Molybdate-reducing and SDS-degrading Enterobacter sp. Strain Neni-13

Abstract

AbstractToxicants removal through microorganism’s action is intensely being sought due to economic reasons. The aim of this paper is to isolate a bacterium that is able to reduce molybdenum blue and at the same time can grow on the detergent Sodium Dodecyl Sulfate (SDS). Biochemical analysis resulted in a tentative identification of the bacterium asEnterobactersp. strain Neni-13. Growth on SDS showed a 100 % removal at 800 mg/L SDS within 12 days. The removal of SDS from media was confirmed through Methylene Blue Active Substances Assay. Molybdenum reduction using sodium molybdate as a substrate was characterized using a microplate assay. The optimum pH and temperature for molybdenum reduction was between 6.0 and 6.5, and at 37 °C, respectively. Glucose was the best electron donor for molybdate reduction. Phosphate and molybdate concentrations of between 2.5 and 5.0 mM and at 15 mM, were optimal for molybdate reduction, respectively. Molybdate reduction was inhibited by the heavy metals mercury, silver, copper and chromium at 2 ppm. The ability of this bacterium to detoxify molybdate and degrade the SDS makes this bacterium an important tool for bioremediation of toxicants in soil.