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Metab Eng. 2019 Jun 17. pii: S1096-7176(19)30111-9. doi: 10.1016/j.ymben.2019.06.006. [Epub ahead of print]

Thermodynamic analysis of the pathway for ethanol production from cellobiose in Clostridium thermocellum.

Author information

1
Department of Chemical Engineering, The Pennsylvania State University, University Park, University Park, PA, USA; Center for Bioenergy Innovation, Oak Ridge National Laboratory, Oak Ridge, TN 37830, USA. Electronic address: satyakam@psu.edu.
2
Thayer School of Engineering at Dartmouth College, Hanover, NH, USA; Center for Bioenergy Innovation, Oak Ridge National Laboratory, Oak Ridge, TN 37830, USA. Electronic address: Daniel.G.Olson@dartmouth.edu.
3
Department of Chemical and Biological Engineering, Colorado State University, Fort Collins, CO, USA; Center for Bioenergy Innovation, Oak Ridge National Laboratory, Oak Ridge, TN 37830, USA. Electronic address: joshua.chan@colostate.edu.
4
Department of Bacteriology, University of Wisconsin, Madison, WI, USA; Center for Bioenergy Innovation, Oak Ridge National Laboratory, Oak Ridge, TN 37830, USA. Electronic address: amadornoguez@wisc.edu.
5
Thayer School of Engineering at Dartmouth College, Hanover, NH, USA; Center for Bioenergy Innovation, Oak Ridge National Laboratory, Oak Ridge, TN 37830, USA. Electronic address: lee.r.lynd@dartmouth.edu.
6
Department of Chemical Engineering, The Pennsylvania State University, University Park, University Park, PA, USA; Center for Bioenergy Innovation, Oak Ridge National Laboratory, Oak Ridge, TN 37830, USA. Electronic address: costas@psu.edu.

Abstract

Clostridium thermocellum is a candidate for consolidated bioprocessing by carrying out both cellulose solubilization and fermentation. However, despite significant efforts the maximum ethanol titer achieved to date remains below industrially required targets. Several studies have analyzed the impact of increasing ethanol concentration on C. thermocellum's membrane properties, cofactor pool ratios, and altered enzyme regulation. In this study, we explore the extent to which thermodynamic equilibrium limits maximum ethanol titer. We used the max-min driving force (MDF) algorithm (Noor et al., 2014) to identify the range of allowable metabolite concentrations that maintain a negative free energy change for all reaction steps in the pathway from cellobiose to ethanol. To this end, we used a time-series metabolite concentration dataset to flag five reactions (phosphofructokinase (PFK), fructose bisphosphate aldolase (FBA), glyceraldehyde-3-phosphate dehydrogenase (GAPDH), aldehyde dehydrogenase (ALDH) and alcohol dehydrogenase (ADH)) which become thermodynamic bottlenecks under high external ethanol concentrations. Thermodynamic analysis was also deployed in a prospective mode to evaluate genetic interventions which can improve pathway thermodynamics by generating minimal set of reactions or elementary flux modes (EFMs) which possess unique genetic variations while ensuring mass and redox balance with ethanol production. MDF evaluation of all generated (336) EFMs indicated that, i) pyruvate phosphate dikinase (PPDK) has a higher pathway MDF than the malate shunt alternative due to limiting CO2 concentrations under physiological conditions, and ii) NADPH-dependent glyceraldehyde-3-phosphate dehydrogenase (GAPN) can alleviate thermodynamic bottlenecks at high ethanol concentrations due to cofactor modification and reduction in ATP generation. The combination of ATP linked phosphofructokinase (PFK-ATP) and NADPH linked alcohol dehydrogenase (ADH-NADPH) with NADPH linked aldehyde dehydrogenase (ALDH-NADPH) or ferredoxin: NADP ​+ ​oxidoreductase (NADPH-FNOR) emerges as the best intervention strategy for ethanol production that balances MDF improvements with ATP generation, and appears to functionally reproduce the pathway employed by the ethanologen Thermoanaerobacterium saccharolyticum. Expanding the list of measured intracellular metabolites and improving the quantification accuracy of measurements was found to improve the fidelity of pathway thermodynamics analysis in C. thermocellum. This study demonstrates even before addressing an organism's enzyme kinetics and allosteric regulations, pathway thermodynamics can flag pathway bottlenecks and identify testable strategies for enhancing pathway thermodynamic feasibility and function.

KEYWORDS:

Clostridium thermocellum; Elementary flux modes; Ethanol inhibition; Genetic interventions; Thermodynamic analysis

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