IGEM:Peking/2007/Count-Conjugation-Procedure: Difference between revisions
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==Make more independent riboregulators== | ==Make more independent riboregulators== | ||
* We choose to use <bbpart> | * We choose to use <bbpart>pSB1A2</bbpart> and <bbpart>BBa_R0010</bbpart>(Plac) to express the taRNA(<bbpart>J23066</bbpart>), and <bbpart>pSB3K3</bbpart> and <bbpart>BBa_R0040</bbpart> to express <bbpart>BBa_E0040</bbpart>, whose translation is under the control of crRNA. | ||
* crRNA is synthesized as two partially overlap ~ | * crRNA is synthesized as two partially overlap ~70bp long primers, and 5 cycles PCR can make it to a dsDNA with some BioBrick cloning sites flanked. | ||
* crRNA should be cut by | * crRNA should be cut by XbaI at 5' and PstI at 3' and cloned into BBa_R0040 to get the full length BioBrick prefix and suffix.--[[User:YangYifan|YangYifan]] 04:19, 9 July 2007 (EDT) | ||
* First, we will try out the UC Berkley riboregulators <bbpart>BBa_J23078</bbpart> and <bbpart>BBa_J23066</bbpart> first. | * First, we will try out the UC Berkley riboregulators <bbpart>BBa_J23078</bbpart> and <bbpart>BBa_J23066</bbpart> first. | ||
* This is '''the exact experimental''' [[IGEM:Peking/2007/Count-Procedure-Riboregulator | '''procedure''']]. | * This is '''the exact experimental''' [[IGEM:Peking/2007/Count-Procedure-Riboregulator | '''procedure''']]. |
Revision as of 04:48, 9 August 2007
Conjugation Test
- We want to do a conjugation efficiency test with wild type F to verify the protocol.
- And then test the conjugation efficiency with all the plasmids at hand.
- This is the exact experimental procedure
Helper plasmids construction
- To construct helper plasmids, we need to knock out the oriT.
- To put conjugation under control, we need to knock out the relaxase.
- The Knockout method: (Anting please explain your method here)
Make more independent riboregulators
- We choose to use <bbpart>pSB1A2</bbpart> and <bbpart>BBa_R0010</bbpart>(Plac) to express the taRNA(<bbpart>J23066</bbpart>), and <bbpart>pSB3K3</bbpart> and <bbpart>BBa_R0040</bbpart> to express <bbpart>BBa_E0040</bbpart>, whose translation is under the control of crRNA.
- crRNA is synthesized as two partially overlap ~70bp long primers, and 5 cycles PCR can make it to a dsDNA with some BioBrick cloning sites flanked.
- crRNA should be cut by XbaI at 5' and PstI at 3' and cloned into BBa_R0040 to get the full length BioBrick prefix and suffix.--YangYifan 04:19, 9 July 2007 (EDT)
- First, we will try out the UC Berkley riboregulators <bbpart>BBa_J23078</bbpart> and <bbpart>BBa_J23066</bbpart> first.
- This is the exact experimental procedure.
Construct the tandem oriT region
- For each conjugation plasmids, we want to construct oriT-taRNA-dbTerm-oriT.
- And Plac to the 5' and GFP to the 3' to test conjugation and deletion.
- Use pSB1A3 as backbone.
- This is the exact experimental procedure.
Put the relaxase under the crRNA control
Assemble the tandem oriT together
Hop count experiement
This is our goal.