Part:BBa_K1172303:Design
Riboflavin synthesis gene cluster from shewanella oneidensis
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal XhoI site found at 1114
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
we isolated the rib-gene-cluster from the genomic sequence of shewanella oneidensis MR-1. We designed our primers in a way that enabled us to use Gibson Assembly to ligate the rib-gene-cluster with pSB1C3. Insofar, we designed four primers to generate homologous overlaps between pSB1C3 and the rib-gene-cluster:
- pSB1C3_fwd_Rib
AGCTTGAACAACAGTTGTAATACTAGTAGCGGCCGCTGCAGTC - pSB1C3_rev_Rib
TCGAGTACTGACCAATTCATCTCTAGAAGCGGCCGCGAATTCC - Rib_fwd
GAATTCGCGGCCGCTTCTAGATGAATTGGTCAGTACTCGATAAC - Rib_rev
CTGCAGCGGCCGCTACTAGTATTACAACTGTTGTTCAAGCTG
- pSB1C3_fwd_Rib
we eliminated three illegal restriction sites: Therefore we substituted one base per illegal restriction site by using PCR. The designed PCR-primers generated homologous overlaps, thus enabling Gibson Assembly afterwards:
- Pst1 at 234 bp (changing CTGCA^G to CTGtAG)
- Pst1 at 1644 bp (changing CTGCA^G to CTGtAG)
- EcoR1 at 1840 bp (changing G^AATTC to GAATTt)
These primers were used to eliminate the illegal restriction sites:
- pst1-234 fwd (38 bp)
TGTCACCTTAGAACCCTGTAGCCATTATGGTCGTACGC - pst1-234 rev (32 bp)
CGACCATAATGGCTACAGGGTTCTAAGGTGAC - pst1-1644 fwd (30 bp)
GTGCCCCATACTGTAGGTGAAACCACGTTG - pst1-1644 rev (34 bp)
AACGTGGTTTCACCTACAGTATGGGGCACAATCG - EcoR1 fwd (43 bp)
GGCACTCAGTTCACTTAGGTATAGAATTTATAACAACAGTCAC - EcoR1 rev (43 bp)
GTGACTGTTGTTATAAATTCTATACCTAAGTGAACTGAGTGCC
- pst1-234 fwd (38 bp)
Source
Shewanella oneidensis MR-1 genomic sequence.
- The strain was kindly provided by Dr. Johannes Gescher (Karlsruher Institut für Technologie)
References
Schicklberger M, Sturm G, Gescher J: Genomic Plasticity Enables a Secondary Electron Transport Pathway in Shewanella oneidensis. Appl Environ Microbiol., 2013 Feb; vol. 79 no. 4 1150-1159.