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Series GSE24944 Query DataSets for GSE24944
Status Public on Dec 31, 2011
Title Butanol Challenge of L. brevis
Organism Levilactobacillus brevis
Experiment type Expression profiling by array
Summary The presence of anti-microbial phenolic compounds, such as the model compound ferulic acid, in biomass hydrolysates poses significant challenges to the widespread use of biomass in conjunction with whole cell biocatalysis or fermentation. Biofuel toxicity must also be overcome to allow for efficient production of next generation biofuels such as butanol, isopropanol, and others for widespread usage. Currently, these inhibitory compounds must be removed through additional downstream processing or sufficiently diluted to create environments suitable for most industrially important microbial strains. This study explores the high ferulic acid and n-butanol tolerance in Lactobacillus brevis (L. brevis), a lactic acid bacteria often found in fermentation processes, by global transcriptional response analysis. The transcriptional profile of L. brevis under ferulic acid and butanol stress reveals that the presence of ferulic acid primarily triggers the expression of membrane proteins to counteract ferulic acid induced changes in membrane fluidity and ion leakage. In contrast to the ferulic acid stress response, butanol addition to growing cultures uniquely induced the entire fatty acid synthesis pathway in the midst of a generalized stress response. Overexpression of the rate-limiting acetyl-CoA carboxylase subunits (AccABCD) in E. coli to increase lipid synthesis had no effect on butanol tolerance, suggesting that additional engineering is necessary to produce sufficient levels of appropriate fatty acids to confer butanol tolerance. Several promising routes for understanding both phenolic acid and butanol tolerance have been identified based upon these findings. These insights may be used to guide further engineering of model industrial organisms to better tolerate both classes of inhibitors in processed biomass used for biofuel production.
 
Overall design Cultures were grown to OD ~ 0.2 in MRS media (baffled flasks), T = 30 C, 100 rpm. Butanol was then added to the cultures. Samples were harvested 15, 75, and 135 min after butanol addition. Each time point has 3 biological replicates, and dye swaps were incorporated into the microarray experiments.
 
Contributor(s) Winkler JD, Kao KC
Citation(s) 21829598
Submission date Oct 26, 2010
Last update date Sep 19, 2012
Contact name James Winkler
E-mail(s) jdwinkler@tamu.edu
Organization name Texas A&M University
Lab Kao Lab
Street address 3122 TAMU
City College Station
State/province TX
ZIP/Postal code 77843
Country USA
 
Platforms (1)
GPL10674 Agilent custom Lactobacillus brevis Microarray (condensed version)
Samples (21)
GSM564264 A492010 FA Array Time Point 1 (15 min)
GSM564265 A492010 FA Array Time Point 2 (135 min)
GSM564266 A4162010 FA Array Time Point 2 (135 min)
Relations
BioProject PRJNA131947

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE24944_RAW.tar 193.2 Mb (http)(custom) TAR (of GPR)
Processed data included within Sample table

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