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Here,a dopa decarboxylase (DDC) from Harmonia axyridis was heterogeneously expressed in Escherichia coli for the efficient biosynthesis of dopamine.For the production of recombinant DDC,the cultivation conditions including IPTG concentration,temperature and induction time were optimized and obtained an optimal specific enzyme activity of 51.72 U·mg-1 crude extracts.After the purification of DDC with a recovery yield of 68.79%,its activity was further characterized.The Vmax,Km,Kcat,and Kcat/Km of DDC for dihydroxyphenylalanine (dopa) were 0.02 mmol·ml-1·s-1,2.328 mmol·ml-1,10435.90 s-1 and 4482.77 ml·mmol-1·s-1,respectively.The highest DDC activity was observed at the condition of pH 7.5 and 45 ℃.With the purified DDC,the feasibility to produce dopamine from L-dopa was evaluated.The optimal yield was determined at the following bioconversion conditions:pH of 7.0,the reaction temper-ature of 40 ℃,0.4 mmol·L-1 of PLP and 4 g·L-1 of L-dopa.Subsequently,a fed-batch process for the pro-duction of dopamine was developed and the effect of oxygen was evaluated.The titer,yield and productivity of dopamine reached up to 21.99 g·L-1,80.88% and 14.66 g·L-1h-1 at 90 min under anaer-obic condition.
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篇名 Characterization and application of a recombinant dopa decarboxylase from Harmonia axyridis for the efficient biosynthesis of dopamine
来源期刊 中国化学工程学报(英文版) 学科
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年,卷(期) 2022,(1) 所属期刊栏目 Biotechnology and Bioengineering
研究方向 页码范围 449-456
页数 8页 分类号
字数 语种 英文
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中国化学工程学报(英文版)
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1004-9541
11-3270/TQ
大16开
北京东城区青年湖南街13号
80-448
1982
eng
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