An Gram negative strain of S. maltophilia, indigenous to environments contaminated by Cr(VI) and identified by biochemical methods and 16S rRNA gene analysis, reduced chromate by 100%, 98–99% and 92% at concentrations in the 10–70, 80–300, and 500 mg/L range, respectively at pH 7 and temperature 37 °C. Increasing concentrations of Cr(VI) in the medium lowered the growth rate but could not be directly correlated with the amount of Cr(VI) reduced. The strain also exhibited multiple resistance to antibiotics and tolerance and resistance to various heavy metals (Ni, Zn and Cu), with the exception of Hg. Hexavalent chromium reduction was mainly associated with the soluble fraction of the cell evaluated with crude cell-free extracts. A protein of molecular weight around 25 kDa was detected on SDS-PAGE gel depending on the concentration of hexavalent chromium in the medium (0, 100 and 500 mg/L). In silico analysis in this contribution, revealed the presence of the chromate reductase gene ChrR in S. maltophilia, evidenced through a fragment of around 468 bp obtained experimentally. High Cr(VI) concentration resistance and high Cr(VI) reducing ability of the strain make it a suitable candidate for bioremediation.

In this research, the presence of microplastics was detected through a differential scanning calorimetry (DSC) analysis of three wastewater treatment plants. One of these plants applied only a preliminary treatment stage while the others applied up to a secondary treatment stage to evaluate their effectiveness. The results showed the presence of polyethylene (PE), polystyrene (PS), polypropylene (PP) and polyethylene terephthalate (PET), which were classified as fragments, fibers or granules. During the evaluation of the plants, it was determined that the preliminary treatment did not remove more than 58% of the microplastics, while the plants applying up to a secondary treatment with activated sludge achieved microplastic removal effectiveness between 90% and 96.9%.