Cite this paper:
MA Chengbo, LI Wenjun, GE Baosheng, LIN Jian, QIN Song. Biosynthesis of phycocyanobilin in recombinant Escherichia coli[J]. HaiyangYuHuZhao, 2020, 38(2): 529-538

Biosynthesis of phycocyanobilin in recombinant Escherichia coli

MA Chengbo1, LI Wenjun2,4, GE Baosheng3, LIN Jian1, QIN Song2,4
1 College of Life Sciences, Yantai University, Yantai 264005, China;
2 Yantai Institute of Coastal Zone Research, Chinese Academy of Sciences, Yantai 264003, China;
3 Center for Bioengineering and Biotechnology, China University of Petroleum (East China), Qingdao 266580, China;
4 Center for Ocean Mega-Science, Chinese Academy of Sciences, Qingdao 266071, China
The recombinant expression of phycocyanobilin (PCB) was carried out in Escherichia coli, and the best fermentation conditions of recombinant E. coli biosynthesized PCB are optimized in the response surface methodology to improve PCB production. The recombinant PCB is extracted, isolated, and purified by methanol and chloroform extraction. Recombinant PCB is validated in UV-vis spectroscopy, high-pressure liquid chromatography, and mass spectrometry. In addition, the anti-oxidant activities of the recombinant PCB are determined. The best induction conditions that optimized by Design Expert 8.0 software include:lactose concentration 4 mmol/L, induction temperature 24.69℃, induction time 4.6 h, and induction duration 13.57 h, under which the PCB expression level reached approximately 13 mg PCB/L, which is more than four times of previously reported 3 mg PCB/L. The maximum absorption peak of the recombinant PCB is located at 680 nm with a high fluorescence intensity of 470 nm. The recombinant PCB has a good ability to scavenge 2,2-diphenyl-1-picrylhydrazyl (DPPH) free radicals.
Key words:    combinational biosynthesis|phycocyanobilin|response surface methodology|antioxidant   
Received: 2019-03-12   Revised: 2019-05-08
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