This report is based on the investigation of the effect of temperature on the removal of Pb 2+ and Cd 2+ in aqueous effluent using C. bicolor biomass in a batch sorption process. The result showed that the most suitable sorption temperature was 40ºC with maximum sorption capacities of 49.02 mg/g and 52.63 mg/g for Pb 2+ and Cd 2+ respectively. Various thermodynamic parameters, such as ∆G o , ∆H o , ∆S o and E a have been calculated. The data showed that the sorption process is spontaneous and exothermic in nature and that lower solution temperatures favours metal ion removal by the biomass. The findings of this investigation suggest that physical sorption plays a role in controlling the sorption rate. The sticking probability model was further employed to assess the applicability of the C. bicolor biomass as an alternative adsorbent for metal ion contaminants in aqueous system.

Alkylating treatments predominantly induce G: C = greater than A:T transitions, consistent with the predicted significance of the miscoding potential of the O6-alG lesion. However, the frequency and distribution of these events induced by any one compound may be diagnostic. SN1 agents that act via an alkyldiazonium cation, such as the N-nitroso compounds, preferentially generate G: C = greater than A:T transitions at 5'-RG-3' sites, while the more SN2 alkylsulfates and alkylalkane-sulfonates do not. The precise nature of this site bias and the possibility of strand bias are target dependent. The extent of this site bias and the contribution of other base substitutions are substituent size dependent. A similar 5'-RT-3' effect is seen for A:T = greater than G:C transitions, presumably directed by O4-alT lesions. The 5'-RG-3' effect, at least, likely reflects a deposition specificity arising from some aspect of helix geometry, although it may be further exaggerated by alkylation-specific repair. Excision repair appears to preferentially reduce the occurrence of ethylation-induced G:C = greater than A:T and A:T = greater than G:C transitions at sites flanked by A:T base pairs. This may be due to an enhancement of the helical distortion imposed by damage at such positions. A similar effect is not seen for methylation-induced mutations and in the case of propyl adducts, the influence of excision repair on the ultimate distribution of mutation cannot be as easily defined with respect to neighbouring sequence.

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