Evidence map›Paper›PMID 40332629›Full record

ArticleStress biology2025

Functional investigation of Zur in metal ion homeostasis, motility and multiple stresses resistance in cyanobacteria Synechocystis sp. PCC 6803.

Han Jin, Xiaoru Han, Chen Zheng, Jingling Xu, Wenjing Zhang, Yanchao Gu, Ying Peng, Jiaxin Han, Lei Xu, Xihui Shen and 1 more

Abstract read
In one paragraph

Article in Stress biology, 2025. 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. Review
  2. Article
  3. Review
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

11 authors.

Han JinState Key Laboratory for Crop Stress Resistance and High-Efficiency Production, Shaanxi Key Laboratory of Agricultural and Environmental Microbiology, College of Life Sciences, Northwest A&F University, Yangling, 712100, China.
Xiaoru HanState Key Laboratory for Crop Stress Resistance and High-Efficiency Production, Shaanxi Key Laboratory of Agricultural and Environmental Microbiology, College of Life Sciences, Northwest A&F University, Yangling, 712100, China.
Chen ZhengState Key Laboratory for Crop Stress Resistance and High-Efficiency Production, Shaanxi Key Laboratory of Agricultural and Environmental Microbiology, College of Life Sciences, Northwest A&F University, Yangling, 712100, China.
Jingling XuState Key Laboratory for Crop Stress Resistance and High-Efficiency Production, Shaanxi Key Laboratory of Agricultural and Environmental Microbiology, College of Life Sciences, Northwest A&F University, Yangling, 712100, China.
Wenjing ZhangState Key Laboratory for Crop Stress Resistance and High-Efficiency Production, Shaanxi Key Laboratory of Agricultural and Environmental Microbiology, College of Life Sciences, Northwest A&F University, Yangling, 712100, China.
Yanchao GuState Key Laboratory for Crop Stress Resistance and High-Efficiency Production, Shaanxi Key Laboratory of Agricultural and Environmental Microbiology, College of Life Sciences, Northwest A&F University, Yangling, 712100, China.
Ying PengState Key Laboratory for Crop Stress Resistance and High-Efficiency Production, Shaanxi Key Laboratory of Agricultural and Environmental Microbiology, College of Life Sciences, Northwest A&F University, Yangling, 712100, China.
Jiaxin HanState Key Laboratory for Crop Stress Resistance and High-Efficiency Production, Shaanxi Key Laboratory of Agricultural and Environmental Microbiology, College of Life Sciences, Northwest A&F University, Yangling, 712100, China.
Lei XuState Key Laboratory for Crop Stress Resistance and High-Efficiency Production, Shaanxi Key Laboratory of Agricultural and Environmental Microbiology, College of Life Sciences, Northwest A&F University, Yangling, 712100, China.
Xihui ShenState Key Laboratory for Crop Stress Resistance and High-Efficiency Production, Shaanxi Key Laboratory of Agricultural and Environmental Microbiology, College of Life Sciences, Northwest A&F University, Yangling, 712100, China. xihuishen@nwsuaf.edu.cn.
Yantao YangState Key Laboratory for Crop Stress Resistance and High-Efficiency Production, Shaanxi Key Laboratory of Agricultural and Environmental Microbiology, College of Life Sciences, Northwest A&F University, Yangling, 712100, China. yyt811113@nwsuaf.edu.cn.ORCID http://orcid.org/0000-0002-2489-7639

Funding

National Key R&D Program of China 2021YFA0909600National Natural Science Foundation of China 31725003National Natural Science Foundation of China 32330004National Natural Science Foundation of China 32370048
6 · The paper itself

Abstract

Zur (zinc uptake regulator), a member of the Fur (ferric uptake regulator) family of transcriptional regulators, plays multifaceted roles by regulating the gene expressions, such as modulating zinc ion uptake by regulating the znuABC gene cluster and influencing bacterial motility by modulating genes associated with flagella or pili. The photosynthetic autotroph Synechocystis sp. PCC 6803 is frequently used as an indicator organism for water pollution and a cell factory for high-value biochemical production in synthetic biology. During its growth, this organism often encounters various abiotic stresses, including oxidative, salt, and antibiotic stress. In this study, we conducted transcriptomic analysis on both Δzur mutant and wild-type (WT) strains to identify potential Zur-regulated genes in Synechocystis sp. PCC 6803. These genes primarily participate in multiple pathways such as inorganic ion transport, carbohydrate transport, energy production and conversion, and cell motility. Zur not only controls zinc ion homeostasis within the cell but also influences the iron balance by directly regulating the expression of the fur gene. In terms of motility, Zur regulates the expression of bacterial pili gene cluster and other motility-related genes, thereby affecting the twitching motility of Synechocystis sp. PCC 6803. Furthermore, Zur plays a crucial role in promoting biofilm formation and enhancing resistance to salt, oxidative, and antibiotic stresses by modulating relative gene expression. In conclusion, as a global transcriptional regulator, Zur plays pivotal roles in metal ion homeostasis, motility, and resistance to multiple stresses in Synechocystis sp. PCC 6803. This study illustrates the Zur regulons in Synechocystis sp. PCC 6803, and underscores the importance of Zur in enhancing the environmental adaptability of cyanobacteria.

Indexed as

Metal ion homeostasisMotilityStress resistanceSynechocystis sp. PCC 6803Transcriptional regulatorZur

Identifiers

PMID40332629
PMCPMC12058595

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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.