Molecular Cloning of cpcU and Heterodimeric Bilin Lyase Activity Analysis of CpcU and CpcS for Attachment of Phycocyanobilin to Cys-82 on the β-Subunit of Phycocyanin in Arthrospira platensis FACHB314.

نویسندگان

  • Fei Wu
  • Xiaonan Zang
  • Xuecheng Zhang
  • Ran Zhang
  • Xiaoyun Huang
  • Lulu Hou
  • Minjie Jiang
  • Chang Liu
  • Chunhong Pang
چکیده

A new bilin lyase gene cpcU was cloned from Arthrospira platensis FACHB314 to study the assembly of the phycocyanin β-Subunit. Two recombinant plasmids, one contained the phycocyanobilin (PCB) producing genes (hoxI and pcyA), while the other contained the gene of the β-Subunit of phycobiliprotein (cpcB) and the lyase gene (cpcU, cpcS, or cpcU/S) were constructed and separately transferred into Escherichia coli in order to test the activities of relevant lyases for catalyzing PCB addition to CpcB during synthesizing fluorescent β-PC of A. platensis FACHB314. The fluorescence intensity examination showed that Cys-82 maybe the active site for the β-Subunit binding to PCBs and the attachment could be carried out by CpcU, CpcS, or co-expressed cpcU/S in A. platensis FACHB314.

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منابع مشابه

BIOGENESIS OF PHYCOBILIPROTEINS. II. CpcS-I AND CpcU COMPRISE THE HETERODIMERIC BILIN LYASE THAT ATTACHES PHYCOCYANOBILIN TO CYS-82 OF β-PHYCOCYANIN AND CYS-81 OF ALLOPHYCOCYANIN SUBUNITS IN SYNECHOCOCCUS SP. PCC 7002*

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عنوان ژورنال:
  • Molecules

دوره 21 3  شماره 

صفحات  -

تاریخ انتشار 2016