2,3-丁二醇
发酵
大肠杆菌
生物过程
生物反应器
化学
产量(工程)
基质(水族馆)
重组DNA
食品科学
色谱法
生物化学
有机化学
材料科学
生物
基因
古生物学
冶金
生态学
作者
Naoya Kataoka,Alisa S. Vangnai,H Ueda,Takahisa Tajima,Yutaka Nakashimada,Junichi Kato
标识
DOI:10.1080/09168451.2014.891933
摘要
(R)-1,3-butanediol ((R)-1,3-BD) is an important substrate for the synthesis of industrial chemicals. Despite its large demand, a bioprocess for the efficient production of 1,3-BD from renewable resources has not been developed. We previously reported the construction of recombinant Escherichia coli that could efficiently produce (R)-1,3-BD from glucose. In this study, the fermentation conditions were optimized to further improve 1,3-BD production by the recombinant strain. A batch fermentation was performed with an optimized overall oxygen transfer coefficient (82.3 h(-1)) and pH (5.5); the 1,3-BD concentration reached 98.5 mM after 36 h with high-yield (0.444 mol (mol glucose)(-1)) and a high maximum production rate (3.63 mM h(-1)). In addition, a fed-batch fermentation enabled the recombinant strain to produce 174.8 mM 1,3-BD after 96 h cultivation with a yield of 0.372 mol (mol glucose)(-1), a maximum production rate of 3.90 mM h(-1), and a 98.6% enantiomeric excess (% ee) of (R)-1,3-BD.
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