Developing a biosurfactant to attenuate arsenic contamination in mining tailings

Abstract

The present study aimed to investigate the ability of a microbial consortium to produce biosurfactant in the presence of two carbon sources and also to evaluate the efficiency of the cell-free supernatant cultures to mobilize As from naturally contaminated soil. Pseudomonas and Stenotrophomonas were the main microorganisms in the microbial consortium. The pH, the incubation time, the temperature, and the glucose and glycerol ratios in the culture medium are the main factors influencing biosurfactant production. The lowest surface tension, 30 mN.m À1 , and the higher emulsification index, 58%, were achieved at the optimum production conditions (OPC), i.e., pH 9.5, a 2.5 glucose/glycerol ratio, after three days of incubation at 25 C. The cell-free extracts containing biosurfactants were more efficient in mobilizing As than distilled water, CaCl 2 0.1 mol.L À1 ; saponin, 0.1%; or sodium dodecyl sulfate, 1% during a sequential soil-flushing procedure. The As mobilization using the supernatants containing biosurfactant was sensitive to pH. The use of OPC cell-free supernatant under alkaline conditions leads to the best-obtained results: 24.6% of As removal (678 mg.kg À1) during sequential extractions. The toxicity reduction of the column eluted solution from the first to the seventh cycle evaluated by the germination index (GI) and morphological structures of Allium cepa in the ecotoxicological assessment confirmed the efficiency of the proposed treatment. Allium cepa seeds and seedlings were sensitive in detecting As in soil and eluted solutions with short time responses to the contaminant. Seeds development increased gradually with arsenic removal. The germination index rose from 0 to 55% after soil decontamination through the proposed soil-flushing procedure.

Biochemical Recurrence in Prostate Cancer Is Associated with the Composition of Lactobacillus: Microbiome Analysis of Prostatic Tissue

“…An Illumina iSeq100 platform was used for 16S rRNA gene sequencing in keeping with a technique already described [ 43 ]. The PCR amplification of DNA was achieved using universal 16S rRNA gene primers for V4 hypervariable section following the pre-established method [ 44 , 45 ].…”