Abstract
The degradation of atrazine under different experimental conditions is monitored. H2 supplied to liquid enrichment cultures accelerated atrazine breakdown. The addition of an energy source (i.e. H2) and not the imposition of a N or a C limitation, makes the bacteria degrade the atrazine molecule. Experiments with [ethyl‐1‐14 C]‐ and [ring‐U‐14 C] atrazine indicate that, thus far, the action of the hydrogenotrophs remained restricted to the sidechains of the triazine molecule.