Swimmy Bacteria : Chiba 2006

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(How it works)
(How it works)
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'''Control the E.coli's movement with light!'''
'''Control the E.coli's movement with light!'''
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=How it works=
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=Design=
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--under construction--
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to stop the e.coli by light, we needed a part that stop the e.coli, and combine this with a light receptor that UCSF made it last year.
to stop the e.coli by light, we needed a part that stop the e.coli, and combine this with a light receptor that UCSF made it last year.
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we chose to control chemotaxis.
we chose to control chemotaxis.
We've found out, from the paper(..see refrences), the chemoreceptor that fix the e.coli tumble.  
We've found out, from the paper(..see refrences), the chemoreceptor that fix the e.coli tumble.  
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it is a fragment of the chemoreceptor "Tsr" (a serin receptor)
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it is a fragment of the chemoreceptor "Tsr" (a serin receptor)from aa 290 to 551. we call this tsr-cw(or tsr290).
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[[Image:Devices.jpg]]
 
<br />
<br />
[[Image:pathway.jpg|pathway]]
[[Image:pathway.jpg|pathway]]
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=Experiments=
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we made the new part rbs-tsrcw by PCR and made a new BioBrick (BBa_J29049).
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==Swarm Plate Assay==
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first we wanted to make sure this parts will work, so we put it suffix in the OmpC-promotor& araC-promotor.
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we found the OmpC promotor (R0082) was not working good, so then we used the araC promotor.
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-- results  under construction --
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==Capillary Assay==
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we wanted to see if the tsr-cw is working good with this assay,too.
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we're waiting for the results...
=Members=
=Members=

Revision as of 16:09, 29 October 2006

Contents

Concept

Swimmy Bacteria -- the E.coli freeze and gather when they are caught by red light.
conceptSwimmy
red light on -> stop
red light off -> move
Control the E.coli's movement with light!

Design

to stop the e.coli by light, we needed a part that stop the e.coli, and combine this with a light receptor that UCSF made it last year.

there was some ways to stop the e.coli running:

  1. making a chemaera with chemotaxis receptor and light sensing receptor
  2. stop the motor protein's expression(motB protein: from last year's parts)
  3. controling chemotaxis

etc

we chose to control chemotaxis. We've found out, from the paper(..see refrences), the chemoreceptor that fix the e.coli tumble. it is a fragment of the chemoreceptor "Tsr" (a serin receptor)from aa 290 to 551. we call this tsr-cw(or tsr290).


pathway

Experiments

we made the new part rbs-tsrcw by PCR and made a new BioBrick (BBa_J29049).

Swarm Plate Assay

first we wanted to make sure this parts will work, so we put it suffix in the OmpC-promotor& araC-promotor. we found the OmpC promotor (R0082) was not working good, so then we used the araC promotor. -- results under construction --


Capillary Assay

we wanted to see if the tsr-cw is working good with this assay,too. we're waiting for the results...

Members

Chiba 2006 team あ

Experiments

light cannon

  • 10/15 we wrote a picture at the solid media.(not finished yet) also we changed the arabinose concentration at the liquid media.
  • 10/14 the Fluorescent lamp was the best light. we could see the on/off clearly in the solid media. we found that the thin media is better than the thicker one.
  • 10/11 we changed the arabinose & S-gal's concentration & the light sorce to find the best condition.

swimmy

  • 10/15 tried the capiraly assay to see chemotaxis. also we washed the e.coli and observed it with the microscope(but it was kind of hard)
  • 10/11 we're finding the suitable media to observe the E.coli's movement(chemotaxis).
  • 8/23 we made the tsr gene parts by PCR & discussed about the locked Tsr mutants.

Todo List

Referenses

Locked Tsr Mutants

  • A.Bren and M.Eisenbach (2000) -- How Signals Are Heard during Bacterial Chemotaxis: Protein-Protein Interactions in Sensory Signal Propagation (J.Bacteriol.)
  • P.Ames and J.S.Parkinson (1988) -- Transmembrane Signaling by Bacterial Chemoreceptors: E.coli Transducers with Locked Signal Output (Cell)
  • P.Ames and J.S.Parkinson (1994) -- Constitutively Signaling Fragments of Tsr, the Escherichia coli Serine Chemoreceptor (J.Bacteriol.)


Experiments

  • Microscope -- Real-time imaging of fluorescent flagellar filaments.J.bacteriol.2000
  • Chemotaxis Assay -- J.Adler -- A Method for Measuring Chemotaxis and Use of the Method to Determine Optimum Conditions for Chemotaxis by Escherichia coli
  • M.K.Slocum and J.S.Parkinson (1985) -- Genetics of Methyl-Accepting Chemotaxis Proteins in Escherichia coli: Null Phenotypes of the tar and tap Genes (J.Bacteriol.)
  • J.S.Parkinson (1976) --- cheA, cheB, and cheC of Escherichia coli and Their Role in Chemotaxis (J.Bacteriol.)

Last Update

  • 10/13 todo list
  • 10/11 swimmy & gene pathway
  • 8/23 refrences
  • 8/7 concept&members --maiko


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