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dc.contributor.authorLakshmanaswamy, Arun Shivkumar
dc.date.accessioned2014-03-04T18:28:33Z
dc.date.available2014-03-04T18:28:33Z
dc.date.issued2010-05
dc.identifier.otherlakshmanaswamy_arun-shivkumar_201005_ms
dc.identifier.urihttp://purl.galileo.usg.edu/uga_etd/lakshmanaswamy_arun-shivkumar_201005_ms
dc.identifier.urihttp://hdl.handle.net/10724/26383
dc.description.abstractThe removal of acetate from biomass hydrolysate is essential for improving microbial production of biochemicals. This research focuses on microbial removal of acetate using the concept of substrate selective degradation. Acetate is selectively removed from glucose-xylose mixtures by metabolically engineered Escherichia coli strain KD840 with mutations in phosphotransferase system (PTS) genes of glucose (ptsG, manZ, crr), glucokinase (glk) and xylose (xylA). In batch cultures, KD840 consumed acetate exclusively at first, and no sugars were consumed up to 30 hours after acetate was exhausted. Six Escherichia coli strains were compared for maximum specific growth rate using 5 g/L acetate as the sole carbon source. MC4100 showed the greatest MAX at 0.368 h-1 while MG1655 showed the lowest MAX at 0.244 h-1. Interestingly, MC4100 does not have a functional acs-yjcH-yjcG operon. ALS1126 (MG1655 acs-yjcH-yjcG) attained a MAX of 0.262 h-1, indicating acs-yjcH-yjcG operon does not affect the growth rate of E. coli on acetate.
dc.languageeng
dc.publisheruga
dc.rightspublic
dc.subjectAcetate
dc.subjectBiomass hydrolysate
dc.subjectEscherichia coli
dc.subjectMetabolic Engineering
dc.subjectOperon
dc.subjectPhosphotransferase system
dc.subjectSubstrate selective degradation
dc.titleSelective consumption of acetate without sugar degradation by metabolically engineered Escherichia coli
dc.typeThesis
dc.description.degreeMS
dc.description.departmentBiological and Agricultural Engineering
dc.description.majorBiological Engineering
dc.description.advisorMark Eiteman
dc.description.committeeMark Eiteman
dc.description.committeeJoy B. Doran-Peterson
dc.description.committeeK.C. Das


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