Difference between revisions of "Part:BBa K3600009"
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===Usage and Biology=== | ===Usage and Biology=== | ||
− | This cassette contains the GSH1 promoter upstream of a reporter gene (mScarlet-i). GSH1 is a stress response gene in s.cerevisiae that is regulated by the YAP1 master regulator<html><a href="#reg"><sup>2</sup></a></html>. | + | This cassette contains the GSH1 promoter upstream of a reporter gene (mScarlet-i). GSH1 is a stress response gene in s.cerevisiae that is regulated by the YAP1 master regulator<html><a href="#reg"><sup>2</sup></a></html>. This cassette is then assembled with a part plasmid containing Lys2 homology sequences (BBa_K36000012) in another Golden Gate BsmBI assembly, to give a final integration cassette (BBa_K3600015). |
<span class='h3bb'>Sequence and Features</span> | <span class='h3bb'>Sequence and Features</span> |
Revision as of 01:54, 28 October 2020
prGSH1-yomScarlet-I-tADH1
This cassette was assembled from 6 part plasmids via Golden Gate assembly using the BsmbBI restriction enzyme. The two connectors (pYTK002 and pYTK072), as well as the terminator (pYTK053) and the Ampicilin resistance/backbone (pYTK095) part plasmids are part of the YTK toolkit developed by Lee et al.1 and can be ordered online.
The promoter part plasmid (BBa_K3600003) and the reporter part plasmid (BBa_K3600010) were synthesized by us.
Usage and Biology
This cassette contains the GSH1 promoter upstream of a reporter gene (mScarlet-i). GSH1 is a stress response gene in s.cerevisiae that is regulated by the YAP1 master regulator2. This cassette is then assembled with a part plasmid containing Lys2 homology sequences (BBa_K36000012) in another Golden Gate BsmBI assembly, to give a final integration cassette (BBa_K3600015).
Sequence and Features
- 10INCOMPATIBLE WITH RFC[10]Illegal EcoRI site found at 1184
Illegal EcoRI site found at 1914
Illegal XbaI site found at 1193
Illegal XbaI site found at 1618
Illegal XbaI site found at 2091
Illegal SpeI site found at 3059
Illegal PstI site found at 3068 - 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 1184
Illegal EcoRI site found at 1914
Illegal SpeI site found at 3059
Illegal PstI site found at 3068
Illegal NotI site found at 1172
Illegal NotI site found at 3078 - 21INCOMPATIBLE WITH RFC[21]Illegal suffix found in sequence at 2661
Illegal EcoRI site found at 1184
Illegal EcoRI site found at 1914
Illegal BglII site found at 1636
Illegal BglII site found at 2532 - 23INCOMPATIBLE WITH RFC[23]Illegal EcoRI site found at 1184
Illegal EcoRI site found at 1914
Illegal XbaI site found at 1193
Illegal XbaI site found at 1618
Illegal XbaI site found at 2091
Illegal SpeI site found at 3059
Illegal PstI site found at 3068 - 25INCOMPATIBLE WITH RFC[25]Illegal EcoRI site found at 1184
Illegal EcoRI site found at 1914
Illegal XbaI site found at 1193
Illegal XbaI site found at 1618
Illegal XbaI site found at 2091
Illegal SpeI site found at 3059
Illegal PstI site found at 3068
Illegal NgoMIV site found at 3016 - 1000COMPATIBLE WITH RFC[1000]