Non-fermentative pathways for synthesis of branched-chain higher alcohols as biofuels

被引:1454
作者
Atsumi, Shota [1 ]
Hanai, Taizo [1 ]
Liao, James C. [1 ,2 ]
机构
[1] Univ Calif Los Angeles, Dept Chem & Biomol Engn, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, UCLA DOE Inst Genom & Proteom, Los Angeles, CA 90095 USA
关键词
D O I
10.1038/nature06450
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Global energy and environmental problems have stimulated increased efforts towards synthesizing biofuels from renewable resources(1-3). 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.
引用
收藏
页码:86 / U13
页数:5
相关论文
共 30 条
  • [1] Engineering yeast transcription machinery for improved ethanol tolerance and production
    Alper, Hal
    Moxley, Joel
    Nevoigt, Elke
    Fink, Gerald R.
    Stephanopoulos, Gregory
    [J]. SCIENCE, 2006, 314 (5805) : 1565 - 1568
  • [2] 3-hydroxypropionaldehyde, an inhibitory metabolite of glycerol fermentation to 1,3-propanediol by enterobacterial species
    Barbirato, F
    Grivet, JP
    Soucaille, P
    Bories, A
    [J]. APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1996, 62 (04) : 1448 - 1451
  • [3] BOGOSIAN G, 1989, J BIOL CHEM, V264, P531
  • [4] CALHOUN DH, 1973, J BIOL CHEM, V248, P3511
  • [5] AMINO-ACID BIOSYNTHESIS IN SPIROCHETE-LEPTOSPIRA - EVIDENCE FOR A NOVEL PATHWAY OF ISOLEUCINE BIOSYNTHESIS
    CHARON, NW
    JOHNSON, RC
    PETERSON, D
    [J]. JOURNAL OF BACTERIOLOGY, 1974, 117 (01) : 203 - 211
  • [6] Biochemical and molecular characterization of α-ketoisovalerate decarboxylase, an enzyme involved in the formation of aldehydes from amino acids by Lactococcus lactis
    de la Plaza, M
    de Palencia, PF
    Peláez, C
    Requena, T
    [J]. FEMS MICROBIOLOGY LETTERS, 2004, 238 (02) : 367 - 374
  • [7] An investigation of the metabolism of valine to isobutyl alcohol in Saccharomyces cerevisiae
    Dickinson, JR
    Harrison, SJ
    Hewlins, MJE
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (40) : 25751 - 25756
  • [8] A C-13 nuclear magnetic resonance investigation of the metabolism of leucine to isoamyl alcohol in Saccharomyces cerevisiae
    Dickinson, JR
    Lanterman, MM
    Danner, DJ
    Pearson, BM
    Sanz, P
    Harrison, SJ
    Hewlins, MJE
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (43) : 26871 - 26878
  • [9] An investigation of the metabolism of isoleucine to active amyl alcohol in Saccharomyces cerevisiae
    Dickinson, JR
    Harrison, SJ
    Dickinson, JA
    Hewlins, MJE
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (15) : 10937 - 10942
  • [10] The catabolism of amino acids to long chain and complex alcohols in Saccharomyces cerevisiae
    Dickinson, JR
    Eshantha, L
    Salgado, J
    Hewlins, MJE
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (10) : 8028 - 8034