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Engineering Pseudomonas putida KT2440 for the production of isobutanol
Authors:Robert Nitschel,Andreas Ankenbauer,Ilona Welsch,Nicolas T. Wirth,Christoph Massner,Naveed Ahmad,Stephen McColm,Fr  d  ric Borges,Ian Fotheringham,Ralf Takors,Bastian Blombach
Affiliation:Robert Nitschel,Andreas Ankenbauer,Ilona Welsch,Nicolas T. Wirth,Christoph Massner,Naveed Ahmad,Stephen McColm,Frédéric Borges,Ian Fotheringham,Ralf Takors,Bastian Blombach
Abstract:We engineered P. putida for the production of isobutanol from glucose by preventing product and precursor degradation, inactivation of the soluble transhydrogenase SthA, overexpression of the native ilvC and ilvD genes, and implementation of the feedback‐resistant acetolactate synthase AlsS from Bacillus subtilis, ketoacid decarboxylase KivD from Lactococcus lactis, and aldehyde dehydrogenase YqhD from Escherichia coli. The resulting strain P. putida Iso2 produced isobutanol with a substrate specific product yield (YIso/S) of 22 ± 2 mg per gram of glucose under aerobic conditions. Furthermore, we identified the ketoacid decarboxylase from Carnobacterium maltaromaticum to be a suitable alternative for isobutanol production, since replacement of kivD from L. lactis in P. putida Iso2 by the variant from C. maltaromaticum yielded an identical YIso/S. Although P. putida is regarded as obligate aerobic, we show that under oxygen deprivation conditions this bacterium does not grow, remains metabolically active, and that engineered producer strains secreted isobutanol also under the non‐growing conditions.
Keywords:isobutanol  ketoacid decarboxylase  metabolic engineering  microaerobic  Pseudomonas putida
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