Difference between revisions of "Part:BBa K2963018"

 
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<partinfo>BBa_K2963018 short</partinfo>
 
<partinfo>BBa_K2963018 short</partinfo>
  
This part contains the pgsB 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. PgsB is mainly responsible for catalysing poly-gamma-glutamic acid synthesis. In our subject, we get the pgsB sequenece by error-prone PCR of Bacillus genome, trying to improve the activity of pgsB protein.
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This part contains the <i>pgsB</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. PgsB is mainly responsible for catalysing poly-γ-glutamic acid synthesis. In our subject, we get the <i>pgsB</i> sequenece from <i>Bacillus sp.</i> genome.
  
 
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Latest revision as of 09:51, 20 October 2019


pgsB - encoding a subunit of poly-γ-glutamic acid synthetase

This part contains the pgsB 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. PgsB is mainly responsible for catalysing poly-γ-glutamic acid synthesis. In our subject, we get the pgsB sequenece from Bacillus sp. genome.

Sequence and Features


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal XbaI site found at 1032
    Illegal PstI site found at 1013
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal PstI site found at 1013
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal XbaI site found at 1032
    Illegal PstI site found at 1013
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal XbaI site found at 1032
    Illegal PstI site found at 1013
  • 1000
    COMPATIBLE WITH RFC[1000]