Previous Article | Next Article ![]()
Applied and Environmental Microbiology, December 2007, p. 7814-7818, Vol. 73, No. 24
0099-2240/07/$08.00+0 doi:10.1128/AEM.01140-07
Copyright © 2007, American Society for Microbiology. All Rights Reserved.
,
S. Atsumi, and
J. C. Liao*
Department of Chemical and Biomolecular Engineering, University of California, Los Angeles, 5531 Boelter Hall, Los Angeles, California 90095
Received 22 May 2007/ Accepted 6 October 2007
A synthetic pathway was engineered in Escherichia coli to produce isopropanol by expressing various combinations of genes from Clostridium acetobutylicum ATCC 824, E. coli K-12 MG1655, Clostridium beijerinckii NRRL B593, and Thermoanaerobacter brockii HTD4. The strain with the combination of C. acetobutylicum thl (acetyl-coenzyme A [CoA] acetyltransferase), E. coli atoAD (acetoacetyl-CoA transferase), C. acetobutylicum adc (acetoacetate decarboxylase), and C. beijerinckii adh (secondary alcohol dehydrogenase) achieved the highest titer. This strain produced 81.6 mM isopropanol in shake flasks with a yield of 43.5% (mol/mol) in the production phase. To our knowledge, this work is the first to produce isopropanol in E. coli, and the titer exceeded that from the native producers.
Published ahead of print on 12 October 2007.
Supplemental material for this article may be found at http://aem.asm.org/.
Permanent address: Laboratory for Bioinformatics, Graduate School of Systems Biosciences, Kyushu University, 6-10-1 Hakozaki, Higashi-ku, Fukuoka 812-8581, Japan.
This article has been cited by other articles:
Copyright © 2009 by the American Society for Microbiology. For an alternate route to Journals.ASM.org, visit: http://intl-journals.asm.org | More Info»