Difference between revisions of "Part:BBa K1959003"
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<partinfo>BBa_K1959003 short</partinfo> | <partinfo>BBa_K1959003 short</partinfo> | ||
− | This part | + | This part contains the coding sequence (CDS) of β-carotene ketolase (BKT, EC 1.14.11.B16) of algae (''Chlamydomonas reinhardti''), which catalyzes the conversion of zeaxanthin to astaxanthin. A ''Pea'' transit peptide of RUBISCO small subunit has been fused to BKT and the codon has been optimized for rice (''Oryza sativa''). |
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===Usage and Biology=== | ===Usage and Biology=== | ||
+ | As a strong antioxidant, astaxanthin synthesis, especially, its biosynthesis attracts much interest of scientists. BKT symmetrically introduces two keto groups to two β-ionone rings of zeaxanthin to generate astaxanthin in algae (Figure.1).<br> In our reconstructed pathway, the CDS of ''BKY'' was codon-optimized for rice. In addition, a ''Pea'' transit peptide was fused to the BKY for proper sorting into the plastid. | ||
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Revision as of 16:03, 19 October 2016
BKT coding sequence fused with Pea transit peptide
This part contains the coding sequence (CDS) of β-carotene ketolase (BKT, EC 1.14.11.B16) of algae (Chlamydomonas reinhardti), which catalyzes the conversion of zeaxanthin to astaxanthin. A Pea transit peptide of RUBISCO small subunit has been fused to BKT and the codon has been optimized for rice (Oryza sativa).
Usage and Biology
As a strong antioxidant, astaxanthin synthesis, especially, its biosynthesis attracts much interest of scientists. BKT symmetrically introduces two keto groups to two β-ionone rings of zeaxanthin to generate astaxanthin in algae (Figure.1).
In our reconstructed pathway, the CDS of BKY was codon-optimized for rice. In addition, a Pea transit peptide was fused to the BKY for proper sorting into the plastid.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal AgeI site found at 1085
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 478
Illegal SapI site found at 900