Difference between revisions of "Part:BBa K3046033"
Line 5: | Line 5: | ||
This part is a long sequence of DNA that are homologous to a part of the <i>albA</i> conidial pigment gene. This homology can be used for homologous recombination of genomic constructs flanked by this IS2 sequence (along with the upstream sequence BBa_K3046032). | This part is a long sequence of DNA that are homologous to a part of the <i>albA</i> conidial pigment gene. This homology can be used for homologous recombination of genomic constructs flanked by this IS2 sequence (along with the upstream sequence BBa_K3046032). | ||
− | |||
− | |||
===Usage and Biology=== | ===Usage and Biology=== | ||
Revision as of 00:29, 22 October 2019
IS2 downstream sequence for A. niger genome integration
This part is a long sequence of DNA that are homologous to a part of the albA conidial pigment gene. This homology can be used for homologous recombination of genomic constructs flanked by this IS2 sequence (along with the upstream sequence BBa_K3046032).
Usage and Biology
Characterization
We have demonstrated that the IS2 up- and downstream sequences work as expected qualitatively speaking. We did this by transforming a GFP reporter into Aspergillus niger ATCC1015, and as shown in figure 1, we were able to make the transformants express GFP as opposed to the wildtype control.
[[File:T--DTU-Denmark--GFPfung2.png]200px|fig.1|left|The two upper pictures show Aspergillus niger ATCC1015 transformed with the pPEA2P1 plasmid. The two pictures in the bottom show the same fungi, transformed with a self replicating AMA1 plasmid containing the PyrG marker]]
Sequence and Features
- 10INCOMPATIBLE WITH RFC[10]Illegal EcoRI site found at 118
Illegal PstI site found at 1262
Illegal PstI site found at 1863 - 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 118
Illegal PstI site found at 1262
Illegal PstI site found at 1863 - 21INCOMPATIBLE WITH RFC[21]Illegal EcoRI site found at 118
Illegal BglII site found at 1360 - 23INCOMPATIBLE WITH RFC[23]Illegal EcoRI site found at 118
Illegal PstI site found at 1262
Illegal PstI site found at 1863 - 25INCOMPATIBLE WITH RFC[25]Illegal EcoRI site found at 118
Illegal PstI site found at 1262
Illegal PstI site found at 1863
Illegal NgoMIV site found at 1250 - 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI site found at 1751
Illegal SapI site found at 2060