Evaluating formulation and storage of Arthrobacter aurescens strain TC1 as a bioremediation tool for terbuthylazine contaminated soils: Efficacy on abatement of aquatic ecotoxicity

Recently, a bioremediation tool consisting of freshly grown cells of the Arthrobacter aurescens strain TC1 proved successful in the cleanup of terbuthylazine (TBA) contaminated soil, with potential to prevent TBA dispersal via the soil-water pathway. The present work aimed at examining the feasibility of preparing and formulating bioaugmentation bacterial cells in advance which retain adequate viability and herbicide-degrading activity during storage and transport to contaminated sites. Three different types of formulation of A. aurescens TC1 cells were performed, namely cell paste, lyophilized, and adsorbed onto the mineral carrier vermiculite. Vermiculite-based cell material and cell paste offered survival rates significantly higher (>= 78% of cells recovered viable, when compared to the initial numbers) than lyophilized cells (>= 65%) after storage at 4 degrees C for up to a maximum period of 30 days. Inocula prepared from the three types of formulated and stored cells supported adequate levels of herbicide-biodegradation activity, ultimately allowing an almost complete removal of TBA from either liquid buffer or soil. In soil microcosms, the efficacy of bioremediation of TBA-contaminated soil in terms of decontamination (%) based on the ecotoxicity assessment of soil eluates towards a freshwater microalga was found to differ within formulations in the order: lyophilized cells (similar to 100% efficacy at the end of one or two weeks of bioremediation treatment with an initial inoculum of similar to 2.5 x 10(7) viable cells/g of soil; similar to fresh cells) > vermiculite-adsorbed cells (81% with similar to 2.4 x 10(8) cells/g) > cell paste (68% with similar to 2.4 x 10(8) cells/g). The limitations and advantages of each type of bacterial formulation, together with the prediction of their applicability in the field are discussed. (C) 2019 Elsevier B.V. All rights reserved.