(567bg) An MILP Approach to the Optimization of Cyanobacteria Metabolic Network for Bioethanol Production | AIChE

(567bg) An MILP Approach to the Optimization of Cyanobacteria Metabolic Network for Bioethanol Production

Authors 

Paulo, C. - Presenter, Planta Piloto de Ingenieria Química ¨(PLAPIQUI) - Universidad Nacional del Sur
Estrada, V. - Presenter, PLAPIQUI (CONICET-UNS)
Di Maggio, J. A. - Presenter, PLAPIQUI (CONICET-UNS)
Diaz, M. - Presenter, Planta Piloto de Ingenieria Quimica-UNS


Different alternatives to fossil fuels are currently being studied to reduce the dependence on non-renewable resources. Biofuels constitute relevant sustainable complements and/or substitutes to petroleum fuels due to energy security reasons, environmental concerns, foreign exchange savings, and socioeconomic issues related to the rural sector. The most common renewable fuel is ethanol derived from corn grain and sugar cane (sucrose). The use of lignocellulosic biomass is an attractive alternative, as second generation pathways for bioethanol production. On the other hand, third generation biofuels are obtained through algae. Cyanobacteria are an abundant and diverse group of ancient autotrophic prokaryotes that perform oxygenic photosynthesis; they played a crucial role in the change of reductive to oxidative atmosphere in the Precambrian period. Cyanobacteria live in freshwater, marine and terrestrial environments and show a wide diversity of morphologies, metabolisms and cell structures, they have several features that make them attractive to obtain commercial interest products in pharmaceutical, nutraceutical, biofuels, and other industries. They reach high cellular densities in culture and have simple growth requirements: light, carbon dioxide, and other inorganic nutrients to growth. Few authors have studied ethanol production from cyanobacteria (Deng & Coleman, 1998; Dexter & Fu, 2009). Ethanol production through cyanobacteria allows the coupling of energy production with the capture of industrial carbon dioxide emissions to reduce greenhouse gasses pollution, without competing with food production. However, current reported ethanol yields still require improvement to make this technology economically attractive. For cost-effective production of ethanol, the metabolic pathways involved in its generation must be engineered and optimized. Advances in metabolic engineering and synthetic biology based on gene sequence, biochemical and physiological data availability in public databases with the constant improvement of the mathematical tools can help to accelerate the development of desired phenotypes for the production of economically viable biofuels (Lee et al. 2008; Picataggio, 2009). In this work, we formulate a mixed-integer linear programming model to represent gene deletions in a metabolic network for the recombinant cyanobacteria Synechocystis sp. strain PCC6803 to maximize ethanol production, while maximizing biomass growth. The model includes more than 800 reactions from the glycolysis, the pentose phosphate pathway, citric acid cycle and Calvin cycle, and gene insertions corresponding to pyruvate decarboxylase (pdc) and alcohol dehydrogenase II (adhII) from obligately Zymomonas mobilis into Synechocystis sp. strain PCC6803 (Dexter and Fu, 2009) to enable the ethanol producing pathway. The model has been implemented in GAMS (Brooke et al., 1997) and solved with CPLEX. Numerical results provide useful insights on understanding of cellular metabolism as well as designing of metabolic engineering strategies for ethanol production using carbon dioxide as carbon source.

References

A. Brooke; Kendrick D.; Meeraus A. (2005) GAMS: A users guide, Scientific Press, Palo Alto, CA. M. Deng & J. Coleman, 1999, Ethanol synthesis by genetic engineering in cyanobacteria, Applied and Environmental Microbiology, 65, 2, 523-528. J. Dexter & P. Fu, 2009, Metabolic engineering of cyanobacteria for ethanol production. Energy and Environmental Sciences, 2, 857-864. J. Di Maggio, J. Diaz Ricci, M.S. Diaz, 2009, Global Sensitivity Analysis in Dynamic Metabolic Networks, Computer Aided Chemical Engineering, 26, 1075-1080. P. Fu (2009) Genome-scale modeling of Synechocystis sp. PCC 6803 and prediction of pathway insertion, J Chem Technol Biotechnol 84, 473?483. S. K. Lee, H. Chou , T. S. Ham, T. S. Lee & J. D. Keasling, 2008, Metabolic engineering of microorganisms for biofuels production: from bugs to synthetic biology to fuels. Curr Opin Biotechnol., 19, 6, 556-563. S. Picataggio, 2009, Potential impact of synthetic biology on the development of microbial systems for the production of renewable fuels and chemicals. Curr Opin Biotechnol., 20, 3, 325-329.