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|300px|thumb|center|]] | ||
| + | <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> | ||
| + | ===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). | ||
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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.
Fig.1 Inducible activity of PcysJ and PcysH[1]
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE 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).