TY - JOUR
T1 - Non-fermentative pathways for synthesis of branched-chain higher alcohols as biofuels
AU - Atsumi, Shota
AU - Hanai, Taizo
AU - Liao, James C.
N1 - Funding Information:
Acknowledgements This work was partially supported by UCLA-DOE Institute for Genomics and Proteomics. We are grateful to H. Bujard for plasmids, and members of the Liao laboratory for discussion and comments on the manuscript.
PY - 2008/1/3
Y1 - 2008/1/3
N2 - Global energy and environmental problems have stimulated increased efforts towards synthesizing biofuels from renewable resources. Compared to the traditional biofuel, ethanol, higher alcohols offer advantages as gasoline substitutes because of their higher energy density and lower hygroscopicity. In addition, branched-chain alcohols have higher octane numbers compared with their straight-chain counterparts. However, these alcohols cannot be synthesized economically using native organisms. Here we present a metabolic engineering approach using Escherichia coli to produce higher alcohols including isobutanol, 1-butanol, 2-methyl-1-butanol, 3-methyl-1-butanol and 2-phenylethanol from glucose, a renewable carbon source. This strategy uses the host's highly active amino acid biosynthetic pathway and diverts its 2-keto acid intermediates for alcohol synthesis. In particular, we have achieved high-yield, high-specificity production of isobutanol from glucose. The strategy enables the exploration of biofuels beyond those naturally accumulated to high quantities in microbial fermentation.
AB - Global energy and environmental problems have stimulated increased efforts towards synthesizing biofuels from renewable resources. Compared to the traditional biofuel, ethanol, higher alcohols offer advantages as gasoline substitutes because of their higher energy density and lower hygroscopicity. In addition, branched-chain alcohols have higher octane numbers compared with their straight-chain counterparts. However, these alcohols cannot be synthesized economically using native organisms. Here we present a metabolic engineering approach using Escherichia coli to produce higher alcohols including isobutanol, 1-butanol, 2-methyl-1-butanol, 3-methyl-1-butanol and 2-phenylethanol from glucose, a renewable carbon source. This strategy uses the host's highly active amino acid biosynthetic pathway and diverts its 2-keto acid intermediates for alcohol synthesis. In particular, we have achieved high-yield, high-specificity production of isobutanol from glucose. The strategy enables the exploration of biofuels beyond those naturally accumulated to high quantities in microbial fermentation.
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U2 - 10.1038/nature06450
DO - 10.1038/nature06450
M3 - Article
C2 - 18172501
AN - SCOPUS:38049001166
SN - 0028-0836
VL - 451
SP - 86
EP - 89
JO - Nature
JF - Nature
IS - 7174
ER -