4.6 Article

Mechanistic studies on the bioremediation of Cr(VI) using Sphingopyxis macrogoltabida SUK2c, a Cr(VI) tolerant bacterial isolate

Journal

BIOCHEMICAL ENGINEERING JOURNAL
Volume 150, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.bej.2019.107292

Keywords

Bioremediation; Cr(VT); Sphingopyxis macrogoltabida SUK2c; Biosorption; Cr(III); Bioreduction

Funding

  1. Indo-French Centre for the Promotion of Advanced Research (CEFIPRA) [5409-1]
  2. Institute of Research for Development (IRD), France
  3. Ministry of Human Resource Development (MHRD), Government of India

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Bioremediation studies of toxic hexavalent chromium (Cr(VI)) were investigated using an indigenous bacterial strain namely, Sphingopyxis macrogoltabida SUK2c, isolated from water samples collected from the Sukinda Valley in Odisha, India. A maximum Cr(VI) biosorption of about 55% could be achieved using the isolate for an initial Cr(VI) concentration of 4 mg L-1. The Cr(VI) biosorption isotherm was found to follow a typical Langmuirian behaviour. The Gibbs free energy value of Cr(VI) biosorption obtained was -25.6 kJ/mol, indicative of the involvement of chemical binding forces. The Cr(VI) biosorption process followed pseudo second order kinetics. FTIR spectral studies revealed that carboxyl, hydroxyl, amino and phosphate groups present on bacterial surface were involved in the complexation process. XPS studies confirmed the involvement of Cr(III) in addition to Cr(VI) ions with the bacterial cell surface. Zeta potential studies showed that the bacterial cells became less negative after interaction with Cr(VI), which further corroborated the binding of positively charged Cr(III) on the cell surface. The marginal shift in iso-electric point for Cr(VI) interacted bacteria further testified to the involvement of chemical binding forces in the bioremediation process. The results of the chromate reductase and Bradford protein assay tests performed on the extracellular component of the isolate also confirmed the involvement of extracellular protein in the reduction of Cr(VI) to Cr(III).

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