Abstract

Biological production of 2,3-butandiol (2,3-BD) has received great attention as an alternative to the petroleum-based 2,3-BD production. In this study, a high production of 2,3-BD in fed-batch fermentation was investigated with a newly isolated bacterium designated as Raoultella ornithinolytica B6. The isolate produced 2,3-BD as the main product using hexoses (glucose, galactose, and fructose), pentose (xylose) and disaccharide (sucrose). The effects of temperature, pH-control schemes, and agitation speeds on 2,3-BD production were explored to optimize the fermentation conditions. Notably, cell growth and 2,3-BD production by R. ornithinolytica B6 were higher at 25°C than at 30°C. When three pH control schemes (no pH control, pH control at 7, and pH control at 5.5 after the pH was decreased to 5.5 during fermentation) were tested, the best 2,3-BD titer and productivity along with reduced by-product formation were achieved with pH control at 5.5. Among different agitation speeds (300, 400, and 500 rpm), the optimum agitation speed was 400 rpm with 2,3-BD titer of 68.27 g/L, but acetic acid was accumulated up to 23.32 g/L. Further enhancement of the 2,3-BD titer (112.19 g/L), yield (0.38 g/g), and productivity (1.35 g/L/h) as well as a significant reduction of acetic acid accumulation (9.71 g/L) was achieved by the overexpression of homologous budABC genes, the 2,3-BD-synthesis genes involved in the conversion of pyruvate to 2,3-BD. This is the first report presenting a high 2,3-BD production by R.ornithinolytica which has attracted little attention with respect to 2,3-BD production, extending the microbial spectrum of 2,3-BD producers.

Highlights

  • The isolate was designated as R. ornithinolytica B6 and deposited in the Korea Culture Center of Microorganisms (KCCM) as KTCM11176-P

  • Because the cultivation of R. ornithinolytica B6 at 25°C appeared to be effective for cell growth and 2,3-BD production, all further studies were done at 25°C

  • R. ornithinolytica B6 did not grow at 37°C which could be a reason for rare infections in humans by R. ornithinolytica

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Summary

Introduction

2,3-butanediol (2,3-BD) is a promising platform material with a wide range of industrial applications as a solvent and a precursor for methyl ethyl ketone, 1,3-butanedien, and 2-butene [1,2]. The production of 2,3-BD by Enterobacter aerogenes, K. pneumoniae and K. oxytoca was reported to be dramatically increased by deletion of NADH-requiring by-product synthesis genes [8,9,10,11] and the overexpression of 2,3-BD synthesis related genes [12,13,14] In addition to those microorganisms, well-known model hosts such as Saccharomyces cerevisiae [3] and Escherichia coli [15] have been engineered to produce 2,3-BD. The results validated that R. ornithinolytica B6 has potential as a high 2,3-BD producer This is the first study on optimization of fermentation conditions and genetic modification for 2,3-BD production with R. ornithinolytica

Materials and Methods
Analytical procedures
Results
Discussion
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