Stanford/BIOE44:Module3:Day2:mercury: Difference between revisions
No edit summary |
No edit summary |
||
Line 13: | Line 13: | ||
'''Promoter Sequence''' | '''Promoter Sequence(repressor protein binds)''' | ||
gaattcgcggccgcttctagagATGGTGATGAACTCCTGGGCCAGGCCCAGACCTGCGAGCGTCAAAGCGGCAAGGATCAGCTTCCTCATACACACCTCCTTGGTGCCGCCGGTAGTATACCCGGCCCTTGCCCTTCTGGCAAGCGCCGCGCGGCCCAGGGAGGGGTTTTTCGCTAGACTAGGGGGTAtactagtagcggccgctgcag | gaattcgcggccgcttctagagATGGTGATGAACTCCTGGGCCAGGCCCAGACCTGCGAGCGTCAAAGCGGCAAGGATCAGCTTCCTCATACACACCTCCTTGGTGCCGCCGGTAGTATACCCGGCCCTTGCCCTTCTGGCAAGCGCCGCGCGGCCCAGGGAGGGGTTTTTCGCTAGACTAGGGGGTAtactagtagcggccgctgcag | ||
'''Mercury Sensitive Transcriptional Regulator Protein Sequence''' | '''Mercury Sensitive Transcriptional Regulator Protein Sequence (merR repressor protein)''' | ||
gaattcgcggccgcttctagATGCCCTACACCATCGGCGAGCTCGCCCGGGCGTTTGGCCTTTCTCCTGATGCCCTCCGCTACTACGAAAGGCTTGGGCTCCTCGCCCCCAGCGGCCGTTCGCCCGGGGGGGTTCGCCTCTACGGGGAGGAGGCCTTCCGCCGCCTCCGCTTCATCAAGGAGGCCCAGGCGGCGGGGCTTAAGCTTGAGGACATCGCCTGGATCCTCCGCGCCGTGGAGGAGGGCCATCCCCCCTGCCGCCACGTGCGGGAGGCCCTGGCCAAGCGCCTGGCGGAGGTGCGGCGTAGGCTCAGGGAGCTCCAGGCCCTGGAAGCGGCCCTGGCCGAACGGCTGGCCTACGCCGAGGCCCACCCTGACCCTGCTTGCGACGGGCGGGACCGCTGCGTCTATTTGGACCCCCTTGACCCTGGAGCACGCTCCAGGGTCTAGTAAtactagtagcggccgctgcag | gaattcgcggccgcttctagATGCCCTACACCATCGGCGAGCTCGCCCGGGCGTTTGGCCTTTCTCCTGATGCCCTCCGCTACTACGAAAGGCTTGGGCTCCTCGCCCCCAGCGGCCGTTCGCCCGGGGGGGTTCGCCTCTACGGGGAGGAGGCCTTCCGCCGCCTCCGCTTCATCAAGGAGGCCCAGGCGGCGGGGCTTAAGCTTGAGGACATCGCCTGGATCCTCCGCGCCGTGGAGGAGGGCCATCCCCCCTGCCGCCACGTGCGGGAGGCCCTGGCCAAGCGCCTGGCGGAGGTGCGGCGTAGGCTCAGGGAGCTCCAGGCCCTGGAAGCGGCCCTGGCCGAACGGCTGGCCTACGCCGAGGCCCACCCTGACCCTGCTTGCGACGGGCGGGACCGCTGCGTCTATTTGGACCCCCTTGACCCTGGAGCACGCTCCAGGGTCTAGTAAtactagtagcggccgctgcag | ||
Revision as of 15:28, 4 May 2010
Purpose
- To create a novel biosensor that senses inorganic mercury and generates a color as an indicator of the presence of mercury pollution in an aquatic environment.
Rationale
Environmental mercury is usually present as dissolved mercury in water, or as Hg2+ ions.
Long Description
- The device is designed to express a color gene as a result of the presence of mercury in water. merR, from Thermus thermophilus HB27, expresses a promoter repressor protein that binds to the promoter region of the mer operon, repressing transcription. In the presence of mercury, the mercury ions bind to the repressor proteins which unbind from the promoter and as a result initiate transcription. In the device, a color generator will be placed downstream of the promoter and merR so that in the presence or mercury, transcription initiates and color is expressed.
Promoter Sequence(repressor protein binds)
gaattcgcggccgcttctagagATGGTGATGAACTCCTGGGCCAGGCCCAGACCTGCGAGCGTCAAAGCGGCAAGGATCAGCTTCCTCATACACACCTCCTTGGTGCCGCCGGTAGTATACCCGGCCCTTGCCCTTCTGGCAAGCGCCGCGCGGCCCAGGGAGGGGTTTTTCGCTAGACTAGGGGGTAtactagtagcggccgctgcag
Mercury Sensitive Transcriptional Regulator Protein Sequence (merR repressor protein) gaattcgcggccgcttctagATGCCCTACACCATCGGCGAGCTCGCCCGGGCGTTTGGCCTTTCTCCTGATGCCCTCCGCTACTACGAAAGGCTTGGGCTCCTCGCCCCCAGCGGCCGTTCGCCCGGGGGGGTTCGCCTCTACGGGGAGGAGGCCTTCCGCCGCCTCCGCTTCATCAAGGAGGCCCAGGCGGCGGGGCTTAAGCTTGAGGACATCGCCTGGATCCTCCGCGCCGTGGAGGAGGGCCATCCCCCCTGCCGCCACGTGCGGGAGGCCCTGGCCAAGCGCCTGGCGGAGGTGCGGCGTAGGCTCAGGGAGCTCCAGGCCCTGGAAGCGGCCCTGGCCGAACGGCTGGCCTACGCCGAGGCCCACCCTGACCCTGCTTGCGACGGGCGGGACCGCTGCGTCTATTTGGACCCCCTTGACCCTGGAGCACGCTCCAGGGTCTAGTAAtactagtagcggccgctgcag
References
- An initial characterization of the mercury resistance (mer) system of the thermophilic bacterium Thermus thermophilus HB27.
- Wang Y, Freedman Z, Lu-Irving P, Kaletsky R, Barkay T.
- FEMS Microbiol Ecol. 2009 Jan;67(1):118-29.
- Department of Biochemistry and Microbiology, Rutgers, The State University of New Jersey, New Brunswick, NJ, USA.
- The genome sequence of the extreme thermophile Thermus thermophilus.
- Nat Biotechnol. 2004 May;22(5):547-53. Epub 2004 Apr 4.
- Henne A, Brüggemann H, Raasch C, Wiezer A, Hartsch T, Liesegang H, Johann A, Lienard T, Gohl O, Martinez-Arias R, Jacobi C, Starkuviene V, Schlenczeck S, Dencker S, Huber R, Klenk HP, :Kramer W, Merkl R, Gottschalk G, Fritz HJ. Göttingen Genomics Laboratory, Institute of Microbiology and Genetics, University of Göttingen, Germany. ahenne@g2l.bio.uni-goettingen.de