Abstract

The current study aimed to characterize Arthrobacter sp. Sphe3 ability to reduce Cr(VI) in suspended cell cultures as well as in immobilized form using Ca-alginate beads. Adaptation studies in the presence of 5mgL−1 Cr(VI) showed a significant increase in specific growth rate from 0.25 to 0.3h−1 and bioremoval percentage from 64% to 94% (p<0.05), whereas Arthrobacter sp. Sphe3 could tolerate up to 50mgL−1 Cr(VI). Optimization of culture conditions resulted in complete reduction of 45mgL−1 Cr(VI) at 30°C, pH 8 and 10gL−1 of glucose. High glucose concentrations helped at reducing (80±2.4)% of initial 100mgL−1 Cr(VI), whereas the bacterial strain could tolerate 850mgL−1 Cr(VI). Cr(III) formation was first evidenced by the appearance of a green insoluble precipitate in the medium. Cell biomass was successfully immobilized in Ca-alginate beads that were evaluated for their stability. Cell release was sharply decreased when 4% Na-alginate was used under non-shaking conditions. Biotransformation efficiency was enhanced when 25–50mgcellsmL−1 Na-alginate from the exponential growth phase were collected and co-encapsulated with either 1% glucose and 0.5% (NH4)2SO4, or 1% LB medium. Immobilized biocatalyst could be reused up to 6 continuous cycles in the presence of 10mgL−1 Cr(VI), but its performance was lowered at higher metal concentrations comparing with free cells that significantly maintained their reducing ability up to 300mgL−1 Cr(VI).

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