bioRxiv Science⌕ Search

Biology subjects

Hackbarth, M.

Publications and source records attributed to Hackbarth, M..

2 recordsLinked to original sources

Oxic microbial electrosynthesis can be more energy efficient for biomass production than knallgas or photosynthesis based processes

Data on the efficiency and development of continuous processes are scarce in the emerging field of oxic microbial electrosynthesis (OMES). Therefore, the recently isolated knallgas bacterium Kyrpidia spormannii was observed in a bioelectrochemical flow cell setup to study biomass formation and energy efficiency of cathode dependent growth. The study revealed that a potential of -500 mV vs. the standard hydrogen electrode (SHE) caused differences in the structure of the biofilm developing on the cathode, but had almost no impact on biomass growth behavior compared to -375 mV vs. SHE. No growth was observed at 0 mV vs SHE. Coulombic efficiency (CE) was calculated for the cultivation at -500 mV vs. SHE. The process can be conducted with the same electron efficiency as traditional gas fermentation. The solar energy demand with 67.89 kWh kg-1 dry biomass is highly competitive to alternative and already established processes for converting (solar) energy to biomass. Additionally, with suggestions for a biomass harvesting method and subsequent recultivation, proof of principle for a continuously operable process was provided. The results pave the way for a new concept in carbon dioxide-based biotechnology. Significance statementTo mitigate global climate change, it is imperative to transition the human economy to a different resource foundation, moving away from fossil fuels and reducing atmospheric carbon dioxide levels. Biotechnological production based on CO2 necessitates a supply of energy and electrons. This study reveals that an oxic process, wherein bacteria are directly cultivated as a biofilm on the cathode surface of a bioelectrochemical system, can exhibit higher energy efficiency than plant-based systems or systems reliant on hydrogen generated through water electrolysis. This technology could be instrumental in establishing carbon dioxide and renewable energy as the foundation for feed, food, and platform chemical production.

bioengineering↗

A scalable, Rotating Disc Bioelectrochemical Reactor (RDBER) suitable for the cultivation of both cathodic and anodic biofilms

This study discusses the construction and operation of a membrane-less bioelectrochemical reactor that employs rotating working electrodes with a surface area of up to 1 m2. As a proof-of-principle for an aerobic microbial electrosynthesis process, Kyrpidia spormannii was cultivated in the reactor. Optical coherence tomography was used to examine the spatial distribution of the cathodic biofilm. After 24 days 87% of the cathode surface was covered with biofilm that was characterized by a radial increase in its biovolume towards the circumcenter of the electrodes reaching up to 92.13 m3 m-2. To demonstrate the versatility of the system, we further operated the reactor as a microbial electrolysis cell employing a co-culture of Shewanella oneidensis and Geobacter sulfurreducens. Anodic current densities of up to 130 A cm-2 were measured during these batch experiments. This resulted in a maximum production rate of 0.43 liters of pure hydrogen per liter reactor volume and day. Graphical Abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=161 SRC="FIGDIR/small/507646v3_ufig1.gif" ALT="Figure 1"> View larger version (55K): org.highwire.dtl.DTLVardef@102fbecorg.highwire.dtl.DTLVardef@e96345org.highwire.dtl.DTLVardef@7476aaorg.highwire.dtl.DTLVardef@1ac358_HPS_FORMAT_FIGEXP M_FIG C_FIG HighlightsO_LIConstruction of a 10 L membrane-less, pressurizable bioelectrochemical reactor C_LIO_LIRotating working electrodes with up to 1 m2 electrode surface C_LIO_LIElectroautotrophic cultivation and quantification of K. spormannii biofilms C_LIO_LIInitial cell density crucial for successful K. spormannii biofilm formation C_LIO_LIAnodic operation as MEC with Shewanella / Geobacter coculture C_LI

microbiology↗