Persistent pollution of surface waters by hydrocarbon compounds is one of the foremost threats to limited global freshwater resources. This study analyzed the abundance, diversity and degradative capacities of hydrocarbon-utilizing bacteria in chronically polluted Kono River in the Nigerian Niger Delta in order to establish the bacterial drivers of ecological regeneration of the river after an oil spill. The study further aimed to develop a specialized bacterial consortium for application in bioremediation interventions. Bacillus, Pseudomonas and Enterobacter spp. were predominant out of the 82 isolates obtained. Klebsiella pneumoniae and two species of Enterobacter cloacae were identified as the most efficient hydrocarbon utilizers. The isolates were also confirmed as biosurfactant producers and possessed the alkB1 and nahAc genes for degradation of aliphatics and aromatics. E. cloacae-K11, K. pneumoniae-K05, E. cloacae-K12 and their consortium were able to degrade the total petroleum hydrocarbons and polycyclic aromatic hydrocarbons in batch systems by 59.37% – 96.06% and 68.40% – 92.46% respectively. K. pneumoniae-K05 showed the greatest petroleum degradation capacity of the three isolates but hydrocarbon degradation was most efficient with the bacterial consortium. The results obtained showed no significant differences at p≤0.05 between the degradation capacities of K. pneumoniae-K05 and the consortium for PAHs but a significant difference (p≤0.05) was seen with TPH degradation. A viable hydrocarbon degrading bacterial consortium was developed at the end of the study and it was concluded that the polluted river water displayed inherent potential for effective natural attenuation.

Consumption of polythene is unavoidable in this era and it is increasing day by day. Polythene’s hazardous waste is adversely effecting environment. In fact any form of polythene is a nuisance to the environment because of strong resistance against degradation thus; they remain in nature for a very long time. Biodegradation is the only promising solution to overcome this problem.  Fungi, a group of saprophytic organisms are evolved to adapt for almost every environment, specially marine and freshwater source. This property drives fungi to grown on polythene even in adverse environment. So, present study was planned to compare biological degradation of low density polythene [LDPE] and biodegradable polythene by potential fungus to find out an eco-friendly and economic solution of polythene waste. Ten fungal strains were isolated from rotting polythene debris those are Penicillium chrysogenum, Rhizopus nigricans, Chaetomium murorum, Memnoniella echinata, Aspergillus fumigatus, Stachybotrys chartarum, Aspergillus niger, Chaetomium globosum, Aspergillus flavus and Fusarium oxysporum, in which Penicillium chrysogenum, Rhizopus nigricans, Aspergillus fumigatus, Aspergillus niger and Aspergillus flavus showed greatest results in terms of degrading both Low density polythene and biodegradable polythene. These isolates also showed good enzymatic reaction and weight loss. SEM analysis of polythene surface was also in support of these findings.

The term bioremediation describes biological machinery of recycling wastes to make them harmless and useful to some extent. Bioremediation is the most proficient tool to manage the polluted environment and recover contaminated river water.  Bioremediation is very much involved in the degradation, eradication, restriction, or reclamation varied chemical and physical hazardous substances from the nearby with the action of all-inclusive microorganisms. The fundamental principle of bioremediation is disintegrating and transmuting pollutants such as hydrocarbons, oil, heavy metal, pesticides and so on. Different microbes like aerobic, anaerobic, fungi and algae are incorporated in bioremediation process. At present, several methods and approaches like bio stimulation, bio augmentation, and monitoring natural recovery are common and functional in different sites around the world for treating contaminated river water. However, all bioremediation procedures it has its own pros and cons due to its own unambiguous application. Above all, utilization of bioremediation paving a minimal inconsiderably contaminated, healthy as well as safe and sound future.

Petroleum-polluted soil samples from Ahvaz oilfield were enriched, using three methods to detect microorganisms with different dibenzothiophene degradation capabilities. Strain NISOC-03, a nitrate-reducing, oxidase negative, catalase, citrate, and urease positive, gram negative rod, showed interesting dibenzothiophene desulfurization behavior, designated as Entreobacter sp. strain NISOC-03 based on phenotype and genotype analyses. Gas chromatography, biomass measurement, and Gibb’s assay showed that in the presence of benzoate as the carbon source, strain NISOC-03 utilized 64% of 0.8 mM dibenzothiophene, producing 0.27 mM phenyl phenol during the exponential growth phase, though the produced phenyl phenol was degraded in the stationary growth phase. In the presence of glucose as the carbon source, however, strain NISOC-03 metabolized only 19.6% of 0.8 mM dibenzothiophene. Furthermore, replacing glucose with ethanol or glycerol led to the same reduction of the dibenzothiophene utilization. It is thus concluded that the chemistry of the potential carbon source(s) in the culture medium has a significant influence on the quality and the rate of dibenzothiophene metablization, and the enrichment designation has a very vital effect on the biodegradation efficiency of the isolated microorganisms.

Environmental threats from the accumulation of plastic trash are getting worse.  It is robust, lightweight, corrosion-resistant, affordable, and durable. Microorganisms play a significant role in protecting our environment by degrading plastic wastes that are harmful either naturally or by chemical modification.  The current study aims to investigate the biodegradation of synthetic polyethylene through the utilization of a laboratory bioreactor. Various types of additives were introduced to the soil samples before subjecting them to a 30-day UV treatment. The degradation of polyethylene was shown through a reduction in weight following a 24-week incubation period with certain bacterial strains. Experimental findings have revealed that models subjected to UV radiation exhibit the highest degree of vulnerability and degradation. Approximately 52% of polyethylene (PE) films underwent degradation when exposed to soil enhanced with peat moss. In contrast, only 40% and 45% of PE films were destroyed when subjected to garden soil that was untreated and treated with UV radiation, respectively. In contrast, the addition of husk resulted in a 48% to 53% reduction in weight for PE films that were buried for the same duration of the experiment.  The highest level of effectiveness was achieved by the disintegration of the plastic material that was introduced into the soil along with organic fertilizers, resulting in a value of 56.60%. The weight loss outcomes have been substantiated by the utilization of the Atomic Force Electron Microscope (AFM) images, which exhibited the highest magnitude in the experimental model using soil supplemented with fertilizers.

Plastic pollution is a threat to the environment because of its slow degradation rate and high usage. The aim of this study is to isolate plastic degrading microorganisms from soils. The soil samples used for this study were collected from dumpsites filled with plastic and plastic materials and the effectiveness of the degradation of plastic materials was studied over a period of six (6) weeks in broth and agar culture under laboratory conditions by weight determination method. Physicochemical and microbiological analysis was carried out on the various soil samples using standard protocols. The biodegradation of polyvinylchloride (PVC) was done in-vitro using the microorganisms isolated from the soil. Microorganisms that were able to degrade a higher percentage of the plastic materials were; Staphylococcus aureus, Streptococcus sp, Bacillus sp, Escherichia coli Aspergillus niger, Aspergillus flavus and Trichoderma viridae. The total viable count for bacteria and fungi were within the range of 11.8x105 CFU/g to 2.0x1010 CFU/g and 3.3x105 CFU/g to 0.1x1011 CFU/g respectively. Staphylococcus aureus, Streptococcus sp, Bacillus sp, Micrococcus sp, Aspergillus niger, Aspergillus flavus, and Trichoderma viridae, degraded plastic up to 25%, 31.2%, 25% 31.2%, 12%, 10% and 10% respectively. These isolates may be used to actively degrade plastics, thereby reducing the rate of plastic pollution in our ecosystem.

Flourene and phenanthrene are organic compounds with high hydrophobicity and toxicity. Being recalcitrant in nature they are accumulating in the environment at an alarming concentration, posing serious threat to living beings. Thus in the present study, microorganisms were screened for their ability to degrade these contaminants at high concentrations in least period of time. Two out of fifteen isolates screened showed growth in basal medium containing 25 mg/l of fluorene/phenanthrene as the only carbon source. These selected isolates were acclimatised with step wise increased concentrations of flourene/phenanthrene for 165 days in basal medium. The acclimatised strains were identified and characterised on the basis of their morphological and biochemical characteristics and 16S rRNA gene sequence analysis. Results showed close relatedness of the isolates to Pseudomonas aeruginosa sp. and Bacillus safensis sp. Biodegradation studies carried out with these acclimatised strains at optimum conditions (pH 7 and temperature 30°C) showed 62.44% degradation of fluorene and 54.21% of phenanthrene in 10 days by Pseudomonas sp. VB92, whereas, Bacillus sp. JK17 degraded 43.64% of fluorene and 59.91% of phenanthrene in 12 days, at an initial concentration of 200 mg/l, as determined by HPTLC. During fluorene degradation by Pseudomonas sp. VB92, one metabolite was identified as fluorene,1,4-dihydro. An anionic biosurfactant (emulsification index of 80%) produced by strain VB92 during growth with PAHs, improved its degradation rate. This showed strong potential of the acclimatised strains for bioremediation and reclamation of polyaromatic hydrocarbon contaminated sites.

The present study has used soil samples from Nigeria, contaminated with Brass crude-oil, to determine its biodegradation through enhanced biostimulation with cow dung and periodic aeration. Over a period of twenty-eight days, the hydrocarbon-utilizing bacteria (HUB) and hydrocarbon-utilizing fungi (HUF) have been counted and identified. Results from biodegradation of the brass crude-oil over the aforementioned period show that amended crude-oil-spiked soil has had 54.82% degradation while for amendment and periodic turning this has been 55.90%, not significantly higher than the former at p≤0.05. Also degradation of spiked soil without cow dung amendment has been 16.13%. The identified HUB are Staphylococcus aureus, Pseudomonas aeruginosa, Bacillus subtilis, and Streptococcus thermophillus, with individual occurrence of 18.52% as well as Proteus vulgaris and Micrococcus luteus with 11.11% and 14.81% occurrence, respectively. Also, the occurrence rate of HUF like Aspergillus flavus, A. niger, Penicillium chrysogenum, Trichothecium roseum, and Penicillium citrinum have been 15.63% each;whilefor Alternaria alternata and Neurospora crazza it has been 6.25% and for Saccharomyces cerevisae and A. fumigatus, 9.38%and3.13%, respectively. The study concludes that amendment with cow dung and periodic turning of the soil enhance degradation of Brass crude-oil significantly. What is more, aeration by periodic turning slightly improves degradation only with cow dung treatment on Days 21 and 28.

Petroleum hydrocarbon contamination is a major global prevalent issue in the petroleum sector. This research focuses on evaluating biodegradation of three Gram-negative bacilli, isolated from cowpea planted soil, contaminated with kerosene. The Gram negative bacilli strains have been characterized and identified, using MicrobactTM ID24E systems for the identification of Enterobacteriaceae and common Miscellaneous Gram-Negative Bacilli (MGNB). The identified organisms include Aeromonas hydrophila, Vibrio parahaemolyticus, and Actinobacillus sp. with the biodegradation indices, monitored for the evaluation of their degrading abilities, being Optical density at 600 nm (OD600nm), pH, and emulsification stability. The chemical profile of single cultures and mixed cultures (consortia) on the jet fuel hydrocarbon has been determined by means of Gas Chromatography Mass Spectrometry (GC-MS), the results of which indicate that all the isolates have undergone above 70% reduction of the hydrocarbon substrates in terms of residual compounds. There has been 48 hydrocarbon compounds in the undegraded jet fuel which, following degradation process, decrease to 5, 13, 7, 10, 6, 9, and 10 compounds for Aeromonas hydrophila, Vibrio parahaemolyticus, Actinobacillus sp., Aeromonas hydrophila and Vibrio parahaemolyticus, Aeromonas hydrophila and Actinobacillus sp., Vibrio parahaemolyticus and Actinobacillus sp., Aeromonas hydrophila, Vibrio parahaemolyticus,and Actinobacillus sp., respectively. The degradation efficiency of the isolates have been relatively high and comparable to the control. Results from this study indicate that all the strains, especially the consortia, are potential candidates for remediating the problem of hydrocarbon contamination in the environment.

Petroleum refining industries produce large amounts of toxic effluents, causing environmental pollution. Iran is an oil-rich country that encounters oil pollution in its soil and water. Bioremediation of these pollutants is an appropriate solution to tackle them, compared to physical and chemical remediation methods. There are some factors that increase the rate of biodegradation; therefore, this study aims to determine the rate of gasoil bioremediation by two indigenous bacterial isolates (from oil-contaminated soils of an oil refinery south of Tehran) in two different media, namely soil and soil-sawdust mixture. The two superior indigenous bacteria has been isolated through three steps with results indicating that in an optimal environmental condition (temperature= 27±2 °C, humidity of 60%, water holding capacity, and daily manual aeration), bacterial isolates are able to degrade about 78.87% and 93.53% of gasoil during 45 days in soil and soil-sawdust mixture media, respectively. These results imply the role of sawdust in improving aeration, water holding capacity, and-consequently- increasing bioavailability of gasoil to bacteria.