TY - JOUR
T1 - Engineering improved ethylene production: Leveraging systems Biology and adaptive laboratory evolution
AU - Vaud, Sophie
AU - Pearcy, Nicole
AU - Hanževački, Marko
AU - Van Hagen, Alexander M.W.
AU - Abdelrazig, Salah
AU - Safo, Laudina
AU - Ehsaan, Muhammad
AU - Jonczyk, Magdalene
AU - Millat, Thomas
AU - Craig, Sean
AU - Spence, Edward
AU - Fothergill, James
AU - Bommareddy, Rajesh Reddy
AU - Colin, Pierre-Yves
AU - Twycross, Jamie
AU - Dalby, Paul
AU - Minton, Nigel
AU - Jäger, Christof M.
AU - Kim, Dong-Hyun
AU - Yu, Jianping
AU - Maness, Pin-Ching
AU - Lynch, Sean
AU - Eckert, Carrie
AU - Conradie, Alex
AU - Bryan, Samantha J.
N1 - Funding information: This work was supported by the Biotechnology and Biological Sciences Research Council (BBSRC; grant number BB/L013940/1) and the Engineering and Physical Sciences Research Council (EPSRC) under the same grant number and the Green Chemicals Beacon of Excellence, University of Nottingham.
PY - 2021/9/1
Y1 - 2021/9/1
N2 - Ethylene is a small hydrocarbon gas widely used in the chemical industry. Annual worldwide production currently exceeds 150 million tons, producing considerable amounts of CO2 contributing to climate change. The need for a sustainable alternative is therefore imperative. Ethylene is natively produced by several different microorganisms, including Pseudomonas syringae pv. phaseolicola via a process catalyzed by the ethylene forming enzyme (EFE), subsequent heterologous expression of EFE has led to ethylene production in non-native bacterial hosts including E. coli and cyanobacteria. However, solubility of EFE and substrate availability remain rate limiting steps in biological ethylene production. We employed a combination of genome scale metabolic modelling, continuous fermentation, and protein evolution to enable the accelerated development of a high efficiency ethylene producing E. coli strain, yielding a 49-fold increase in production, the most significant improvement reported to date. Furthermore, we have clearly demonstrated that this increased yield resulted from metabolic adaptations that were uniquely linked to the EFE enzyme (WT vs mutant). Our findings provide a novel solution to deregulate metabolic bottlenecks in key pathways, which can be readily applied to address other engineering challenges.
AB - Ethylene is a small hydrocarbon gas widely used in the chemical industry. Annual worldwide production currently exceeds 150 million tons, producing considerable amounts of CO2 contributing to climate change. The need for a sustainable alternative is therefore imperative. Ethylene is natively produced by several different microorganisms, including Pseudomonas syringae pv. phaseolicola via a process catalyzed by the ethylene forming enzyme (EFE), subsequent heterologous expression of EFE has led to ethylene production in non-native bacterial hosts including E. coli and cyanobacteria. However, solubility of EFE and substrate availability remain rate limiting steps in biological ethylene production. We employed a combination of genome scale metabolic modelling, continuous fermentation, and protein evolution to enable the accelerated development of a high efficiency ethylene producing E. coli strain, yielding a 49-fold increase in production, the most significant improvement reported to date. Furthermore, we have clearly demonstrated that this increased yield resulted from metabolic adaptations that were uniquely linked to the EFE enzyme (WT vs mutant). Our findings provide a novel solution to deregulate metabolic bottlenecks in key pathways, which can be readily applied to address other engineering challenges.
KW - Systems biology
KW - Adaptive evolution
KW - Directed evolution
KW - Metabolic engineering
KW - Fermentation
UR - http://www.scopus.com/inward/record.url?scp=85111223211&partnerID=8YFLogxK
U2 - 10.1016/j.ymben.2021.07.001
DO - 10.1016/j.ymben.2021.07.001
M3 - Article
SN - 1096-7176
VL - 67
SP - 308
EP - 320
JO - Metabolic Engineering
JF - Metabolic Engineering
ER -