Difference between revisions of "Part:BBa K518003"

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Escherichia coli and other organisms have a gene cluster activated in case of emergency, which is called "SOS genes". It is well-documented that in E. coli, most of those SOS genes are repressed by LexA protein. When the cell is exposed to excess stress, RecA is up-produced, which promotes the self-degradation of LexA. As a result, many LexA-regulated genes become expressed.
 
Escherichia coli and other organisms have a gene cluster activated in case of emergency, which is called "SOS genes". It is well-documented that in E. coli, most of those SOS genes are repressed by LexA protein. When the cell is exposed to excess stress, RecA is up-produced, which promotes the self-degradation of LexA. As a result, many LexA-regulated genes become expressed.
Combined with RecA and SOS promoters (for instance, [[Part:BBa_K518010 |sulAp]]), a stress-responsive gene-expression circuit was assembled. For experimental details, see [http://2011.igem.org/Team:UT-Tokyo our page].
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Combined with RecA and SOS promoters (for instance, [[Part:BBa_K518010 |sulAp]]), a stress-responsive gene-expression circuit was assembled.
  
 
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Revision as of 14:56, 3 October 2011

LexA - a repressor for LexA-regulated SOS promoters -

Escherichia coli and other organisms have a gene cluster activated in case of emergency, which is called "SOS genes". It is well-documented that in E. coli, most of those SOS genes are repressed by LexA protein. When the cell is exposed to excess stress, RecA is up-produced, which promotes the self-degradation of LexA. As a result, many LexA-regulated genes become expressed. Combined with RecA and SOS promoters (for instance, sulAp), a stress-responsive gene-expression circuit was assembled.

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI.rc site found at 684