Abstract
1,3-propanediol (1,3-PDO) is one of the most important industrial chemicals due to its highly desired properties and its wide applications as a key component of the emerging polymer industry. Biotechnology route has been one of the most interesting methods for 1,3-PDO production, whereas, the dha genes were essential to 1,3-PDO biosynthesis. In this study, we cloned and placed the dha cassettes under the control of a glyceraldehyde 3-phosphate dehydrogenase gene promoter pGAP and homologous ZrFPS1 gene promoter pZrfps1; these two promoters were further integrated into the chromosome of Z. rouxii JL2011 to generate recombinant strain JL2011-GZ and JL2011-ZZ, respectively. The results showed that the two strains could produce 1,3-PDO from glucose with a final yield of 6.9 and 10.3 g/l, respectively. The engineered strain JL2011-ZZ showed a 2.3- and 1.5-fold increase in the specific activities and final concentration of 1,3-PDO, respectively, with respect to JL2011-GZ. Batch fermentation with aerobic/micro-aerobic combined strategy of JL2011-ZZ resulted a titer of 17.1 g/l and a yield from glucose of 8.6 %. These results demonstrated that JL2011-ZZ would be a potential strain for 1,3-PDO production from glucose.
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Acknowledgments
This work was supported by the Zhejiang key project of innovative team (2009R500273), Zhejiang S&T project (2010C32063), Zhejiang Province Natural Science Foundation (LQ12C14004, LY12C140046), and National Basic Research Program of China (973 Program; No.2011CB111602, 2012CB114100). We are grateful to Dr. Zhiming Rao for his support in the early stage of this work and Dr. Bin Zhuge for his helpful suggestion.
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Ma, Z., Bian, Y., Shentu, X. et al. Development of a novel recombinant strain Zygosacharomyces rouxii JL2011 for 1,3-propanediol production from glucose. Appl Microbiol Biotechnol 97, 4055–4064 (2013). https://doi.org/10.1007/s00253-012-4501-6
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DOI: https://doi.org/10.1007/s00253-012-4501-6