From 2009.igem.org

Discussed how genetic amplifiers work, including transient and steady state response
Looked at ways in which a latch might be made, by positive feedback, mutual inhibition, or other schemes

Positive feedback relies in part on an amplifier component: this would need to be fixed on toxicity grounds before the secondary application could be used.

Plan for tomorrow

Prepare trimethoprim stock solution
Make LB agar and trimethoprim plates as well as LB agar and copper + tyrosine plates
Complete proceedure for making competant cells (transfer bacteria into big flask, wash with HEPES, and aliquot into glycerol)
Attempt transformations by electroporation

pPSX plasmid (violet)
melA plasmid (brown)
biobricks

Wednesday

Competent Cell Procedure

Completed (see protocol page for details of the procedure). Competent cells stored in aliquots at -80 degrees.

Planned and Prepared for Electroporation Tomorrow

Made up 4 LB agar and 100ug/ml Ampicillin, 0.2mg/mL tyrosine (NOTE: protocol actually calls for 0.3mg/mL), 15 ug/mL CuSO4 plates
Plan to transform TOP10 competent bacteria with

Melanin plasmid, pTRCmelA plasmid -- Plate onto tyrosine/copper/ampicillin plate
Violacein plasmid,Plasmid pPSX-Vio+ -- Plate onto trimethoprim plate
Orange biobrick, BBa_K152005 -- Plate onto ampicillin plate
Promoter, R0011 -- Plate onto ampicillin plate
More?

Need to make trimethoprim stock solution 10mg/mL acetone, and plate at 50ug/mL

Tried to make the stock solution today, couldn't get the solid trimethoprim to dissolve in acetone

Need to work out exact volumes of plasmid to be added to the cell (concentrations written on the side of the bottles)

Thursday

Electroporation

Transformed Top10 competent cells, incubated the following plates:

Top10 + pTRCmelA plasmid on tyrosine/copper/ampicillin plate
Top10 + Plasmid pPSX-Vio+ on trimethoprim plate
Top10 + BBa_K152005 on ampicillin plate
Top 10 + R0011 on ampicillin plate
1:10 dilutions of each were also plated

All plates were stored overnight in the 37 degree incubator

Making BioBricks

With the aim of making a brown-pigmented BioBrick, we looked at constructing primers to cut out the MelA gene from the plasmid, add the prefix and suffix, and remove the two forbidden restriction sites. This would then be pasted into one of the recommended vectors and could be submitted to the registry.

Input and Processing systems

We split into groups to plan and discuss the following possible ideas for input systems:

Mike and Shuna = Amplifier
Siming and Alan = Bistable switch
Crispian and Megan = Population control and growth
Viv = Coloured spores (Idea discarded due to high levels of complexity involved in understanding, designing and working with the spore system. It also required the use of a chassis that was not E-Coli.)

Plans for Friday

Meeting at 10am to discuss ideas Meeting with faculty at 2.30pm to further discuss ideas and present work done so far

Wet work = colony PCR (to be explained by James) and observation of (hopefully!) coloured plates

Friday

Results of Wet Work

All transformations were completed sucessfully. Single cononies were observed on the 1/10 dilution plates and could easily be picked out for plasmid propagation procedure (to be started on Monday). However no colours were observed.

Reasons:

Melanin plasmid = plasmid required the addition of IPTG
pPSX plasmid (violet) = the pigment is on a low copy number plasmid

The melanin plates were left out on the bench to see if the brown pigment developed over time. The rest of the plates were stored in the fridge for making plasmid stocks (procedure starting next week).

BioBrick Construction

Used ApE to examine the melanin plasmid:

This contains only two forbidden restriction sites within the actual gene. These could be removed by PCR.

Also looked at the vio operon:

As this contains a large number of the forbidden biobrick restriction sites, it would be impossible to prepare the biobrick using PCR alone. The operon would have to be synthesised with these sites removed to be feasible as a biobrick.

The other possible pigments are the orange biobrick system and the pseudomonas red/green pigment.

Pigment Plans

Melanin

Chemistry of Pigment Production:

The MelA gene is a tyrosinase. Tyrosinases catalyze two reactions, as described in the figure below. Melanin is a macromolecular compound produced by the polymerization of the quinone product of the second reaction, and has a characteristic brown colour.

From H. Claus and H. Decker, Bacterial tyrosinases, Syst. Appl. Microbiol. 29 (2006), pp. 3–14. [http://www.sciencedirect.com/science?_ob=ArticleURL&_udi=B7GVX-4H21K91-1&_user=1495569&_coverDate=01%2F24%2F2006&_fmt=full&_orig=search&_cdi=20442&view=c&_acct=C000053194&_version=1&_urlVersion=0&_userid=1495569&md5=de451c5e1d1d18ad12b7e39b10b80408&ref=full]

Forward plans:

Troubleshoot pigment production
Make our own plasmid stocks
As above, make the pigment into a biobrick
Characterize the pigment by making an absorbance spectrum (max absorption at 400 nm); incidentally, the melanin gene we have is actually a mutant, and maximum pigment production was achieved in a strain that over-produces tyrosine, as described in:

Santos, C. N., and G. Stephanopoulos. 2008. Melanin-based high-throughput screen for L-tyrosine production in Escherichia coli. Appl. Environ. Microbiol. 74:1190-1197. [http://aem.asm.org/cgi/content/abstract/74/4/1190]

Goal: To use as a single BioBrick output (possibly as a 'fall-back' pigment to test processing systems)

Violacin

Chemistry of pigment production:

There are 4 genes that convert tryptophan into violacein; the biosynthetic pathway is detailed below

Molecule 5 is Cyan coloured, allowing two different colour states to be produced by this system.

From P.R. August, T.H. Grossman, C. Minor, M.P. Draper, I.A. MacNeil, J.M. Pemberton, K.M. Call, d. Holt, and M. S. Osbourne, Sequence Analysis and Functional Characterization of the Violacein Biosynthetic Pathway from Chromobacterium violaceum, J. Mol. Microbiol. Biotechnol. (2000) 2(4): 513-519. [http://www.horizonpress.com/jmmb/v2/v2n4/26.pdf]

Forward plans:

troubleshoot pigment production
make our own plasmid sticks
As above, synthesize the operon with the biobrick prefix and suffix
Use the synthesized operon as a template to PCR out the individual genes
Characterize both violacein and the cyan molecule by making an absorption spectrum for each.
Explore the possibilities of constructing logic gates

For example,

Need to analyze the flux through the pathway
The products of the reactions catalyzed by VioD and VioA are combined in a 1:1 ratio by VioB; what happens to the production of cyan and violacein if flux through VioD is much greater than flux through VioA? Which might be the case if VioD and VioA are induced by different inputs that are not reliably equal.
What are the dynamics of the flux through VioC? Would analyze by producing cyan, and then switching on VioC and measuring absorbance. Considerations for biosensors - if presence of whatever the biosensor is sensing causes cyan production, and then low rate of VioC expression slowly turns cyan into violet, violet being an indication that the sensor is old and past its shelf life .

Red and Green from Pseudomonas

Chemistry of the pigment

From Mavrodi, D. V., R. F. Bonsall, S. M. Delaney, M. J. Soule, G. Phillips, and L. S. Thomashow. 2001. Functional analysis of genes for biosynthesis of pyocyanin and phenazine-1-carboxamide from Pseudomonas aeruginosa PAO1. J. Bacteriol. 183:6454-6465. [http://jb.asm.org/cgi/content/abstract/183/21/6454?ijkey=41531d004be13e87d3ba32abcbbd672bcc9d6cf3&keytype2=tf_ipsecsha]

Pyocyanin is a green pigment that diffuses out of the cell, the red pigment also diffuses out of the cell.

Currently waiting for the arrival of plasmids containing PhzM and PhzS; if they do arrive, hoping to explore logic gate construction.

Planning a Processing System

Amplification:

An amplifier consists of a ribosome binding site, a protein coding region, a terminator and a promoter. The protein produced in the device binds to the promoter as an activator, such that an incoming gene transcription will be amplified to various levels with appropriate choices of activator and promoter. The Cambridge team in 2007 looked at these devices.

We are taking this idea forward.

Population Control:

If we had three different pigments in a single plate, we would like to make sure that the colonies all grow to the same size.

We therefore looked into an AHL-regulated arrangement, where the slowest-growing strain would produce signalling molecules, allowing the faster strains to grow. The medium speed strain could also have a signalling molecule for induction of the fast strain.

The idea has a good chance of working in a liquid medium, where the relevant signalling molecules can easily disperse. However, on a plate, spatial effects have to be considered. Due to this difficulty, we chose not to continue this idea further.

Bioswitch:

A basic bistable switch requires two inverters, and some way of making it change state.

Important papers on this concept in synthetic biology include:

"Construction of a genetic toggle switch in Escherichia coli" Gardner, Cantor & Collins 2000 http://www.nature.com/nature/journal/v403/n6767/pdf/403339a0.pdf

This paper was followed up with a second, "Programmable cells: Interfacing natural and engineered gene networks", 2004 http://www.pnas.org/content/101/22/8414.figures-only

The authors showed in 2000 that a genetic toggle switch was possible. They investigated using different promoters, and found only some combinations to give bistability.

Many iGEM teams have attempted to recreate a bistable switch; none have so far fully succeeded! The most recent were Peking 2007 and Bologna 2008.

Peking 2007 designed a bistable circuit as part of their "push on, push off" device. They connected together two mutual inhibitors, and showed that this gave an agar spread that had red in places and green in others. This suggests that they made a bistable device. However, they did not progress to activation by external sources.

Bologna's iGEM project in 2008 was a bistable circuit, called "E.coli PROM". They performed extensive modelling of the device, but did not complete fabrication.

This leaves an iGEM team with a good opportunity. Building on Peking and Bologna, amongst others, a working, and inducible bistable could be made, an iGEM first.

However, we decided that given the large amount of work which we need to do on pigments, and the fact that a non-functioning bistable would not be novel, we would not progress further with this idea.

Weekend

RED

Looked at red pigment synthesis briefly as optional easy extra link to relevant paper - https://static.igem.org/mediawiki/2009/f/ff/1128.pdf

Degredation tags

Interesting articles:

Engineering controllable protein degredation [http://www.sciencedirect.com/science?_ob=ArticleURL&_udi=B6WSR-4K47X21-G&_user=1495569&_rdoc=1&_fmt=&_orig=search&_sort=d&_docanchor=&view=c&_searchStrId=967086878&_rerunOrigin=google&_acct=C000053194&_version=1&_urlVersion=0&_userid=1495569&md5=8603cc30cea1e63c39b7a605a8f2a477]

Primers for melanin designed!

Team:Cambridge/Notebook/Week2

From 2009.igem.org

Categories :

Project :

Notebook :

Team Logistics :

Week 2 - The Project

Monday

Objectives

Goals for Wet Work

Tuesday

Proceedure to make competant cells started

Planned and prepared for transformation

Dry work