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Growth phase-dependant enzyme profile of pyruvate catabolism and end-product formation in Clostridium thermocellum ATCC 27405
Authors:Thomas Rydzak   David B. Levin   Nazim Cicek  Richard Sparling  
Affiliation:aDeparment of Microbiology, University of Manitoba, Winnipeg, Manitoba, Canada R3T 2N2;bDepartment of Biosystems Engineering, University of Manitoba, Winnipeg, Manitoba, Canada R3T 3V6
Abstract:End-product synthesis and enzyme activities involved in pyruvate catabolism, H2 synthesis, and ethanol production in mid-log (OD600 not, vert, similar 0.25), early stationary (OD600 not, vert, similar 0.5), and stationary phase (OD600 not, vert, similar 0.7) cell extracts were determined in Clostridium thermocellum ATCC 27405 grown in batch cultures on cellobiose. Carbon dioxide, hydrogen, ethanol, acetate and formate were major end-products and their production paralleled growth and cellobiose consumption. Lactate dehydrogenase, pyruvate:formate lyase, pyruvate:ferredoxin oxidoreductase, methyl viologen-dependant hydrogenase, ferredoxin-dependant hydrogenase, NADH-dependant hydrogenase, NADPH-dependant hydrogenase, NADH-dependant acetaldehyde dehydrogenase, NADH-dependant alcohol dehydogenase, and NADPH-dependant alcohol dehydrogenase activities were detected in all extracts, while pyruate dehydrogenase and formate dehydrogenase activities were not detected. All hydrogenase activities decreased (2–12-fold) as growth progressed from early exponential to stationary phase. Alcohol dehydrogenase activities fluctuated only marginally (<45%), while lactate dehydrogenase, pyruvate:formate lyase, and pyruvate:ferredoxin oxidoreductase remained constant in all cell extracts. We have proposed a pathway involved in pyruvate catabolism and end-product formation based on enzyme activity profiles in conjunction with bioinformatics analysis.
Keywords:Clostridium thermocellum   Consolidated bioprocessing   Pyruvate catabolism   Hydrogen synthesis   Ethanol synthesis   Enzyme activity shift
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