Several studies have explored the utilization of soil microorganisms, to address the environmental issues associated with glyphosate use and enhance crop yields. In our investigation, screening on Agar plate and broth medium  Luria Bertani was carried out after isolating bacterial strains from rhizospheric agricultural soil in Mascara,  Algeria, to biodegrade glyphosate, following that by testing the Plant Growth-Promoting Rhizobacteria and evaluate the effects of glyphosate on these proprieties. Our findings indicate that five bacterial strains exhibited growth in the presence of glyphosate concentrations up to 25 mg/ml, beyond this concentration the strains have developed tolerance. Following a partial examination of the 16S rRNA sequences, the bacterial strains were identified as belonging to the genus of Enterobacter. After 10 days of incubation with the glyphosate, Phosphate solubilization decreased in broth and agar Pikovskaya medium and the bacterial strains synthetized less of indole-3-acetic acid compared to the control, indicating the impact of glyphosate on these outcomes, high concentration of glyphosate inhibited nitrogen fixation, and various doses of glyphosate were found to restrict the growth of biofilms in these strains. The results of HPLC examination of secondary metabolites revealed that the primary degradation products of glyphosate in all strains were Sarcosine and Glycine. So, it seemed that the strain could both biodegrade glyphosate and use it for growth ,while also possessing rhizobacteria properties that promote plant development, enabling the use of the strains in the bioremediation of glyphosate-contaminated soils.

In this study, a strain of lactic acid bacteria Streptococcus salivarius was studied for its capacity to remove hexavalent chromium (Cr (VI)) from a liquid medium and to form biofilm. Both properties are useful for using the strain in bioremediation of metal-contaminated effluents. For biofilm formation capacity, three methods were used: the tube method (TM), the Congo red agar method (CRA) and adherence to polystyrene tissue culture plate method (TCP). S. salivarius, showed a positive-biofilm and a correlation between the three methods was noted. The bacterial surface hydrophobicity was studied using the microbial adhesion to solvents method (MATS). On AISI-316 L stainless steel, the strain with a hydrophobic surface showed a good adhesion on this support after 18 h incubation. The colonization of the supports and the biofilms formation by the bacterial cell was observed using scanning electron microscopy (SEM). The minimum inhibitory concentration (MIC) of Cr(VI) on S. salivarius was determined on MRS broth, it was relatively high and equal to 400mg/l. In addition, it displayed a remarkable capacity to reduce Cr(VI) concentration on the liquid medium containing initially 50 mg/l of Cr(VI) ; the percent removal rate was equal to approximately 42% after 72 h of incubation at 37 °C. In addition to its GRAS status, the obtained results suggested that S. salivarius could be successfully used in Cr(VI) bioremediation.