Photosynthetic production of ethanol from carbon dioxide in genetically engineered cyanobacteria

Zhengxu Gao, Hui Zhao, Zhimin Li, Xiaoming Tan, Xuefeng Lü

Energy & Environmental Science · 2012 · 369 citations · 31 references

Concepts

TL;DR

The growing demand for energy and concerns over CO₂ emissions have spurred interest in renewable biofuels, yet bioethanol production remains limited by food competition and cost. The authors aimed to integrate photosynthetic biomass production with microbial ethanol conversion in Synechocystis sp. PCC6803 through a consolidated bioprocessing strategy. They engineered PCC6803 to convert CO₂ to ethanol, cloned and expressed nine cyanobacterial alcohol dehydrogenases in E. coli, and evaluated culture conditions such as tap water, metal ions, and anoxic aeration.

Abstract

The rapidly growing demand for energy and the environmental concerns about carbon dioxide emissions make the development of renewable biofuels more and more attractive. Tremendous academic and industrial efforts have been made to produce bioethanol, which is one major type of biofuel. The current production of bioethanol is limited for commercialization because of issues with food competition (from food-based biomass) or cost effectiveness (from lignocellulose-based biomass). In this report we applied a consolidated bioprocessing strategy to integrate photosynthetic biomass production and microbial conversion producing ethanol together into the photosynthetic bacterium, Synechocystis sp. PCC6803, which can directly convert carbon dioxide to ethanol in one single biological system. A Synechocystis sp. PCC6803 mutant strain with significantly higher ethanol-producing efficiency (5.50 g L−1, 212 mg L−1 day−1) compared to previous research was constructed by genetically introducing pyruvate decarboxylase from Zymomonas mobilis and overexpressing endogenous alcohol dehydrogenase through homologous recombination at two different sites of the chromosome, and disrupting the biosynthetic pathway of poly-β-hydroxybutyrate. In total, nine alcohol dehydrogenases from different cyanobacterial strains were cloned and expressed in E. coli to test ethanol-producing efficiency. The effects of different culturing conditions including tap water, metal ions, and anoxic aeration on ethanol production were evaluated.

References

31