Difference between revisions of "Part:BBa K3098001"

 
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<partinfo>BBa_K3098001 short</partinfo>
 
<partinfo>BBa_K3098001 short</partinfo>
  
GxCesA protein is a GT-2 glycosyltransferase containing transmembrane helices and the catalytic subunit of cellulose synthase. The gene of cesA is found in all living cellulose-producing organisms, whereas the other genes are specific to bacterial cellulose synthase.
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GxCesA protein is a GT-2 glycosyltransferase containing transmembrane helices and the catalytic subunit of cellulose synthase.
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The first cellulose synthase gene was identified in Gluconacetobacter xylinus (formly Acetobacter xylinum). In this bacterium, four genes are clustered in one operon, namely, gxcesA, gxcesB, gxcesC and gxcesD (formly bcsA, bcsB, bcsC and bcsD). The gene of cesA is found in all living cellulose-producing organisms, whereas the other genes are specific to bacterial cellulose synthase.
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In the case of bacteria, the CesA and CesB proteins represent the minimum subunit requirements for cellulose synthesis.
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This part cannot work along. See Cellulose Synthase (BBa_K3098005).
  
 
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Revision as of 11:19, 21 October 2019


GxCesA

GxCesA protein is a GT-2 glycosyltransferase containing transmembrane helices and the catalytic subunit of cellulose synthase. The first cellulose synthase gene was identified in Gluconacetobacter xylinus (formly Acetobacter xylinum). In this bacterium, four genes are clustered in one operon, namely, gxcesA, gxcesB, gxcesC and gxcesD (formly bcsA, bcsB, bcsC and bcsD). The gene of cesA is found in all living cellulose-producing organisms, whereas the other genes are specific to bacterial cellulose synthase. In the case of bacteria, the CesA and CesB proteins represent the minimum subunit requirements for cellulose synthesis.

This part cannot work along. See Cellulose Synthase (BBa_K3098005).

Sequence and Features


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal EcoRI site found at 580
    Illegal PstI site found at 742
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal EcoRI site found at 580
    Illegal PstI site found at 742
  • 21
    INCOMPATIBLE WITH RFC[21]
    Unknown
  • 23
    INCOMPATIBLE WITH RFC[23]
    Unknown
  • 25
    INCOMPATIBLE WITH RFC[25]
    Unknown
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI.rc site found at 1717