ETHZ/Biology/Lab

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<center>[[ETHZ | Main Page]] &nbsp;&nbsp;&nbsp;&nbsp; [[ETHZ/Model | System Modeling]] &nbsp;&nbsp;&nbsp;&nbsp; [[ETHZ/Simulation | Simulations]] &nbsp;&nbsp;&nbsp;&nbsp; [[ETHZ/Biology | System Implementation]] &nbsp;&nbsp;&nbsp;&nbsp; [[ETHZ/Biology/Lab| Lab Notes]] &nbsp;&nbsp;&nbsp;&nbsp; [[ETHZ/Meet_the_team | Meet the Team]] &nbsp;&nbsp;&nbsp;&nbsp; [[ETHZ/Internal | Team Notes]] &nbsp;&nbsp;&nbsp;&nbsp; [[ETHZ/Pictures | Pictures!]]</center><br>
<center>[[ETHZ | Main Page]] &nbsp;&nbsp;&nbsp;&nbsp; [[ETHZ/Model | System Modeling]] &nbsp;&nbsp;&nbsp;&nbsp; [[ETHZ/Simulation | Simulations]] &nbsp;&nbsp;&nbsp;&nbsp; [[ETHZ/Biology | System Implementation]] &nbsp;&nbsp;&nbsp;&nbsp; [[ETHZ/Biology/Lab| Lab Notes]] &nbsp;&nbsp;&nbsp;&nbsp; [[ETHZ/Meet_the_team | Meet the Team]] &nbsp;&nbsp;&nbsp;&nbsp; [[ETHZ/Internal | Team Notes]] &nbsp;&nbsp;&nbsp;&nbsp; [[ETHZ/Pictures | Pictures!]]</center><br>
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<a href="https://2007.igem.org/wiki/index.php?title=ETHZ#Introduction">Introduction Section</a>
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<a href="https://2007.igem.org/wiki/index.php?title=ETHZ#Introduction">Introduction</a>
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<a href="https://2007.igem.org/wiki/index.php?title=ETHZ#Team_Members">Team Members</a>
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<a href="https://2007.igem.org/wiki/index.php?title=ETHZ#Acknowledgments">Acknowledgments Section</a>
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<a href="https://2007.igem.org/wiki/index.php?title=ETHZ#Acknowledgments">Acknowledgments</a>
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<a href="https://2007.igem.org/wiki/index.php?title=ETHZ#Site_Map">Site map Section</a>
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<a href="https://2007.igem.org/wiki/index.php?title=ETHZ/Model#Introduction">Introduction Section</a>
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<a href="https://2007.igem.org/wiki/index.php?title=ETHZ/Model#Introduction">Introduction</a>
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<a href="https://2007.igem.org/wiki/index.php?title=ETHZ/Model#Model_Overview">Model Overview Section</a>
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<a href="https://2007.igem.org/wiki/index.php?title=ETHZ/Model#Model_Overview">Model Overview</a>
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<a href="https://2007.igem.org/wiki/index.php?title=ETHZ/Model#Detailed_Model">Detailed Model</a>
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<a href="https://2007.igem.org/wiki/index.php?title=ETHZ/Model#Final_Model">Final Model Section</a>
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<a href="https://2007.igem.org/wiki/index.php?title=ETHZ/Model#Final_Model">Final Model</a>
<a href="https://2007.igem.org/wiki/index.php?title=ETHZ/Modeling_Basics">Modeling Basics Page</a>
<a href="https://2007.igem.org/wiki/index.php?title=ETHZ/Modeling_Basics">Modeling Basics Page</a>
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<a href="https://2007.igem.org/wiki/index.php?title=ETHZ/Model#Mathematical_Model">Mathematical Model Section</a>
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<a href="https://2007.igem.org/wiki/index.php?title=ETHZ/FSM">FSM View Page</a>
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<a href="https://2007.igem.org/wiki/index.php?title=ETHZ/Simulation#Introduction">Introduction Section</a>
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<a href="https://2007.igem.org/wiki/index.php?title=ETHZ/Simulation#Introduction">Introduction</a>
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<a href="https://2007.igem.org/wiki/index.php?title=ETHZ/Biology#Introduction">Introduction Section</a>
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<a href="https://2007.igem.org/wiki/index.php?title=ETHZ/Biology#Introduction">Introduction</a>
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<a href="https://2007.igem.org/wiki/index.php?title=ETHZ/Biology#The_Complete_System">The Complete System Section</a>
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<a href="https://2007.igem.org/wiki/index.php?title=ETHZ/Biology#The_Complete_System">The Complete System</a>
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<a href="https://2007.igem.org/wiki/index.php?title=ETHZ/Biology#System_Phases">System Phases Section</a>
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<a href="https://2007.igem.org/wiki/index.php?title=ETHZ/Biology#System_Phases">System Phases</a>
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<a href="https://2007.igem.org/wiki/index.php?title=ETHZ/Biology#Current_Cloning_Status">Current Cloning Status</a>
<a href="https://2007.igem.org/wiki/index.php?title=ETHZ/Biology/parts">System Parts Page</a>
<a href="https://2007.igem.org/wiki/index.php?title=ETHZ/Biology/parts">System Parts Page</a>
<a href="https://2007.igem.org/wiki/index.php?title=ETHZ/Biology/Lab">Lab Notes Page</a>
<a href="https://2007.igem.org/wiki/index.php?title=ETHZ/Biology/Lab">Lab Notes Page</a>
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<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>
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<a href="https://2007.igem.org/wiki/index.php?title=ETHZ/Internal">Brainstorming Page</a>
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__NOTOC__
__NOTOC__
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== Introduction ==
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= Introduction =
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For all our cloning procedures we used standard protocols according to SAMBROOK and RUSSELL Molecular Cloning: A Laboratory Manual.
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On this page, you can find information about how educatETH <i>E.coli</i> 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, you can find [[ETHZ/Biology/Labbook| here]] an (unfortunately not complete) electronic copy of our lab notebook. If you are here because you are interested in implementing educatETH <i>E.coli</i> in your lab, then our System Implementation and the System Parts pages may be of help to you!
 +
For all our cloning procedures we used standard protocols according to ''SAMBROOK and RUSSELL'' Molecular Cloning: A Laboratory Manual [1].
== Strains ==
== Strains ==
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[http://openwetware.org/wiki/E._coli_genotypes#TOP10_.28Invitrogen.29|<b><i>E. coli </i>Top10 (Invitrogen):</b>] <br>  
[http://openwetware.org/wiki/E._coli_genotypes#TOP10_.28Invitrogen.29|<b><i>E. coli </i>Top10 (Invitrogen):</b>] <br>  
 +
*You can find this strain at [http://partsregistry.org/Part:BBa_V1009 BBa_V1009]
*This strain has a streptomycin resistance <br>  
*This strain has a streptomycin resistance <br>  
*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
*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
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[http://openwetware.org/wiki/E._coli_genotypes#JM101|<b><i>E. coli </i>JM101:</b>] <br>
[http://openwetware.org/wiki/E._coli_genotypes#JM101|<b><i>E. coli </i>JM101:</b>] <br>
 +
*You can find this strain at [http://partsregistry.org/Part:BBa_I739301 BBa_I739301]
*We call them <i>Jimmys</i>
*We call them <i>Jimmys</i>
*This strain is the original blue/white cloning strain
*This strain is the original blue/white cloning strain
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*<i>Reference</i>:
*<i>Reference</i>:
**Messing, J. et al. (1981) Nucleic Acids Res. 9, 309; Yanisch-Perron, C., Vieira, J., and Messing, J. (1985) Gene 33, 103
**Messing, J. et al. (1981) Nucleic Acids Res. 9, 309; Yanisch-Perron, C., Vieira, J., and Messing, J. (1985) Gene 33, 103
 +
== Plasmids ==
== Plasmids ==
 +
For our system we needed three plasmids with different origins of replication and antibiotic resistances. We decided to take low copy plasmids. We also decided to use the following plasmids, which we wanted to modify so that they would become compatible to the Biobrick Library multiple cloning site:
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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 ===
=== Basic plasmids ===
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! Plasmid !! Resistances !! Copy number !! Origin !! Map  
! Plasmid !! Resistances !! Copy number !! Origin !! Map  
|-
|-
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| [[ETHZ/pbr322| pBR322]] [2,3] || width=505px | Ampicillin, Tetracyline || 15-20 [4] || width=96px | pMB1 || [[Image:Mappbr322.jpg|center|thumb|pBR322 Map|100px]]
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| [[ETHZ/pbr322| pBR322]] || Ampicillin, Tetracyline || 15-20 [1] || pMB1 || [[Image:Mappbr322.jpg|center|thumb|pBR322 Map|100px]]
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|-
|-
-
 
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| [[ETHZ/pck01| pCK01]] [5] || Chloramphenicol|| 5-12 [4] || pSC101 || [[Image:Mappck01.jpg|center|thumb|pCK01 Map|100px]]
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| [[ETHZ/pck01| pCK01]] || Chloramphenicol|| 5-12 [1]|| pSC101 || [[Image:Mappck01.jpg|center|thumb|pCK01 Map|100px]]
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|-
|-
-
 
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| [[ETHZ/pacyc177| pACYC177]] [6,7] || Ampicillin, Kanamycin|| 10-12 [4] || p15A || [[Image:Mappacyc177.jpg|center|thumb|pACYC177 Map|100px]]
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| [[ETHZ/pacyc177| pACYC177]] || Ampicillin, Kanamycin|| 10-12 [1] || p15A || [[Image:Mappacyc177.jpg|center|thumb|pACYC177 Map|100px]]
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|-
|-
|}
|}
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<br>
=== Changes to the plasmids ===
=== 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:
In order to get the Biobrick multiple cloning site into the plasmids, we had to make several changes to the plasmids:
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{| class="wikitable" border="1" cellspacing="0" cellpadding="2" style="text-align:left; margin: 1em 1em 1em 0; background: #f9f9f9; border: 1px #aaa solid; border-collapse: collapse;"
{| class="wikitable" border="1" cellspacing="0" cellpadding="2" style="text-align:left; margin: 1em 1em 1em 0; background: #f9f9f9; border: 1px #aaa solid; border-collapse: collapse;"
|-
|-
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! Plasmid !! Changes !! New plasmid name !! New resistance !! Map  
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! Plasmid !! Changes !! width=85px| New name !! New resistance !! New Map  
|-
|-
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| width=94px | [http://partsregistry.org/Part:BBa_I739201 BBa_I739201]
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| [[ETHZ/pbr322| pBR322]]  
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|
-
|  
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*Site directed mutagenesis: Changed the GCA codon of the PstI site of the bla gene into GTA
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*Site directed mutagenisis: Changed the GCA codon of the PstI site in bla gene to GTA
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*Cloned in [[ETHZ/pbr322-3| linker oligos]] (EcoRI/BamHI)
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*Cloned in linker oligos (EcoRI/BamHI)  
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|
-
| BBa_I739201 
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[[ETHZ/pbr322| pBR322]]
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| Ampicillin
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|
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| [[Image:Mappbr322.jpg|center|thumb|pBR322 Map|100px]]
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Ampicillin  
 +
|
 +
[[Image:MapI739201.jpg|center|thumb|BBa_I739201 Map|100px]]
|-
|-
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| [http://partsregistry.org/Part:BBa_I739203 BBa_I739203]  
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| [[ETHZ/pbr322| pBR322]]  
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|
-
|  
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*Cloned in [[ETHZ/pbr322-1| linker oligos]] (EcoRI/PstI)
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*Cloned in linker oligos (EcoRI/PstI)  
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|
-
| BBa_I739203
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[[ETHZ/pbr322| pBR322]]
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| Tetracyline
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|
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| [[Image:Mappbr322.jpg|center|thumb|pBR322 Map|100px]]
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Tetracycline
 +
|
 +
[[Image:MapI739203.jpg|center|thumb|BBa_I739203 Map|100px]]
|-
|-
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| [http://partsregistry.org/Part:BBa_I739202 BBa_I739202]
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| [[ETHZ/pck01| pCK01]]  
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|
-
|  
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*[[ETHZ/primer_pcr_killspe_up| Site directed mutagenesis]]: Changed the ACT codon of the SpeI site in the origin of replication into ATT
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*Site directed mutagenisis: Changed the xxx codon of the SpeI site into xxx
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*Cloned in [[ETHZ/pck01-3| linker oligos]] (AgeI/AseI)
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*Cloned in linker oligos (AgeI/AseI)
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|
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| BBa_I739202
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[[ETHZ/pck01| pCK01]]
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| Chloramphenicol  
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|
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| [[Image:Mappck01.jpg|center|thumb|pCK01 Map|100px]]
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Chloramphenicol
 +
|
 +
[[Image:MapI739202.jpg|center|thumb|BBa_I739202 Map|100px]]
|-
|-
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| [http://partsregistry.org/Part:BBa_I739204 BBa_I739204]
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| [[ETHZ/pacyc177| pACYC177]]  
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|
-
|  
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*Cloned in [[ETHZ/pacyc177-1| linker oligos]] (BamHI/PstI)
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*Cloned in linker oligos (BamHI/PstI)
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|
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| BBa_I739204
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[[ETHZ/pacyc177| pACYC177]]
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| Kanamycin
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|
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| [[Image:Mappacyc177.jpg|center|thumb|pACYC177 Map|100px]]
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Kanamycin  
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| [[Image:MapI739204.jpg|center|thumb|BBa_I739204 Map|100px]]
|-
|-
|}
|}
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<br>
 +
==Cloning plan==
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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])
 
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==Cloning plan==
 
===Parts assignment into plasmids===
===Parts assignment into plasmids===
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The plan was to put the following parts into the three plasmids (for the detailed cloning procedure see below):
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Three plasmids are used for the EducatETH <i>E.coli</i> system parts as follows:
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{| class="wikitable" border="1" cellspacing="0" cellpadding="2" style="text-align:left; margin: 1em 1em 1em 0; background: #f9f9f9; border: 1px #aaa solid; border-collapse: collapse;"
{| class="wikitable" border="1" cellspacing="0" cellpadding="2" style="text-align:left; margin: 1em 1em 1em 0; background: #f9f9f9; border: 1px #aaa solid; border-collapse: collapse;"
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|+'''Plasmids and contents'''
 
|-
|-
! plasmid !! resistance !! copy type!! contents !! comments
! plasmid !! resistance !! copy type!! contents !! comments
|-
|-
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| [[ETHZ/pbr322| pbr322]] || ampicillin || high || 1,2,3 || constitutive subsystem
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| [http://partsregistry.org/Part:BBa_I739201 BBa_I739201] || ampicillin || low || [http://partsregistry.org/Part:BBa_I739001 BBa_I739001(TetR) ], [http://partsregistry.org/Part:BBa_I739002 BBa_I739002(LacI) ], [http://partsregistry.org/Part:BBa_I739003 BBa_I739003(LuxR) ] || constitutive subsystem
|-
|-
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| [[ETHZ/pck01| pck01]] || chloramphenicol|| low || 4,5,8,9 || reporting subsystem
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| [http://partsregistry.org/Part:BBa_I739202 BBa_I739202] || chloramphenicol|| low || [http://partsregistry.org/Part:BBa_I739004 BBa_I739004(P22 cII) ], [http://partsregistry.org/Part:BBa_E0430 BBa_E0430(EYFP) ], [http://partsregistry.org/Part:BBa_I739008 BBa_I739008(cI) ], [http://partsregistry.org/Part:BBa_I739009 BBa_I739009(ECFP) ] || reporting subsystem
|-
|-
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| [[ETHZ/pacyc177| pacyc177]] || kanamycin|| low || 6,7,10,11 || learning subsystem, reporting subsystem
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| [http://partsregistry.org/Part:BBa_I739204 BBa_I739204] || kanamycin|| low || [http://partsregistry.org/Part:BBa_I739006 BBa_I739006(cI) ], [http://partsregistry.org/Part:BBa_I739007 BBa_I739007(P22 cII) ], [http://partsregistry.org/Part:BBa_I739010 BBa_I739010(RFP) ], [http://partsregistry.org/Part:BBa_I739011 BBa_I739011(GFP) ] || learning subsystem, reporting subsystem
|-
|-
|}
|}
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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.
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:
+
=== Cloning 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]. [[Image:Assembly _process.png|thumb|300px|DNA assembly process [8]]] 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'''.
-
{| class="wikitable" border="1" cellspacing="0" cellpadding="2" style="text-align:left; margin: 1em 1em 1em 0; background: #f9f9f9; border: 1px #aaa solid; border-collapse: collapse;"
 
-
|+'''Linkers for plasmids'''
 
-
|-
 
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! Linker!! Plasmid
 
-
|-
 
-
| [[ETHZ/pbr322-1| pbr322-1]]|| pbr322
 
-
|-
 
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| [[ETHZ/pbr322-2| pbr322-2]]|| pbr322
 
-
|-
 
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| [[ETHZ/pbr322-3| pbr322-3]]|| pbr322
 
-
|-
 
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| [[ETHZ/pbr322-4| pbr322-4]]|| pbr322
 
-
|-
 
-
| [[ETHZ/pck01| pck01]] || pck01
+
==== Plasmid 1 ''([http://partsregistry.org/Part:BBa_I739201 BBa_I739201])'' ====
-
|-
+
-
| [[ETHZ/pCK01-2| pck01-2]] || pck01
+
-
|-
+
-
| [[ETHZ/pacyc177-1| pacyc177-1]] || pacyc177
 
-
|-
 
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| [[ETHZ/pacyc177-2| 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.
+
# Digest '''[http://partsregistry.org/Part:BBa_I739001 I739001(TetR)]''' and [http://partsregistry.org/Part:BBa_I739201 BBa_I739201] plasmid with EcoRI/PstI and ligate them afterwards.
 +
# Digest '''[http://partsregistry.org/Part:BBa_I739002 I739002(LacI)]''' and '''[http://partsregistry.org/Part:BBa_I739003 I739003(LuxR)]''' with XbaI/PstI
 +
# Digest '''[http://partsregistry.org/Part:BBa_I739001 I739001(TetR)]''' in [http://partsregistry.org/Part:BBa_I739201 BBa_I739201] with SpeI/PstI.
 +
# Ligate digested '''[http://partsregistry.org/Part:BBa_I739001 I739001(TetR)]''' in [http://partsregistry.org/Part:BBa_I739201 BBa_I739201] with digested '''[http://partsregistry.org/Part:BBa_I739002 I739002(LacI)]'''. You get a plasmid containing a '''[http://partsregistry.org/Part:BBa_I739001 I739001(TetR)].[http://partsregistry.org/Part:BBa_I739002 I739002(LacI)]''' composite part.
 +
# Digest '''[http://partsregistry.org/Part:BBa_I739001 I739001(TetR)].[http://partsregistry.org/Part:BBa_I739002 I739002(LacI)]''' with SpeI/PstI.
 +
# Ligate digested '''[http://partsregistry.org/Part:BBa_I739001 I739001(TetR)].[http://partsregistry.org/Part:BBa_I739002 I739002(LacI)]''' with digested '''[http://partsregistry.org/Part:BBa_I739003 I739003(LuxR)]'''. You get the completed '''[http://partsregistry.org/Part:BBa_I739001 I739001(TetR)].[http://partsregistry.org/Part:BBa_I739002 I739002(LacI)].[http://partsregistry.org/Part:BBa_I739003 I739003(LuxR)]''' composite part in the [http://partsregistry.org/Part:BBa_I739201 BBa_I739201] plasmid.
-
=== 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]. [[Image:Assembly _process.png|thumb|300px|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)'' ====
+
==== Plasmid 2 ''([http://partsregistry.org/Part:BBa_I739202 BBa_I739202])''====
-
# Put parts 1,2,3 in  pbr322ap plasmids.
 
-
# Merge plasmid containing part '''2''' ''(donor)'' with plasmid containing part '''3''' ''(acceptor)''. You should get a plasmid containing a '''2.3''' composite part.
 
-
# 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)''====
+
# Digest '''[http://partsregistry.org/Part:BBa_I739004 BBa_I739004(P22 cII)]''', '''[http://partsregistry.org/Part:BBa_I739008 BBa_I739008(cI)]''' and the plasmid [http://partsregistry.org/Part:BBa_I739202 BBa_I739202] with EcoRI/PstI.
 +
# Digest '''[http://partsregistry.org/Part:BBa_E0430 BBa_E0430(EYFP)]''' and '''[http://partsregistry.org/Part:BBa_I739009 BBa_I739009(ECFP)]''' with XbaI/PstI.
 +
# Ligate digested '''[http://partsregistry.org/Part:BBa_I739004 BBa_I739004(P22 cII)]''' and digested plasmid [http://partsregistry.org/Part:BBa_I739202 BBa_I739202].
 +
# Ligate digested '''[http://partsregistry.org/Part:BBa_I739008 BBa_I739008(cI)]''' and the plasmid [http://partsregistry.org/Part:BBa_I739202 BBa_I739202].
 +
# Digest '''[http://partsregistry.org/Part:BBa_I739004 BBa_I739004(P22 cII)]''' in [http://partsregistry.org/Part:BBa_I739202 BBa_I739202] with SpeI/PstI.
 +
# Digest '''[http://partsregistry.org/Part:BBa_I739008 BBa_I739008(cI)]''' in [http://partsregistry.org/Part:BBa_I739202 BBa_I739202] with SpeI/PstI.
 +
# Ligate digested '''[http://partsregistry.org/Part:BBa_I739004 BBa_I739004(P22 cII)]''' in [http://partsregistry.org/Part:BBa_I739202 BBa_I739202] with digested '''[http://partsregistry.org/Part:BBa_E0430 BBa_E0430(EYFP)]'''. You get a plasmid containing a '''[http://partsregistry.org/Part:BBa_I739004 BBa_I739004(P22 cII)].[http://partsregistry.org/Part:BBa_E0430 BBa_E0430(EYFP)]''' composite part.
 +
# Ligate digested '''[http://partsregistry.org/Part:BBa_I739008 BBa_I739008(cI)]''' in [http://partsregistry.org/Part:BBa_I739202 BBa_I739202] with '''[http://partsregistry.org/Part:BBa_I739009 BBa_I739009(ECFP)]'''. You get a plasmid containing a '''[http://partsregistry.org/Part:BBa_I739008 BBa_I739008(cI)].[http://partsregistry.org/Part:BBa_I739009 BBa_I739009(ECFP)]''' composite part.
 +
# Digest '''[http://partsregistry.org/Part:BBa_I739004 BBa_I739004(P22 cII)].[http://partsregistry.org/Part:BBa_E0430 BBa_E0430(EYFP)]''' with SpeI/PstI.
 +
# Digest '''[http://partsregistry.org/Part:BBa_I739008 BBa_I739008(cI)].[http://partsregistry.org/Part:BBa_I739009 BBa_I739009(ECFP)]''' with XbaI/PstI.
 +
# Ligate digested '''[http://partsregistry.org/Part:BBa_I739004 BBa_I739004(P22 cII)].[http://partsregistry.org/Part:BBa_E0430 BBa_E0430(EYFP)]''' and digested '''[http://partsregistry.org/Part:BBa_I739008 BBa_I739008(cI)].[http://partsregistry.org/Part:BBa_I739009 BBa_I739009(ECFP)]'''. You get the completed plasmid containing the '''[http://partsregistry.org/Part:BBa_I739004 BBa_I739004(P22 cII)].[http://partsregistry.org/Part:BBa_E0430 BBa_E0430(EYFP)].[http://partsregistry.org/Part:BBa_I739008 BBa_I739008(cI)].[http://partsregistry.org/Part:BBa_I739009 BBa_I739009(ECFP)]''' composite part.
-
# Put parts 4,5,8,9 in  pck01cm plasmids.
 
-
# Merge plasmid containing part '''4''' ''(donor)'' with plasmid containing part '''5''' ''(acceptor)''. You should get a plasmid containing a '''4.5''' composite part.
 
-
# 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.
 
-
# 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)''====
 
-
# Put parts 6,7,10,11 in  pacyc177km plasmids.
+
====Plasmid 3 ''([http://partsregistry.org/Part:BBa_I739204 BBa_I739204])''====
-
# Merge plasmid containing part '''6''' ''(donor)'' with plasmid containing part '''7''' ''(acceptor)''. You should get a plasmid containing a '''6.7''' composite part.
+
-
# 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.
+
-
# 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.
+
-
== [[ETHZ/Biology/Labbook| Labbook]] ==
 
 +
# Digest '''[http://partsregistry.org/Part:BBa_I739006 BBa_I739006(cI)]''', '''[http://partsregistry.org/Part:BBa_I739010 BBa_I739010(RFP)]''' and the plasmid [http://partsregistry.org/Part:BBa_I739204 BBa_I739204] with EcoRI/PstI.
 +
# Digest '''[http://partsregistry.org/Part:BBa_I739007 BBa_I739007(P22 cII)]''' and '''[http://partsregistry.org/Part:BBa_I739011 BBa_I739011(GFP)]''' with XbaI/PstI.
 +
# Ligate digested '''[http://partsregistry.org/Part:BBa_I739006 BBa_I739006(cI)]''' and digested plasmid [http://partsregistry.org/Part:BBa_I739204 BBa_I739204].
 +
# Ligate digested '''[http://partsregistry.org/Part:BBa_I739010 BBa_I739010(RFP)]''' and the plasmid [http://partsregistry.org/Part:BBa_I739204 BBa_I739204].
 +
# Digest '''[http://partsregistry.org/Part:BBa_I739006 BBa_I739006(cI)]''' in [http://partsregistry.org/Part:BBa_I739204 BBa_I739204] with SpeI/PstI.
 +
# Digest '''[http://partsregistry.org/Part:BBa_I739010 BBa_I739010(RFP)]''' in [http://partsregistry.org/Part:BBa_I739204 BBa_I739204] with SpeI/PstI.
 +
# Ligate digested '''[http://partsregistry.org/Part:BBa_I739006 BBa_I739006(cI)]''' in [http://partsregistry.org/Part:BBa_I739204 BBa_I739204] with digested '''[http://partsregistry.org/Part:BBa_I739007 BBa_I739007(P22 cII)]'''. You get a plasmid containing a '''[http://partsregistry.org/Part:BBa_I739006 BBa_I739006(cI)].[http://partsregistry.org/Part:BBa_I739007 BBa_I739007(P22 cII)]''' composite part.
 +
# Ligate digested '''[http://partsregistry.org/Part:BBa_I739010 BBa_I739010(RFP)]''' in [http://partsregistry.org/Part:BBa_I739204 BBa_I739204] with '''[http://partsregistry.org/Part:BBa_I739011 BBa_I739011(GFP)]'''. You get a plasmid containing a '''[http://partsregistry.org/Part:BBa_I739010 BBa_I739010(RFP)].[http://partsregistry.org/Part:BBa_I739011 BBa_I739011(GFP)]''' composite part.
 +
# Digest '''[http://partsregistry.org/Part:BBa_I739006 BBa_I739006(cI)].[http://partsregistry.org/Part:BBa_I739007 BBa_I739007(P22 cII)]''' with SpeI/PstI.
 +
# Digest '''[http://partsregistry.org/Part:BBa_I739010 BBa_I739010(RFP)].[http://partsregistry.org/Part:BBa_I739011 BBa_I739011(GFP)]''' with XbaI/PstI.
 +
# Ligate digested '''[http://partsregistry.org/Part:BBa_I739006 BBa_I739006(cI)].[http://partsregistry.org/Part:BBa_I739007 BBa_I739007(P22 cII)]''' and digested '''[http://partsregistry.org/Part:BBa_I739010 BBa_I739010(RFP)].[http://partsregistry.org/Part:BBa_I739011 BBa_I739011(GFP)]'''. You get the completed plasmid containing the '''[http://partsregistry.org/Part:BBa_I739006 BBa_I739006(cI)].[http://partsregistry.org/Part:BBa_I739007 BBa_I739007(P22 cII)].[http://partsregistry.org/Part:BBa_I739010 BBa_I739010(RFP)].[http://partsregistry.org/Part:BBa_I739011 BBa_I739011(GFP)]''' composite part.
 +
<br>
==References==
==References==
-
<p>[1] [http://www1.qiagen.com/faq/faqview.aspx?faqid=350&SearchText=&FaqCategoryId=0&MenuItemId=0&catalog=1&ProductLineId=1000228  QIAGEN FAQs]</p>
+
 
-
<p>[x] [http://partsregistry.org/Assembly:Standard_assembly Standard Assembly Process]</p>
+
[http://www.MolecularCloning.com &#91;1&#93; Sambrook J and Russel DW] <i>"Molecular Cloning: A Laboratory Manual"</i>, Cold Spring Harbour Laboratory Press, 3rd edition, 2001<br />
 +
&#91;2&#93; Bolivar F, Rodriguez RL, Greene PJ, Betlach MC, Heynecker HL and Boyer HW <i>"Construction of useful cloning vectors"</i>, Gene 2: 95-113, 1977<br />
 +
&#91;3&#93; Watson N <i>"A new revision of the sequence of plasmid pBR322"</i>, Gene 70: 399-403, 1988<br /> 
 +
[http://www1.qiagen.com/faq/faqview.aspx?faqid=350&SearchText=&FaqCategoryId=0&MenuItemId=0&catalog=1&ProductLineId=1000228  &#91;4&#93; QIAGEN FAQs]<br />
 +
[http://www.blackwell-synergy.com/doi/abs/10.1111/j.1365-2958.1995.tb02293.x &#91;5&#93; Fernández S et al.] <i>"Activation of the transcriptional regulator XylR of Pseudomonas putida by release of repression between functional domains"</i>, Mol Microbiol 16(2):205-213, 1995]<br />
 +
&#91;6&#93; Chang ACY and Cohen SN <i>"Construction and characterization of amplifiable multicopy DNA cloning vehicles derived from the P15A cryptic miniplasmid"</i>, J Bacteriol 134: 1141-1156, 1978<br />
 +
&#91;7&#93; Rose, R.E., <i>"The nucleotide sequence of pACYC177"</i>, Nucleic Acids Res, 16(1): 356, 1988<br />
 +
[http://partsregistry.org/Assembly:Standard_assembly &#91;8&#93; Standard Assembly Process]<br />

Latest revision as of 20:03, 26 October 2007

ETHZ banner.png

 


Introduction

On this page, you can 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, you can 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!

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:


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

  • You can find this strain at [http://partsregistry.org/Part:BBa_V1009 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 [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:]

  • You can find this strain at [http://partsregistry.org/Part:BBa_I739301 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 [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 also decided to use the following plasmids, which we wanted to modify so that they would become compatible to the Biobrick Library multiple cloning site:


Basic plasmids

Plasmid Resistances Copy number Origin Map
pBR322 [2,3] Ampicillin, Tetracyline 15-20 [4] pMB1
pBR322 Map
pCK01 [5] Chloramphenicol 5-12 [4] pSC101
pCK01 Map
pACYC177 [6,7] Ampicillin, Kanamycin 10-12 [4] 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
[http://partsregistry.org/Part:BBa_I739201 BBa_I739201]
  • Site directed mutagenesis: Changed the GCA codon of the PstI site of the bla gene into GTA
  • Cloned in linker oligos (EcoRI/BamHI)

pBR322

Ampicillin

BBa_I739201 Map
[http://partsregistry.org/Part:BBa_I739203 BBa_I739203]

pBR322

Tetracycline

BBa_I739203 Map
[http://partsregistry.org/Part:BBa_I739202 BBa_I739202]

pCK01

Chloramphenicol

BBa_I739202 Map
[http://partsregistry.org/Part:BBa_I739204 BBa_I739204]

pACYC177

Kanamycin

BBa_I739204 Map


Cloning plan

Parts assignment into plasmids

The plan was to put the following parts into the three plasmids (for the detailed cloning procedure see below):

plasmid resistance copy type contents comments
[http://partsregistry.org/Part:BBa_I739201 BBa_I739201] ampicillin low [http://partsregistry.org/Part:BBa_I739001 BBa_I739001(TetR) ], [http://partsregistry.org/Part:BBa_I739002 BBa_I739002(LacI) ], [http://partsregistry.org/Part:BBa_I739003 BBa_I739003(LuxR) ] constitutive subsystem
[http://partsregistry.org/Part:BBa_I739202 BBa_I739202] chloramphenicol low [http://partsregistry.org/Part:BBa_I739004 BBa_I739004(P22 cII) ], [http://partsregistry.org/Part:BBa_E0430 BBa_E0430(EYFP) ], [http://partsregistry.org/Part:BBa_I739008 BBa_I739008(cI) ], [http://partsregistry.org/Part:BBa_I739009 BBa_I739009(ECFP) ] reporting subsystem
[http://partsregistry.org/Part:BBa_I739204 BBa_I739204] kanamycin low [http://partsregistry.org/Part:BBa_I739006 BBa_I739006(cI) ], [http://partsregistry.org/Part:BBa_I739007 BBa_I739007(P22 cII) ], [http://partsregistry.org/Part:BBa_I739010 BBa_I739010(RFP) ], [http://partsregistry.org/Part:BBa_I739011 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.


Cloning 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 [8]
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 ([http://partsregistry.org/Part:BBa_I739201 BBa_I739201])

  1. Digest [http://partsregistry.org/Part:BBa_I739001 I739001(TetR)] and [http://partsregistry.org/Part:BBa_I739201 BBa_I739201] plasmid with EcoRI/PstI and ligate them afterwards.
  2. Digest [http://partsregistry.org/Part:BBa_I739002 I739002(LacI)] and [http://partsregistry.org/Part:BBa_I739003 I739003(LuxR)] with XbaI/PstI
  3. Digest [http://partsregistry.org/Part:BBa_I739001 I739001(TetR)] in [http://partsregistry.org/Part:BBa_I739201 BBa_I739201] with SpeI/PstI.
  4. Ligate digested [http://partsregistry.org/Part:BBa_I739001 I739001(TetR)] in [http://partsregistry.org/Part:BBa_I739201 BBa_I739201] with digested [http://partsregistry.org/Part:BBa_I739002 I739002(LacI)]. You get a plasmid containing a [http://partsregistry.org/Part:BBa_I739001 I739001(TetR)].[http://partsregistry.org/Part:BBa_I739002 I739002(LacI)] composite part.
  5. Digest [http://partsregistry.org/Part:BBa_I739001 I739001(TetR)].[http://partsregistry.org/Part:BBa_I739002 I739002(LacI)] with SpeI/PstI.
  6. Ligate digested [http://partsregistry.org/Part:BBa_I739001 I739001(TetR)].[http://partsregistry.org/Part:BBa_I739002 I739002(LacI)] with digested [http://partsregistry.org/Part:BBa_I739003 I739003(LuxR)]. You get the completed [http://partsregistry.org/Part:BBa_I739001 I739001(TetR)].[http://partsregistry.org/Part:BBa_I739002 I739002(LacI)].[http://partsregistry.org/Part:BBa_I739003 I739003(LuxR)] composite part in the [http://partsregistry.org/Part:BBa_I739201 BBa_I739201] plasmid.


Plasmid 2 ([http://partsregistry.org/Part:BBa_I739202 BBa_I739202])

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


Plasmid 3 ([http://partsregistry.org/Part:BBa_I739204 BBa_I739204])

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


References

[http://www.MolecularCloning.com [1] Sambrook J and Russel DW] "Molecular Cloning: A Laboratory Manual", Cold Spring Harbour Laboratory Press, 3rd edition, 2001
[2] Bolivar F, Rodriguez RL, Greene PJ, Betlach MC, Heynecker HL and Boyer HW "Construction of useful cloning vectors", Gene 2: 95-113, 1977
[3] Watson N "A new revision of the sequence of plasmid pBR322", Gene 70: 399-403, 1988
[http://www1.qiagen.com/faq/faqview.aspx?faqid=350&SearchText=&FaqCategoryId=0&MenuItemId=0&catalog=1&ProductLineId=1000228 [4] QIAGEN FAQs]
[http://www.blackwell-synergy.com/doi/abs/10.1111/j.1365-2958.1995.tb02293.x [5] Fernández S et al.] "Activation of the transcriptional regulator XylR of Pseudomonas putida by release of repression between functional domains", Mol Microbiol 16(2):205-213, 1995]
[6] Chang ACY and Cohen SN "Construction and characterization of amplifiable multicopy DNA cloning vehicles derived from the P15A cryptic miniplasmid", J Bacteriol 134: 1141-1156, 1978
[7] Rose, R.E., "The nucleotide sequence of pACYC177", Nucleic Acids Res, 16(1): 356, 1988
[http://partsregistry.org/Assembly:Standard_assembly [8] Standard Assembly Process]