Difference between revisions of "Part:BBa K174008"

 
 
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Metallothionein protein can bind to heavy metals such as cadmium, arsenic, mercury, silver. By fusing CotC spore coat protein from ''Bacillus subtilis'', it can be localized to the spore coat, hence trap the metals into bacterial spores. It is also fused with Gfp to see the spores with the proteins using a microscope.
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This part is designed to allow heavy metals to be incorporated into ''Bacillus subtilis'' spores.
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SmtA metallothionein protein from ''E. coli'' can bind to heavy metals [1,2,3]. Metallothioneins have a tendency to bind to cationic metal ions such as cadmium, copper, arsenic, mercury, silver.  
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By translationally fusing CotC spore coat protein from ''Bacillus subtilis'', SmtA can be localized to the spore coat, hence trapping heavy metals into bacterial spores. SmtA is also fused with Gfp to facilitate the visualisation of spores using a fluorescent microscope.
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We designed this device to sequester cadmium into ''B. subtilis'' spores. The device is expressed using a ''sigK'' type promoter which becomes active under sporulation conditions. Hence metals are soaked up when the cells are undergoing sporulation.
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For more information, go to Newcastle iGEM 2009 [http://2009.igem.org/Team:Newcastle/Metals Metal Sequester] and [http://2009.igem.org/Team:Newcastle/Project/Overview Overview] pages.
  
 
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===References===
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#Cretì, P., F. Trinchella, et al. "Heavy metal bioaccumulation and metallothionein content in tissues of the sea bream Sparus aurata from three different fish farming systems." Environmental Monitoring and Assessment.
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#Morby, A. P., J. S. Turner, et al. (1993). SmtB is a metal-dependent repressor of the cyanobacterial metallothionein gene smtA: identification of a Zn inhibited DNA-protein complex. 21: 921-925.
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#Waldron, K. J. and N. J. Robinson (2009). "How do bacterial cells ensure that metalloproteins get the correct metal?" Nat Rev Micro 7(1): 25-35.

Latest revision as of 22:21, 21 October 2009

SmtA metallothionein protein with CotC and Gfp fusion

This part is designed to allow heavy metals to be incorporated into Bacillus subtilis spores.

SmtA metallothionein protein from E. coli can bind to heavy metals [1,2,3]. Metallothioneins have a tendency to bind to cationic metal ions such as cadmium, copper, arsenic, mercury, silver.

By translationally fusing CotC spore coat protein from Bacillus subtilis, SmtA can be localized to the spore coat, hence trapping heavy metals into bacterial spores. SmtA is also fused with Gfp to facilitate the visualisation of spores using a fluorescent microscope.

We designed this device to sequester cadmium into B. subtilis spores. The device is expressed using a sigK type promoter which becomes active under sporulation conditions. Hence metals are soaked up when the cells are undergoing sporulation.

For more information, go to Newcastle iGEM 2009 [http://2009.igem.org/Team:Newcastle/Metals Metal Sequester] and [http://2009.igem.org/Team:Newcastle/Project/Overview Overview] pages.

Sequence and Features


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Unknown
  • 12
    INCOMPATIBLE WITH RFC[12]
    Unknown
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal AgeI site found at 1234
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI.rc site found at 1046


References

  1. Cretì, P., F. Trinchella, et al. "Heavy metal bioaccumulation and metallothionein content in tissues of the sea bream Sparus aurata from three different fish farming systems." Environmental Monitoring and Assessment.
  2. Morby, A. P., J. S. Turner, et al. (1993). SmtB is a metal-dependent repressor of the cyanobacterial metallothionein gene smtA: identification of a Zn inhibited DNA-protein complex. 21: 921-925.
  3. Waldron, K. J. and N. J. Robinson (2009). "How do bacterial cells ensure that metalloproteins get the correct metal?" Nat Rev Micro 7(1): 25-35.