(→Random ideas from Superphage (Forrest))
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Ideas to chew on
- Chitin synthesis and localization in cell division cycle mutants of Saccharomyces cerevisiae
- Chs1p and Chs3p, two proteins involved in chitin synthesis, populate a compartment of the Saccharomyces cerevisiae endocytic pathway
- Chitin synthetase zymogen is attached to the yeast plasma membrane
- Activating System of Chitin Synthetase from Saccharomyces cerevisiae
More Random Ideas
(based on some articles but I'm not sure if any are feasible)
- Bacteria that will help turn rock into fertile soil and can live in extreme environments to colonize Mars
- or maybe create a self-sustaining biosystem of extremophiles
- bacteria to degrade trash
- styrofoam: 
- Other issues: Waterlogging, Oil spill cleanup, water filtration, non-chemical alternative to pesticides
- Harvesting Light Energy (this is nothing new, but it is now possible to convert e.coli in a single step) 
- perhaps we could try to take this further by turning the mechanical energy of the bacteria into another form (electrical,biofuel...)that can be used by humans?
- oscillatory system (biological clock)
- bacteria to produce chitosan(currently used in bandages)layer to protect open wounds (burns) from infection and encourage healing/clotting
Possible Project Ideas from the 5.23.07 Meeting (Apologies if some of these are repeats)
- Building a biofilm: a mechanism to adhere yeast to surfaces when stimulated (through amino acids)
- Similar to mollusk muscles
- A “lab kit” – for quick separations (make wanted bacteria sticky and then save the rest)
- Separate different types/kinds of bacteria?
- Squid reflective (crystal) plates [a reflective protein]
- Tyr, Trp, Met – pumps protein out through secretory valves (six types?)
- Possible problem could arise because proteins are not soluble?
- De-salinization (?)
- Biofilm with pores – selectively push ions to desired positions [like spider silk?]
- Making efficient/earth-friendly fuel
- Healthy/nutritious bacteria for consumption (vegemite?)
- Bacteria in the gut that could digest lactase OR insulin, etc.
- Possible barrier could occur when testing bacteria unless we used model system
- Bacteria that synthesize vitamins (such as D, A, B12)
- Possible problem could be overdosing on certain vitamin
_ _ _ _ _
I just finished a class on microfluidic devices and engineering with cells, etc. if we possibly want to incorporate that sort of technology into our final project? (I don’t think it’d be feasible to use microfluidics as the actual basis of the project…but just in case…)
Request for Scope
The ideas are great, guys, and thanks for the links too. But can someone go through the ideas and give them a sense of complexity? A lot of these sound really cool but I'm scared they are beyond the scope of a summer project.--Toan 01:16, 2 June 2007 (EDT)
Some ideas from 4/23/07 meeting
M1. Bacteria with squid reflecting protein (reflectin) NO
- Brian: 6 family members, all highly homologous
- Brian: biggest issue could be solubility problems (E. Coli)
- Brian: try expression in different systems where folding more likely to be correct (yeast, streptomyces, etc)
- Brian: only 1 major publication, so very little known about possible chaperones (see reference)
- Forrest: Paper on Methionine-Rich Repeat Proteins (MRRPs)
- Robbie: Nature materials paper from the air force research laboratory describing the production of reflectin in E. coli. They purified the reflectin and made a biofilm of it. 
M2. Self mini-prepping bacteria
- comments: once triggered, will lyse, express RNases, and precipitate proteins and genomic DNA
M3. Bacteria with limited lifetime (telomeres)
- Brian: streptomyces bacteria have linear genome
- Brian: e. coli w/ linear genomes have been constructed (see reference)
- tk: The N15 plasmid (works in E. coli, commercially available from Lucigen) is linear.
M4. Bacteria with removed/non-functional DNA
- comments: "minicells" will grow for several weeks
M5. Incorporating biobrick parts into minicell
- comments: difficult to produce in large quatities
M6. Magnetic alignment of bacteria
- Brian: surface display of peptide which binds magnetic nanoparticles (iron oxide, cobalt oxide)
- Brian: can we control number of bound nanoparticles via concentration (i.e. one NP per bacteria)?
- Brian: feasibility: can we generate enough force and torque on NP to align bacteria (calculations)
- Forrest: Iron oxide nanoparticles tend to fall off the protein surface near neutral pH; cobalt oxide adheres better, but the synthesis conditions are quite toxic for cells
M7. Bacteria that illuminate when dark
M8. Bacteria which synthesize vitamins
- comments: Major vitamin deficiencies
- Brian: One of the most serious vitamin deficiencies in the current world is that of vitamin D (described as an epidemic in the USA). Although it can be produced by humans, the synthesis requires sunlight and many people do not receive sufficient UV radiation to produce the minimum daily requirement. Vitamin D is required for efficient calcium absorption in the gut, and deficiency leads to many bone disorders (rickets, osteoporosis, etc) as well as increasing the risk of autoimmune disease, diabetes, cancer, and cardiovascular disease. Current methods to synthesize vitamin D use extraction from sheep's wool. For more info on vitamin D, see wikipedia page epidemic cancer
- Brian: Another option is Vitamin B12, which is the main vitamin lacking in vegan diets (deficiency causes pernicious anemia). It is produced ONLY in prokaryotic organisms...
- Brian: Beriberi is caused by deficiency in thiamine (vitamin B1). It is very prevalent in Asian countries where many people rely entirely on white rice for their diet.
M9. Sensing pH
- Brian: idea -- use anthocyanins as pH sensor (expressed in plants such as red cabbage)
- Brian: E. Coli have been metabolically engineered to produce anthocyanin (see reference)
M10. Bacteria with kill switch
M11. Bacteria battle
- Forrest: Austin mentioned during the 4/23/07 meeting that this could be done in 2-D (on a dish)
- Forrest: Environmental conditions/stimuli can skew the outcome (e.g. shinning light or lowering pH causes on colony to have advantage over another)
- Brian: Could use F factor (bacterial conjugation) as the "weapon", where Strain A delivers a repressor gene lethal to Strain B and so on.
- Brian: Could have multiple fighting strains (e.g., A kills B, B kills C, C kills A)
- Brian: Possible to see population oscillations? Could easily model the system...
- tk: The idea of "phage wars" was an early incarnation of the IGEM competition. We rejected it because it seemed too yucky.
M12. Plastic binding bacteria
- comments: credit to Reshma
- Brian: bacteria bind to polymer plastic via surface display peptides
- Brian: one idea: couple to growth phase -- bacteria in stationary phase bind to side of plastic tube, which those still growing can be poured out (easy separation)
- Forrest: We have peptide sequences that bind to an electically conducting polymer (PPyCl) (NATURE MATERIALS 4 (6): 496-502 JUN 2005)
- tk: wouldn't a plastic making bacterium be more interesting?
- Forrest: Perhaps the bacteria can produce keratin, i.e. the plastic-like structural material in bird feathers; it would be very interesting to produce different keratin compositions (e.g. include pigments for color or strenghening) and microstructures (e.g. to diffract light like some feathers do)
- Forrest: Plastic Made by Bacteria Commercialized (Apr '07)
- Forrest: Some pionnering work is lead by MIT's Anthony Sinskey (Biopolymer Engineering)
M13. Luciferase Lava Lamp
- comments: credit to Reshma
M14. Organic Transister?
- using conductive M13 phage nanowires?
- Forrest: For electrical transister, M13 phage is not suitable because it's difficult to program both the head and tail to bind to electrodes. In the past, someone has been able to bind the tail end to an electrode and play with flow to get the head to make contact with another electrode. Not sure how much more we can improve on...
Random ideas from Superphage (Forrest)
F1. Engineering bacteria to operate in extreme environment (extremophiles)
- bacteria that die when not in artificially harsh environments (i.e. bacteria that 'escaped' from lab would not thrive)
- Genes from Syntrophus bacterium
F2. High protein bacteria/fungus
- Easy to grow, and highly-nutritious
- To be made into bread spread for poor or disaster-striken communities
- Jess: Whey protein (whey is milk plasma, the liquid that remains after milk is curdled) is used by athletes and body builders to increase muscle mass. It's mostly beta-lactoglobulin (~65%), alpha-lactalbumin (~25%), and serum albumin (~8%), so maybe we could engineer bacteria to create these proteins. (Perhaps make them a byproduct of storage medium digestion for easy transportation to the communities.)
- Whey Protein
F3. Blood clotting phage/bacteria
- function like Chitosan bandaids
F4. Bacteria that process animal waste to recover nutrients
- Recover proteins and other substances from pool of farm animal waste (e.g. the edible stuff floats to the top) and add back to animal feed
F5. Food spoilage detection
- Add non-harmful bacteria to milk, meat packaging, etc; these bacteria grow slightly more easily that the usual bacteria that make people sick, and are highly visible (e.g. bright purple) when they grow
- If consumer sees purple, if means that the food is possibly spoiled
F6. Fungus-based sensors
- Sensing: ammonia (NH3), CO2, light, stresses (osmotic shock, temperature, salt), UV, other fungi
- Fungi as sensors
- Fungus engineering
- Fungus eats radiation for breakfast
Random ideas from Cookb (Brian)
B1. RNA oligo synthesizing bacteria
- bacteria that produce and secrete RNA (mRNA, siRNA, RNAi, microRNA, etc)
- could be used to mass produce RNA-based therapies
- benefit from high-fidelity biological production (no error-prone commercial synthesis)
- commercial synthesis is limited to <20 bp (maybe 50 bp max)
- purification by HPLC later (and analyze by MS)
- protect RNA (chemicals protect 2'OH, could secrete as dsRNA)
- F factor secretion?
Olfactory sensing systems
- The idea is to capture the very wide diversity of the olfactory sensing systems in mammalian noses.
- Like antibodies, there is a very wide range of sequenced olfactory systems, especially from the new Dog genome.
- Here is a list of possible readings. Short version: proofs of concept in yeast have been made.
- Katada S, Nakagawa T, Kataoka H, and Touhara K. . pmid:12767924.
- Pajot-Augy E, Crowe M, Levasseur G, Salesse R, and Connerton I. . pmid:14626444.
- Levasseur G, Persuy MA, Grebert D, Remy JJ, Salesse R, and Pajot-Augy E. . pmid:12823561.
- Minic J, Sautel M, Salesse R, and Pajot-Augy E. . pmid:15853708.
- Minic J, Persuy MA, Godel E, Aioun J, Connerton I, Salesse R, and Pajot-Augy E. . pmid:15654890.
- Touhara K. . pmid:12203691.
- Shirokova E, Schmiedeberg K, Bedner P, Niessen H, Willecke K, Raguse JD, Meyerhof W, and Krautwurst D. . pmid:15598656.
- Radhika V, Proikas-Cezanne T, Jayaraman M, Onesime D, Ha JH, and Dhanasekaran DN. . pmid:17486045.
- Brian -- I work on olfactory receptors (ORs), so I have a good deal of experience with them. But they are difficult to express (especially in bacteria and yeast) and this could be tricky to do in a summer, especially if trying to use multiple OR proteins.
Stick-to-everything proteins from mussels
- Hwang DS, Yoo HJ, Jun JH, Moon WK, and Cha HJ. . pmid:15184131.
- Hwang DS, Gim Y, and Cha HJ. . pmid:15932281.
- Hwang DS, Gim Y, Yoo HJ, and Cha HJ. . pmid:17507090.
- Hwang DS, Gim Y, Kang DG, Kim YK, and Cha HJ. . pmid:16979252.
- Lee H, Scherer NF, and Messersmith PB. . pmid:16920796.
- Lin Q, Gourdon D, Sun C, Holten-Andersen N, Anderson TH, Waite JH, and Israelachvili JN. . pmid:17360430.
- Wang J, Liu C, Lu X, and Yin M. . pmid:17475323.
- Forrest -- ref.13 points:
- adhesive properties are from an "unusual amino acid 3,4-dihydroxy-l-phenylalanine (dopa)"
- "On inorganic surfaces the unoxidized dopa forms high-strength yet reversible coordination bonds, whereas on organic surfaces oxidized dopa is capable of adhering via covalent bond formation."
- Forrest --
- could perhaps express dopa on p3 (tail) or p8 (main body) protein of M13 phage
- after discussing with Rana, it seems that phage is probably not appropriate b/c 1) it is difficult/impossible to engineer phage to express tyrosine (perhaps too bulky) and 2) a phagemid approach would incorporate dopa arbitrarily and sparsely on phage; our best bet would be to engineer p3 of phage (p3 engineering is generally more forgiving than p8)
- Forrest --
- we can create a bacteria smart glue: a substance that becomes sticky when a certain temperature is reached, or if a certain chemical is present, etc (a "programmable glue", so to speak)
- Brian -- could express on E. Coli using fusion to surface proteins (e.g., OmpA, OmpX, FhuA, or LamB). see references below
- also possible to express on flagella via the Invitrogen FliTrx system
- a good consensus peptide appears to be AKPSYPPTYK, with tyrosines getting converted to L-DOPA. Also reported to have prolines converted to hydroxyproline, but not sure if required for stickiness.
- can convert tyrosine residues to L-DOPA by adding tyrosine hydroxylase (later could have bacteria secrete it)
- main question/concern is will bacteria stick to each other and clump up? separations obviously won't work if sticky (+) bacteria adhere to the non-sticky (-) bacteria we are trying to separate from.
- some papers on bacterial surface display:
- Rice JJ, Schohn A, Bessette PH, Boulware KT, and Daugherty PS. . pmid:16600968.
- Bessette PH, Rice JJ, and Daugherty PS. . pmid:15531628.
- Etz H, Minh DB, Schellack C, Nagy E, and Meinke A. . pmid:11698382.
- Hall SS, Mitragotri S, and Daugherty PS. . pmid:17469847.
- Samuelson P, Gunneriusson E, Nygren PA, and Ståhl S. . pmid:12039531.
- Wernérus H and Ståhl S. . pmid:15035661.
Adhesive bacteria with surface specificity
- Non-specific binding (mussel peptide) has certain disadvantages, such as exotic amino acids (DOPA, hydroxyproline) and possibility of cell clumping.
- Instead could investigate adhesive peptides which specifically bind common plastic/polymer surfaces.
- Reference (below): polystyrene binding peptides
- Gebhardt K, Lauvrak V, Babaie E, Eijsink V, and Lindqvist BH. . pmid:9048419.
- Kenan DJ, Walsh EB, Meyers SR, O'Toole GA, Carruthers EG, Lee WK, Zauscher S, Prata CA, and Grinstaff MW. . pmid:16873017.
- Adey NB, Mataragnon AH, Rider JE, Carter JM, and Kay BK. . pmid:7737512.
- Menendez A and Scott JK. . pmid:15620878.
Comment from Brian (email): As for the sticky bacteria, we had a bunch of ideas concerning the control of crosslinking (via oxidation/reduction). Perhaps even to use crosslinking (bacteria sticking/clumping) as a sensor readout. Possibility also of using leucine zippers (protein/protein interaction) for cells clumping.
Getting it unstuck?
- Brian-- Once bacteria have adhered to surface, how do we get them off?
- Easy way would be to engineer a protease cleavage site into the displayed peptide. For instance, have a trypsin cleavage sequence and just add trypsin so cut the cells off the surface (just as is done in adherent mammalian cell culture).
- Hopefully the protease would not cause excessive damage to the bacteria
- Forrest-- have light as stimulus (e.g. rhodopsin approach), and stickiness as response (e.g. dopa or other peptide sequence); expose biofilm to light to cause stickiness
- Brian-- can do 3D printing; concerned about exposure time (might take too long)
- Forrest-- time for bacterial photography is 4-12hrs; does seem like a long time, but might be acceptable for project if we can make it work
- Forrest-- can also do lithography; portions of film exposed to light stick together to the substrate, and unexposed regions can be washed away or killed
Some applications of bacterial glue (from news)
- Water is collected from a river (or other source) into a filtration setup
- Bacteria is added to the water
- The bacteria bind to or take in metals or other pollutants (input 1: detection/uptake of pollutant)
- Input causes bacteria to be able to bind to the filter material (output 1: stickiness to filter material)
- The water is now pollutant-free
- The filter can be cleaned by rinsing/soaking it with water while shining light on it (input 2: light)
- This second input causes the bacteria to unbind from the filter material (output 2: loss of stickiness to filter material)