Difference between revisions of "Part:BBa K4192142:Design"
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===Design Notes=== | ===Design Notes=== | ||
| − | + | This element showed no inducibility in Pseudomonas fluorescein and resulted in 85% bacterial death, probably due to essential Escherichia coli regulatory elements. | |
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===Source=== | ===Source=== | ||
| − | + | All individual components were derived from E. coli. | |
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===References=== | ===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). | [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). | ||
Latest revision as of 04:50, 12 October 2022
PcysJ-mazE-mazF
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 283
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
This element showed no inducibility in Pseudomonas fluorescein and resulted in 85% bacterial death, probably due to essential Escherichia coli regulatory elements.
Source
All individual components were derived from E. coli.
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).