Introduction of the exogenous NADH coenzyme regeneration system and its influence on intracellular metabolic flux of Paenibacillus polymyxa
•pMA5 plasmid and P43 promoter provide a new tool for expression of exogenous genes in P. polymyxa.•The NAD+-dependent formate dehydrogenase was successfully expressed in P. polymyxa.•There is no need to supplement formic acid during fermentation.•The yield of R,R-2,3-butanediol was improved through...
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Veröffentlicht in: | Bioresource technology 2016-02, Vol.201, p.319-328 |
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Sprache: | eng |
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Zusammenfassung: | •pMA5 plasmid and P43 promoter provide a new tool for expression of exogenous genes in P. polymyxa.•The NAD+-dependent formate dehydrogenase was successfully expressed in P. polymyxa.•There is no need to supplement formic acid during fermentation.•The yield of R,R-2,3-butanediol was improved through the NADH regeneration system.•The study provides a new strategy for promoting synthesis of NADH-dependent products.
The NAD+-dependent formate dehydrogenase (FDH) gene from Candida boidinii was introduced into Paenibacillus polymyxa ZJ-9. The effects of this exogenous gene on the growth of the recombinant strain P. polymyxa XG-1, FDH activity, intracellular NADH and NAD+ level and the synthesis of R,R-2,3-butanediol (R,R-2,3-BD) were determined. Results from the fermentation in the 7.5L bioreactor showed that the exogenous FDH was highly expressed in the recombinant strain. The titers of NADH, lactic acid, ethanol, NADH/NAD+, and CO2 excretion rate (CER) of the recombinant strain increased considerably, while acetoin and formic acid decreased significantly. The highest titers of R,R-2,3-BD by the recombinant strain in batch and fed-batch fermentation were 36.8g/L and 51.3g/L, increased 10.2% and 8.0% compared with the parent strain, respectively. This study confirmed that coenzyme regeneration system can manipulate substance metabolism in bacteria, and is an efficient way for promoting the synthesis of NADH-dependent products. |
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ISSN: | 0960-8524 1873-2976 |
DOI: | 10.1016/j.biortech.2015.11.067 |