Part:BBa_K1351003:Design
Laminin-derived peptide binding to NADH Oxidase of S. pneumoniae
- 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
For generation of the part's nucleotide sequence, the amino acid sequence of the peptide (Muchnik et. al., 2013) was reverse transcribed with regard to the codon usage of Bacillus subtilis.
Oligos were designed as precut by EcoRI and PstI to shorten the synthesized fragments and to simplify the cloning into pSB1C3.
Source
The part was generated by annealing of artificially synthesized oligonucletides:
L5P_ENX_SD_Ngo_precutEP_fwd: AATTCgcggccgctTCTAGAgtaaggaggaaGCCGGCATG TGTCAAGAATGTTCACCGGGATTT ACCGGTtaatACTAGTagcggccgCTGCA
L5P_SNP_Age_precutEP_rev: GcggccgctACTAGTattaACCGGT AAATCCCGGTGAACATTCTTGACA CATGCCGGCttcctccttacTCTAGAagcggccgcG
References
Muchnik, L., A. Adawi, A. Ohayon, S. Dotan, I. Malka, S. Azriel, M. Shagan, M. Portnoi, D. Kafka, H. Nahmani, A. Porgador, J. M. Gershoni, D. A. Morrison, A. Mitchell, M. Tal, R. Ellis, R. Dagan and Y. M. Nebenzahl. "Nadh Oxidase Functions as an Adhesin in Streptococcus Pneumoniae and Elicits a Protective Immune Response in Mice." PLoS One 8, no. 4 (2013): e61128. [http://www.ncbi.nlm.nih.gov/pubmed/23577197 PubMed]