Daily Notebook
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==JUN 10== | ==JUN 10== |
Latest revision as of 16:30, 24 June 2008
Home | The Team | The Project | Parts Submitted to the Registry | Modeling | Notebook |
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Contents |
TO NAVIGATE THIS SECTION, PLEASE CLICK ON THE BRAINSTORMING LINK OR ANY GIVEN DATE (LINKS ABOVE) TO SEE MORE DETAIL
Brainstorming
JUN 10
JUN 16
Summary of individual tasks to research:
- S. Mutans metabolism pathway-Asad
- L. bulgaricus metabolism pathway-Allin
- secretion (full or partial)-John
- other secretion systems (introduction of)-Sara
- T7 as a promoter (L. bulgaricus)-Prarthna
- L. bulgaricus transformation/protocols-Derek
- binding assay protocols-Andrew
Linear Sequence/Design
Ex-promoter-RBS-ATG-signal-epitope-p1025-linker (TEV cleavage site)-GFP-His-TAATAA-termination-SP (see top of page)
- Base pairs: 35-10-3-90-30-60-45-700-15-6-8
- potential eptiopes
- FLAG (Asp-Tyr-Lys-Asp-Asp-Asp-Asp-Lys)
- C-myc (E Q K L I S E E D L)
- HA (Y P Y D U P D Y A: #2)
DNA/Plasmid Editor
- http://www.biology.utah.edu/jorgensen/wayned/ape/
Peptide Sequence Manipulations
- http://slam.bs.jhmi.edu/gd/
Primer Analyzer Tool (check temperature & GC content)
- http://www.idtdna.com/analyzer/Applications/OligoAnalyzer/Default.aspx
- primers should be 17-28 bases in length;
- base composition should be 50-60% (G+C);
- primers should end (3') in a G or C, or CG or GC: this prevents "breathing" of ends and increases efficiency of priming;
- Tms between 55-80oC are preferred;
- 3'-ends of primers should not be complementary (ie. base pair), as otherwise primer dimers will be synthesised preferentially to any other product;
- primer self-complementarity (ability to form 2o structures such as hairpins) should be avoided;
- runs of three or more Cs or Gs at the 3'-ends of primers may promote mispriming at G or C-rich sequences (because of stability of annealing), and should be avoided.
- http://bioweb.uwlax.edu/GenWeb/Molecular/Seq_Anal/Primer_Design/primer_design.htm
Parts/Construction
- Construction
- GFP
- Synthetic peptide
- L. bulgaricus vector
- Assay
- L. bulgaricus
- S. Mutans
To Do/To Buy:
- finalize DNA sequence
- primer
- synthesis
- reagents
TEV Protease cut site
- Amino Acid Sequence : Glu-Asn-Leu-Tyr-Phe-Gln-Gly (Cuts between Gln-Gly)
- Base Pair Sequence: GAAAACCTGTACTTCCAGGGT
JUN 17
Links to sites from individual research topics
- T7 as a promoter in L. bulgaricus/Other viable promoter options
- LacS promoter
- http://www.patentstorm.us/patents/5639644/description.html
- http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=161534
- http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=123959
- http://jb.asm.org/cgi/content/full/184/4/928
- LacS promoter
- Secretion signal peptide
- [http://www.pubmedcentral.nih.gov/picrender.fcgi?artid=178052&blobtype=pdf cleavage site]
P4 Revised
- reverse sequence: CTG CAG CGG CCG CTA CTA GTA AGA GAA TAT AAA AAG CCA GAT TAT TAA TCC GGC TTT TTT ATT ATT TTT ATT AGT GGT GAT GGT GAT GAT GTT TGT ATA GTT CAT CCA TGC
- length = 111 bp
- melting temp = 69.6 C
- GC content % = 36.0
JUN 18
- [[../lbulgaricus |Lactobacillus delbrueckii subsp. bulgaricus Information & Protocols]]
- [[../toothbindingassay | Tooth binding assay protocol]]
Home | The Team | The Project | Parts Submitted to the Registry | Modeling | Notebook |
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- http://www.freewebs.com/naguiar/ (S. mutans Information)
- http://pubs.acs.org/cgi-bin/abstract.cgi/jafcau/2002/50/i05/abs/jf010958t.html (S. mutans adsorption to HA Beads)
- http://www.blackwell-synergy.com/doi/full/10.1111/j.1399-302X.2007.00412.x (Influence of Starch and Sucrose on S. mutans)
Friday Meeting breakdown
- Andrew: primers
- Derek: L. bulgaricus procedures
- Allin: metabolism
- John: binding assay
- Sara: secretion
- Asad: S. Mutans/Binding Assay
- Prarthna: promoters