Evidence map›Paper›PMID 35152320›Full record

ArticleArchives of microbiology2022

A soil-borne Mn(II)-oxidizing bacterium of Providencia sp. exploits a strategy of superoxide production coupled to hydrogen peroxide consumption to generate Mn oxides.

Sha Chen, Zhexu Ding, Jinyuan Chen, Jun Luo, Xiaofang Ruan, Zongpei Li, Fengfeng Liao, Jing He, Ding Li

Abstract read
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In one paragraph

Article in Archives of microbiology, 2022. 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. Draft genomes of multidrug-resistantMicrobiology resource announcements · 2025
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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

9 authors.

Sha ChenSchool of Life Sciences and Chemistry, Hunan University of Technology, Zhuzhou, 412007, China.
Zhexu DingSchool of Life Sciences and Chemistry, Hunan University of Technology, Zhuzhou, 412007, China.
Jinyuan ChenSchool of Life Sciences and Chemistry, Hunan University of Technology, Zhuzhou, 412007, China.
Jun LuoSchool of Life Sciences and Chemistry, Hunan University of Technology, Zhuzhou, 412007, China.
Xiaofang RuanSchool of Life Sciences and Chemistry, Hunan University of Technology, Zhuzhou, 412007, China.
Zongpei LiSchool of Life Sciences and Chemistry, Hunan University of Technology, Zhuzhou, 412007, China.
Fengfeng LiaoSchool of Life Sciences and Chemistry, Hunan University of Technology, Zhuzhou, 412007, China.
Jing HeSchool of Life Sciences and Chemistry, Hunan University of Technology, Zhuzhou, 412007, China.
Ding LiSchool of Life Sciences and Chemistry, Hunan University of Technology, Zhuzhou, 412007, China. liding@hut.edu.cn.ORCID http://orcid.org/0000-0001-6721-6680

Funding

National Natural Science Foundation of China 32171622National Natural Science Foundation of China 5177412Natural Science Foundation of Hunan Province 2019JJ50143Natural Science Foundation of Hunan Province 2021JJ50003Natural Science Foundation of Hunan Province 2021JJ50034Scientific Research Projects of Hunan Education Department 18C0491Scientific Research Projects of Hunan Education Department 20B187Scientific Research Projects of Hunan Education Department 20C0588
6 · The paper itself

Abstract

Bacterial non-enzymatic Mn(II) oxidation involving reactive oxygen species (ROS) (i.e., indirect oxidation), initially discovered from a marine alpha-proteobacterium, is believed to be of importance in controlling biogeochemical cycles. For soil-borne bacteria, however, evidence of indirect Mn(II) oxidation remains unclear. In this study, the indirect Mn(II) oxidation was evidenced in a soil-borne bacterium, Providencia sp. LLDRA6. First, with and without 50 mM of Mn(II) exposure for LLDRA6, 300 differentially expressed genes were found to be linked to Mn(II) exposure via transcriptome sequencing. Among them, an operon, responsible for phenylacetic acid catabolism, was sharply upregulated in transcription, drawing us a special attention, since its transcriptional upregulation has recently shown to be important for withstanding ROS. Next, a fluorometric probe, 2',7'-Dichlorofluorescin diacetate (DCFDA), was used to qualitatively detect ROS from cells, showing a distinct increase in fluorescence intensities of ROS during Mn(II) exposure. Furthermore, concentrations of superoxide and hydrogen peroxide from cells were detected, respectively, with and without Mn(II) exposure, exhibiting that when Mn(II) oxidation occurred, superoxide concentration significantly increased but hydrogen peroxide concentration significantly decreased. Particularly, superoxide produced by LLDRA6 was proven to be the oxidant for Mn(II) in the formation of Mn oxides. Finally, we predicted links between phenylacetic acid metabolism pathway and ROS during Mn(II) exposure, proposing that the excessive ROS, generated in response to Mn(II) exposure, transcriptionally activate phenylacetic acid catabolism presumably by increasing concentrations of highly reactive oxepins.

Indexed as

OxidesSuperoxidesBacteriaHydrogen PeroxideManganeseOxidation-ReductionProvidenciaSoilHydrogen PeroxideManganeseOxidesSoilSuperoxidesMn(II) oxidationPhenylacetic acid catabolismProvidencia sp.Reactive oxygen species

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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.