Assessment of s-Triazine Catabolic Potential in Soil Bacterial Isolates Applying atz Genes as Functional Biomarkers

Fluorescence in situ hybridization (FISH) technique and qPCR analyses, targeting atz genes, were applied to detect the presence of simazine-degrading bacteria in an agricultural soil with a history of herbicide application. atz B-targeted bacteria detected by FISH represented 5% of total soil bacteria with potential capability to metabolize the herbicide. The soil natural attenuation capacity was confirmed in soil microcosms by measuring simazine degradation. Moreover, four bacterial strains were isolated from the soil and identified as Acinetobacter lwoffii , Pseudomonas putida , Rhizobium sp. and Pseudomonas sp. The isolates were able to grow using different s -triazine compounds and related metabolites as the sole carbon source. Growth parameters in presence of simazine were calculated using the Gompertz model. Rhizobium sp. showed the highest simazine degradation (71.2%) and mineralization (38.7%) rates, whereas the lowest values were found to A. lwoffii —50.4% of degradation and 22.4% of mineralization. Results from qPCR analyses of atz A, atz B and atz C genes revealed their presence in Rhizobium sp. and A. lwoffii , being atz B and atz C the most abundant functional genes. Rhizobium sp. showed a higher amount of the three biomarkers compared to A. lwoffii : the atz A, atz B and atz C gene copy number per microlitre were, respectively, 10 1 , 10 2 and 10 3 -fold higher in the former. Therefore the proposed molecular approaches based on the use of atz genes as biomarkers can be considered as useful tools to evaluate the presence and potential capability of degrading- s -triazines soil microorganisms.