TY - JOUR
T1 - The ethanol pathway from Thermoanaerobacterium saccharolyticum improves ethanol production in Clostridium thermocellum
AU - Hon, Shuen
AU - Olson, Daniel G.
AU - Holwerda, Evert K.
AU - Lanahan, Anthony A.
AU - Murphy, Sean J.L.
AU - Maloney, Marybeth I.
AU - Zheng, Tianyong
AU - Papanek, Beth
AU - Guss, Adam M.
AU - Lynd, Lee R.
N1 - Publisher Copyright:
© 2017 International Metabolic Engineering Society
PY - 2017/7
Y1 - 2017/7
N2 - Clostridium thermocellum ferments cellulose, is a promising candidate for ethanol production from cellulosic biomass, and has been the focus of studies aimed at improving ethanol yield. Thermoanaerobacterium saccharolyticum ferments hemicellulose, but not cellulose, and has been engineered to produce ethanol at high yield and titer. Recent research has led to the identification of four genes in T. saccharolyticum involved in ethanol production: adhE, nfnA, nfnB and adhA. We introduced these genes into C. thermocellum and observed significant improvements to ethanol yield, titer, and productivity. The four genes alone, however, were insufficient to achieve in C. thermocellum the ethanol yields and titers observed in engineered T. saccharolyticum strains, even when combined with gene deletions targeting hydrogen production. This suggests that other parts of T. saccharolyticum metabolism may also be necessary to reproduce the high ethanol yield and titer phenotype in C. thermocellum.
AB - Clostridium thermocellum ferments cellulose, is a promising candidate for ethanol production from cellulosic biomass, and has been the focus of studies aimed at improving ethanol yield. Thermoanaerobacterium saccharolyticum ferments hemicellulose, but not cellulose, and has been engineered to produce ethanol at high yield and titer. Recent research has led to the identification of four genes in T. saccharolyticum involved in ethanol production: adhE, nfnA, nfnB and adhA. We introduced these genes into C. thermocellum and observed significant improvements to ethanol yield, titer, and productivity. The four genes alone, however, were insufficient to achieve in C. thermocellum the ethanol yields and titers observed in engineered T. saccharolyticum strains, even when combined with gene deletions targeting hydrogen production. This suggests that other parts of T. saccharolyticum metabolism may also be necessary to reproduce the high ethanol yield and titer phenotype in C. thermocellum.
UR - http://www.scopus.com/inward/record.url?scp=85021427979&partnerID=8YFLogxK
U2 - 10.1016/j.ymben.2017.06.011
DO - 10.1016/j.ymben.2017.06.011
M3 - Article
C2 - 28663138
AN - SCOPUS:85021427979
SN - 1096-7176
VL - 42
SP - 175
EP - 184
JO - Metabolic Engineering
JF - Metabolic Engineering
ER -