氨基葡萄糖
大肠杆菌
重组DNA
补料分批培养
生物化学
N-乙酰氨基葡萄糖
化学
食品科学
生物
酶
发酵
基因
作者
Xin Chen,Long Liu,Jianghua Li,Jie Liu,Guocheng Du,Jian Chen
出处
期刊:Journal of Industrial Microbiology & Biotechnology
[Oxford University Press]
日期:2011-10-18
卷期号:39 (2): 359-365
被引量:26
标识
DOI:10.1007/s10295-011-1046-0
摘要
In this work, a recombinant Escherichia coli was constructed by overexpressing glucosamine (GlcN) synthase and GlcN-6-P N-acetyltransferase for highly efficient production of GlcN and N-acetylglucosamine (GlcNAc). For further enhancement of GlcN and GlcNAc production, the effects of different glucose feeding strategies including constant-rate feeding, interval feeding, and exponential feeding on GlcN and GlcNAc production were investigated. The results indicated that exponential feeding resulted in relatively high cell growth rate and low acetate formation rate, while constant feeding contributed to the highest specific GlcN and GlcNAc production rate. Based on this, a multistage glucose supply approach was proposed to enhance GlcN and GlcNAc production. In the first stage (0-2 h), batch culture with initial glucose concentration of 27 g/l was conducted, whereas the second culture stage (2-10 h) was performed with exponential feeding at μ (set) = 0.20 h⁻¹, followed by feeding concentrated glucose (300 g/l) at constant rate of 32 ml/h in the third stage (10-16 h). With this time-variant glucose feeding strategy, the total GlcN and GlcNAc yield reached 69.66 g/l, which was enhanced by 1.59-fold in comparison with that of batch culture with the same total glucose concentration. The time-dependent glucose feeding approach developed here may be useful for production of other fine chemicals by recombinant E. coli.
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