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==mreB Project Description==
==mreB Project Description==
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The goal of our project is to clone the gene, mreB, from ''Caulobacter crescentus'' (stalked shaped cell) into ''Escherchia coli'' (rod shaped cell)to see if mreB will affect ''E. coli's'' cell shape in some way. We expect to see the ''E. coli cells'' lyse or change from their normal rod shape.  
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The goal of our project is to clone the gene, mreB, from ''Caulobacter crescentus'' (stalked shaped cell) into ''Escherchia coli'' (rod shaped cell) to see if mreB will affect ''E. coli's'' cell shape in some way. We expect to see the ''E. coli'' cells lyse or change from their normal rod shape.  
MreB is a rod-shape determining gene that appears as bands or spirals encircling the cell. It is known to associate with mreC and penicillin-binding proteins to catalyze precursors for the peptidoglycan cell wall and correctly position polar bacterial proteins. It is also homologous of actin in eukaryotes.   
MreB is a rod-shape determining gene that appears as bands or spirals encircling the cell. It is known to associate with mreC and penicillin-binding proteins to catalyze precursors for the peptidoglycan cell wall and correctly position polar bacterial proteins. It is also homologous of actin in eukaryotes.   
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Parts  
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'''Parts'''
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* Tissue Source: wild type ''C. crescentus'' CB15N (generously donated from the lab of Christine Jacobs-Wagner at Yale University)
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* Gene of Interest: mreB from ''C. crescentus''
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Accession # NC_011916
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1,044 base pairs
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No introns
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* Primers
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Forward primer: the first 34 bases of our gene sequence. We also added in the Biobrick enzymes EcoR1 and Xba1 in front of the primer.
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Reverse primer: the last 20 bases of our gene sequence. We also added in the Biobrick enzymes Pst1 and Spe1 in front of the primer.
 +
 
 +
* Promoter: BBa_K206000 (pBad Strong Promoter)
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This promoter is inducible by L-arabinose. When induced, AraC binds and changes the conformation interacting with Aral1 and Aral2 operator sites, permitting transcription.
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* Plasmid Vector: pSB1A3
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Biobrick part containing ampicillin marker gene.
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* Intron Removal: not necessary because our organism is a prokaryote.
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'''Procedure'''
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1. Grow ''C. crescentus'' and ''E. coli'' on the respective medias
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2. PCR to extract mreB gene + Biobrick (BB) enzymes
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3. Isolate and purify mreB + BB enzymes
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4. Cut mreB + BB enzymes and ligate with pSB1A3
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5. Perform bacterial transformation to import the plasmid into ''E. coli''
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6. Grow E. coli bacteria on experimental plates (No ampicillin, ampicillin, and ampicillin + L-arabinose)
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7. Verification testing by examining the physical cell shapes under a light microscope and sequence verification by sending a sample of cloned DNA to Iowa State.
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* List all the steps that are needed to complete your project
 
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* Do not go into experimental details and don't list procedures. Just list the major steps necessary to complete your project
 
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* Please also make yourself familiar with uploading pictures and *.ppt files
 
==Important Results and Milestones==
==Important Results and Milestones==

Revision as of 19:49, 9 September 2012

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Team Tango Alpha

  • Bess Lippmann
  • Colby Swanson

mreB Project Description

The goal of our project is to clone the gene, mreB, from Caulobacter crescentus (stalked shaped cell) into Escherchia coli (rod shaped cell) to see if mreB will affect E. coli's cell shape in some way. We expect to see the E. coli cells lyse or change from their normal rod shape.

MreB is a rod-shape determining gene that appears as bands or spirals encircling the cell. It is known to associate with mreC and penicillin-binding proteins to catalyze precursors for the peptidoglycan cell wall and correctly position polar bacterial proteins. It is also homologous of actin in eukaryotes.

Parts

  • Tissue Source: wild type C. crescentus CB15N (generously donated from the lab of Christine Jacobs-Wagner at Yale University)
  • Gene of Interest: mreB from C. crescentus

Accession # NC_011916 1,044 base pairs No introns

  • Primers

Forward primer: the first 34 bases of our gene sequence. We also added in the Biobrick enzymes EcoR1 and Xba1 in front of the primer.

Reverse primer: the last 20 bases of our gene sequence. We also added in the Biobrick enzymes Pst1 and Spe1 in front of the primer.

  • Promoter: BBa_K206000 (pBad Strong Promoter)

This promoter is inducible by L-arabinose. When induced, AraC binds and changes the conformation interacting with Aral1 and Aral2 operator sites, permitting transcription.

  • Plasmid Vector: pSB1A3

Biobrick part containing ampicillin marker gene.

  • Intron Removal: not necessary because our organism is a prokaryote.

Procedure 1. Grow C. crescentus and E. coli on the respective medias 2. PCR to extract mreB gene + Biobrick (BB) enzymes 3. Isolate and purify mreB + BB enzymes 4. Cut mreB + BB enzymes and ligate with pSB1A3 5. Perform bacterial transformation to import the plasmid into E. coli 6. Grow E. coli bacteria on experimental plates (No ampicillin, ampicillin, and ampicillin + L-arabinose) 7. Verification testing by examining the physical cell shapes under a light microscope and sequence verification by sending a sample of cloned DNA to Iowa State.


Important Results and Milestones

  • keep track of your most important results and refer to the corresponding page in your notebook
  • upload important pictures (don't forget to label them! Powerpoint is very convenient). Remember: these will become quite handy later in your summary report or final presentation. If you do label and upload the pictures as soon as you got them, your summary report can be written much more effortlessly (do you usually procrastinate? This is chance to do some work before hand that frees you up for finals week).

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