ETHZ/Biology/Lab

From 2007.igem.org

(Difference between revisions)
Line 72: Line 72:
<a href="https://2007.igem.org/wiki/index.php?title=ETHZ/Meet_the_team#The_ETH_Zurich_07_Team">The ETH Zurich 07 Team</a>
<a href="https://2007.igem.org/wiki/index.php?title=ETHZ/Meet_the_team#The_ETH_Zurich_07_Team">The ETH Zurich 07 Team</a>
<a href="https://2007.igem.org/wiki/index.php?title=ETHZ/Meet_the_team#Team_Description">Team Description</a>
<a href="https://2007.igem.org/wiki/index.php?title=ETHZ/Meet_the_team#Team_Description">Team Description</a>
 +
<a href="https://2007.igem.org/wiki/index.php?title=ETHZ/Internal">Brainstorming Page</a>
</div>
</div>

Revision as of 23:46, 24 October 2007

ETH banner.png

 


On this page, you may find information about how educatETH e.coli was implemented in the lab. More specifically, you will find information on the plasmid strains we used, the modifications we did to them in order to be compatible with the Biobrick library and our cloning plan. Moreover, in this page you may find here an (unfortunately not complete) electronic copy of our lab notebook. If you are here because you are interested in implementing educatETH E.coli in your lab, then our System Implementation and the System Parts pages may be of help to you!


Introduction

For all our cloning procedures we used standard protocols according to SAMBROOK and RUSSELL Molecular Cloning: A Laboratory Manual [1].

Strains

We used the following E. coli strains:


E. coli Top10 (Invitrogen):

  • You can find this strain at BBa_V1009
  • This strain has a streptomycin resistance
  • Genotype: F’ {tetR}, mcrA, Δ(mrr-hsdRMS-mcrBC), φ80 lacZ ΔM15, ΔlacX74, deoR, recA1, araD139 Δ(ara-leu)7679, galU, galK, λ-, rpsL,endA1, nupG
  • For further information please click here
  • References:
    • Casdaban, M. and Cohen, S. (1980) J Mol Biol 138:179 PMID 6997493
    • Grant, S.G.N. et al. (1990) Proc. Natl. Acad. Sci. USA 87: 4645-4649 PMID 2162051


E. coli JM101:

  • You can find this strain at BBa_I739301
  • We call them Jimmys
  • This strain is the original blue/white cloning strain
  • Genotype: glnV44, thi-1, Δ(lac-proAB), F'[lacIqZΔM15 traD36 proAB+]
  • For further information please click here
  • Reference:
    • Messing, J. et al. (1981) Nucleic Acids Res. 9, 309; Yanisch-Perron, C., Vieira, J., and Messing, J. (1985) Gene 33, 103


Plasmids

For our system we needed three plasmids with different origins of replication and antibiotic resistances. We decided to take low copy plasmids. We decided to use the following plasmids, which we wanted modify so that they would become compatible to the Biobrick Library multiple cloning site:


Basic plasmids

Plasmid Resistances Copy number Origin Map
pBR322 [2] Ampicillin, Tetracyline 15-20 [3] pMB1
pBR322 Map
pCK01 [4] Chloramphenicol 5-12 [3] pSC101
pCK01 Map
[[ETHZ/pacyc177| pACYC177 [5]] Ampicillin, Kanamycin 10-12 [3] p15A
pACYC177 Map

Changes to the plasmids

In order to get the Biobrick multiple cloning site into the plasmids, we had to make several changes to the plasmids:


Plasmid Changes New name New resistance New Map
pBR322
  • Site directed mutagenesis: Changed the GCA codon of the PstI site of the bla gene into GTA
  • Cloned in linker oligos (EcoRI/BamHI)

BBa_I739201

Ampicillin

BBa_I739201 Map
pBR322

BBa_I739203

Tetracycline

BBa_I739203 Map
pCK01

BBa_I739202

Chloramphenicol

BBa_I739202 Map
pACYC177

BBa_I739204

Kanamycin

BBa_I739204 Map


Cloning plan

Parts assignment into plasmids

The plan was to put the following parts into the three plasmids:

plasmid resistance copy type contents comments
BBa_I739201 ampicillin low BBa_I739001(TetR) , BBa_I739002(LacI) , BBa_I739003(LuxR) constitutive subsystem
BBa_I739202 chloramphenicol low BBa_I739004(P22 cII) , BBa_E0430(EYFP) , BBa_I739008(cI) , BBa_I739009(ECFP) reporting subsystem
BBa_I739204 kanamycin low BBa_I739006(cI) , BBa_I739007(P22 cII) , BBa_I739010(RFP) , BBa_I739011(GFP) learning subsystem, reporting subsystem

It is important to insert parts responsible for the production of fluorescent proteins in low copy plasmids, as they are potentially harmful for the cell. Unfortunately, working with low copy plasmids makes the procedure more demanding in the lab.


Procedure

The standard BioBrick assembly will be used to put the parts in the plasmids. Detailed information on how the BioBrick part fabrication works can be found here. For a shorter explanation of how to assemble 2 parts together check here.
DNA assembly process [6]
Note that the composite part is constructed from the end to the beginning, i.e. each new part is inserted before the existing one. Composite parts made of parts a and b are denoted a.b.


Plasmid 1 (BBa_I739201)

  1. Digest I739001(TetR) and BBa_I739201 plasmid with EcoRI/PstI and ligate them afterwards.
  2. Digest I739002(LacI) and I739003(LuxR) with XbaI/PstI
  3. Digest I739001(TetR) in BBa_I739201 with SpeI/PstI.
  4. Ligate digested I739001(TetR) in BBa_I739201 with digested I739002(LacI). You get a plasmid containing a I739001(TetR).I739002(LacI) composite part.
  5. Digest I739001(TetR).I739002(LacI) with SpeI/PstI.
  6. Ligate digested I739001(TetR).I739002(LacI) with digested I739003(LuxR). You get the completed I739001(TetR).I739002(LacI).I739003(LuxR) composite part in the BBa_I739201 plasmid.


Plasmid 2 (BBa_I739202)

  1. Digest BBa_I739004(P22 cII), BBa_I739008(cI) and the plasmid BBa_I739202 with EcoRI/PstI.
  2. Digest BBa_E0430(EYFP) and BBa_I739009(ECFP) with XbaI/PstI.
  3. Ligate digested BBa_I739004(P22 cII) and digested plasmid BBa_I739202.
  4. Ligate digested BBa_I739008(cI) and the plasmid BBa_I739202.
  5. Digest BBa_I739004(P22 cII) in BBa_I739202 with SpeI/PstI.
  6. Digest BBa_I739008(cI) in BBa_I739202 with SpeI/PstI.
  7. Ligate digested BBa_I739004(P22 cII) in BBa_I739202 with digested BBa_E0430(EYFP). You get a plasmid containing a BBa_I739004(P22 cII).BBa_E0430(EYFP) composite part.
  8. Ligate digested BBa_I739008(cI) in BBa_I739202 with BBa_I739009(ECFP). You get a plasmid containing a BBa_I739008(cI).BBa_I739009(ECFP) composite part.
  9. Digest BBa_I739004(P22 cII).BBa_E0430(EYFP) with SpeI/PstI.
  10. Digest BBa_I739008(cI).BBa_I739009(ECFP) with XbaI/PstI.
  11. Ligate digested BBa_I739004(P22 cII).BBa_E0430(EYFP) and digested BBa_I739008(cI).BBa_I739009(ECFP). You get the completed plasmid containing the BBa_I739004(P22 cII).BBa_E0430(EYFP).BBa_I739008(cI).BBa_I739009(ECFP) composite part.


Plasmid 3 (BBa_I739204)

  1. Digest BBa_I739006(cI), BBa_I739010(RFP) and the plasmid BBa_I739204 with EcoRI/PstI.
  2. Digest BBa_I739007(P22 cII) and BBa_I739011(GFP) with XbaI/PstI.
  3. Ligate digested BBa_I739006(cI) and digested plasmid BBa_I739204.
  4. Ligate digested BBa_I739010(RFP) and the plasmid BBa_I739204.
  5. Digest BBa_I739006(cI) in BBa_I739204 with SpeI/PstI.
  6. Digest BBa_I739010(RFP) in BBa_I739204 with SpeI/PstI.
  7. Ligate digested BBa_I739006(cI) in BBa_I739204 with digested BBa_I739007(P22 cII). You get a plasmid containing a BBa_I739006(cI).BBa_I739007(P22 cII) composite part.
  8. Ligate digested BBa_I739010(RFP) in BBa_I739204 with BBa_I739011(GFP). You get a plasmid containing a BBa_I739010(RFP).BBa_I739011(GFP) composite part.
  9. Digest BBa_I739006(cI).BBa_I739007(P22 cII) with SpeI/PstI.
  10. Digest BBa_I739010(RFP).BBa_I739011(GFP) with XbaI/PstI.
  11. Ligate digested BBa_I739006(cI).BBa_I739007(P22 cII) and digested BBa_I739010(RFP).BBa_I739011(GFP). You get the completed plasmid containing the BBa_I739006(cI).BBa_I739007(P22 cII).BBa_I739010(RFP).BBa_I739011(GFP) composite part.


References

[1] Sambrook and Russel, "Molecular Cloning: A Laboratory Manual", Cold Spring Harbour Laboratory Press, 3rd edition, 2001

[3] QIAGEN FAQs

[4] Fernández et al., "Molecular Microbiology", 16:205-213, 1995

[6] Standard Assembly Process