Mixtures of Pseudomonas putida CECT 5279 cells of different ages: Optimization as biodesulfurization catalyst

Sulfur content in fossil fuels is known to be the most important anthropogenic cause of sulfur oxide emissions to the atmosphere. In order to avoid health, environmental and technical problems caused by this compound, legislation imposes restrictive limitations to fuel sulfur content. Biodesulfurization (BDS) can become a complementary technology to hydrodesulfurization (HDS) to face this situation. Pseudomonas putida CECT 5279 is a genetically modified microorganismwhich can act as a desulfurizing biocatalyst. This microorganism has the ability of performing the metabolic 4S pathway from Rhodococcus erythropolis IGTS8, in order to desulfurize DBT, as a model compound. Maximum in vivo activities of monooxygenase enzymes (DszA and DszC) are shown when late exponential growth phase is reached (23h), while desulfinase enzymeDszB presents amaximum activity during the early exponential growth phase (5h), as previously reported [1]. Also, it has been proved that the combined utilization of these two ibenzothiophene S route cell ages yields excellent results when used as biocatalyst for desulfurization [2]. The aim of this work is to optimize the ratio and total biomass concentration of both 5h and 23h growth time cells in a complex biocatalyst for desulfurization by performing resting cells biodesulfurization assays using dibenzothiophene (DBT) as sulfur model compound. The best combination of cells was determined aiming for the highest desulfurization in the shortest time of operation while investing the minimum concentration of biomass. A particular cell mixture, containing 66.7% of 23h growth time cells, was found to work as the ation most effective desulfuriz