Applied Biochemistry and Biotechnology

, Volume 142, Issue 1, pp 52–59

Combinational Biosynthesis of a Fluorescent Cyanobacterial Holo-α-Phycocyanin in Escherichia coli by Using One Expression Vector

Authors

  • Xiangyu Guan
    • College of Marine Life Science, Faculty of Life Science and TechnologyOcean University of China
  • Song Qin
    • Institute of OceanologyChinese Academy of Sciences
  • Zhongliang Su
    • Qingdao University of Science & Technology
  • Fangqing Zhao
    • Institute of OceanologyChinese Academy of Sciences
  • Baosheng Ge
    • Institute of OceanologyChinese Academy of Sciences
  • Fuchao Li
    • Institute of OceanologyChinese Academy of Sciences
    • College of Marine Life Science, Faculty of Life Science and TechnologyOcean University of China
Article

DOI: 10.1007/s12010-007-8000-7

Cite this article as:
Guan, X., Qin, S., Su, Z. et al. Appl Biochem Biotechnol (2007) 142: 52. doi:10.1007/s12010-007-8000-7

Abstract

The phycobiliproteins (PBSs) are large pigment proteins found in certain algae that play a central role in harvesting light energy for photosynthesis. Phycocyanin (PC) is one type of PBSs that gains increasing attention owing to its various biological and pharmacological properties. In this paper, an expression vector containing five essential genes in charge of biosynthesis of cyanobacterial C-phycocyanin (C-PC) holo-α subunit (holo-CpcA) was successfully constructed resulting in over-expression of a fluorescent holo-CpcA in E. coli BL21. The vector harbored two cassettes: one cassette carried genes hox1 and pcyA required for conversion of heme to phycocyanobilin (PCB), and the other cassette carried cpcA encoding CpcA along with cpcE and cpcF both of which were necessary and sufficient for the correct addition of PCB to CpcA. The vector system contained a His-tag for protein purification. The purified protein showed correct molecular weight on SDS-PAGE gel and emitted orange fluorescence by UV excitation. The maximum peak of absorbance spectrum was at 623 nm, and the maximum peak of fluorescence emission and excitation were at 648 and 633 nm, respectively, which were similar to those of native C-PC. This study provides an efficient method for large-scale production of the fluorescent holo-CpcA in biotechnological applications.

Keywords

EscherichiacoliPhycocyaninFluorescenceHolo-HT-CpcA

Abbreviations

PBS

phycobiliproteins

CpcA

α subunit of C-phycocyanin

CpcE and CpcF

subunits of the heterodimeric phycocyanin α-subunit phycocyanobilin lyase

Hox1

heme oxygenase 1

HT

His-tag

PCB

phycocyanobilin

PcyA

3Z-phycocyanobilin: ferredoxin oxidoreductase

Sp

spectinomycin

Km

kanamycin

Copyright information

© Humana Press Inc. 2007