Difference between revisions of "Part:BBa K3600007"
(2 intermediate revisions by one other user not shown) | |||
Line 3: | Line 3: | ||
<partinfo>BBa_K3600007 short</partinfo> | <partinfo>BBa_K3600007 short</partinfo> | ||
− | |||
− | + | 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.<html><a href="#Lee2015"><sup>1</sup></a></html> and can be ordered online. | |
+ | The promoter part plasmid (BBa_K3600001) and the reporter part plasmid (BBa_K3600010) were synthesized by us. | ||
+ | |||
===Usage and Biology=== | ===Usage and Biology=== | ||
− | + | This cassette contains the TRX2 promoter upstream of a reporter gene (mScarlet-i). TRX2 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_K3600014). | |
+ | |||
<span class='h3bb'>Sequence and Features</span> | <span class='h3bb'>Sequence and Features</span> | ||
<partinfo>BBa_K3600007 SequenceAndFeatures</partinfo> | <partinfo>BBa_K3600007 SequenceAndFeatures</partinfo> | ||
Line 17: | Line 19: | ||
<partinfo>BBa_K3600007 parameters</partinfo> | <partinfo>BBa_K3600007 parameters</partinfo> | ||
<!-- --> | <!-- --> | ||
+ | |||
+ | ===References=== | ||
+ | <HTML><a name=Lee2015 style="color:black"> | ||
+ | [1] Lee, M. E., DeLoache, W. C., Cervantes, B. & Dueber, J. E. A Highly Characterized Yeast Toolkit for Modular, Multipart Assembly. ACS Synth. Biol. 4, 975–986 (2015). | ||
+ | </a></html> | ||
+ | |||
+ | <HTML><a name=reg style="color:black"> | ||
+ | [2] Kuge S, Jones N. YAP1 dependent activation of TRX2 is essential for the response of Saccharomyces cerevisiae to oxidative stress by hydroperoxides. The EMBO journal. 1994 Feb;13(3):655-64. | ||
+ | </a></html> |
Latest revision as of 02:52, 28 October 2020
prTRX2-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_K3600001) and the reporter part plasmid (BBa_K3600010) were synthesized by us.
Usage and Biology
This cassette contains the TRX2 promoter upstream of a reporter gene (mScarlet-i). TRX2 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_K3600014).
Sequence and Features
- 10INCOMPATIBLE WITH RFC[10]Illegal EcoRI site found at 936
Illegal EcoRI site found at 1666
Illegal XbaI site found at 945
Illegal XbaI site found at 1843
Illegal SpeI site found at 2811
Illegal PstI site found at 2820 - 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 936
Illegal EcoRI site found at 1666
Illegal SpeI site found at 2811
Illegal PstI site found at 2820
Illegal NotI site found at 924
Illegal NotI site found at 2830 - 21INCOMPATIBLE WITH RFC[21]Illegal suffix found in sequence at 2413
Illegal EcoRI site found at 936
Illegal EcoRI site found at 1666
Illegal BglII site found at 2284 - 23INCOMPATIBLE WITH RFC[23]Illegal EcoRI site found at 936
Illegal EcoRI site found at 1666
Illegal XbaI site found at 945
Illegal XbaI site found at 1843
Illegal SpeI site found at 2811
Illegal PstI site found at 2820 - 25INCOMPATIBLE WITH RFC[25]Illegal EcoRI site found at 936
Illegal EcoRI site found at 1666
Illegal XbaI site found at 945
Illegal XbaI site found at 1843
Illegal SpeI site found at 2811
Illegal PstI site found at 2820
Illegal NgoMIV site found at 2768 - 1000COMPATIBLE WITH RFC[1000]