Evidence map›Paper›PMID 40442147›Full record

ArticleScientific reports2025

Cloning and expression of chromate reductase from Bacillus paramycoides S48 for chromium remediation.

Kalsoom Kalsoom, Salah Ud Din, Esma Ceylan, Fariha Hasan, Samiullah Khan, Malik Badshah, Sabriye Çanakçi, Ali Osman Belduz, Aamer Ali Shah

Abstract read
In one paragraph

Article in Scientific reports, 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

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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. Review
  2. Survival tactics ofFrontiers in microbiology · 2025
    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

9 authors.

Kalsoom KalsoomDepartment of Microbiology, Faculty of Biological Sciences, Quaid-I-Azam University, Islamabad, 45320, Pakistan.
Salah Ud DinDepartment of Microbiology, Faculty of Biological Sciences, Quaid-I-Azam University, Islamabad, 45320, Pakistan.
Esma CeylanDepartment of Biology, Karadeniz Technical University, Trabzon, Turkey.
Fariha HasanDepartment of Microbiology, Faculty of Biological Sciences, Quaid-I-Azam University, Islamabad, 45320, Pakistan.
Samiullah KhanDepartment of Microbiology, Faculty of Biological Sciences, Quaid-I-Azam University, Islamabad, 45320, Pakistan.
Malik BadshahDepartment of Microbiology, Faculty of Biological Sciences, Quaid-I-Azam University, Islamabad, 45320, Pakistan.
Sabriye ÇanakçiDepartment of Biology, Karadeniz Technical University, Trabzon, Turkey.
Ali Osman BelduzDepartment of Biology, Karadeniz Technical University, Trabzon, Turkey. belduz@ktu.edu.tr.
Aamer Ali ShahDepartment of Microbiology, Faculty of Biological Sciences, Quaid-I-Azam University, Islamabad, 45320, Pakistan. alishah@qau.edu.pk.

Funding

Government of Turkiye Burslari Scholarship Grant 20PK038055Higher Education Commission, Pakistan 50043034
6 · The paper itself

Abstract

This study explores the production and characterization of chromium reductase from Bacillus paramycoides S48, focusing on its ability to effectively reduce toxic hexavalent chromium to less harmful chromium. The strain exhibited 65% reduction in Cr(VI) within 96 h at 30 °C. Clear morphological and functional group shifts on strain S48 cell surface treated with metal were noted using analytical tools i.e. SEM-EDX and FT-IR. The physico-chemical conditions such as temperature, pH and nutritional factors were optimized for better chromate reductase yield using Placket-Burman and Central Composite design software. The purified chromate reductase, obtained through size exclusion column chromatography, demonstrated a specific activity of 1416.5 U/mg, and 6.6-fold increase in purity, with a molecular mass of approximately 35 kDa. The enzyme exhibited stability at temperature 30-40 °C and pH 5.0-8.0. Furthermore, the purified chromium reductase achieved, 80% reduction of toxic Cr(VI) at temperature 35 °C after 96 h. The BparChR gene was successfully cloned into the pET-28a vector, expressed in E. coli BL21, and purified through Ni-Affinity ion exchange chromatography. The recombinant BparChR protein displayed a specific activity of 1680 U/mg, and a purification fold of 5.73 times. The BparChR exhibited a remarkable 90% reduction in chromium after 96 h, surpassing the efficacy of whole-cell and native chromium reductase. This study concludes that B. paramycoides S48, holds promise for the cost-effective and environmentally friendly detoxification of chromium in contaminated industrial effluents.

Indexed as

BacillusBacterial ProteinsChromiumOxidoreductasesBiodegradation, EnvironmentalCloning, MolecularEnzyme StabilityEscherichia coliHydrogen-Ion ConcentrationRecombinant ProteinsTemperatureBacterial Proteinschromate reductaseChromiumchromium hexavalent ionOxidoreductasesRecombinant ProteinsBacillus paramycoidesBioremediationBparChR geneChromate reductaseCloning

Identifiers

PMID40442147
PMCPMC12123004

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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.