Difference between revisions of "Part:BBa K4192041"
 
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The regulatory mechanism of cysHp is still not clear.
 
The regulatory mechanism of cysHp is still not clear.
  
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[[File:Inducible_activity_of_PcysJ_and_PcysH.png|600px|thumb|center|]]
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[[File:Inducible_activity_of_PcysJ_and_PcysH.png|300px|thumb|center|]]
 
<p style="text-align: center;"><b>Fig.1 Inducible activity of PcysJ and PcysH[1]</b></p >
 
<p style="text-align: center;"><b>Fig.1 Inducible activity of PcysJ and PcysH[1]</b></p >
  
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<partinfo>BBa_K4192041 SequenceAndFeatures</partinfo>
 
<partinfo>BBa_K4192041 SequenceAndFeatures</partinfo>
  
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===References===
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[1]. Liu, Y.N., et al., Developing a high-throughput screening method for threonine overproduction based on an artificial promoter. Microbial Cell Factories, 2015. 14(1).
  
 
<!-- Uncomment this to enable Functional Parameter display  
 
<!-- Uncomment this to enable Functional Parameter display  

Latest revision as of 14:45, 12 October 2022


PcysH

Novel threonine sensing promoters including PcysJ and PcysH were discovered by proteomic analyses of Escherichia coli in response to extracellular threonine challenges.

The regulatory mechanism of cysHp is still not clear.

Inducible activity of PcysJ and PcysH.png

Fig.1 Inducible activity of PcysJ and PcysH[1]


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
    COMPATIBLE WITH RFC[1000]

References

[1]. Liu, Y.N., et al., Developing a high-throughput screening method for threonine overproduction based on an artificial promoter. Microbial Cell Factories, 2015. 14(1).