Bacteria with dual resistance to elevated concentrations of heavy metals and antibiotics in Nigerian contaminated systems

Samples of soil, water, and sediments from industrial estates in Lagos were collected and analyzed for heavy metals and physicochemical composition. Bacteria that are resistant to elevated concentrations of metals (Cd^2?+?, Co^2?+?, Ni^2?+?, Cr^6?+?, and Hg^2?+?) were isolated from the samples, and they were further screened for antibiotic sensitivity. The minimum tolerance concentrations (MTCs) of the isolates with dual resistance to the metals were determined. The physicochemistry of all the samples indicated were heavily polluted. Twenty-two of the 270 bacterial strains isolated showed dual resistances to antibiotics and heavy metals. The MTCs of isolates to the metals were 14 mM for Cd^2?+?, 15 mM for Co^2?+? and Ni^2?+?, 17 mM for Cr^6?+?, and 10 mM for Hg^2?+?. Five strains (Pseudomonas aeruginosa, Actinomyces turicensis, Acinetobacter junni, Nocardia sp., and Micrococcus sp.) resisted all the 18 antibiotics tested. Whereas Rhodococcus sp. and Micrococcus sp. resisted 15 mM Ni^2?+?, P. aeruginosa resisted 10 mM Co^2?+?. To our knowledge, there has not been any report of bacterial strains resisting such high doses of metals coupled with wide range of antibiotics. Therefore, dual expressions of antibiotics and heavy-metal resistance make the isolates, potential seeds for decommissioning of sites polluted with industrial effluents rich in heavy metals, since the bacteria will be able to withstand in situ antibiosis that may prevail in such ecosystems.     

Synthesis of zinc-carboxylate metal-organic frameworks for the removal of emerging drug contaminant (amodiaquine) from aqueous solution

We herein report the removal of amodiaquine, an emerging drug contaminant from aqueous solution using [Zn2(fum)2(bpy)] and [Zn4 O(bdc)3](fum = fumaric acid; bpy =4,4-bipyridine; bdc = benzene-1,4-dicarboxylate) metal–organic frameworks(MOFs) as adsorbents. The adsorbents were characterized by elemental analysis, Fourier transform infrared(FT-IR) spectroscopy, and powder X-ray diffraction(PXRD). Adsorption process for both adsorbents were found to follow the pseudo-first-order kinetics, and the adsorption equilibrium data fitted best into the Freundlich isotherm with the R~2 values of 0.973 and0.993 obtained for [Zn_2(fum)_2(bpy)] and [Zn_4 O(bdc)_3] respectively. The maximum adsorption capacities foramodiaquine in this study were found to be 0.478 and 47.62 mg/g on the[Zn_2(fum)_2(bpy)] and [Zn_4 O(bdc)_3] MOFs respectively, and were obtained at p H of 4.3 for both adsorbents. FT-IR spectroscopy analysis of the MOFs after the adsorption process showed the presence of the drug. The results of the study showed that the prepared MOFs could be used for the removal of amodiaquine from wastewater.     

Flame ionization gas chromatographic determination of phthalate esters in water, surface sediments and fish species in the Ogun river catchments, Ketu, Lagos, Nigeria

The detection and quantification of four phthalate esters??dimethyl phthalate (DMP), diethyl phthalate (DEP), dibutyl phthalate (DBP), and diethylhexyl phthalate (DEHP)??in water, sediment, and some fish species were carried out using flame ionization gas chromatography. The samples were collected from the Ogun river catchments, Ketu, Lagos. The DMP was not detected in the water and fish samples but was detected in sediments collected from four of the six sampling sites. The concentration of DEP, DBP, and DEHP in the fish species ranged from 320.0?C810.0, 380.0?C1,080.0, and 40.0?C150.0 ??g/kg in Tilapia sp.; 310.0?C860.0, 400.0?C1,170.0, and 40.0?C110.0 ??g/kg in Chrysichthys sp.; and 320.0?C810.0, 400.0?C3,970.0, and 30.0?C300.0 ??g/kg (DEHP) in Synodontis sp., respectively. The differences in fish phthalate levels are not statistically significant at p?<?0.05, an indication that phthalate esters accumulation is not fish species dependent. The DEP, DBP, and DEHP values recorded are considerably higher than the maximum allowed concentrations for drinking water prescribed by the US Environmental Protection Agency. The phthalate pollution index and biosediment accumulation factor values were also calculated.     

Effects of Polluting Soil with Cassava Mill Effluent on the Bacteria and Fungi Populations of a Soil Cultivated with Maize

The study was carried out to investigate the effects of application of cassava mill effluent on bacteria and fungi types and population in a soil grown to maize (Zea Mays L.) Microbial populations were determined before pollution of soil with cassava mill effluent, six weeks after pollution with effluent and at the end of the experiment. Results obtained showed that bacteria and fungi populations increased with time as rates of pollution increased. It was also observed that some bacteria present in the soil at the beginning of the experiment and up to the sixth week after pollution with effluent became extinct at the end of the experiment.     

Efficiency of cassava steep liquor for bioremediation of diesel oil-contaminated tropical agricultural soil

Soil artificially contaminated with diesel oil, treated with cassava steep liquor (CSL) and designated EXPS. Similar polluted soil without CSL amendment (CSS1) and uncontaminated soil (CSS2) served as controls. There were dramatic changes in the physico-chemistry of systems EXPS and CSS1 with utilization of the inorganic nutrients to near-depletion in the former than the latter. In contrast, the properties of CSS2 remained relatively stable throughout the investigated period. Similarly, the population densities of microflora in the polluted soils showed an initial decrease between days 0 and 5 before assuming an increasing trend with percent hydrocarbon-utilizers ranging significantly (P < 0.05) from 0.56 to 6.6, 0.1 to 2.46 and 0.56 to 0.26, respectively for EXPS, CSS1, and CSS2. In EXPS, the residual oil decreased from 98,045 to 1,102.3 mg/kg soil at day 35 representing about 98.88% degradation. The corresponding value for CSS1 was 98,106.1 to 52,110 mg/kg soil, amounting to 46.88% oil disappearance. The GC fingerprints of alkane fractions of the recovered oil reduced significantly by day 15 for EXPS with near-similar results of CSS1. However, by day 35, there was complete disappearance of all peaks including the pristane and phytane molecules in the former whereas in CSS1, there were no observable changes. The germination and growth profiles of maize seed plants as evidence of recovery of oil-impacted soils were poor in CSS1 (10%) with pronounced abnormal morphology when compared with the data obtained for EXPS (74%) and CSS2 (80%). These results suggest that CSL could be an indispensable tool in bioremediation of environments contaminated with hydrocarbons. The technology of application is simple, rapid and cost-effective and may be appropriate for use in developing countries to ameliorate the problems of petroleum pollution.     

Chromium (VI) biosorption properties of multiple resistant bacteria isolated from industrial sewerage

Chromium (VI) [Cr (VI)] biosorption by four resistant autochthonous bacterial strains was investigated to determine their potential for use in sustainable marine water-pollution control. Maximum exchange between Cr (VI) ions and protons on the cells surfaces were at 30–35 °C, pH?2.0 and 350–450 mg/L. The bacterial strains effectively removed 79.0–90.5 % Cr (VI) ions from solution. Furthermore, 85.3–93.0 % of Cr (VI) ions were regenerated from the biomasses, and 83.4–91.7 % of the metal was adsorbed when the biomasses was reused. Langmuir isotherm performed better than Freundlich isotherm, depicting that Cr (VI) affinity was in the sequence Rhodococcus sp. AL03Ni?>?Burkholderia cepacia AL96Co?>?Corynebacterium kutscheri FL108Hg?>?Pseudomonas aeruginosa CA207Ni. Biosorption isotherms confirmed that Rhodococcus sp. AL03Ni was a better biosorbent with a maximum uptake of 107.46 mg of Cr (VI) per g (dry weight) of biomass. The results highlight the high potential of the organisms for bacteria-based detoxification of Cr (VI) via biosorption.     

Differential degradation of crude oil （Bonny Light） by four Pseudomonas strains

Four hydrocarbon degraders isolated from enriched oil- and asphalt-contaminated soils in Lagos, Nigeria, were tested for their petroleum degradation potentials. All the isolates were identified as species of Pseudomonas. Pseudomonas putida P11 demonstrated a strong ability to degrade kerosene, gasoline, diesel, engine oil and crude oil while P. aeruginosa BB3 exhibited fair degradative ability on crude oil, gasoline, engine oil, anthracene and pyrene but weak on kerosene, diesel and dibenzothiophene. Pseudomonas putida WL2 and P. aeruginosa MVL1 grew on crude oil and all its cuts tested with the latter possessing similar polycyclic aromatic potentials as P11. All the strains grew logarithmically with 1–2 orders of magnitude and with generation time ranging significantly between 3.07 and 8.55 d at 0.05 level of confidence. Strains WL2 and MVL1 utilized the oil substrate best with more than 70% in 6 d experimental period, whereas the same feat was achieved by P11 in 12 d period. BB3 on the other hand degraded only 46% within 6 d. Interestingly, data obtained from gas chromatographic analysis of oil recovered from the culture fluids of MVL1 confirmed near-disappearance of major peaks (including aliphatics and aromatics) in the hydrocarbon mixture.     

Total petroleum hydrocarbons and trace heavy metals in roadside soils along the Lagos–Badagry expressway, Nigeria

This study reports the level of total petroleum hydrocarbons (TPH) and trace heavy metals (lead, copper, and cadmium) in soil samples collected randomly from Iyana–Iba garage, Lagos State University bus stop, Adeniran Ogunsanya College of Education bus stop, and a control site off Lusada–Atan road, near Crawford University, Igbesa, Ogun state. TPH was estimated gravimetrically after Soxhlet extraction and column clean up, while soil metals were determined by atomic absorption spectrometry using mineral acid digestion. For TPH, the sites have mean values of 19.43 ± 1.27, 16.11 ± 1.85, and 11.43 ± 4.33 mg/g with a control mean value of 0.33 ± 0.16 mg/g. For trace heavy metals, cadmium was not detected. However, the mean levels of lead are 4.24 ± 3.10, 3.72 ± 0.60, and 3.70 ± 1.32 μg/g, respectively, whereas mean copper concentrations are 20.63 ± 9.02, 19.35 ± 3.61, and 16.76 ± 3.02 μg/g in all sites, respectively, compared to the control mean of 0.25 ± 0.13 and 5.99 ± 1.23 μg/g for lead and copper, respectively. Sites studied have higher levels of TPH and metals compared to the control soil samples. This is indicated by a statistically significant difference found between the concentration of analyzed elements in soils collected along Lagos–Badagry expressway and the control site.     

Pseudomonas sp. (Strain 10–1B): A potential inoculum candidate for green and sustainable remediation

Soil pollution caused by polycyclic aromatic hydrocarbons (PAHs) is a consequence of various industrial processes which destabilizes the ecosystem. Bioremediation by bacteria is a cost‐effective and environmentally safe solution for reducing or eliminating pollutants in soils. In the present study, we artificially polluted agricultural soil with used automobile engine oil with a high PAH content and then isolated bacteria from the soil after 10 weeks. Pseudomonas sp. strain 10–1B was isolated from the bacterial community that endured this artificial pollution. We sequenced its genomic DNA on Illumina MiSeq sequencer and evaluated its ability to solubilize phosphate, fix atmospheric nitrogen, and produce indoleacetic acid, in vitro, to ascertain its potential for contribution to soil fertility. Its genome annotation predicted several dioxygenases, reductases, ferredoxin, and Rieske proteins important in the ring hydroxylation initiating PAH degradation. The strain was positive for the soil fertility attributes evaluated. Such combination of attributes is important for any potential bacterium partaking in sustainable bioremediation of PAH‐polluted soil.