TY - JOUR
T1 - Open microbiome dominated by Clostridium and Eubacterium converts methanol into i-butyrate and n-butyrate
AU - Huang, Shengle
AU - Kleerebezem, Robbert
AU - Rabaey, Korneel
AU - Ganigué, Ramon
PY - 2020
Y1 - 2020
N2 - Isobutyrate (i-butyrate) is a versatile platform chemical, whose acid form is used as a precursor of plastic and emulsifier. It can be produced microbially either using genetically engineered organisms or via microbiomes, in the latter case starting from methanol and short-chain carboxylates. This opens the opportunity to produce i-butyrate from non-sterile feedstocks. Little is known on the ecology and process conditions leading to i-butyrate production. In this study, we steered i-butyrate production in a bioreactor fed with methanol and acetate under various conditions, achieving maximum i-butyrate productivity of 5.0 mM day−1, with a concurrent production of n-butyrate of 7.9 mM day−1. The production of i-butyrate was reversibly inhibited by methanogenic inhibitor 2-bromoethanesulfonate. The microbial community data revealed the co-dominance of two major OTUs during co-production of i-butyrate and n-butyrate in two distinctive phases throughout a period of 54 days and 28 days, respectively. The cross-comparison of product profile with microbial community composition suggests that the relative abundance of Clostridium sp. over Eubacterium sp. is correlated with i-butyrate productivity over n-butyrate productivity.
AB - Isobutyrate (i-butyrate) is a versatile platform chemical, whose acid form is used as a precursor of plastic and emulsifier. It can be produced microbially either using genetically engineered organisms or via microbiomes, in the latter case starting from methanol and short-chain carboxylates. This opens the opportunity to produce i-butyrate from non-sterile feedstocks. Little is known on the ecology and process conditions leading to i-butyrate production. In this study, we steered i-butyrate production in a bioreactor fed with methanol and acetate under various conditions, achieving maximum i-butyrate productivity of 5.0 mM day−1, with a concurrent production of n-butyrate of 7.9 mM day−1. The production of i-butyrate was reversibly inhibited by methanogenic inhibitor 2-bromoethanesulfonate. The microbial community data revealed the co-dominance of two major OTUs during co-production of i-butyrate and n-butyrate in two distinctive phases throughout a period of 54 days and 28 days, respectively. The cross-comparison of product profile with microbial community composition suggests that the relative abundance of Clostridium sp. over Eubacterium sp. is correlated with i-butyrate productivity over n-butyrate productivity.
KW - Carboxylate platform
KW - Chain elongation
KW - Isobutyrate production
KW - Methanol
KW - Mixed culture fermentation
UR - http://www.scopus.com/inward/record.url?scp=85082962614&partnerID=8YFLogxK
U2 - 10.1007/s00253-020-10551-w
DO - 10.1007/s00253-020-10551-w
M3 - Article
AN - SCOPUS:85082962614
SN - 0175-7598
VL - 104
SP - 5119
EP - 5131
JO - Applied Microbiology and Biotechnology
JF - Applied Microbiology and Biotechnology
IS - 11
ER -