Abstract

Electroautotrophy is a novel and fascinating microbial metabolism, with tremendous potential for CO2 storage and valorization into chemicals and materials made thereof. Research attention has been devoted toward the characterization of acetogenic and methanogenic electroautotrophs. In contrast, here we characterize the electrophysiology of a sulfate-reducing bacterium, Desulfosporosinus orientis, harboring the Wood-Ljungdahl pathway and, thus, capable of fixing CO2 into acetyl-CoA. For most electroautotrophs the mode of electron uptake is still not fully clarified. Our electrochemical experiments at different polarization conditions and Fe0 corrosion tests point to a H2- mediated electron uptake ability of this strain. This observation is in line with the lack of outer membrane and periplasmic multi-heme c-type cytochromes in this bacterium. Maximum planktonic biomass production and a maximum sulfate reduction rate of 2 ± 0.4 mM day–1 were obtained with an applied cathode potential of −900 mV vs. Ag/AgCl, resulting in an electron recovery in sulfate reduction of 37 ± 1.4%. Anaerobic sulfate respiration is more thermodynamically favorable than acetogenesis. Nevertheless, D. orientis strains adapted to sulfate-limiting conditions, could be tuned to electrosynthetic production of up to 8 mM of acetate, which compares well with other electroacetogens. The yield per biomass was very similar to H2/CO2 based acetogenesis. Acetate bioelectrosynthesis was confirmed through stable isotope labeling experiments with Na-H13CO3. Our results highlight a great influence of the CO2 feeding strategy and start-up H2 level in the catholyte on planktonic biomass growth and acetate production. In serum bottles experiments, D. orientis also generated butyrate, which makes D. orientis even more attractive for bioelectrosynthesis application. A further optimization of these physiological pathways is needed to obtain electrosynthetic butyrate production in D. orientis biocathodes. This study expands the diversity of facultative autotrophs able to perform H2-mediated extracellular electron uptake in Bioelectrochemical Systems (BES). We characterized a sulfate-reducing and acetogenic bacterium, D. orientis, able to naturally produce acetate and butyrate from CO2 and H2. For any future bioprocess, the exploitation of planktonic growing electroautotrophs with H2-mediated electron uptake would allow for a better use of the entire liquid volume of the cathodic reactor and, thus, higher productivities and product yields from CO2-rich waste gas streams.

Highlights

  • Microbial Electrochemical Technologies (MET) represent an innovative biotechnological solution for CO2-valorisation and surplus electricity storage (Zhang and Tremblay, 2018)

  • Since some bacteria of the class of Clostridia are able to use amino acids as carbon and energy source (Fonknechten et al, 2010), we evaluated the influence of cysteine, which is used as a reducing agent in our media, on our biocathode performance (Supplementary Material Section 2)

  • The data presented in this work demonstrated the ability of D. orientis to perform a mediated electron uptake from cathodes in the presence of abiotically produced or biologically induced H2

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Summary

Introduction

Microbial Electrochemical Technologies (MET) represent an innovative biotechnological solution for CO2-valorisation and surplus electricity storage (Zhang and Tremblay, 2018). In reductive bioelectrochemical processes electrical energy is used to accomplish cathodic fixation of CO2-rich gas streams into valuable products (Bajracharya et al, 2017) This Microbial Electrosynthesis (MES) is based on the special metabolic ability of electroautotrophic microorganisms: they acquire energy by taking up electrons directly or indirectly from electrodes, while using CO2 as inorganic carbon source and terminal electron acceptor (Nevin et al, 2010). The oxidative pathway of acetogens is rather based on the cytoplasmatic electron-bifurcating [FeFe] hydrogenase complex, that coupled Ferrodoxin and NAD(P) reduction with H2 oxidation These bifurcating-hydrogenases contribute to the energy conservation pathway of aceteogens, providing reduced Ferrodixin for the Rnf complex or the Ech complex, in which exergonic electron flow is coupled to vectorial ion transport out of the cell. The results showed that not all species were able to perform MES and that a more efficient metabolism in H2CO2-fed flasks does not necessarily translate into better electrosynthetic performance (Aryal et al, 2017)

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