ETHZ/Biology/Lab

From 2007.igem.org

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| [[Image:Mappbr322.jpg|center|thumb|pBR322 Map|100px]]
 
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| [[ETHZ/pbr322| pBR322]]
 
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*Cloned in linker oligos (EcoRI/PstI)
 
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| Tetracyline
 
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| [[Image:Mappbr322.jpg|center|thumb|pBR322 Map|100px]]
 
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| [[ETHZ/pck01| pCK01]]
 
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*Site directed mutagenisis: Changed the ACT codon of the SpeI site in the origin of replication into ATT
 
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| [[Image:Mappck01.jpg|center|thumb|pCK01 Map|100px]]
 
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| [[ETHZ/pacyc177| pACYC177]]
 
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*Cloned in linker oligos (BamHI/PstI)
 
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In this page, you can find information on laboratory conducted to construct EducatETH <i>E.coli</i>. The system parts are presented again, their assembly into plasmids and the cloning plan are explained and all lab notes taken by the ETH Zurich team are accessible. If you are trying to construct EducatETH <i>E.coli</i> at your lab, the section [https://2007.igem.org/ETHZ/Biology/Lab#.::_Problems_we_faced_::. Problems we faced] might be useful to you. If you want to see the whole biological design of the system, please visit the [[ETHZ/Biology | Biology Pespective]]. Finally, photos of our lab experience are accessible under [[ETHZ/Pictures | Pictures!]]
 
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Todo: decide what happens with lab book ([https://2007.igem.org/ETHZ/Lab_book here])
 
==Cloning plan==
==Cloning plan==

Revision as of 19:58, 24 October 2007

Eth zh logo 4.png

 


Introduction

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


Strains

We used the following E. coli strains:


[http://openwetware.org/wiki/E._coli_genotypes#TOP10_.28Invitrogen.29|E. coli Top10 (Invitrogen):]

  • 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 [http://openwetware.org/wiki/E._coli_genotypes#TOP10_.28Invitrogen.29| 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


[http://openwetware.org/wiki/E._coli_genotypes#JM101|E. coli JM101:]

  • 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 [http://openwetware.org/wiki/E._coli_genotypes#JM101| 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 Ampicillin, Tetracyline 15-20 [1] pMB1
pBR322 Map
pCK01 Chloramphenicol 5-12 [1] pSC101
pCK01 Map
pACYC177 Ampicillin, Kanamycin 10-12 [1] 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 plasmid name New resistance Map
pBR322
  • Site directed mutagenisis: Changed the GCA codon of the PstI site in the bla gene into GTA
  • Cloned in linker oligos (EcoRI/BamHI)
BBa_I739201 Ampicillin

Cloning plan

Parts assignment into plasmids

Three plasmids are used for the EducatETH E.coli system parts as follows:

Plasmids and contents
plasmid resistance copy type contents comments
pbr322 ampicillin high 1,2,3 constitutive subsystem
pck01 chloramphenicol low 4,5,8,9 reporting subsystem
pacyc177 kanamycin low 6,7,10,11 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.

Linkers

Because the plasmids used were not standard plasmids found in the registry, but came from the lab where we work, linkers compatible with the standard BioBrick assembly have to be used in order to work with them. The list of all linkers is the following:

Linkers for plasmids
Linker Plasmid
pbr322-1 pbr322
pbr322-2 pbr322
pbr322-3 pbr322
pbr322-4 pbr322
pck01 pck01
pck01-2 pck01
pacyc177-1 pacyc177
pacyc177-2 pacyc177

Note that four linkers are tested for pbr322, as two are used for the tetracycline-resistance version of pbr322 and two are used for the ampicillin-resistnace version.

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 [http://openwetware.org/wiki/Synthetic_Biology:BioBricks/Part_fabrication here]. For a shorter explanation of how to assemble 2 parts together check [http://partsregistry.org/Assembly:Standard_assembly here].
DNA assembly process ([1]) (Fig. 4)
Note that the composite part is constructed from the end to the beginning, i.e. each new part is inserted before the existing one. In the following, the plasmid containing the new part to be inserted will be referred to as the donor and the plasmid accepting the new part will be referred to as the acceptor. Composite pars made of parts a and b are denoted a.b.

Plasmid 1 (pbr322ap)

  1. Put parts 1,2,3 in pbr322ap plasmids.
  2. Merge plasmid containing part 2 (donor) with plasmid containing part 3 (acceptor). You should get a plasmid containing a 2.3 composite part.
  3. Merge plasmid containing part 1 (donor) with plasmid containing composite part 2.3 (acceptor). You should get a plasmid containing a 1.2.3 composite part.

Plasmid 2 (pck01cm)

  1. Put parts 4,5,8,9 in pck01cm plasmids.
  2. Merge plasmid containing part 4 (donor) with plasmid containing part 5 (acceptor). You should get a plasmid containing a 4.5 composite part.
  3. Merge plasmid containing part 8 (donor) with plasmid containing part 9 (acceptor). You should get a plasmid containing a 8.9 composite part. Note: this step can be done simultaneously with the above.
  4. Merge plasmid containing composite part 4.5 (donor) with plasmid containing composite part 8.9 (acceptor). You should get a plasmid containing a 4.5.8.9 composite part.

Plasmid 3 (pacyc177km)

  1. Put parts 6,7,10,11 in pacyc177km plasmids.
  2. Merge plasmid containing part 6 (donor) with plasmid containing part 7 (acceptor). You should get a plasmid containing a 6.7 composite part.
  3. Merge plasmid containing part 10 (donor) with plasmid containing part 11 (acceptor). You should get a plasmid containing a 10.11 composite part. Note: this step can be done simultaneously with the above.
  4. Merge plasmid containing composite part 6.7 (donor) with plasmid containing composite part 10.11 (acceptor). You should get a plasmid containing a 6.7.10.11 composite part.

Labbook

References

[1] [http://www1.qiagen.com/faq/faqview.aspx?faqid=350&SearchText=&FaqCategoryId=0&MenuItemId=0&catalog=1&ProductLineId=1000228 QIAGEN FAQs]

[x] [http://partsregistry.org/Assembly:Standard_assembly Standard Assembly Process]
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