Difference between revisions of "Part:BBa K2963003"

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<partinfo>BBa_K2963003 short</partinfo>
 
<partinfo>BBa_K2963003 short</partinfo>
  
This part contains the capB gene for poly-gamma-glutamic acid synthetase. This enzyme is involved in poly-gamma-glutamic acid synthesis,which converts the glutamate to poly-gamma-glutamic acid. CapB is mainly responsible for catalysing poly-gamma-glutamic acid synthesis. In our subject, we get the capB sequenece by error-prone PCR of Bacillus genome, trying to improve the activity of CapB protein.
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This part contains the <i>capB</i> gene which encodes a subunit for poly-γ-glutamic acid synthetase. This enzyme is involved in poly-γ-glutamic acid synthesis, which converts the glutamate to poly-γ-glutamic acid. CapB is mainly responsible for catalysing poly-γ-glutamic acid synthesis. In our subject, we get the <i>capB</i> sequenece from <i>Bacillus sp.</i> genome and we used the mutant of <i>capB</i> gene.
  
 
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Revision as of 09:57, 20 October 2019


capB* - a subunit of poly-γ-glutamic acid synthetase

This part contains the capB gene which encodes a subunit for poly-γ-glutamic acid synthetase. This enzyme is involved in poly-γ-glutamic acid synthesis, which converts the glutamate to poly-γ-glutamic acid. CapB is mainly responsible for catalysing poly-γ-glutamic acid synthesis. In our subject, we get the capB sequenece from Bacillus sp. genome and we used the mutant of capB gene.

Sequence and Features


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal EcoRI site found at 737
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal EcoRI site found at 737
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal EcoRI site found at 737
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal EcoRI site found at 737
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal EcoRI site found at 737
  • 1000
    COMPATIBLE WITH RFC[1000]