Part:BBa_K3138000:Design
Metallothionein-IV promoter Uniprot Q9HFC9-1
- 10INCOMPATIBLE WITH RFC[10]Illegal EcoRI site found at 95
- 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 95
- 21INCOMPATIBLE WITH RFC[21]Illegal EcoRI site found at 95
Illegal BglII site found at 380
Illegal BglII site found at 492 - 23INCOMPATIBLE WITH RFC[23]Illegal EcoRI site found at 95
- 25INCOMPATIBLE WITH RFC[25]Illegal EcoRI site found at 95
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
Characterization
The promoter region was used to induce lycopene biosynthesis by Yarrowia lipolytica after exposure of the cells to heavy metals (Cd, Cu, Pb) in the growth medium.
Verification of metallotionein respons to heavy metals using real-time PCR
The gene responding to heavy metals was identified using real-time PCR followed by its promoter region sequence being used for further analysis. The cells were grown in Erlenmeyer flasks containing 50 ml of YPD medium. To identify genes reposnding to heavy metals three different ions in different concentrations were used: Cd (10 mM) Cu (28 mM), Pb (50 mM). The control medium in this experiment was YPD medium without any heavy metals. The concentration of metal ions were taken from the available literature [1]. Actine gene was used as a reference gene for qRT-PCR experiment. Five different genes were analyzed: YALI0A02416g, YALI0E08387g, YALI0F11275g, YALI0C18481g, YALI0C22394g.
The RNA was extracted from the cells harvested at 72h of the culture.
Source
This part was isolated from chromosome C on Yarrowia lipolityca A101 genome.
References
- García S, Prado M, Dégano R and Domínguez A (2002) A copper-responsive transcription factor, CRF1, mediates copper and cadmium resistance in Yarrowia lipolytica. Journal of Biological Chemistry 277(40): 37359–37368.