Team:Heidelberg/Templates/M-15-05-13
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Contents |
State of the lab
backbones
- psB4K5 for Del A-P is ready
- psB6A1 for DelH not
- psB1C3 for Indigoidine is ready
DelH
- two parts via SalI (8 kb and 10 kb) successfully amplified
- will be integrated into plasmid for electroporation in E. coli
Further plan
methylmalonyl-CoA-strain
- K207-3 is not available
- we get BAP1
- Lambda-red plasmid
- FLP plasmid
- Template plasmid
DelH
- Expression in E. coli end of may
Indigoidine and NRPS library
- problems concerning RFC10
- Gibson Info Freiburg required
- Washington standard: contact Washington team! (Fanny?)
Gibson assembly
- maybe method of choice
- are there protocols or do we have to delelop standard protocols
- small fragments could be a problem (PCP-domain)
- develop Gibson RFC standard for NRPS library?
Gibson approach, Indigoidine and NRPS library
- problems with RFC10 restriction sites and gene size
DelA-P Cloning strategy
- leave out not necessary genes like DelC
- five cluster fragments
- use Gibson cloning
- Dominik: mid of next week we will get further information
- avoid too big PCR-constructs; 10 kb has been very difficult to amplify
Indigoidine
- try plasmid, reproduction of paper
- seperate domains (A, T, TE) and fuse again to proove modularity
- maybe exchange domains with domains from other pathways
- Müller Plasmid -> new problem of 11 restriction sites
- How do we want to assemble NRPS modules in our project?
- maybe Berkeley RFC21 standard because it works very good for our gene clusters
- compatible with linkers
- allows fusion protein
- not accepted by iGEM registry
- BglIII cannot be heat-inactivated
- benign scar (GS)
Washington pGA
- Gibson Assembly Toolkit
- based on RFC21 backbone
standards...
- mix and match domains not using biobrick standard but another strategy
- it is too much work to get our parts conform to RFC10 and the NRPS-pathways are not realy compatible with RFC10 at all
- after first experiments consider codon optimized synthesis for part submission
- other NRPS not standardised, but propose a new standard
- few characterized parts are of more value than a hundret useless ones
conclusion
- why not omit RFC and start with Gibson at the first point
- get expertise in Gibson cloning (read papers)
- Hanna and Julia (TA) should try Gibson assembly together
Software
iGEM pulse
- use scrapy (python) to get data from last years wikis -> MySQL (first subgroup)
- develop parameters for iGEM oulse webpage (second subgroup)
- First Deadline: May 24
- detailed plan on data mining and parameter design
- Second Deadline: End of June
- valuable product
NRPS software
- NRPS library software starting after proof of cencept in Indigoidine
- predict required domains for input structure and propose cloning protocol
Budget
- possible sponsors
- Klaus Tschira as main sponsor
- talk to other sponsors for small fundings (connections...)
- university funding, helmholtz, biotech,
- sponsorship benefits?
- logos on Shirt, Website, presentation
Miscellaneous
- reservation of lufthansa flights for Boston!
- group tickets are cheaper
- greater flexibility
- book hotels/ guest houses in Lyon!
- marketing will be done by professionals
- They will need the project description with loads of random pictures (domains, gold, electronic waste, cash, ...)
- will be there at the next meeting
Conclusion
- start Indigoidine subproject with Gibson cloning (faster!)
- take care about hotels, flight (Sophie)
- project proposal, sponsor list (coordinated by Fanny)
- creative input for marketing people
Agenda for next meeting with Advisors (06.06.2013)
- talk to marketing people
- progress in labwork
- DelA-P
- Indigoidine
- DelH
- travel agency
- project proposal, sponsor list