We developed two novel bio-photovoltaic devices in the frame of this project.
(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.