Environmental pollution threatens global ecosystems and public health, while driving global climate change. Although bioremediation is a sustainable and cost-effective alternative to traditional chemical treatments, natural bacteria are often limited by slow degradation rates and an inability to break down highly resilient materials. To overcome these limits, genetic engineering and targeted mutation are used to improve bacterial metabolism and increase the production of key degrading enzymes. This review examines recent progress in genetically altering established pollutant-degrading bacteria through various mutation methods. Specifically, we evaluate how well these engineered strains clean up synthetic plastics, heavy metals, and crude oil hydrocarbons. We also outline practical strategies for large-scale field use, including direct bioaugmentation, cell encapsulation, ex situ bioreactors, and root-associated plant partnerships. Finally, the paper addresses critical biosafety and ethical concerns, focusing on the risk of altered genes transferring to native microbes. To prevent these modified bacteria from persisting in nature, we discuss synthetic safety controls like genetic kill switches and metabolic dependencies. Ultimately, this review provides a clear framework to guide future research toward developing highly efficient, scalable, and environmentally safe biotechnology for ecological restoration.
| Published in | Frontiers in Environmental Microbiology (Volume 12, Issue 3) |
| DOI | 10.11648/j.fem.20261203.12 |
| Page(s) | 43-57 |
| Creative Commons |
This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited. |
| Copyright |
Copyright © The Author(s), 2026. Published by Science Publishing Group |
Mutation, Bacteria, Heavy Metals, Hydrocarbons, Plastics, Pollutants, Environment
Feature | Wild-Type Limitation | GM Strain Example | Key Genetic Modification | Remediation Target compounds | References |
|---|---|---|---|---|---|
Expanded Substrate Range | Inability to degrade complex artificial chemicals. | Pseudomonas putida KT2440 | Insertion of the BPH (biphenyl) operon. | PCBs and halogenated aromatics. | [51, 52] |
Metal Sequestration | Low binding capacity; sensitive to toxicity. | Escherichia coli | Overexpression of metallothionein (MT2). | Cadmium (Cd) and Mercury (Hg). | [53] |
Enhanced Kinetics | Slow natural enzyme turnover. | Ideonella sakaiensis (Mutant) | Engineered PETase (e.g., S238F/W159H). | PET Plastics (faster crystallinity breakdown) | [54] |
In Situ Monitoring | Hard to track cleanup progress. | Pseudomonas fluorescens HK44 | Fusion of luxCDABE to the salicylate promoter. | Naphthalene (bacteria glow during degradation). | [55] |
Solvent Tolerance | Cell membrane lysis in high oil/fuel zones. | Pseudomonas putida S12 | Upregulation of solvent efflux pumps (srpABC). | Toluene and organic solvents. | [56] |
Biomineralization | Slow natural precipitation of metals. | Citrobacter sp. | Insertion of phoN (acid phosphatase). | Uranium (U) and Nickel (Ni). | [57] |
Microorganism / Enzyme | Modification Method | Plastic Type | Key Results / Improvements over wild-type strains | References |
|---|---|---|---|---|
Pseudomonas aeruginosa D5 | UV Irradiation | LDPE | 9% better weight reduction than wild type (28 days). | [64] |
Ideonella sakaiensis (PETase) | Active site mutation | PET | 2.5x higher activity; 22.5 mg per μmol L⁻¹ per day. | [65] |
Pseudomonas putida | UV Mutation | LDPE | 34% weight loss vs. 11% in wild type (60 days). | [66] |
E. coli PHL628 | BIND Strategy (Genetic Fusion) | PET (Microplastics) | Degraded microplastics from bottles and water plants. | [67] |
Thermobifida fusca (TfCut2) | Single-site substitution | PET | 2.7-fold increase in weight loss. | [68] |
E. coli (from P. aestuansigri) | Gene Cloning | Amorphous PET | 2.5x higher degradation than parental strain. | [69] |
Stenotrophomonas pavanii | Overexpression (DuraPETase) | PET (BHET) | 100% degradation of BHET within 4 hours at 30 °C. | [70] |
PES-H1 (Variant L92F/Q94Y) | Protein Engineering | PET Waste | 3.4-fold improved activity against real-world waste. | [71] |
Bacterium XZ-A | ARTP Mutagenesis | PE (Microplastics) | 53.65% increase in degradation efficiency. | [37] |
P. putida | Genomic Integration | PET / PBAT | Successfully metabolised terephthalic acid (TA). | [72] |
Cutinase-CBMCenA | Site-directed mutagenesis | PET Fiber | 1.4–15fold improvement in catalytic efficiency. | [73] |
Modified Cutinase | Genetic Modification | PET | 12 mg/h/mg vs 0.05 mg/h/mg for native enzyme. | [74] |
BS-10L | Plasma Treatment | LDPE | 27.78% mass loss vs. 13.40% for untreated. | [75] |
Bacillus velezensis (BCAv-PEase) | Pathway Engineering | PE (Microplastics) | Enhanced MP degradation and microbial abundance. | [76] |
Amidases (PA_PBM fusion) | Enzyme Absorption Improvement | Polyurethane | 4x more active than the native enzyme. | [77] |
Cutinases | DM Strategy | PBAT | Achieved complete biodegradation to monomers. | [78] |
PAHs | Polycyclic Aromatic Hydrocarbons |
MNPs | Micro- and Nano-plastics |
PFAS | Per- and Polyfluoroalkyl Substances |
UV | Ultraviolet |
PNP | p-Nitrophenol |
PCB | Polychlorinated Biphenyl |
PET | Polyethylene Terephthalate |
LDPE | Low-Density Polyethylene |
BHET | Bis(2-Hydroxyethyl) Terephthalate |
PBAT | Polybutylene Adipate Terephthalate |
GMOs | Genetically Modified Organisms |
GEMs | Genetically Engineered Microorganisms |
ARTP | Atmospheric and Room Temperature Plasma |
DNA | Deoxyribonucleic Acid |
HGT | Horizontal Gene Transfer |
GMM | Genetically Modified Microorganism |
CRISPR | Clustered Regularly Interspaced Short Palindromic Repeats |
UNESCO | United Nations Educational, Scientific and Cultural Organization |
EPA | Environmental Protection Agency |
EFSA | European Food Safety Authority |
BSL | Biosafety Level |
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APA Style
Oluwole, O. A., Olowomofe, T. O., Olaniyan, I. G. (2026). Mutant Bacteria in Bioremediation: Harnessing Modified Microbes for Cleanup of Environmental Pollutants. Frontiers in Environmental Microbiology, 12(3), 43-57. https://doi.org/10.11648/j.fem.20261203.12
ACS Style
Oluwole, O. A.; Olowomofe, T. O.; Olaniyan, I. G. Mutant Bacteria in Bioremediation: Harnessing Modified Microbes for Cleanup of Environmental Pollutants. Front. Environ. Microbiol. 2026, 12(3), 43-57. doi: 10.11648/j.fem.20261203.12
@article{10.11648/j.fem.20261203.12,
author = {Olusola Adeoye Oluwole and Temitayo Omotunde Olowomofe and Ikeoluwa Gloria Olaniyan},
title = {Mutant Bacteria in Bioremediation: Harnessing Modified Microbes for Cleanup of Environmental Pollutants},
journal = {Frontiers in Environmental Microbiology},
volume = {12},
number = {3},
pages = {43-57},
doi = {10.11648/j.fem.20261203.12},
url = {https://doi.org/10.11648/j.fem.20261203.12},
eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.fem.20261203.12},
abstract = {Environmental pollution threatens global ecosystems and public health, while driving global climate change. Although bioremediation is a sustainable and cost-effective alternative to traditional chemical treatments, natural bacteria are often limited by slow degradation rates and an inability to break down highly resilient materials. To overcome these limits, genetic engineering and targeted mutation are used to improve bacterial metabolism and increase the production of key degrading enzymes. This review examines recent progress in genetically altering established pollutant-degrading bacteria through various mutation methods. Specifically, we evaluate how well these engineered strains clean up synthetic plastics, heavy metals, and crude oil hydrocarbons. We also outline practical strategies for large-scale field use, including direct bioaugmentation, cell encapsulation, ex situ bioreactors, and root-associated plant partnerships. Finally, the paper addresses critical biosafety and ethical concerns, focusing on the risk of altered genes transferring to native microbes. To prevent these modified bacteria from persisting in nature, we discuss synthetic safety controls like genetic kill switches and metabolic dependencies. Ultimately, this review provides a clear framework to guide future research toward developing highly efficient, scalable, and environmentally safe biotechnology for ecological restoration.},
year = {2026}
}
TY - JOUR T1 - Mutant Bacteria in Bioremediation: Harnessing Modified Microbes for Cleanup of Environmental Pollutants AU - Olusola Adeoye Oluwole AU - Temitayo Omotunde Olowomofe AU - Ikeoluwa Gloria Olaniyan Y1 - 2026/10/14 PY - 2026 N1 - https://doi.org/10.11648/j.fem.20261203.12 DO - 10.11648/j.fem.20261203.12 T2 - Frontiers in Environmental Microbiology JF - Frontiers in Environmental Microbiology JO - Frontiers in Environmental Microbiology SP - 43 EP - 57 PB - Science Publishing Group SN - 2469-8067 UR - https://doi.org/10.11648/j.fem.20261203.12 AB - Environmental pollution threatens global ecosystems and public health, while driving global climate change. Although bioremediation is a sustainable and cost-effective alternative to traditional chemical treatments, natural bacteria are often limited by slow degradation rates and an inability to break down highly resilient materials. To overcome these limits, genetic engineering and targeted mutation are used to improve bacterial metabolism and increase the production of key degrading enzymes. This review examines recent progress in genetically altering established pollutant-degrading bacteria through various mutation methods. Specifically, we evaluate how well these engineered strains clean up synthetic plastics, heavy metals, and crude oil hydrocarbons. We also outline practical strategies for large-scale field use, including direct bioaugmentation, cell encapsulation, ex situ bioreactors, and root-associated plant partnerships. Finally, the paper addresses critical biosafety and ethical concerns, focusing on the risk of altered genes transferring to native microbes. To prevent these modified bacteria from persisting in nature, we discuss synthetic safety controls like genetic kill switches and metabolic dependencies. Ultimately, this review provides a clear framework to guide future research toward developing highly efficient, scalable, and environmentally safe biotechnology for ecological restoration. VL - 12 IS - 3 ER -