Periodic Reporting for period 1 - EnergUP (Development of alga-based photovoltaic devices: Electron transport from photosynthesis via the cell wall to electrodes)
Okres sprawozdawczy: 2020-09-01 do 2022-08-31
Alga-based current production could be advantageous for several reasons, such as 1) being an environmental friendly way of sunlight energy conversion, and 2) the potential to decrease the energy consumption of alga biomass production by including self-sustainable bioreactors in the production system. The fact that these photosynthetic algae capture CO2 while produce O2, is a further positive aspect.
Although BPVs provide a promising alternative for producing energy, the efficiency of the available systems is inadequite for industrial use. The aim of the EnergUP project was to improve the alga-based, light-dependent current production by targeting various elements of the process.
Objectives of this Marie Skłodowska Curie Action (MSCA) have been to (1) enhance the electron flow from alga cells towards the electrodes of the BPVs by modofying internal electron transport processes, to (2) investigate the possible barrier effect of the wall surrounding the cells, and to (3) establish an alga cell immobilization method for a more efficient current production.
Overall, the rate of current production was sustantially increased by certain specific electron transport mutations in the green algae cells. On the other hand, it turned out that the presence of the cell wall has minor or no effect on the the current production. However, wild-type cells of various origin can have huge variation in the current producing capacity, most probably due to differences in their cellular metabolism. In the frame of the present project, various alga species have been screened using two newly developed bio-photovoltaic setups and strains with high current production capacity were identified.
(1) We designed a small-volume BPV device to carry out measurements on up to eight samples simultaneously. This setup enables varying the light intensity and to test its effect on current production. This device requires a small culture volume and it is designed to carry out short term measurements (up to one hour). The major application of this bio-photovoltaic setup is to screen algae strains and test the effects of various treatments for the identification of potential target points for increasing the rate of current production.
Using the small-volume BPV, we tested the effects of several treatments and conditions, including dark pre-treatments and light treatments at various intensities on the efficacy of current production. In parallel, various physiological parameters were also measured to obtain information on culture fitness before and after applying the current production protocol. These measurements helped us to pinpoint which conditions are best suited for producing high current and maintaining cell viability.
The above mentioned BPV device was applied to study various mutant strains affected in photosynthetic electron transport. Our data revealed that the redox state of the photosynthetic electron transport, namely the plastoquinone (PQ) pool has vital role in the current production by green algae. With specific mutations increasing the reduction level of the PQ-pool, we could increase 5 to 10 fold the maximal current production of the cells. Maximum current production was obtained at moderately high light intensities (in the range of 500 µmol photons m-2s-1, which is less than the maximum intensity of sunlight).
In addition, we investigated alga strains with eliminated or modified cell wall, but found no clear connection to the current production capacity. Thus, we concluded that the cell wall is not a limiting factor for the electron transfer feeding current production and current production cannot be enhanced by modifying it.
(2) We constructed a large-volume BPV device for liquid cell cultures for long-term measurements. This experimental setup enables measuring the light induced current production for several days and it does not require specific pretreatment of the cell culture, such as harvesting or concentrating. The obtained currents are outstanding, i.e. several times higher than reported so far, and this experimental system does not require expensive or toxic materials. This large-volume PBV device allows testing the previously preselected (using small-scale BPV device) strains in a larger volume, and less stressful conditions. It also provides a great opportunity for testing the effect of immobilisation on the current producing capacity of the cells.
During the project, we aimed at optimizing the measuring conditions not only for obtaining maximal current production of the alga cells but also to maintain their viability. During the construction of the devices and setting up the measuring protocols we were searching for low cost and low toxicity materials to ensure the sustainability in future industrial scale applications.