TY - JOUR
T1 - Evolution of microbial communities growing with carbon monoxide, hydrogen, and carbon dioxide
AU - Esquivel-Elizondo, Sofia
AU - Delgado, Anca
AU - Krajmalnik-Brown, Rosa
N1 - Funding Information:
This work was supported in part by the Engineering Research Center program of the National Science Foundation (NSF) under NSF Cooperative Agreement Number EEC-1 449 501, and CAREER Award number 1 053 939. Any opinions, findings and conclusions, or recommendations expressed in this material are those of the author(s) and do not necessarily reflect those of the NSF.
Funding Information:
SEE was partially supported by the Mexican National Council for Science and Technology (CONACyT for its initials in Spanish).
Publisher Copyright:
© FEMS 2017. All rights reserved.
PY - 2017/6
Y1 - 2017/6
N2 - Microbial anaerobic conversion of carbon monoxide (CO) and syngas (mainly composed of CO, CO2 and H2) leads to the production of important industrial products, such as acetate and ethanol. The composition of CO- and syngas-converting microbial communities and the microbial interactions involved are still largely unknown. The main objectives of this study were (i) to understand the effects of CO, CO2, and H2 on the structure and function of a CO-consuming microbial community, and (ii) to identify key carboxidotrophs in the mixed culture. For this, sludge was anaerobically enriched with CO as the sole carbon/energy source at incrementally increasing CO partial pressures (PCO). Phylotypes of Methanobacteriaceae and methane production were detected at PCO ≤ 44.1 kPa. At higher PCO, enriched phylotypes were Acetobacterium, Oscillospira and Pleomorphomonas, and acetate was the main end product. The addition of CO2/HCO3- or H2 to CO fermentation increased the acetate/ethanol ratio and species diversity, compared to growth with CO as sole substrate. Phylotypes associated with Pleomorphomonas and Acetobacterium increased in relative abundance during exponential CO utilization. The Pleomorphomonas-like isolate produced H2:CO2, whereas the Acetobacterium-like isolate produced ethanol, when CO was the only electron/carbon source. These findings shed light on the interplay between syngas components and microbial communities.
AB - Microbial anaerobic conversion of carbon monoxide (CO) and syngas (mainly composed of CO, CO2 and H2) leads to the production of important industrial products, such as acetate and ethanol. The composition of CO- and syngas-converting microbial communities and the microbial interactions involved are still largely unknown. The main objectives of this study were (i) to understand the effects of CO, CO2, and H2 on the structure and function of a CO-consuming microbial community, and (ii) to identify key carboxidotrophs in the mixed culture. For this, sludge was anaerobically enriched with CO as the sole carbon/energy source at incrementally increasing CO partial pressures (PCO). Phylotypes of Methanobacteriaceae and methane production were detected at PCO ≤ 44.1 kPa. At higher PCO, enriched phylotypes were Acetobacterium, Oscillospira and Pleomorphomonas, and acetate was the main end product. The addition of CO2/HCO3- or H2 to CO fermentation increased the acetate/ethanol ratio and species diversity, compared to growth with CO as sole substrate. Phylotypes associated with Pleomorphomonas and Acetobacterium increased in relative abundance during exponential CO utilization. The Pleomorphomonas-like isolate produced H2:CO2, whereas the Acetobacterium-like isolate produced ethanol, when CO was the only electron/carbon source. These findings shed light on the interplay between syngas components and microbial communities.
KW - Acetobacterium
KW - CO enrichment
KW - CO partial pressure
KW - Pleomorphomonas
KW - carbon monoxide (CO)
KW - carboxidotroph
UR - http://www.scopus.com/inward/record.url?scp=85029361733&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85029361733&partnerID=8YFLogxK
U2 - 10.1093/femsec/fix076
DO - 10.1093/femsec/fix076
M3 - Article
C2 - 28575426
AN - SCOPUS:85029361733
SN - 0168-6496
VL - 93
JO - FEMS Microbiology Ecology
JF - FEMS Microbiology Ecology
IS - 6
M1 - fix076
ER -