Difference between revisions of "Part:BBa K3600004"
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The GLR1 gene encodes the glutathione reductase, which catalyses the reduction of the oxidized form of glutathione (GSSG) to Glutathione (GSH).<html><a href="#Grant1996"><sup>1</sup></a></html> | The GLR1 gene encodes the glutathione reductase, which catalyses the reduction of the oxidized form of glutathione (GSSG) to Glutathione (GSH).<html><a href="#Grant1996"><sup>1</sup></a></html> | ||
This promoter is regulated by the transcription factor Yap1p. | This promoter is regulated by the transcription factor Yap1p. | ||
| − | The binding site for Yap1p, in the promoter GLR1, is TTACTAA.<html><a href="#Kuge1994"><sup> | + | The binding site for Yap1p, in the promoter GLR1, is TTACTAA.<html><a href="#Kuge1994"><sup>2</sup></a></html> |
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| − | <span | + | <span class='h3bb'>Sequence and Features</span> |
<partinfo>BBa_K3600004 SequenceAndFeatures</partinfo> | <partinfo>BBa_K3600004 SequenceAndFeatures</partinfo> | ||
Revision as of 17:53, 27 October 2020
GLR1 promoter part plasmid
GLR1 promoter part plasmid was made in order to create a part plasmid which contains the GLR1 promoter and is compatible with the Yeast Toolkit.
To create a promoter part plasmid compatible with the yeast toolkit, at first, we designed a gBlock consisting of the 500bp promoter region, that was retrieved from the yeast genome database, and two linking sequences which were added to the ends of the promoter. Then, the gBlock was inserted into the part plasmid entry vector (pYTK001) through a BsmBI assembly.
Usage and Biology
The GLR1 gene encodes the glutathione reductase, which catalyses the reduction of the oxidized form of glutathione (GSSG) to Glutathione (GSH).1 This promoter is regulated by the transcription factor Yap1p. The binding site for Yap1p, in the promoter GLR1, is TTACTAA.2
Sequence and Features
- 10INCOMPATIBLE WITH RFC[10]Illegal XbaI site found at 778
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23INCOMPATIBLE WITH RFC[23]Illegal XbaI site found at 778
- 25INCOMPATIBLE WITH RFC[25]Illegal XbaI site found at 778
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 624
Illegal BsaI.rc site found at 1145