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    <identifier>10.57760/sciencedb.07431</identifier>
    <datestamp>2023-02-15T15:52:40Z</datestamp>
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  <dc:date>2023-02-15</dc:date>
  <dc:title>Efficient Biosynthesis of Phycobiliprotein in Escherichia coli</dc:title>
  <dc:identifier>doi:10.57760/sciencedb.07431</dc:identifier>
  <dc:language>en</dc:language>
  <dc:description>&amp;nbsp;In this work, a pathway for SLA-PEB (a fusion protein of streptavidin and allophycocyanin that covalently binds phycoerythrobilin (PEB)) biosynthesis in E. coli was constructed using a single-expression plasmid strategy. Compared with a previous E. coli strain transformed with dual plasmids, the E. coli strain transformed with a single plasmid showed increased plasmid stability and produced SLA-PEB with a higher chromophorylation ratio. To achieve full chromophorylation of SLA-PEB, directed evolution was employed to improve the catalytic performance of lyase CpcS. In addition, the catalytic abilities of heme oxygenases from different cyanobacteria were investigated based on biliverdin IX&amp;alpha; and PEB accumulation. Upregulation of the heme biosynthetic pathway genes was also carried out to increase heme availability and PEB biosynthesis in E. coli. Fed-batch fermentation was conducted for the strain V5ALD, which produced recombinant SLA-PEB with a chromophorylation ratio of 96.7%.</dc:description>
  <dc:subject>藻胆蛋白; 藻胆色素; 质粒稳定性; 大肠杆菌</dc:subject>
  <dc:creator>Huaxin Chen</dc:creator>
  <dc:creator>Peng Jiang</dc:creator>
  <dc:rights>PUBLIC</dc:rights>
  <dc:rights>https://creativecommons.org/publicdomain/zero/1.0/</dc:rights>
  <dc:type>dataset</dc:type>
  <dc:relation>http://www.doi.org/https://doi.org/10.1186/s12934-019-1100-6</dc:relation>
  <dc:publisher>Science Data Bank</dc:publisher>
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