Difference between revisions of "Part:BBa K3717014"
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+ | <b>Figure 1: Endo-β-galactosidase from 2014 Tuebingen with T7 promoter, RBS, and a terminator. | ||
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+ | <b><font size="+1.2">Contruct Design</font></b> | ||
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+ | Endo-β-galactosidase an enzyme that catalyzes the cleavage of the A and B type blood antigens (trisaccharides) such that the remaining sugar can be classified as a H antigen, which the anti-A and anti-B antibodies are unable to recognize and thus does not elicit an immune response in the human body. Thus, the enzyme can convert both A and B blood types to universal O type. The enzyme has been previously shown to successfully convert A,B, and AB type erythrocytes to O type but lacked a cost-effective method of production. | ||
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+ | We obtained the amino acid sequence of the endo-β-galactosidase protein, derived from Clostridium perfringens, from the iGEM DNA Repository Plate (BBa_K1483001), which served as our Open Reading Frame (ORF). We attached a T7 promoter, derived from the T7 phage, and strong ribosome binding site (RBS; BBa_K525998) upstream of the open reading frame (ORF). The composite gene was synthesized through DNA cloning. | ||
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Revision as of 08:39, 19 October 2021
Endo-β-Galactosidase with T7 promoter and strong RBS
Figure 1: Endo-β-galactosidase from 2014 Tuebingen with T7 promoter, RBS, and a terminator.
<b>Contruct Design
Endo-β-galactosidase an enzyme that catalyzes the cleavage of the A and B type blood antigens (trisaccharides) such that the remaining sugar can be classified as a H antigen, which the anti-A and anti-B antibodies are unable to recognize and thus does not elicit an immune response in the human body. Thus, the enzyme can convert both A and B blood types to universal O type. The enzyme has been previously shown to successfully convert A,B, and AB type erythrocytes to O type but lacked a cost-effective method of production.
We obtained the amino acid sequence of the endo-β-galactosidase protein, derived from Clostridium perfringens, from the iGEM DNA Repository Plate (BBa_K1483001), which served as our Open Reading Frame (ORF). We attached a T7 promoter, derived from the T7 phage, and strong ribosome binding site (RBS; BBa_K525998) upstream of the open reading frame (ORF). The composite gene was synthesized through DNA cloning.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]