Difference between revisions of "Part:BBa K1124008:Design"
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===Design Notes=== | ===Design Notes=== | ||
− | + | This part was generated by site-directed mutagenesis on MicC-sRNA scaffold([[BBa_K1124005]]), in which the target-binding sequence was added to the scaffold. | |
− | + | The target binding sequence was designed complementary to the hycA gene of ''E. coli'' K-12 strain. | |
===Source=== | ===Source=== | ||
+ | We designed oligo DNA complementary to the first 24nt of hycA CDS as the target binding sequence. Then, we integrated it with MicC sRNA scaffold ([[BBa_K1124005]]) using PCR technique. | ||
− | + | ===References=== | |
+ | Viviana Sanchez-Torres,1 Toshinari Maeda,and Thomas K.(2009). Wood -Protein Engineering of the Transcriptional Activator FhlA To Enhance Hydrogen Production in Escherichia coli- APPLIED AND ENVIRONMENTAL MICROBIOLOGY, Sept. 5639–5646 | ||
− | + | Yoo, S. M., Na, D., & Lee, S. Y. (2013). Design and use of synthetic regulatory small RNAs to control gene expression in Escherichia coli. Nature protocols, 8(9), 1694-1707. |
Latest revision as of 14:10, 27 September 2013
anti-hycA sRNA
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
This part was generated by site-directed mutagenesis on MicC-sRNA scaffold(BBa_K1124005), in which the target-binding sequence was added to the scaffold. The target binding sequence was designed complementary to the hycA gene of E. coli K-12 strain.
Source
We designed oligo DNA complementary to the first 24nt of hycA CDS as the target binding sequence. Then, we integrated it with MicC sRNA scaffold (BBa_K1124005) using PCR technique.
References
Viviana Sanchez-Torres,1 Toshinari Maeda,and Thomas K.(2009). Wood -Protein Engineering of the Transcriptional Activator FhlA To Enhance Hydrogen Production in Escherichia coli- APPLIED AND ENVIRONMENTAL MICROBIOLOGY, Sept. 5639–5646
Yoo, S. M., Na, D., & Lee, S. Y. (2013). Design and use of synthetic regulatory small RNAs to control gene expression in Escherichia coli. Nature protocols, 8(9), 1694-1707.