Pathogenic microorganisms such as bacteria, virus, and fungi present in water matrices are cause of infections and epidemic diseases worldwide. Photocatalytic deactivation is emerging as a promising, powerful method for water disinfection and microbial control. Transition metal oxide semiconductor photocatalysts has been widely investigated, being non-toxic, eco-friendly, and cost effective. However, their use in practical applications is limited due to their relatively wide band gap, reducing their optical absorption range to the UV domain of the solar radiation, and high recombination rate of photo-induced electron-hole pairs. The synthesised Mg doped TiO₂ / graphene-like reduced graphene oxide nanocomposites are highly effective in deactivating nucleic acid molecules extracted from model Saccharomyces cerevisiae yeast cells as well as Saccharomyces cerevisiae yeast cells cultures, both under simulated sunlight and visible-light irradiation. The morphology, structure, and composition of the layers were thoroughly investigated by high resolution scanning electron microscopy, transmission electron microscopy, high-angle annular dark field scanning transmission microscopy, energy dispersive X-ray spectroscopy, as well as X-ray photoelectron spectroscopy. In accordance with the energy band structure of the synthesised nanocomposite catalysts, hydrogen peroxide and hydroxyl radicals are the major oxidative species (ROS) involved in the deactivation process. This study reveals a highly efficient approach for ROS generation for cell components decomposition and pathogen deactivation under visible light, and it can serve as an essential confirmation of the efficiency of visible-light-responsive photocatalysts in water disinfection.