Crude oil-derived hydrocarbons constitute the largest group of environmental pollutants worldwide. The number of reports concerning their toxicity and emphasizing the ultimate need to remove them from marine and soil environments confirms the unceasing interest of scientists in this field. Among the various techniques used for clean-up actions, bioremediation seems to be the most acceptable and economically justified. Analysis of recent reports regarding unsuccessful bioremediation attempts indicates that there is a need to highlight the fundamental aspects of hydrocarbon microbiology in a clear and concise manner. Therefore, in this review, we would like to elucidate some crucial, but often overlooked, factors. First, the formation of crude oil and abundance of naturally occurring hydrocarbons is presented and compared with bacterial ability to not only survive but also to utilize such compounds as an attractive energy source. Then, the significance of nutrient limitation on biomass growth is underlined on the example of a specially designed experiment and discussed in context of bioremediation efficiency. Next, the formation of aerobic and anaerobic conditions, as well as the role of surfactants for maintaining appropriate C:N:P ratio during initial stages of biodegradation is explained. Finally, a summary of recent scientific reports focused on the removal of hydrocarbon contaminants using bioaugmentation, biostimulation and introduction of surfactants, as well as biosurfactants, is presented. This review was designed to be a comprehensive source of knowledge regarding the unique aspects of hydrocarbon microbiology that may be useful for planning future biodegradation experiments. In addition, it is a starting point for wider debate regarding the limitations and possible improvements of currently employed bioremediation strategies.

Coupling of power-to-gas processes with underground gas storage could effectively allow surplus electricity to be stored for later use. Depleted hydrocarbon reservoirs could be used as stores, but practical experience of hydrogen storage in such sites is limited. Here we present data from a field trial that stored 119,353 m³ of hydrogen admixed to natural gas in a depleted hydrocarbon reservoir. After 285 days, hydrogen recovery was 84.3%, indicating the process’s technical feasibility. Additionally, we report that microbes mediated hydrogen conversion to methane. In laboratory experiments studying mesocosms that mimic real reservoirs, hydrogen and carbon dioxide were converted to methane (0.26 mmol l⁻¹ h⁻¹ evolution rate) reproducibly over 14 cycles in 357 days. This rate theoretically allows 114,648 m³ of methane per year to be produced in the test reservoir (equivalent to ~1.08 GWh). Our research demonstrates the efficiency of hydrogen storage and the importance of geo-methanation in depleted hydrocarbon reservoirs.

This laboratory study investigates the potential of two innovative laccase-mediator systems for removing PAHs from historically contaminated field soil and focuses on the treatment effect on the accessible and desorption resistant PAH fraction. Laccase degraded accessible PAHs when applied in combination with the mediator TEMPO (up to 24 % within 48 h). The mediator HBT did not induce degradation but mobilized desorption resistant PAHs from high affinity sorption sites via a competitive sorption mechanism. Enzymatic degradation of inaccessible PAHs was not observed with neither of the two enzyme-mediator systems. To verify a potential radical susceptibility of contaminants inaccessible to microorganisms, PAH contaminated biochar was treated with hydroxyl radicals generated by Fenton's reaction. These radical species reduced the desorption resistant fraction of phenanthrene (13 ± 10 %), fluoranthene (33 ± 8 %) and benzo(a)pyrene (69 ± 5 %). In conclusion, laccase-mediator systems can interact with accessible and inaccessible PAHs, whereas direct degradation of desorption resistant contaminants required highly active hydroxyl radicals. Further studies should develop enzyme-mediator systems establishing a sufficient oxidation potential to attack the desorption resistant contaminant fraction.