Co‑cultivation of anaerobic fungi with Clostridium acetobutylicum bolsters butyrate and butanol production from cellulose and lignocellulose

Author:

Brown Jennifer L1,Perisin Matthew A2,Swift Candice L1,Benyamin Marcus2,Liu Sanchao2,Singan Vasanth3,Zhang Yu3ORCID,Savage Emily3,Pennacchio Christa3,Grigoriev Igor V34,O'Malley Michelle A15ORCID

Affiliation:

1. Department of Chemical Engineering, University of California Santa Barbara , Rm 3357 Engineering II, Santa Barbara, CA 93117 , USA

2. Biological and Biotechnology Sciences Division, DEVCOM Army Research Laboratory , 2800 Powder Mill Road, Adelphi, MD 20783 , USA

3. US Department of Energy Joint Genome Institute, Lawrence Berkeley National Laboratory , Berkeley, CA 94720 , USA

4. Department of Plant and Microbial Biology, University of California Berkeley , Berkeley, CA 94720 , USA

5. Joint BioEnergy Institute, Lawrence Berkeley National Laboratory , Berkeley, CA 94608 , USA

Abstract

Abstract A system for co-cultivation of anaerobic fungi with anaerobic bacteria was established based on lactate cross-feeding to produce butyrate and butanol from plant biomass. Several co-culture formulations were assembled that consisted of anaerobic fungi (Anaeromyces robustus, Neocallimastix californiae, or Caecomyces churrovis) with the bacterium Clostridium acetobutylicum. Co-cultures were grown simultaneously (e.g., ‘one pot’), and compared to cultures where bacteria were cultured in fungal hydrolysate sequentially. Fungal hydrolysis of lignocellulose resulted in 7–11 mM amounts of glucose and xylose, as well as acetate, formate, ethanol, and lactate to support clostridial growth. Under these conditions, one-stage simultaneous co-culture of anaerobic fungi with C. acetobutylicum promoted the production of butyrate up to 30 mM. Alternatively, two-stage growth slightly promoted solventogenesis and elevated butanol levels (∼4–9 mM). Transcriptional regulation in the two-stage growth condition indicated that this cultivation method may decrease the time required to reach solventogenesis and induce the expression of cellulose-degrading genes in C. acetobutylicum due to relieved carbon-catabolite repression. Overall, this study demonstrates a proof of concept for biobutanol and bio-butyrate production from lignocellulose using an anaerobic fungal-bacterial co-culture system.

Funder

U.S. Army Research Office

Institute for Collaborative Biotechnologies

Department of Energy Office of Science

DOE Office of Science

Publisher

Oxford University Press (OUP)

Subject

Applied Microbiology and Biotechnology,Biotechnology,Bioengineering

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