Bioslurping 2
Bioslurping 2
Review
Recent Strategies for Bioremediation of Emerging Pollutants:
A Review for a Green and Sustainable Environment
Saroj Bala 1,† , Diksha Garg 1,† , Banjagere Veerabhadrappa Thirumalesh 2,† , Minaxi Sharma 3 ,
Kandi Sridhar 4 , Baskaran Stephen Inbaraj 5, * and Manikant Tripathi 6, *
Abstract: Environmental pollution brought on by xenobiotics and other related recalcitrant com-
pounds have recently been identified as a major risk to both human health and the natural envi-
ronment. Due to their toxicity and non-biodegradability, a wide range of pollutants, such as heavy
metals, polychlorinated biphenyls, plastics, and various agrochemicals are present in the environ-
ment. Bioremediation is an effective cleaning technique for removing toxic waste from polluted
environments that is gaining popularity. Various microorganisms, including aerobes and anaerobes,
are used in bioremediation to treat contaminated sites. Microorganisms play a major role in bioreme-
Citation: Bala, S.; Garg, D.; diation, given that it is a process in which hazardous wastes and pollutants are eliminated, degraded,
Thirumalesh, B.V.; Sharma, M.; detoxified, and immobilized. Pollutants are degraded and converted to less toxic forms, which is a
Sridhar, K.; Inbaraj, B.S.; Tripathi, M. primary goal of bioremediation. Ex situ or in situ bioremediation can be used, depending on a variety
Recent Strategies for Bioremediation of of factors, such as cost, pollutant types, and concentration. As a result, a suitable bioremediation
Emerging Pollutants: A Review for a method has been chosen. This review focuses on the most recent developments in bioremediation
Green and Sustainable Environment. techniques, how microorganisms break down different pollutants, and what the future holds for
Toxics 2022, 10, 484. https://
bioremediation in order to reduce the amount of pollution in the world.
doi.org/10.3390/toxics10080484
Academic Editor: Mariusz Cycoń Keywords: bioremediation; microbes; pollutants; environment; sustainable technologies
lot of waste and pollution, so they are not valued [3]. Bioremediation is a cost-effective and
practical solution for removing environmental contaminants [4]. Plant growth promotion,
insect control, soil conservation, nutrient recycling, and pollutant reduction are all key
functions of soil microorganisms [5]. Bioremediation has come a long way in terms of
efficiency, cost, and social acceptability [6]. Bioremediation research has largely focused on
bacterial processes, which have numerous applications. Archaea are known to play a role in
bioremediation in many applications where bacteria are involved. Many hostile situations
have degraded, requiring bioremediation. Microbes can also assist in the elimination of
pollutants from hyperthermal, acidic, hypersaline, or basic industrial waste [7,8]. Recent
research suggests that using more than one living organism will improve the efficiency
and results, and allow for greater microbial diversity in bioremediation [8,9]. Many re-
searchers employed bioremediation technology for the removal of organic and inorganic
pollutants [10–12]. In a study, bioremediation technology was used for the treatment of
various pollutants, including organophosphate pesticides such as chlorpyrifos, methyl
parathion, and profenofos, by Aspergillus sydowii, and chloramphenicol by endophytic
fungi, respectively [13,14]. In another study, Cymbella sp. has been shown to detoxify
naproxen-polluted water with an efficiency of 97.1% [15].
A bioremediation approach requires the use of microbial enzymes to break down
hydrocarbons into less harmful compounds. The widespread use of genetically-modified
microorganisms that can also help to eliminate petroleum, naphthalene, toluene, benzene,
and other xenobiotic chemicals is now being studied [16]. Several factors, such as tem-
perature of the surrounding environment, aerobic or anaerobic conditions, and nutrient
availability, all influence bioremediation for better outcomes. Emerging environmental pol-
lutants, such as persistent organic compounds, heavy metals, toxins, and air pollutants that
are of synthetic or natural origin, reach ecosystems mainly through anthropogenic activities
and pose adverse threats to lifeforms like plants, animals, and humans [17]. One of the most
economical and environmentally favorable biotechnological innovations is bioremediation.
Waste management mainly relies on bioremediation. It can remove persistent organic
pollutants, which are hard to breakdown and are thought to be heterologous biological
substances. This review addresses the recent approaches and updated information of
bioremediation strategies for eco-friendly detoxification and the effective degradation of
various organic and inorganic contaminants to control environmental pollution.
2.1. Aerobic
Several microorganisms have the ability to bioremediate different types of environmental
pollutants under aerobic conditions. Bacillus, Pseudomonas, Sphingomonas, Flavobacterium, Nocar-
dia, Rhodococcus, and Mycobacterium are aerobic bacteria that can degrade a variety of complex
organic compounds [20]. Pesticides, alkane hydrocarbons, and polyaromatic compounds have
been shown to be degraded by these microbes. Several of these microorganisms make use
of these contaminants as a source of carbon and energy [21]. In the aerobic bioremediation
process, oxygen is the limiting factor for the growth of microorganisms.
Toxics 2022, 10, 484 3 of 24
2.2. Anaerobic
Amphibious bacteria that degrade and convert pollutants to fewer toxic forms are be-
coming increasingly popular for the bioremediation of polychlorinated biphenyls, chlorine
compounds, and the chlorinated solvents, trichlorethylene and chloroform [22]. Several
bacteria, such as Pseudomonas, Aeromonas, and sulfate-reducing bacteria, have been used in
the bioremediation process under anaerobic conditions. Garg and Tripathi [23] reported
microbial discoloration of azo dyes under different environmental situations. Azo dyes
can decompose anaerobically through reduction reactions using electrons produced by the
oxidation of the organic substrate(s). Due to such controlled dye decolorization events,
microbe electrochemical properties would have a major impact on the effectiveness of
color removal. Dyes were anaerobically decolored for industrial activities to progressively
acquire such time-variant decolorized-metabolites (DMs). However, external augmentation
of DMs gathered under certain conditions was carried out for improved research so that a
precise system can be used [24].
Table 1. Cont.
4. Principle of Bioremediation
When organic wastes are biologically degraded under controlled conditions, “biore-
mediation” is the term used to describe this process. Using bioremediation, harmful
substances can be degraded or detoxified by providing the organisms with the nutrients
and other chemicals they need to function optimally. Enzymes play a critical role in every
stage of the metabolic process [24,43]. It is part of the family of oxidoreductases, lyases,
transferases, and hydrolases. Non-specific and specific substrate affinities allow many
enzymes to degrade a wide range of substrates. There must be enzymatic action on the
pollutants in order for bioremediation to be successful. In order to speed up microbial
growth and degradation, environmental parameters must often be manipulated during
Toxics 2022, 10, 484 5 of 24
bioremediation [38,43]. This is because bioremediation only works when the environment
is right for microbes to grow and move around.
Living organisms and fertilizers can aid in the process of bioremediation, which
occurs naturally and is encouraged. Biodegradation is a key component of bioremediation
technology. It’s the process of converting harmful organic pollutants like carbon dioxide
and water into non-toxic or naturally-occurring inorganic compounds that are safe for use
by humans, plants, animals, and aquatic life [44].
5. Types of Bioremediations
Bioremediation can be used in a plethora of ways, and some of the most commonly
used methods are presented here (Figure 1).
5.1. Biopile
In bioremediation, aeration and nutrient supplementation are used to enhance micro-
bial metabolic activities in the piled-up polluted soil above ground. Aeration, nutrients,
irrigation, leachate collection, and treatment bed systems are all included in this procedure.
When it comes to ex situ biodegradation, this method is becoming increasingly popular
because of its cost-effectiveness and useful features, such as pH and nutrient control. Us-
ing the biopile to clean up polluted cold environments and treat low-molecular-weight
volatile pollutants is an option [15,45]. The biopile’s adaptability allows for a reduction in
remediation time by increasing microbial activity and contaminant availability while also
increasing biodegradation rate. When warm air is introduced into the biopile system to
provide air and heat simultaneously, bioremediation is improved. The biopile’s remediation
process has been helped by the addition of bulking agents like straw, sawdust, or wood
chips. To replenish the air supply to polluted piled soil in biopiles, ex situ bioremediation
techniques such as land farming, biosparging, and bioventing can be applied [46]. How-
ever, these techniques are expensive to implement and require a power supply at remote
locations. Bioremediation may be slowed down by extreme air temperatures that dry soil
and make it more likely to be vaporized than to be broken down by living organisms [47].
Bio-available organic carbon (BOC) plays an important role in bioremediation through the
biopile method. Petroleum contaminated soil has been bioremediated using mesophillic
conditions (30 ◦ C–40 ◦ C) and a low aeration rate for the removal of total petroleum hydro-
carbon (TPH) using alpha, beta, and gamma proteobacteria [48]. Biopile systems have also
Toxics 2022, 10, 484 6 of 24
been utilized for treating the diesel contaminated soil of the sub-Antarctic region. A total
of 93% of the total petroleum hydrocarbon (TPH) was removed using the biopile system
within one year [49].
5.2. Windrows
Windrows boosts bioremediation by enhancing the biodegradation processes of native
and transitory hydrocarbon plastic found in the contaminated soils when spinning the
heaped contaminated soils. The aeration, mineralization, and biotransformation of toxic
soil can be performed through acclimation, biological treatment, and mineralization [50],
can speed up bioremediation. The biopile approach can remove more hydrocarbons from
soil than windrow treatment [15,51], which was more efficient in terms of hydrocarbon
removal. The periodic rotation connected with windrow remediation is not a better selection
approach for the bioremediation of soil affected by harmful volatile chemicals. Windrow
treatment is a source of greenhouse gas (CH4 ) due to the anaerobic system generated
inside the heaped contaminated soil [52]. The windrow method of has been applied for
the bioremediation of the Gurugram–Faridabad dumpsite in Bandhwari, India by forming
terraces and windrows and utilizing bio-culture, and the results showed a decrease in the
garbage [53].
5.4. Bioreactor
Following a series of biological reactions, bioreactors transform raw materials into
specific products. Bioremediation thrives in a bioreactor, which provides the ideal con-
ditions for growth [58]. The remediation samples are placed in a bioreactor. There are a
number of advantages to using a bioreactor to treat contaminated soil as opposed to ex
situ bioremediation methods. An efficient bioremediation process based on bioreactors
that can precisely regulate pH, agitation, temperature, aeration, substrate concentration,
and inoculum concentration significantly reduce the time required for bioremediation [59].
Biological reactions can take place when the bioreactor can be controlled and manipulated.
Given their adaptability, bioreactor designs are able to maximize microbial degradation
while abiotic losses are kept to a minimum.
5.5. Bioventing
Bioventing is a technique that uses controlled airflow to increase the activity of in-
digenous microbes for bioremediation by delivering oxygen to the unsaturated zone. The
bioremediation process is aided by the addition of nutrients and moisture during the
bioventing process. This will lead to the microbial transformation of pollutants into harm-
less substances. Other in situ bioremediation methods have flocked to this one in recent
years [69]. Bioventing is a technique that helps in stimulating the indigenous microflora
through ample amounts of aeration to enhance the biodegradation ability of the various
microbes and promote decontamination of the heavy metal pollutants by precipitation [70].
5.6. Bioslurping
A direct oxygen supply and stimulation of contaminant biodegradation are used
in conjunction with vacuum-assisted pumping, bioventing, and soil vapour extraction
(SVE) in order to reach soil and groundwater levels for restoration [71]. This approach can
be used to recover unsaturated and saturated zones as well as light non-aqueous phase
liquids (LNAPLs). This technology can be used to remediate soils contaminated with
flammable and moderately-flammable organic substances. Liquid is drawn from the free
product layer by means of a “slurp” that spreads into the layer. LNAPLs are lifted to the
surface by the pumping machine, where they are separated from the surrounding air and
water [72]. To reduce microbial activity, soil moisture is used in this technique to reduce air
permeability and oxygen transfer rate. Given that it uses less groundwater, this method
saves money on storage, disposal, and treatment, even though it’s not ideal for remediation
in low-permeable soils. Bioslurping requires 25 feet of digging below the ground surface
and then the contaminants floating on the water can be removed. It combines both the
approaches of bioventing, which utilize aerobic bioremediation of contaminated soil in
situ. Free product is recovered by a vacuum-enhanced system that utilizes LNAPLs from
Toxics 2022, 10, 484 8 of 24
the capillary fringe [73]. Free product is “slurped” up the bioslurping tube into a trap or
oil–water separator for further treatment after the bioslurping tube is vacuumed. When the
LNAPL is removed, the height of the LNAPL drops, which encourages the flow of LNAPL
from distant locations into the bioslurping well. The bioslurping tube starts to remove
vapours from the unsaturated zone when the fluid level in the bioslurping well decreases
as a result of the vacuum extraction of LNAPL. This vapour extraction encourages soil gas
movement, which in turn boosts aerobic biodegradation and aeration [74].
5.7. Biosparging
Air is introduced into the soil’s core, just like bioventing, to encourage microbiolog-
ical activity, which in turn removes pollutants from polluted sites. As an alternative to
conventional biodegradation methods, bioventing involves injecting air into a saturated
zone in order to encourage the movement of flammable organic chemicals upward to an
unsaturated zone nearby [75]. The success of biosparging is dependent on soil porosity
and contaminant biodegradability. When it comes to bioventing and soil vapour extrac-
tion (SVE), in situ air sparging (IAS) uses high air-flow rates to volatilize contaminants,
while biosparging encourages microbial degradation [76]. It is common practice to use
biosparging to remove diesel and kerosene from water supplies. In order to hasten the
biodegradation processes, oxygen is supplied into microorganisms during enhanced biore-
mediation [77]. The removal of organic pollutants (BTEX) can be accomplished using a
variety of technologies, including adsorption, microbial degradation, biosparging, PRBs,
and the use of modified or synthesized zeolites. However, there aren’t many investigations
on readily available, inexpensive materials like natural zeolite for BTEX adsorption [78].
5.8. Phytoremediation
Contaminated soils can be cleaned up using phytoremediation. In contaminated areas,
this method uses plant interactions at the physical, biological, chemical, biochemical, and
microbiological levels to reduce pollutant toxicity. Depending on the quantity and form of
the pollutant, phytoremediation employs a variety of processes [79]. Extraction, sequestra-
tion, and transformation are common methods for removing pollutants like heavy metals.
When using plants like willow or alfalfa, the decay, immobilization, rhizoremediation, and
evaporation of organic contaminants such as oils and chloro-compounds is feasible [80].
Tap root system or fibrous root system, penetration, toxicity levels, adaptability to the harsh
environmental conditions of the contaminants, plant annual growth, supervision, and,
notably, the time needed to reach standard of cleanliness are all important factors in plants
that serve as phytoremediators. The plant must also be disease and insect resistant [81]. An
important part of phytoremediation is removing pollutants from the roots and shoots. The
movement of water and nutrients is also dependent on transpiration and partitioning [82].
When it comes to contaminants and plant nature, it is possible to alter this process. Phy-
toremediation can be accomplished with the help of the majority of the plants present at
a polluted site. In polluted environments, native plants can be bioaugmented by natural
or anthropogenic plants, or a combination of both. Phytomining, the process of extracting
precious metals from polluted sites with plants, is one of them [83].
Numerous plants (over 300) are better candidates for phytoremediation because they
ideally absorb Cu, Zn, and Ni. Phytostabilization, sometimes referred to as in situ in-
activation or immobilisation of heavy metals, reduces their bioavailability and prevents
their off-site transfer. At the plant roots, it absorbs metals and restores them. Several
species, notably Acanthus ilicifolius and Virola surinamensis, are capable of Cd photostability.
Cinnamomum camphora, Osmanthus fragrans, Euonymus japonicus, Ligustrum vicaryi, and
Loropetalum chinense are five decorative plants chosen for their capacity to phytostabilize
Cd [84]. Water from various places that has been contaminated with metal can be success-
fully treated using bacterially-aided phytoremediation. The phytoremediation method
of metal reduction in wastewater utilising plants can be used by coalitions of growth-
Toxics 2022, 10, 484 9 of 24
promoting rhizobacteria, degrading bacteria, as well as endophytic bacteria [85]. There are
a few limitations to bioremediation techniques, as presented in Table 2.
genes, as well as the extracellular enzymatic activity (in the case of bacteria) (fungal
degradation process). The varying environmental conditions that affect the microbe growth
pattern further complicate these processes [94].
A successfully bioengineered microbe requires the identification of the relevant species
and strains for each substrate. A viable alternative to the recombinant degradation of
resistant organic compounds is biodegradation by microbes using readily-available organic
carbon and energy sources in the surrounding environment. Microbes use the fluctuation
in chemical gradients in their environment to determine the most favourable conditions for
growth. This allows them to thrive in an optimal environment [95]. Microbial consortia and
microbial fuel cells (MFCs and bioreactors) are two new developments in microbiological
bioremediation that are being used to degrade recalcitrant organic compounds. Toxic
organics can be remedied more effectively using fungi rather than bacteria because the
latter cannot grow at high concentrations of toxic organics [96]. For example, the enzymes,
laccase (LAC), lignin peroxidase (Lip), and manganese decarboxylase (MDA), are active
in the metabolism of lignocellulosic compounds by the white rot fungus Phanerochaete
chrysosporium [97].
Table 3. Potentially hazardous organic and inorganic pollutants and their degrading microbes
(bacteria, fungi, and algae).
7.1.2. Genomics
There is a new field in genomics for the study of bioremediation microbes. This
strategy is based on microbes’ ability to fully analyze their genetic information within the
cell. Bioremediation uses a wide variety of microorganisms [138]. To better understand the
biodegradation process, genomic tools such as PCR, analysis of isotope distribution, DNA
hybridization, molecular connectivity, metabolic footprinting, and metabolic engineering
are used. For genotypic fingerprinting, a variety of PCR-based techniques are available,
including amplified fragment length polymorphisms (AFLP), amplified ribosomal DNA
restriction analysis (ARDRA), automated ribosomal intergenic spacer analysis (ARISA),
terminal-restriction fragment length polymorphism (T-RFLP), randomly amplified poly-
morphic DNA analysis (RAPD), single strand conformation polymorphism (SSCP), and
length heterogeneity [139]. When it comes to studying soil microbial communities, RAPD
can be utilized for assessing inherently related bacterial species, constructing functional
structural models, and generating genetic fingerprints [140]. In microbial communities,
LH-PCR may be used to detect natural length variations of various SSU rRNA genes.
Multiple taxonomic groups of microbes can be profiled simultaneously using T-RFLP [141].
Research into how soil microbes interact with natural factors can also make use of a combi-
nation of molecular tools, such as genetic fingerprinting, microradiography, FISH, stable
isotope probing, and quantitative PCR. A PCR-based quantitative analysis of soil microbial
communities can be used to determine the abundance and appearance of taxonomic and
operational gene markers in the soil. Techniques for analysing a person’s DNA use ampli-
fied PCR products as a starting point for the direct analysis of specific molecular biomarker
genes [142]. In order to better understand the relationship between diverse microbial com-
Toxics 2022, 10, 484 13 of 24
et al. [154] synthesized silver nanoparticles using whole cells of the fungi Trichoderma spp.
for its application.
a simple, environmentally-friendly, and fast method for removing and degrading persistent
xenobiotic compounds by microorganisms [134,145]. Enzyme-producing microorganisms
have been isolated and characterized with the limitation of low productivity. Insecti-
cides’ main ingredients, organophosphates (OP) and organochlorines (OC), are found in
agricultural soil and run-off into waterways.
Genetically-engineered microorganisms have demonstrated successful bioremediation
of hexachlorocyclohexane and methyl parathion [135,146]. Genetically-modified P. putida
KT2440 was used in organophosphate and pyrethroid bioremediation experiments [168].
The degradation and catabolism of a variety of persistent compounds has been documented
since the advent of metabolic engineering. Sphingobium japonicum and Pseudomonas sp.
WBC-3 showed bioremediation of methyl parathion and -hexachlorocyclohexane degrada-
tion pathways [169]. When three enzymes from two different microorganisms are combined
in E. coli, a persistent fumigant called 1-, 2-, 3-trichloropropane is released into the envi-
ronment via heterologous catabolism [137,148]. To do this, microbes can be used to turn
persistent compounds into minerals [49].
Author Contributions: Conceptualization, M.T., M.S., K.S. and B.S.I.; Writing—original draft prepara-
tion, S.B., D.G. and B.V.T.; Writing—review and editing, M.S., M.T., K.S. and B.V.T.; visualization, S.B.
and D.G.; supervision, M.T., M.S., K.S. and B.S.I. All authors have read and agreed to the published
version of the manuscript.
Funding: This research received no external funding.
Institutional Review Board Statement: Not applicable.
Informed Consent Statement: Not applicable.
Data Availability Statement: Data that support these findings available within the article.
Acknowledgments: The author M.T. grateful to the Biotechnology Program, Department of Biochem-
istry, Dr. Rammanohar Lohia Avadh University, Ayodhya, India, for providing us with the research
environment.
Conflicts of Interest: The authors declare no conflict of interest.
References
1. Masindi, V.; Osman, M.S.; Tekere, M. Mechanisms and Approaches for the Removal of Heavy Metals from Acid Mine Drainage
and Other Industrial Effluents. In Water Pollution and Remediation: Heavy Metals; Springer: Berlin/Heidelberg, Germany, 2021;
pp. 513–537. [CrossRef]
2. Briffa, J.; Sinagra, E.; Blundell, R. Heavy metal pollution in the environment and their toxicological effects on humans. Heliyon
2020, 6, e04691. [CrossRef]
3. Rebello, S.; Sivaprasad, M.S.; Anoopkumar, A.N.; Jayakrishnan, L.; Aneesh, E.M. Cleaner technologies to combat heavy metal
toxicity. J. Environ. Manag. 2021, 296, 113231. [CrossRef]
4. Tripathi, M.; Singh, D.N.; Prasad, N.; Gaur, R. Advanced Bioremediation Strategies for Mitigation of Chromium and Organics
Pollution in Tannery. In Rhizobiont in Bioremediation of Hazardous Waste; Kumar, V., Prasad, R., Kumar, M., Eds.; Springer:
Singapore, 2021; pp. 195–215. [CrossRef]
5. Tripathi, M.; Gaur, R. Bioactivity of soil microorganisms for agriculture development. In Microbes in Land Use Change Management;
Singh, J.S., Tiwari, S., Singh, C., Singh, A.K., Eds.; Elsevier: Amsterdam, The Netherlands; Academic Press: Cambridge, MA,
USA, 2021; pp. 197–220. [CrossRef]
6. Alaira, S.; Padilla, C.; Alcantara, E.; Aggangan, N. Social Acceptability of the Bioremediation Technology for the Rehabilita-tion of
an Abandoned Mined-Out Area in Mogpog, Marinduque, Philippines. J. Environ. Sci. Manag. 2021, 24. [CrossRef]
7. Krzmarzick, M.J.; Taylor, D.K.; Fu, X.; McCutchan, A.L. Diversity and niche of archaea in bioremediation. Archaea 2018, 2018,
3194108. [CrossRef] [PubMed]
8. Kour, D.; Kaur, T.; Devi, R.; Yadav, A.; Singh, M.; Joshi, D. Beneficial microbiomes for bioremediation of diverse contaminated
environments for environmental sustainability: Present status and future challenges. Environ. Sci. Pollut. Res. 2021, 28,
24917–24939. [CrossRef] [PubMed]
9. Sharma, P.; Pandey, A.K.; Kim, S.H.; Singh, S.P.; Chaturvedi, P.; Varjani, S. Critical review on microbial community during in-situ
bioremediation of heavy metals from industrial wastewater. Environ. Technol. Innov. 2021, 24, 101826. [CrossRef]
10. Tripathi, M.; Vikram, S.; Jain, R.K.; Garg, S.K. Isolation and growth characteristics of chromium (VI) and penta-chlorophenol
tolerant bacterial isolate from treated tannery effluent for its possible use in simultaneous bioremediation. Indian J. Microbiol.
2011, 51, 61–69. [CrossRef] [PubMed]
11. Tripathi, M.; Garg, S.K. Dechlorination of chloroorganics, decolorization and simultaneous bioremediation of Cr6+ from real
tannery effluent employing indigenous Bacillus cereus isolate. Environ. Sci. Pollut. Res. 2014, 21, 5227–5241. [CrossRef]
12. Sonawane, J.M.; Rai, A.K.; Sharma, M.; Tripathi, M.; Prasad, R. Microbial biofilms: Recent advances and progress in envi-
ronmental bioremediation. Sci. Total Environ. 2022, 824, 153843. [CrossRef]
13. Soares, P.R.S.; Birolli, W.G.; Ferreira, I.M.; Porto, A.L.M. Biodegradation pathway of the organophosphate pesticides chlorpyrifos,
methyl parathion and profenofos by the marine-derived fungus Aspergillus sydowii CBMAI 935 and its poten-tial for methylation
reactions of phenolic compounds. Mar. Pollut. Bull. 2021, 166, 112185. [CrossRef]
14. Holanda, F.H.; Birolli, W.G.; Morais, E.D.S.; Sena, I.S.; Ferreira, A.M.; Faustino, S.M.M.; Solon, L.G.D.S.; Porto, A.L.; Ferreira, I.M.
Study of biodegradation of chloramphenicol by endophytic fungi isolated from Bertholletia excelsa (Brazil nuts). Biocatal. Agric.
Biotechnol. 2019, 20, 101200. [CrossRef]
15. Ding, T.; Lin, K.; Yang, B.; Yang, M.; Li, J.; Li, W.; Gan, J. Biodegradation of naproxen by freshwater algae Cymbella sp. and
Scenedesmus quadricauda and the comparative toxicity. Bioresour. Technol. 2017, 238, 164–173. [CrossRef] [PubMed]
16. Singh, S.; Singh, S.; Kushwaha, R. Bioremediation of hydrocarbons and xenobiotic compounds. In Bioremdiation: Challenges
and Advancements; Tripathi, M., Singh, D.N., Eds.; Bentham Science Publishers: Sharjah, United Arab Emirates, 2022; pp. 1–48.
[CrossRef]
Toxics 2022, 10, 484 18 of 24
17. Bhavya, G.; Belorkar, S.A.; Mythili, R.; Geetha, N.; Shetty, H.S.; Udikeri, S.S.; Jogaiah, S. Remediation of emerging environ-mental
pollutants: A review based on advances in the uses of eco-friendly biofabricated nanomaterials. Chemosphere 2021, 275, 129975.
[CrossRef] [PubMed]
18. Enerijiofi, K.E. Bioremediation of environmental contaminants: A sustainable alternative to environmental management. In
Bioremediation for Environmental Sustainability; Elsevier: Amsterdam, The Netherlands, 2021; pp. 461–480. [CrossRef]
19. Hussain, A.; Rehman, F.; Rafeeq, H.; Waqas, M.; Asghar, A.; Afsheen, N.; Rahdar, A.; Bilal, M.; Iqbal, H.M. In-situ, Ex-situ, and
nano-remediation strategies to treat polluted soil, water, and air—A review. Chemosphere 2022, 289, 133252. [CrossRef] [PubMed]
20. Giri, B.S.; Geed, S.; Vikrant, K.; Lee, S.S.; Kim, K.H.; Kailasa, S.K.; Vithanage, M.; Chaturvedi, P.; Rai, B.N.; Singh, R.S. Progress in
bioremediation of pesticide residues in the environment. Environ. Eng. Res. 2021, 26, 200446. [CrossRef]
21. Tarekegn, M.M.; Salilih, F.Z.; Ishetu, A.I. Microbes used a tool for bioremediation of heavy metals from the environment. Cogent
Food Agric. 2020, 6, 1783174. [CrossRef]
22. Tegene, B.G.; Tenkegna, T.A. Mode of Action, Mechanism and Role of Microbes in Bioremediation Service for Environmental
Pollution Management. J. Biotechnol. Bioinform. Res. 2020, 2, 1–18. [CrossRef]
23. Garg, S.K.; Tripathi, M. Microbial strategies for discoloration and detoxification of azo dyes from textile effluents. Res. J. Microbiol.
2017, 12, 1–19. [CrossRef]
24. Chen, B.Y.; Ma, C.M.; Han, K.; Yueh, P.L.; Qin, L.J.; Hsueh, C.C. Influence of textile dye and decolorized metabolites on mi-crobial
fuel cell-assisted bioremediation. Bioresour. Technol. 2016, 200, 1033–1038. [CrossRef]
25. Nannipieri, P.; Kandeler, E.; Ruggiero, P. Enzyme activities and microbiological and biochemical processes in soil. In Enzymes in
the Environment; CRC Press: Boca Raton, FL, USA, 2002; pp. 1–33.
26. Khalid, F.; Hashmi, M.Z.; Jamil, N.; Qadir, A.; Ali, M.I. Microbial and enzymatic degradation of PCBs from e-waste-contaminated
sites: A review. Environ. Sci. Pollut. Res. 2021, 28, 10474–10487. [CrossRef]
27. Garg, S.K.; Tripathi, M.; Srinath, T. Strategies for chromium bioremediation of tannery effluent. Rev. Environ. Contam. Toxicol.
2012, 217, 75–140. [CrossRef] [PubMed]
28. Abatenh, E.; Gizaw, B.; Tsegaye, Z.; Wassie, M. The role of microorganisms in bioremediation—A review. J. Environ. Biol. 2017, 2,
38–46. [CrossRef]
29. Alvarez, A.; Saez, J.M.; Costa, J.S.D.; Colin, V.L.; Fuentes, M.S.; Cuozzo, S.A.; Benimeli, C.S.; Polti, M.A.; Amoroso, M.J.
Actinobacteria: Current research and perspectives for bioremediation of pesticides and heavy metals. Chemosphere 2017, 166,
41–62. [CrossRef] [PubMed]
30. Maier, R.M.; Gentry, T.J. Microorganisms and organic pollutants. In Environmental Microbiology; Academic Press: Cambridge, MA,
USA, 2015; pp. 377–413. [CrossRef]
31. Alegbeleye, O.O.; Opeolu, B.O.; Jackson, V.A. Polycyclic aromatic hydrocarbons: A critical review of environmental occurrence
and bioremediation. Environ. Manag. 2017, 60, 758–783. [CrossRef]
32. Sodhi, K.K.; Kumar, M.; Singh, D.K. Insight into the amoxicillin resistance, ecotoxicity, and remediation strategies. J. Water Process.
Eng. 2021, 39, 101858. [CrossRef]
33. Mazumder, M.A.R.; Jubayer, M.F.; Ranganathan, T.V. Biodegradation of Plastics by Microorganisms. In Biotechnology for Zero
Waste: Emerging Waste Management Techniques; John Wiley & Sons: Hoboken, NJ, USA, 2022; pp. 123–141. [CrossRef]
34. Jangir, C.K.; Kumar, S.; Meena, R.S. Significance of soil organic matter to soil quality and evaluation of sustainability. In Sustainable
agriculture; Scientific Publisher: Jodhpur, India, 2019; pp. 357–381. [CrossRef]
35. Kebede, G.; Tafese, T.; Abda, E.M.; Kamaraj, M.; Assefa, F. Factors influencing the bacterial bioremediation of hydrocarbon
contaminants in the soil: Mechanisms and impacts. J. Chem. 2021, 2021, 9823362. [CrossRef]
36. Mupambwa, H.A.; Mnkeni, P.N.S. Optimizing the vermicomposting of organic wastes amended with inorganic materials for
production of nutrient-rich organic fertilizers: A review. Environ. Sci. Pollut. Res. 2018, 25, 10577–10595. [CrossRef]
37. Sharma, P.; Singh, S.P.; Parakh, S.K.; Tong, Y.W. Health hazards of hexavalent chromium (Cr (VI)) and its microbial reduction.
Bioengineered 2022, 13, 4923–4938. [CrossRef]
38. Ren, X.; Zeng, G.; Tang, L.; Wang, J.; Wan, J.; Wang, J. The potential impact on the biodegradation of organic pollutants from
composting technology for soil remediation. Waste Manag. 2018, 72, 138–149. [CrossRef]
39. Rajkumar, R.; Kurinjimalar, C. Microbes and plant mineral nutrition. In Microbiological Activity for Soil and Plant Health Management;
Springer: Singapore, 2021; pp. 111–132. [CrossRef]
40. Sangwan, S.; Dukare, A. Microbe-Mediated Bioremediation: An Eco-friendly Sustainable Approach for Environmental Clean-up.
In Advances in Soil Microbiology: Recent Trends and Future Prospects; Springer Nature: Singapore, 2018; pp. 145–163. [CrossRef]
41. Padhan, D.; Rout, P.P.; Kundu, R.; Adhikary, S.; Padhi, P.P. Bioremediation of heavy metals and other toxic substances by
microorganisms. In Soil Bioremediation: An Approach Towards Sustainable Technology; John Wiley & Sons: Hoboken, NJ, USA, 2021;
pp. 285–329. [CrossRef]
42. Boopathy, R. Factors limiting bioremediation technologies. Bioresour. Technol. 2000, 74, 63–67. [CrossRef]
43. Malik, S.; Dhasmana, A.; Kishore, S.; Kumari, M. Microbes and Microbial Enzymes for Degradation of Pesticides. In Bioremediation
and Phytoremediation Technologies in Sustainable Soil Management; Apple Academic Press: New York, NY, USA, 2022; pp. 95–127.
[CrossRef]
44. Priyadarshanee, M.; Das, S. Biosorption and removal of toxic heavy metals by metal tolerating bacteria for bioremediation of
metal contamination: A comprehensive review. J. Environ. Chem. Eng. 2021, 9, 104686. [CrossRef]
Toxics 2022, 10, 484 19 of 24
45. Sutherland, D.L.; Ralph, P.J. Microalgal bioremediation of emerging contaminants-Opportunities and challenges. Water Res. 2019,
164, 114921. [CrossRef] [PubMed]
46. Arora, S.; Saxena, S.; Sutaria, D.; Sethi, J. Bioremediation: An ecofriendly approach for the treatment of oil spills. In Advances in
Oil-Water Separation; Elsevier: Amsterdam, The Netherlands, 2022; pp. 353–373. [CrossRef]
47. Ojha, N.; Karn, R.; Abbas, S.; Bhugra, S. Bioremediation of Industrial Wastewater: A Review. In IOP Conference Series: Earth and
Environmental Science; IOP Publishing: Philadelphia, PA, USA, 2021; Volume 796, p. 012012. [CrossRef]
48. Naeem, U.; Qazi, M.A. Leading edges in bioremediation technologies for removal of petroleum hydrocarbons. Environ. Sci. Pollut.
Res. 2020, 27, 27370–27382. [CrossRef] [PubMed]
49. Jaain, R.; Patel, A. Bioremediation of Gurugram–Faridabad Dumpsite at Bandhwari. In Waste Valorisation and Recycling; Springer:
Singapore, 2019; pp. 433–440. [CrossRef]
50. Rayu, S.; Karpozas, D.G.; Singh, B.K. Emerging technologies in bioremediation: Constraints and opportunities. Biodegradation
2012, 23, 917–926. [CrossRef]
51. Yap, H.S.; Zakaria, N.N.; Zulkharnain, A.; Sabri, S.; Gomez-Fuentes, C.; Ahmad, S.A. Bibliometric analysis of hydrocarbon
bioremediation in cold regions and a review on enhanced soil bioremediation. Biology 2021, 10, 354. [CrossRef]
52. Sivashankar, R.; Sathya, A.B.; Vasantharaj, K.; Nithya, R.; Sivasubramanian, V. Biotechnology and Its Significance in Environmental
Protection. In Bioprocess Engineering for a Green Environment; CRC Press: Boca Raton, FL, USA, 2018; pp. 1–31. [CrossRef]
53. Fortin Faubert, M.; Hijri, M.; Labrecque, M. Short rotation intensive culture of willow, spent mushroom substrate and ramial
chipped wood for bioremediation of a contaminated site used for land farming activities of a former petrochemical plant. Plants
2021, 10, 520. [CrossRef]
54. Janssen, D.B.; Stucki, G. Perspectives of genetically engineered microbes for groundwater bioremediation. Environ. Sci. Process.
Impacts 2020, 22, 487–499. [CrossRef]
55. Guerin, T.F. Prototyping of co-composting as a cost-effective treatment option for full-scale on-site remediation at a decommis-
sioned refinery. J. Clean. Prod. 2021, 302, 127012. [CrossRef]
56. Patel, A.K.; Singhania, R.R.; Albarico, F.P.J.B.; Pandey, A.; Chen, C.W.; Dong, C.D. Organic wastes bioremediation and its changing
prospects. Sci. Total Environ. 2022, 824, 153889. [CrossRef]
57. Wang, L.; Rinklebe, J.; Tack, F.M.; Hou, D. A review of green remediation strategies for heavy metal contaminated soil. Soil Use
Manag. 2021, 37, 936–963. [CrossRef]
58. Gomes, H.I.; Dias-Ferreira, C.; Ribeiro, A.B. Overview of in situ and ex situ remediation technologies for PCB-contaminated soils
and sediments and obstacles for full-scale application. Sci. Total Environ. 2013, 445, 237–260. [CrossRef] [PubMed]
59. Davoodi, S.M.; Miri, S.; Taheran, M.; Brar, S.K.; Galvez-Cloutier, R.; Martel, R. Bioremediation of unconventional oil contaminated
ecosystems under natural and assisted conditions: A review. Environ. Sci. Technol. 2020, 54, 2054–2067. [CrossRef] [PubMed]
60. Azubuike, C.C.; Chikere, C.B.; Okpokwasili, G.C. Bioremediation techniques–classification based on site of application: Principles,
advantages, limitations and prospects. World J. Microbiol. Biotechnol. 2016, 32, 180. [CrossRef] [PubMed]
61. Tekere, M.; Jacob-Lopes, E.; Zepka, L.Q. Microbial bioremediation and different bioreactors designs applied. In Biotechnology and
Bioengineering; IntechOpen: Rijeka, Croatia, 2019; pp. 1–19. [CrossRef]
62. Gurkok, S. Important parameters necessary in the bioreactor for the mass production of biosurfactants. In Green Sustainable Process
for Chemical and Environmental Engineering and Science; Elsevier: Amsterdam, The Netherlands, 2021; pp. 347–365. [CrossRef]
63. Sharma, J. Advantages and limitations of in situ methods of bioremediation. Recent Adv. Biol. Med. 2019, 5, 10941. [CrossRef]
64. Akubude, V.C.; Oyewusi, T.F.; Okafor, V.C.; Obumseli, P.C.; Igwe, A.O. Application of Nanomaterials in the Bioaugmentation of
Heavily Polluted Environment. In Bioaugmentation Techniques and Applications in Remediation; CRC Press: Boca Raton, FL, USA,
2020; pp. 87–101. [CrossRef]
65. Yadav, B.; Mathur, S.; Ch, S.; Yadav, B.K. Simulation-Optimization approach for the consideration of well clogging during cost
estimation of in situ bioremediation system. J Hydrol. Eng. 2018, 23, 04018001. [CrossRef]
66. Cecchin, I.; Reginatto, C.; Siveris, W.; Schnaid, F.; Thomé, A.; Reddy, K.R. Remediation of Hexavalent Chromium Contaminated
Clay Soil by Injection of Nanoscale Zero Valent Iron (nZVI). Water Air Soil Pollut. 2021, 232, 268. [CrossRef]
67. Zhang, Y.; Zhang, Y.; Akakuru, O.U.; Xu, X.; Wu, A. Research progress and mechanism of nanomaterials-mediated in-situ
remediation of cadmium-contaminated soil: A critical review. J. Environ. Sci. 2021, 104, 351–364. [CrossRef]
68. Kumar, V. Mechanism of microbial heavy metal accumulation from a polluted environment and bioremediation. In Microbial Cell
Factories; CRC Press: Boca Raton, FL, USA, 2018; pp. 149–174. [CrossRef]
69. da Silva, S.; Gonçalves, I.; Gomes de Almeida, F.C.; Padilha da Rocha e Silva, N.M.; Casazza, A.A.; Converti, A.; Asfora-Sarubbo,
L. Soil bioremediation: Overview of technologies and trends. Energies 2020, 13, 4664. [CrossRef]
70. Anekwe, I.M.S.; Isa, Y.M. Comparative evaluation of wastewater and bioventing system for the treatment of acid mine drainage
contaminated soils. Water-Energy Nexus 2021, 4, 134–140. [CrossRef]
71. Anekwe, I.M.; Isa, Y.M. Wastewater and Bioventing Treatment Systems for Acid Mine Drainage–Contaminated Soil. Soil Sediment
Contam. Int. J. 2021, 30, 518–531. [CrossRef]
72. Tong, W. Groundwater Hydrology, Soil and Groundwater Contamination Assessment and Monitoring. In Fundamentals of
Environmental Site Assessment and Remediation; CRC Press: Boca Raton, FL, USA, 2018; pp. 70–99. [CrossRef]
73. SookhakLari, K.; Rayner, J.L.; Davis, G.B. Toward optimizing LNAPL remediation. Water Resour. Res. 2019, 55, 923–936. [CrossRef]
Toxics 2022, 10, 484 20 of 24
74. Beretta, G.; Mastorgio, A.F.; Pedrali, L.; Saponaro, S.; Sezenna, E. Support tool for identifying in situ remediation technology for
sites contaminated by hexavalent chromium. Water 2018, 10, 1344. [CrossRef]
75. Gautam, K.; Gaur, P.; Sharma, P. Bioremediation of Radioactive Contaminants/Radioactive Metals. In Bioremediation: Challenges
and Advancements; Tripathi, M., Singh, D.S., Eds.; Bentham Science Publishers: Singapore, 2022; pp. 90–117.
76. Philp, J.C.; Atlas, R.M. Bioremediation of contaminated soils and aquifers. In Bioremediation: Applied Microbial Solutions for
Real-World Environmental Cleanup; John Wiley & Sons: Hoboken, NJ, USA, 2005; pp. 139–236. [CrossRef]
77. Maitra, S. In situ bioremediation—An overview. Res. J. Life Sci. Bioinfo. Pharmaceu. Chem. Sci. 2018, 4, 576–598. [CrossRef]
78. Ahmadnezhad, Z.; Vaezihir, A.; Schüth, C.; Zarrini, G. Combination of zeolite barrier and bio sparging techniques to en-hance
efficiency of organic hydrocarbon remediation in a model of shallow groundwater. Chemosphere 2021, 273, 128555. [CrossRef]
79. Wei, Z.; Van Le, Q.; Peng, W.; Yang, Y.; Yang, H.; Gu, H.; Lam, S.S.; Sonne, C. A review on phytoremediation of contaminants in
air, water and soil. J. Hazard. Mater. 2021, 403, 123658. [CrossRef]
80. Odoh, C.K.; Zabbey, N.; Sam, K.; Eze, C.N. Status, progress and challenges of phytoremediation—An African Scenario. J. Environ.
Manag. 2019, 237, 365–378. [CrossRef]
81. Chakrabartty, M.; Harun-Or-Rashid, G.M. Feasibility Study of the Soil Remediation Technologies in the Natural Environment.
Am. J. Civ. Eng. 2021, 9, 91–98. [CrossRef]
82. Ali, S.; Abbas, Z.; Rizwan, M.; Zaheer, I.E.; Yavaş, İ.; Ünay, A.; Abdel-Daim, M.M.; Bin-Jumah, M.; Hasanuzzaman, M.; Kalderis,
D. Application of floating aquatic plants in phytoremediation of heavy metals polluted water: A review. Sustainability 2020, 12,
1927. [CrossRef]
83. Nkrumah, P.; Echevarria, G.; Erskine, P.; van der Ent, A. Phytomining: Using plants to extract valuable metals from mineralised
wastes and uneconomic resources. In Extracting Innovations: Mining, Energy, and Technological Change in the Digital Age; CRC Press:
Boca Raton, FL, USA, 2018; pp. 313–324. [CrossRef]
84. Zeng, P.; Guo, Z.; Cao, X.; Xiao, X.; Liu, Y.; Shi, L. Phytostabilization potential of ornamental plants grown in soil contaminated
with cadmium. Int. J. Phytoremediat. 2018, 20, 311–320. [CrossRef]
85. Capuana, M. A review of the performance of woody and herbaceous ornamental plants for phytoremediation in urban areas.
iForest-Biogeosci. For. 2020, 13, 139. [CrossRef]
86. Oualha, M.; Al-Kaabi, N.; Al-Ghouti, M.; Zouari, N. Identification and overcome of limitations of weathered oil hydrocar-bons
bioremediation by an adapted Bacillus sorensis strain. J. Environ. Manag. 2019, 250, 109455. [CrossRef] [PubMed]
87. Cózar, A.; Aliani, S.; Basurko, O.C.; Arias, M.; Isobe, A.; Topouzelis, K.; Rubio, A.; Morales-Caselles, C. Marine litter windrows: A
strategic target to understand and manage the ocean plastic pollution. Front. Mar. Sci. 2021, 8, 571796. [CrossRef]
88. Deeb, M.; Groffman, P.M.; Blouin, M.; Egendorf, S.P.; Vergnes, A.; Vasenev, V.; Cao, D.L.; Walsh, D.; Morin, T.; Séré, G. Using
constructed soils for green infrastructure–challenges and limitations. Soil 2020, 6, 413–434. [CrossRef]
89. Kim, S.Y.; Garcia, H.A.; Lopez-Vazquez, C.M.; Milligan, C.; Livingston, D.; Herrera, A.; Matosic, M.; Curko, J.; Brdjanovic, D.
Limitations imposed by conventional fine bubble diffusers on the design of a high-loaded membrane bioreactor (HL-MBR).
Environ. Sci. Pollut. Res. 2019, 26, 34285–34300. [CrossRef]
90. Kumar, V.; Shahi, S.K.; Singh, S. Bioremediation: An eco-sustainable approach for restoration of contaminated sites. In Microbial
Bioprospecting for Sustainable Development; Springer: Singapore, 2018; pp. 115–136. [CrossRef]
91. Yaashikaa, P.R.; Kumar, P.S.; Jeevanantham, S.; Saravanan, R. A review on bioremediation approach for heavy metal detox-ification
and accumulation in plants. Environ. Pollut. 2022, 301, 119035. [CrossRef]
92. Bhatt, P.; Verma, A.; Gangola, S.; Bhandari, G.; Chen, S. Microbial glycoconjugates in organic pollutant bioremediation: Recent
advances and applications. Microb. Cell Fact. 2021, 20, 72. [CrossRef]
93. Leung, K.T.; Jiang, Z.H.; Almzene, N.; Nandakumar, K.; Sreekumari, K.; Trevors, J.T. Biodegradation and bioremediation of
organic pollutants in soil. In Modern Soil Microbiology; CRC Press: Boca Raton, FL, USA, 2019; pp. 381–402. [CrossRef]
94. Bharagava, R.N.; Saxena, G.; Mulla, S.I. Introduction to industrial wastes containing organic and inorganic pollutants and
bioremediation approaches for environmental management. In Bioremediation of Industrial Waste for Environmental Safety; Springer:
Singapore, 2020; pp. 1–18. [CrossRef]
95. Mbé, B.; Monga, O.; Pot, V.; Otten, W.; Hecht, F.; Raynaud, X.; Garnier, P. Scenario modelling of carbon mineralization in 3D soil
architecture at the microscale: Toward an accessibility coefficient of organic matter for bacteria. Eur. J. Soil Sci. 2022, 73, e13144.
[CrossRef]
96. Hu, R.; Cao, Y.; Chen, X.; Zhan, J.; Luo, G.; Ngo, H.H.; Zhang, S. Progress on microalgae biomass production from wastewater
phycoremediation: Metabolic mechanism, response behavior, improvement strategy and principle. J. Chem. Eng. 2022, 137187, in
press. [CrossRef]
97. Sharma, K.R.; Giri, R.; Sharma, R.K. Efficient bioremediation of metal containing industrial wastewater using white rot fungi. Int.
J. Environ. Sci. Technol. 2022, 1–8. [CrossRef]
98. Lawal, A.T. Polycyclic aromatic hydrocarbons. A review. Cogent Environ. Sci. 2017, 3, 1339841. [CrossRef]
99. Joutey, N.T.; Bahafid, W.; Sayel, H.; El Ghachtouli, N. Biodegradation: Involved microorganisms and genetically engineered
microorganisms. In Biodegradation—Life of Science; IntechOpen: London, UK, 2013; Volume 1, pp. 289–320. [CrossRef]
100. Thakare, M.; Sarma, H.; Datar, S.; Roy, A.; Pawar, P.; Gupta, K.; Pandit, S.; Prasad, R. Understanding the holistic approach to
plant-microbe remediation technologies for removing heavy metals and radionuclides from soil. Curr. Res. Biotechnol. 2021, 3,
84–98. [CrossRef]
Toxics 2022, 10, 484 21 of 24
101. Masindi, V.; Muedi, K.L. Environmental contamination by heavy metals. Heavy Met. 2018, 10, 115–132. [CrossRef]
102. Gałwa-Widera, M. Biochar—Production, Properties, and Service to Environmental Protection against Toxic Metals. In Handbook of
Assisted and Amendment: Enhanced Sustainable Remediation Technology; John Wiley & Sons: Hoboken, NJ, USA, 2021; pp. 53–75.
[CrossRef]
103. Anning, C.; Asare, M.O.; Wang, J.; Geng, Y.; Lyu, X. Effects of physicochemical properties of Au cyanidation tailings on cyanide
microbial degradation. J. Environ. Sci. Health Part A 2021, 56, 413–433. [CrossRef] [PubMed]
104. Xia, X.; Wu, S.; Zhou, Z.; Wang, G. Microbial Cd (II) and Cr (VI) resistance mechanisms and application in bioremediation. J.
Hazard. Mater. 2021, 401, 123685. [CrossRef]
105. Van der Veken, D.; Hollanders, C.; Verce, M.; Michiels, C.; Ballet, S.; Weckx, S.; Leroy, F. Genome-Based Characterization of a
Plasmid-Associated Micrococcin P1 Biosynthetic Gene Cluster and Virulence Factors in Mammaliicoccus sciuri IM-DO-S72. Appl.
Environ. Microbiol. 2022, 88, e0208821. [CrossRef]
106. Kunze, M.; Zerlin, K.F.; Retzlaff, A.; Pohl, J.O.; Schmidt, E.; Janssen, D.B.; Reineke, W. Degradation of chloroaromatics by
Pseudomonas putida GJ31: Assembled route for chlorobenzene degradation encoded by clusters on plasmid pKW1 and the
chromosome. Microbiology 2009, 155, 4069–4083. [CrossRef]
107. Giriyan, A.L.; Berde, V.B.; Pereira, E.J.; Parulekar-Berde, C.V. Microbial Bioremediation of Heavy Metals: A Genetic and Omics
Approach. In Handbook of Research on Microbial Remediation and Microbial Biotechnology for Sustainable Soil; IGI Global: Hershey, PA,
USA, 2021; pp. 417–439. [CrossRef]
108. Mohapatra, B.; Phale, P.S. Microbial degradation of naphthalene and substituted naphthalenes: Metabolic diversity and genomic
insight for bioremediation. Front. Bioeng. Biotechnol. 2021, 9, 144. [CrossRef]
109. Meehan, C.; Banat, I.M.; Mcmullan, G.; Nigam, P.; Smyth, F. Decolorization of REMAZOL BLACK-B using a thermotolerant yeast.
Kluyveromyces marxianus IMB3. Environ. Int. 2000, 26, 75–79. [CrossRef]
110. Tripathi, M.; Garg, S.K. Response surface modeling for co-remediation of Cr6+ and pentachlorophenol by Bacillus cereus RMLAU1:
Bioreactor trial, structural and functional characterization by SEM-EDS and FT-IR analyses. Bioremediat. J. 2014, 18, 328–344.
[CrossRef]
111. Sen, S.K.; Patra, P.; Das, C.R.; Raut, S.; Raut, S. Pilot-scale evaluation of bio-decolorization and biodegradation of reactive textile
wastewater: An impact on its use in irrigation of wheat crop. Water Resour. Ind. 2019, 21, 100106. [CrossRef]
112. Basu, S.; Rabara, R.C.; Negi, S.; Shukla, P. Engineering PGPMOs through gene editing and systems biology: A solution for
phytoremediation? Trends Biotechnol. 2018, 36, 499–510. [CrossRef] [PubMed]
113. Gaur, N.; Narasimhulu, K.; PydiSetty, Y. Recent advances in the bio-remediation of persistent organic pollutants and its effect on
environment. J. Clean. Prod. 2018, 198, 1602–1631. [CrossRef]
114. Bustard, M.; McMullan, G.; McHale, A.P. Biosorption of textile dyes by biomass derived from Kluyveromyces marxianus IMB3.
Bioprocess Eng. 1998, 19, 427–430. [CrossRef]
115. Halak, S.; Basta, T.; Bürger, S.; Contzen, M.; Stolz, A. Characterization of the genes encoding the 3-carboxy-cis, cis-muconate-
lactonizing enzymes from the 4-sulfocatechol degradative pathways of Hydrogenophaga intermedia S1 and Agrobacterium radiobacter
S2. Microbiology 2006, 152, 3207–3216. [CrossRef] [PubMed]
116. Liu, Z.; Shao, B.; Zeng, G.; Chen, M.; Li, Z.; Liu, Y.; Yan, M. Effects of rhamnolipids on the removal of 2, 4, 2, 4-tetrabrominated
biphenyl ether (BDE-47) by Phanerochaete chrysosporium analyzed with a combined approach of experiments and molecular
docking. Chemosphere 2018, 210, 922–930. [CrossRef] [PubMed]
117. Raquel, S.; Natalia, G.; Luis Fernando, B.; Maria Carmen, M. Biodegradation of high-molecular-weight polycyclic aromatic
hydrocarbons by a wood-degrading consortium at low temperatures. FEMS Microbiol. Ecol. 2013, 83, 438–449. [CrossRef]
118. Sangkharak, K.; Choonut, A.; Rakkan, T.; Prasertsan, P. The degradation of phenanthrene, pyrene, and fluoranthene and its
conversion into medium-chain-length polyhydroxyalkanoate by novel polycyclic aromatic hydrocarbon-degrading bacteria. Curr.
Microbiol. 2020, 77, 897–909. [CrossRef]
119. Phulpoto, A.H.; Qazi, M.A.; Mangi, S.; Ahmed, S.; Kanhar, N.A. Biodegradation of oil-based paint by Bacillus species monocul-
tures isolated from the paint warehouses. Int. J. Environ. Sci. Technol. 2016, 13, 125–134. [CrossRef]
120. Krab-Hüsken, L. Production of Catechols: Microbiology and Technology. Ph.D. Thesis, Wageningen University and Research,
Wageningen, The Netherlands, 2002. [CrossRef]
121. Miri, S.; Rasooli, A.; Brar, S.K.; Rouissi, T.; Martel, R. Biodegradation of p-xylene—A comparison of three psychrophilic
Pseudomonas strains through the lens of gene expression. Environ. Sci. Pollut. Res. 2022, 29, 21465–21479. [CrossRef]
122. Pande, V.; Pandey, S.C.; Sati, D.; Pande, V.; Samant, M. Bioremediation: An emerging effective approach towards environment
restoration. Environ. Sustain. 2020, 3, 91–103. [CrossRef]
123. Duc, H.D.; Hung, N.V.; Oanh, N.T. Anaerobic Degradation of Endosulfans by a Mixed Culture of Pseudomonas sp. and
Staphylococcus sp. Appl. Biochem. Microbiol. 2021, 57, 327–334. [CrossRef]
124. Garg, S.K.; Tripathi, M.; Singh, S.K.; Singh, A. Pentachlorophenol dechlorination and simultaneous Cr6+ reduction by Pseudomonas
putida SKG-1 MTCC (10510): Characterization of PCP dechlorination products, bacterial structure and functional groups. Environ.
Sci. Pollut. Res. 2013, 20, 2288–2304. [CrossRef] [PubMed]
125. Kharangate-Lad, A.; D’Souza, N.C. Current Approaches in Bioremediation of Toxic Contaminants by Application of Microbial
Cells; Biosurfactants and Bioemulsifiers of Microbial Origin. In Rhizobiont in Bioremediation of Hazardous Waste; Springer: Singapore,
2021; pp. 217–263. [CrossRef]
Toxics 2022, 10, 484 22 of 24
126. Unuofin, J.O.; Falade, A.O.; Aladekoyi, O.J. Applications of microbial laccases in bioremediation of environmental pollutants: Po-
tential issues, challenges, and prospects. In Bioremediation for Environmental Sustainability; Elsevier: Amsterdam, The Netherlands,
2021; pp. 519–540. [CrossRef]
127. Gaur, V.K.; Tripathi, V.; Manickam, N. Bacterial-and fungal-mediated biodegradation of petroleum hydrocarbons in soil. In
Development in Wastewater Treatment Research and Processes; Elsevier: Amsterdam, The Netherlands, 2022; pp. 407–427. [CrossRef]
128. Sravya, K.; Sangeetha, S. Feasibility study on bioremediation techniques to contaminated soils. Mater. Today Proc. 2022, 51,
2556–2560. [CrossRef]
129. Shah, H.; Jain, S. Bioremediation: An approach for environmental pollutants detoxification. In Waste to Energy: Prospects and
Applications; Springer: Singapore, 2020; pp. 121–142. [CrossRef]
130. Geetha, N.; Bhavya, G.; Abhijith, P.; Shekhar, R.; Dayananda, K.; Jogaiah, S. Insights into nanomycoremediation: Secretomics and
mycogenic biopolymer nanocomposites for heavy metal detoxification. J. Hazard. Mater. 2021, 409, 124541. [CrossRef] [PubMed]
131. Aregbesola, O.A.; Kumar, A.; Mokoena, M.P.; Olaniran, A.O. Cloning, overexpression, purification, characterization and structural
modelling of a metabolically active Fe2+ dependent 2, 6-dichloro-p-hydroquinone 1, 2-dioxygenase (CpsA) from Bacillus cereus
strain AOA-CPS_1. Int. J. Biol. Macromol. 2020, 161, 247–257. [CrossRef]
132. Song, J.; Zhang, S.; Xie, Y.; Li, Q. Purification and characteristics of an aflatoxin B1 degradation enzyme isolated from Pseudomonas
aeruginosa. FEMS Microbiol. Lett. 2019, 366, fnz034. [CrossRef]
133. Yergeau, E.; Sanschagrin, S.; Beaumier, D.; Greer, C.W. Metagenomic analysis of the bioremediation of diesel-contaminated
Canadian high Arctic soils. PLoS ONE 2012, 7, e30058. [CrossRef]
134. Zheng, Y.; Li, Y.; Long, H.; Zhao, X.; Jia, K.; Li, J.; Zhang, D. bifA regulates biofilm development of Pseudomonas putida MnB1 as a
primary response to H2 O2 and Mn2+ . Front. Microbiol. 2018, 9, 1490. [CrossRef]
135. Vega-Páez, J.D.; Rivas, R.E.; Dussán-Garzón, J. High Efficiency Mercury Sorption by Dead Biomass of Lysinibacillussphaercus—New
Insights into the Treatment of Contaminated Water. Materials 2019, 12, 1296. [CrossRef]
136. Sar, P.; Islam, E. Metagenomic Approaches in Microbial Bioremediation of Metals and Radionuclides. In Microrganisms in
Environmental Management; Springer: Dordrecht, The Netherlands, 2012; pp. 525–546. [CrossRef]
137. Villegas-Plazas, M.; Sanabria, J.; Junca, H. A composite taxonomical and functional framework of microbiomes under acid mine
drainage bioremediation systems. J. Env. Manag. 2019, 251, 109581. [CrossRef]
138. Jaiswal, S.; Singh, D.K.; Shukla, P. Gene editing and systems biology tools for pesticide bioremediation: A review. Front. Microbiol.
2019, 10, 87. [CrossRef] [PubMed]
139. Hakeem, K.R.; Bhat, R.A.; Qadri, H. Bioremediation and Biotechnology; Springer: Cham, Switzerland, 2020. [CrossRef]
140. Rodríguez, A.; Castrejón-Godínez, M.L.; Sánchez-Salinas, E.; Mussali-Galante, P.; Tovar-Sánchez, E.; Ortiz-Hernández, M.
Pesticide Bioremediation: OMICs Technologies for Understanding the Processes. In Pesticides Bioremediation; Springer: Cham,
Switzerland, 2022; pp. 197–242. [CrossRef]
141. Gupta, K.; Biswas, R.; Sarkar, A. Advancement of omics: Prospects for bioremediation of contaminated soils. In Microbial
Bioremediation & Biodegradation; Springer: Singapore, 2020; pp. 113–142. [CrossRef]
142. Yunusa, Y.R.; Umar, Z.D. Effective microbial bioremediation via the multi-omics approach: An overview of trends, problems and
prospects. UMYU J. Microbiol. Res. 2021, 6, 127–145. [CrossRef]
143. Sharma, P.; Singh, S.P.; Iqbal, H.M.; Tong, Y.W. Omics approaches in bioremediation of environmental contaminants: An integrated
approach for environmental safety and sustainability. Environ. Res. 2022, 211, 113102. [CrossRef] [PubMed]
144. Singh, D.; Geat, N.; Mehriya, M.; Rajawat, M.V.S.; Prasanna, R.; Kumar, A.; Kumari, G.; Jha, M.N. Omics (genomics, proteomics,
metabolomics, etc.) tools to study the environmental microbiome and bioremediation. In Waste to Energy: Prospects and Applications;
Springer: Singapore, 2020; pp. 235–260. [CrossRef]
145. Haque, S.; Srivastava, N.; Pal, D.B.; Alkhanani, M.F.; Almalki, A.H.; Areeshi, M.Y.; Naidu, R.; Gupta, V.K. Functional micro-biome
strategies for the bioremediation of petroleum-hydrocarbon and heavy metal contaminated soils: A review. Sci. Total Environ.
2022, 833, 155222. [CrossRef] [PubMed]
146. Lawrence, M.; Huber, W.; Pages, H.; Aboyoun, P.; Carlson, M.; Gentleman, R.; Carey, V.J. Software for computing and an-notating
genomic ranges. PLoS Comput. Biol. 2013, 9, e1003118. [CrossRef] [PubMed]
147. Zhang, W.; Li, F.; Nie, L. Integrating multiple ‘omics’ analysis for microbial biology: Application and methodologies. Microbiology
2010, 156, 287–301. [CrossRef]
148. Tripathi, M.; Singh, D.N.; Vikram, S.; Singh, V.S.; Kumar, S. Metagenomic approach towards bioprospection of novel biomolecule(s)
and environmental bioremediation. Ann. Res. Rev. Biol. 2018, 22, 1–12. [CrossRef]
149. Gaur, V.K.; Gautam, K.; Sharma, P.; Gupta, P.; Dwivedi, S.; Srivastava, J.K.; Varjani, S.; Ngo, H.H.; Kim, S.H.; Chang, J.S.; et al.
Sustainable strategies for combating hydrocarbon pollution: Special emphasis on mobil oil bioremediation. Sci. Total Environ.
2022, 832, 155083. [CrossRef]
150. Bharagava, R.N.; Purchase, D.; Saxena, G.; Mulla, S.I. Applications of metagenomics in microbial bioremediation of pollutants:
From genomics to environmental cleanup. In Microbial Diversity in the Genomic Era; Academic Press: Cambridge, MA, USA, 2019;
pp. 459–477. [CrossRef]
151. Sanghvi, G.; Thanki, A.; Pandey, S.; Singh, N.K. Engineered bacteria for bioremediation. In Bioremediation of Pollutants; Elsevier:
Amsterdam, The Netherlands, 2020; pp. 359–374. [CrossRef]
Toxics 2022, 10, 484 23 of 24
152. Vázquez-Núñez, E.; Molina-Guerrero, C.E.; Peña-Castro, J.M.; Fernández-Luqueño, F.; de la Rosa-Álvarez, M. Use of nano-
technology for the bioremediation of contaminants: A review. Processes 2020, 8, 826. [CrossRef]
153. Shukla, P. Microbial nanotechnology for bioremediation of industrial wastewater. Front. Microbiol. 2020, 11, 590631. [CrossRef]
154. Ramos, M.M.; dos Morais, E.; da Sena, I.; Lima, A.L.; de Oliveira, F.R.; de Freitas, C.M.; Fernandes, C.P.; de Carvalho, J.C.T.;
Ferreira, I.M. Silver nanoparticle from whole cells of the fungi Trichoderma spp. isolated from Brazilian Amazon. Biotechnol. Lett.
2020, 42, 833–843. [CrossRef] [PubMed]
155. Tripathi, S.; Sanjeevi, R.; Anuradha, J.; Chauhan, D.S.; Rathoure, A.K. Nano-Bioremediation: Nanotechnology and Bioremediation.
In Research Anthology on Emerging Techniques in Environmental Remediation; IGI Global: Hershey, PA, USA, 2022; pp. 135–149.
[CrossRef]
156. Nwuche, C.O.; Igbokwe, V.C.; Ajagbe, D.D.; Onwosi, C.O. Nanoparticles, Biosurfactants and Microbes in Bioremediation. In
Rhizomicrobiome Dynamics in Bioremediation; CRC Press: Boca Raton, FL, USA, 2021; pp. 162–179. [CrossRef]
157. Dangi, A.K.; Sharma, B.; Hill, R.T.; Shukla, P. Bioremediation through microbes: Systems biology and metabolic engineering
approach. Crit. Rev. Biotechnol. 2019, 39, 79–98. [CrossRef] [PubMed]
158. Sharma, M.; Sharma, S.; Mazumder, S.; Negi, R.K. Application of “OMICs” Approaches in Bioremediation. In Bioremediation:
Challenges and Advancements; Tripathi, M., Singh, D.S., Eds.; Bentham Science Publisher: Singapore, 2022; Volume 69, pp. 191–223.
[CrossRef]
159. Phale, P.S.; Mohapatra, B.; Malhotra, H.; Shah, B.A. Eco-physiological portrait of a novel Pseudomonas sp. CSV86: An ideal
host/candidate for metabolic engineering and bioremediation. Environ. Microbiol. 2022, 24, 2797–2816. [CrossRef] [PubMed]
160. Mohapatra, B.; Malhotra, H.; Saha, B.K.; Dhamale, T.; Phale, P.S. Microbial metabolism of aromatic pollutants: High-throughput
OMICS and metabolic engineering for efficient bioremediation. In Current Developments in Biotechnology and Bioengineering;
Elsevier: Amsterdam, The Netherlands, 2022; pp. 151–199. [CrossRef]
161. Techtmann, S.M.; Hazen, T.C. Metagenomics applications in environmental monitoring and bioremediation. J. Ind. Microbiol.
Biotechnol. 2016, 43, 1345–1354. [CrossRef]
162. Jaiswal, S.; Shukla, P. Alternative strategies for microbial remediation of pollutants via synthetic biology. Front. Microbiol. 2020,
11, 808. [CrossRef]
163. Chen, S.; Zhan, H. Biodegradation of synthetic pyrethroid insecticides. In Microbial Metabolism of Xenobiotic Compounds; Springer:
Singapore, 2019; pp. 229–244. [CrossRef]
164. Wang, C.; Sun, H.; Li, J.; Li, Y.; Zhang, Q. Enzyme activities during degradation of polycyclic aromatic hydrocarbons by white rot
fungus Phanerochaete chrysosporium in soils. Chemosphere 2009, 77, 733–738. [CrossRef]
165. Baker, P.; Tiroumalechetty, A.; Mohan, R. Fungal enzymes for bioremediation of xenobiotic compounds. In Recent Advancement in
White Biotechnology through Fungi; Springer: Cham, Switzerland, 2019; pp. 463–489. [CrossRef]
166. Ahsan, Z.; Kalsoom, U.; Bhatti, H.N.; Aftab, K.; Khalid, N.; Bilal, M. Enzyme-assisted bioremediation approach for synthetic dyes
and polycyclic aromatic hydrocarbons degradation. J. Basic Microbiol. 2021, 61, 960–981. [CrossRef]
167. Bosco, F.; Mollea, C. Mycoremediation in soil. In Environmental Chemistry and Recent Pollution Control Approaches; IntechOpen:
London, UK, 2019; p. 173. [CrossRef]
168. Gong, T.; Xu, X.; Dang, Y.; Kong, A.; Wu, Y.; Liang, P.; Wang, S.; Yu, H.; Xu, P.; Yang, C. An engineered Pseudomonas putida can
simultaneously degrade organophosphates, pyrethroids and carbamates. Sci. Total Environ. 2018, 628, 1258–1265. [CrossRef]
169. Siddavattam, D.; Yakkala, H.; Samantarrai, D. Lateral transfer of organophosphate degradation (opd) genes among soil bacteria:
Mode of transfer and contributions to organismal fitness. J. Genet. 2019, 98, 23. [CrossRef]
170. Sharma, B.; Shukla, P. Designing synthetic microbial communities for effectual bioremediation: A review. Biocatal. Biotransforma-
tion. 2020, 38, 405–414. [CrossRef]
171. Sharma, B.; Shukla, P. Futuristic avenues of metabolic engineering techniques in bioremediation. Biotechnol. Appl. Biochem. 2022,
69, 51–60. [CrossRef] [PubMed]
172. Romero, M.; Gallego, D.; Blaz, J.; Lechuga, A.; Martínez, J.F.; Barajas, H.R.; Hayano-Kanashiro, C.; Peimbert, M.; Cruz-Ortega, R.;
Molina-Freaner, F.E.; et al. Rhizosphere metagenomics of mine tailings colonizing plants: Assembling and selecting synthetic
bacterial communities to enhance in situ bioremediation. bioRxiv 2019, 664805. [CrossRef]
173. Che, S.; Men, Y. Synthetic microbial consortia for biosynthesis and biodegradation: Promises and challenges. J. Ind. Microbiol.
Biotechnol. 2019, 46, 1343–1358. [CrossRef] [PubMed]
174. Nikel, P.I.; de Lorenzo, V. Metabolic engineering for large-scale environmental bioremediation. Metab. Eng 2021, 13, 859–890.
[CrossRef]
175. Sharma, N.; Sodhi, K.K.; Kumar, M.; Singh, D.K. Heavy metal pollution: Insights into chromium eco-toxicity and recent
advancement in its remediation. Environ. Nanotechnol. Monit. Manag. 2021, 15, 100388. [CrossRef]
176. Sharma, I. Bioremediation techniques for polluted environment: Concept, advantages, limitations, and prospects. In Trace Metals
in the Environment—New Approaches and Recent Advances; IntechOpen: London, UK, 2020. [CrossRef]
177. Dar, A.; Naseer, A. Recent Applications of Bioremediation and Its Impact. In Hazardous Waste Management; IntechOpen: London,
UK, 2022; p. 49. [CrossRef]
178. Lee, H.; Jun, Z.; Zahra, Z. Phytoremediation: The sustainable strategy for improving indoor and outdoor air quality. Environments
2021, 8, 118. [CrossRef]
Toxics 2022, 10, 484 24 of 24
179. Kadosaki, M.; Terasawa, T.; Tanino, K.; Tatuyama, C. Exploration of highly sensitive oxide semiconductor materials to in-door-air
pollutants. IEEJ Trans. Sens. Micromach. 1999, 119, 383–389. [CrossRef]
180. Khasawneh, O.F.S.; Palaniandy, P. Occurrence and removal of pharmaceuticals in wastewater treatment plants. Process Saf.
Environ. Prot. 2021, 150, 532–556. [CrossRef]
181. Shahsavari, A.; Akbari, M. Potential of solar energy in developing countries for reducing energy-related emissions. Renew. Sustain.
Eng. Rev. 2018, 90, 275–291. [CrossRef]
182. Prasad, M.N.V. (Ed.) Transgenic Plant Technology for Remediation of Toxic Metals and Metalloids; Academic Press: Cambridge, MA,
USA, 2018. [CrossRef]
183. Kumar, R.S.; Singh, D.; Bose, S.K.; Trivedi, P.K. Biodegradation of environmental pollutant through pathways engineering and
genetically modified organisms approaches. In Microorganisms for Sustainable Environment and Health; Elsevier: Amsterdam, The
Netherlands, 2020; pp. 137–165. [CrossRef]