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Background  Isobutanol is a candidate to replace gasoline from fossil resources. This higher alcohol can be produced from sugars using genetically modified microorganisms.  Shimwellia blattae  (p424IbPSO) is a robust strain resistant to high concentration of isobutanol that can achieve a high production rate of this alcohol. Nevertheless, this strain, like most strains developed for isobutanol production, has some limitations in its metabolic pathway. Isobutanol production under anaerobic conditions leads to a depletion of NADPH, which is necessary for two enzymes in the metabolic pathway. In this work, two independent approaches have been studied to mitigate the co-substrates imbalance: (i) using a NADH-dependent alcohol dehydrogenase to reduce the NADPH dependence of the pathway and (ii) using a transhydrogenase to increase NADPH level.    Results  The addition of the NADH-dependent alcohol dehydrogenase from  Lactococcus lactis  (AdhA) to  S. blattae  (p424IbPSO) resulted in a 19.3% higher isobutanol production. The recombinant strain  S. blattae  (p424IbPSO, pIZpntAB) harboring the PntAB transhydrogenase produced 39.0% more isobutanol than the original strain, reaching 5.98 g L −1  of isobutanol. In both strains, we observed a significant decrease in the yields of by-products such as lactic acid or ethanol.    Conclusions  The isobutanol biosynthesis pathway in  S. blattae  (p424IbPSO) uses the endogenous NADPH-dependent alcohol dehydrogenase YqhD to complete the pathway. The addition of NADH-dependent AdhA leads to a reduction in the consumption of NADPH that is a bottleneck of the pathway. The higher consumption of NADH by AdhA reduces the availability of NADH required for the transformation of pyruvate into lactic acid and ethanol. On the other hand, the expression of PntAB from  E. coli  increases the availability of NADPH for IlvC and YqhD and at the same time reduces the availability of NADH and thus, the production of lactic acid and ethanol. In this work it is shown how the expression of AdhA and PntAB enzymes in  Shimwellia blattae  increases yield from 11.9% to 14.4% and 16.4%, respectively.

Modulating redox metabolism to improve isobutanol production in Shimwellia blattae