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Improved production of 1-deoxynojirymicin in Escherichia coli through metabolic engineering

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Abstract

Azasugars, such as 1-deoxynojirymicin (1-DNJ), are associated with diverse pharmaceutical applications, such as antidiabetic, anti-obesity, anti-HIV, and antitumor properties. Different azasugars have been isolated from diverse microbial and plant sources though complicated purification steps, or generated by costly chemical synthesis processes. But the biosynthesis of such potent molecules using Escherichia coli as a heterologous host provides a broader opportunity to access these molecules, particularly by utilizing synthetic biological, metabolic engineering, and process optimization approaches. This work used an integrated approach of synthetic biology, enzyme engineering, and pathway optimization for rational metabolic engineering, leading to the improved production of 1-DNJ. The production of 1-DNJ in recombinant E. coli culture broth was confirmed by enzymatic assays and mass spectrometric analysis. Specifically, the pathway engineering for its key precursor, fructose-6-phosphate, along with optimized media condition, results in the highest production levels. When combined, 1-DNJ production was extended to ~ 273 mg/L, which is the highest titer of production of 1-DNJ reported using E. coli.

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Acknowledgements

This work was supported by the National Research Foundation of Korea (NRF) Grant funded by the Korea government (MEST) (NRF-2017R1A2A2A05000939).

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Correspondence to Jae Kyung Sohng.

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All the authors read the manuscript and agreed on the contents of manuscript. All authors declare that they have no conflict of interest.

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This article does not include any studies with human participants or animals models.

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Rayamajhi, V., Dhakal, D., Chaudhary, A.K. et al. Improved production of 1-deoxynojirymicin in Escherichia coli through metabolic engineering. World J Microbiol Biotechnol 34, 77 (2018). https://doi.org/10.1007/s11274-018-2462-3

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  • DOI: https://doi.org/10.1007/s11274-018-2462-3

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