Difference between revisions of "Part:BBa K2665012"
Line 6: | Line 6: | ||
It increases glycerol synthesis which work as compatible solute. So, it may raise osmotolerance in yeast. | It increases glycerol synthesis which work as compatible solute. So, it may raise osmotolerance in yeast. | ||
− | <!-- Add more about the biology of this part here | + | <!-- Add more about the biology of this part here--> |
==Usage and Biology== | ==Usage and Biology== | ||
This part sequence can be used directly because it contains promoter and terminator, but promoter is TDH3 promoter so it can't express in <i>E. coli</i>. If need to use the protein in <i>E. coli</i>, please note that you have to change promoter and terminator. ZrGPD1 is the gene that codes a glycerol-3-phosphate dehydrogenase which controls glycerol synthesis. | This part sequence can be used directly because it contains promoter and terminator, but promoter is TDH3 promoter so it can't express in <i>E. coli</i>. If need to use the protein in <i>E. coli</i>, please note that you have to change promoter and terminator. ZrGPD1 is the gene that codes a glycerol-3-phosphate dehydrogenase which controls glycerol synthesis. |
Revision as of 02:30, 9 October 2018
TDH3-ZrGPD1-6xHis-CYC
ZrGPD1 is the gene that codes a glycerol-3-phosphate dehydrogenase which controls glycerol synthesis in Zygosaccharomyces rouxii. It increases glycerol synthesis which work as compatible solute. So, it may raise osmotolerance in yeast.
Usage and Biology
This part sequence can be used directly because it contains promoter and terminator, but promoter is TDH3 promoter so it can't express in E. coli. If need to use the protein in E. coli, please note that you have to change promoter and terminator. ZrGPD1 is the gene that codes a glycerol-3-phosphate dehydrogenase which controls glycerol synthesis.
Characterization
We used this part in order to enhance the solt tolerance of yeast. We assessed the tolerance in our method(please refer to [http://http://2018.igem.org/Team:Kyoto/Protocol our Wiki's Special Protocol] ). Result is showed below.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 1923
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal AgeI site found at 1454
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 1129
Illegal BsaI site found at 1889
Illegal BsaI.rc site found at 1271
Reference
[1] Hou,Lihua Wang,Meng Wang,Cong Wang,Chunling Wang,Haiyong (2013) Analysis of salt-tolerance genes in zygosaccharomyces rouxii, Applied Biochemistry and Biotechnoloogy 1417-1425