<abstract xmlns="http://www.w3.org/1999/xhtml"> Microbes play significant roles in remediation of heavy metal polluted industrial effluent using the mechanisms of biosorption and bioaccumulation. In the present study, six heavy metal resistant autochthonous bacteria species namely Bacillus cereus, B. megaterium, B. subtilis, Flavobacterium aquatile, Pseudomonas flourescens and Pseudomonas putida were isolated from effluent samples collected from Paper-mill industry (PMI), Paints and Chemicals Industry (PCI), and Steel-rolling Industry (SRI). The isolates were studied for their heavy metal tolerant capacities at different aqueous salt concentrations. Elemental analysis of the industrial effluent samples collected indicated the presence of heavy metals such as Copper (Cu2+), Manganese (Mn2+), Iron (Fe2+) and Lead (Pb2+) at varying concentrations in μg/ml. Generally, there were variations in the minimum inhibitory concentrations (MIC) of the heavy metal salt to each of the bacteria understudy. The MIC value of each of the bacterial isolates to aqueous solution of Cu2SO4 showed that B. megaterium, B. subtilis, Pseudomonas flourescens and Pseudomonas putida had the same MIC value of 20 ± 1.5 μg/mL while Bacillus cereus and Flavobacterium aquatile had MIC values of 13 ± 1.3 μg/mL and 25 ± 2.1 μg/mL respectively. This variation was also noticeable in aqueous salts of Mn2SO4, Fe2SO4 and Pb2SO4. The bacteria isolates showed sensitivity to heavy metals with increasing zone of inhibition as concentration increased with each isolate showing varying degree of metalotolerance. The effectiveness of the autochthonous bacteria as a means to bio-augment the remediation of heavy metal polluted industrial effluent was further proven and recommended.</abstract>

Metalotolerance Capacity of Autochthonous Bacteria Isolated From Industrial Waste Effluent

<abstract xmlns="http://www.w3.org/1999/xhtml"> Kinetics of oxidation of Lysine (Lys) and mechanisms by μ-peroxo bis[bis(ethylenediamine)succinimidato-dicobalt(III)]dinitratedihydrate; [LCo(μ-O2)CoL](NO3)2.2H2O (L = suc(en)2), hereafter the complex, was investigated at 420 nm wavelength of maximum absorption of the complex under the conditions hydrogen ions concentration = 1.8 × 10-2 mol dm-3, temperature = 24 ± 1 °C, [LCo(μ-O2)CoL2+] = 1.4 × 10-4 mol dm-3 and ionic strength = 0.5 mol dm-3. First order in [LCo(μ- O2)CoL2+] and [Lys] were obtained but inverse first order in [H+]. The proposed overall rate equation is as shown: Rate of the reaction decreases when hydrogen ions concentration increase and exhibited converse effect with increase in concentration of ionic strength from 0.1 - 1.3 mol dm-3. Added cations and anions affected the reaction rate and the Michaelis-Menten plot passed through the origin indicating no absence of intermediate complex in the electron transfer processes. Putting all the results obtained together, the most probable reaction mechanism is in favour of outer-sphere and an appropriate rate law is established using steady state approximation.</abstract>

The Kinetics of the Oxidation of Lysine by μ-Peroxo-Bridged Binuclear Cobalt (III) Complex of Succinimide in Aqueous Hydrochloric Acid Medium

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Metalotolerance Capacity of Autochthonous Bacteria Isolated From Industrial Waste Effluent

The Kinetics of the Oxidation of Lysine by μ-Peroxo-Bridged Binuclear Cobalt (III) Complex of Succinimide in Aqueous Hydrochloric Acid Medium

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