From 2007.igem.org

Introduction | Project Design ( 1.Sticky Hands | 2.Communication | 3.Size Control ) | Making Marimos | Our Goal || Team Members | メンバ連絡簿

Size Control

Our Aim

Since produced AHL diffuses all around the bacteria culture, all receivers can ultimately aggregate to one huge marimo with their sticky hands. This final state is not the case of real marimos. Thus our idea for controlling the size of Bacteria Marimos is based on the high performance quorum sensing or AHL-diffusing inhibition.

1. Raise the AHL productivity of Sender
2. Increase the AHL sensitivity of Receiver
3. Use the AHL degrading enzyme aiiA to localize AHL

1.Improving Sender

Design

AHL is synthesized from methionine by the enzyme MetK and LuxI.
We tested in the hope of combined overexpression of these 2 genes will enhance the sender capacity.

Experiment

Sender

Ptet-LuxI

• Synthesize AHL constantly

metK Sender

• Synthesize AHL and express metK constantly

Receiver

Method(Fig3.)

1. Inoculated sender, MetK sender, and receiver in each liquid medias. Incubated at 37℃ 12h.
2. Checked OD. Dispensed receiver in each tube equally. Spin downed senders and resuspended with fresh liquid media.
3. Diluted senders to adjust cell population (5x10⁸,5x10⁷,......, 5x10²).
4. Mix receivers and senders.
5. Incubated for 1h to 3h at room tempature
6. Spindowned and UV checked.

Result

• No difference was seen.
  
• 何と何の間の違いが見られないのかな？byとよたろ
  

Discussion

• No efficiency was observed.
• Our Assumption:S-adenosyl methionine was synthesized enough or consumed in other path way.
• Sequencing riquired.

2.Improving Receiver

Design

Collins et.al. described the hyper-sensitive variants of luxR to AHL.(Collins, C. H., Arnold, F. H. & Leadbetter, J. R. Directed evolution of Vibrio fischeri LuxR for increased sensitivity to a broad spectrum of acyl-homoserine lactones. Mol. Microbiol. 55, 712–723 (2005))
We created two types of sensitive luxR mutants.　理由．

• 理由ということでもいいし、何かを期待して行った、ってことでもいいと思います。byとよたろ

Experiment

sensitive luxR mutants の性能を以下の２つの方法で評価した。

• ここに上がっているデータは一つですよ？１つだけでも構わないので、どんな実験を行ったのかな。。。byとよたろ

Result

• mutant(I45F,S116A)はAHLを添加しなくてもGFPを発現した。
• mutant(I45F)はwild typeよりもGFPの発現が多くなった。(AHL 10nM)

Discussion

3.Localizing AHL

Design1

AiiA expression is regulated by pLac, which makes it express constantly to inactivate AHL.

Experiment

1. Inoculate E.coli carries this aiiA receiver plasmid in Liquid Media.
2. At the same time, inoculate AHL sender E.coli in Liquid Media.
3. Dilute receiver cells and spread on agar plate, and spot sender 1μL. Incubate at 37℃
4. Check plate.(GFP expressed?)

Result

GFP did not express on the plate.

Discussion

Excessive amounts of　aiiA is expressed to generate concentration gradient. We expected aiiA express more moderate to make it.

Design2

図のように，AHLのシグナルが入るとaiiaを合成するような回路を考えた．Marimo全体がAHL quencherとして働く．Marimoの内側でAHLを分解し、Marimoの外側のAHL濃度の上昇を抑える．

Experiment

Result

• BBa_T9002との比較ではGFPははじめ発現しないが、しばらくするとGFPが発現するようになる。

(Assumption:GFPは細胞内で分解されにくいからではないだろうか）

Discussion

• 発現し始めた時が、AHLの濃度がaiiAの分解る能力を超えた時だと考えられる。

Design3

Above picture describes aiiA is regulated inverted lux promoter with CI inverter．

• High AHL concentration: no aiiA expression, no AHL degrade.
• Low AHL concentration: aiiA expressed, AHL degraded.

図のようにインバーターをかませた．高い濃度ではaiiAが発現しないためAHLは分解されない．AHLが低い濃度ではaiiAが発現しAHLを分解する．

よってマリモの中心付近ではAHLを分解せず，外側へ行くと分解される．

Experiment

We could not finish assembling this part. It'll be our future work. このパーツを作ろうとしたが、inverterを組み合わせた時点で終わってしまった。

Subpart:BBa_S03840