial ProteinsAcid stressLactiplantibacillus plantarumMalolactic fermentationOenococcus oeniTranscriptome

Identifiers

PMID39342090
PMCPMC11438414

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.