Latest revision as of 04:25, 30 October 2008

Home Voltage Signalling Bacillus Modelling Protocols People

Bacillus Overview Transformation RBS & Promoters Primers InFusion Superfolder GFP Lab Notebook

x

To build more complex cellular systems, new tools and techniques are required. We are generating standardized parts, tools, and techniques for the gram-positive chassis B. subtillis. Easy to handle and transform, this bacterium offers many adantages to E. coli', including the ability to secrete proteins and integrate DNA into the chromosome. We have designed, built, and submitted gram-positive RBSes, promoters, and shuttle vectors.As a part of this work we have confirmed single copy chromosomal insertion, demonstrated InFusion assembly, and characterized an improved GFP variant. You can find our Bacillus protocols here.

Improved GFP

Superfolder GFP along with other variants under UV light

We created a codon-optimized and biobricked version of the 'Superfolder' GFP engineered by Pédelacq et al (2006). This GFP variant folds faster and glows brighter than other GFP variants. Read more...

Creating new Biobrick-compatible B.subtilis vectors

[http://partsregistry.org/cgi/partsdb/pgroup.cgi?pgroup=iGEM2008&group=Cambridge Vectors submitted:] We are using the [http://bioinfo.clontech.com/infusion/ In-Fusion™ PCR method from ClonTech] to create new Biobrick-compatible integrative and episomal vectors. These vectors will allow us to insert Biobricks into the Bacillus subtilis genome at the AmyE locus and as a 3-5 copy plasmid that will replicate autonomously in Bacillus.

Successful transformation of Bacillus

Transformation with episomal vectors

ECE166 : High-level constitutive expression of a Green Fluorescent Protein (with the promoter Pupp) Read more...

Observation with microscope (x20) : B.S. transformed with ECE166

Transformation with integration vectors

ECE153 and ECE112 : Transformation in IA751 : Amylase test

IA751 transformed with ECE153 : SUCCESFUL TRANSFORMATION, no zone of clearing

IA751 transformed with ECE112 : SUCCESFUL TRANSFORMATION for 4 colonies out of 5, no zone of clearing

B. subtilis Promoters Designed

[http://partsregistry.org/cgi/partsdb/pgroup.cgi?pgroup=iGEM2008&group=Cambridge Biobricks submitted:]

Pupp - a strong constitutive Bacillus cereus promoter present on B. subtilis vector ECE166
- Successfully expressed in an episomal vector...
Ppac - constitutive, present on B. subtilis vector ECE151
Pspac - IPTG inducible, present on B. subtilis vector ECE151
Pxyl - xylose inducible, present on B. subtilis vector ECE153

Information about the B. subtilis vectors can be found here.

x

@@ Line 1: / Line 1: @@
-<hr width="810px">
+{{Cambridge/Notitle}}
-<div id="about">
+<div class=bodytable>
-{|{{table}} width="800"
+{{Cambridge08}}
-|align="center" style="background-color: #444444;" |
+{{Cambridge08bacillus}}
-[[Image:Bacillus_button.gif|300px]]
-{{Cambridge08a}}
-</div>
-<hr width="810px">
 __NOTOC__
+__NOEDITSECTION__
+<html>
+<table style="background:#444444; padding:15px;">
+<table align=left width= border="0" style="background:#444444; padding:5px;">
+<tr>
+<td style="width:100%; height: 400; padding-left: 15px;">
+    <b class="b1f"></b><b class="b2f"></b><b class="b3f"></b><b class="b4f"></b>
+    <div class="contentf">
+    <div style="height: 400; background: white; line-height:170% padding: 5px;">
+<div style="color: white; font: 2px;">x</div>
+</html>
+'''To build more complex cellular systems, new tools and techniques are required. We are generating standardized parts, tools, and techniques for the gram-positive chassis ''B. subtillis''. Easy to handle and transform, this bacterium offers many adantages to ''E. coli', including the ability to secrete proteins and integrate DNA into the chromosome. We have designed, built, and submitted gram-positive RBSes, promoters, and shuttle vectors.As a part of this work we have confirmed single copy chromosomal insertion, demonstrated InFusion assembly, and characterized an improved GFP variant.  You can find our  [[IGEM:Cambridge/2008/Turing Pattern Formation/Experiments/Bacillus subtilis transfomation| ''Bacillus'' protocols here]].'''
-{|{{table}}
-{|cellspacing="5" cellpadding="10" style="background:#444444"
-|-valign="top"
-|style="background:#FFFFFF"|
-<font style="color:#000000">
+==Improved GFP==
-=Working with ''B.subtilis''=
+[[Image:plate picture.jpg| thumb | 300px | center | Superfolder GFP along with other variants under UV light]]
-Building on the work of the last year's Cambridge iGEM team, we are exploring applications of the gram-positive chassis ''B.subtillis''. Easy to handle and transform, this bacterium is much better to use than ''E.coli'' wherever protein import/export is concerned, e.g. in our signalling project. An important part of our effort is to establish standard protocols and parts to work in ''B.subtillis'', characterise control elements, and develop new vectors. You can find our  [[IGEM:Cambridge/2008/Turing Pattern Formation/Experiments/Bacillus subtilis transfomation| ''Bacillus'' protocols here]].
+We created a codon-optimized and biobricked version of the 'Superfolder' GFP engineered by Pédelacq et al (2006). This GFP variant folds faster and glows brighter than other GFP variants. [[Team:Cambridge/Improved_GFP|Read more...]]
-=Creating new Biobrick-compatible ''B.subtilis'' vectors=
+==Creating new Biobrick-compatible ''B.subtilis'' vectors==
+[http://partsregistry.org/cgi/partsdb/pgroup.cgi?pgroup=iGEM2008&group=Cambridge Vectors submitted:]
-We are using the In-Fusion™ PCR method from ClonTech to create new Biobrick-compatible integrative and episomal vectors. These vectors will allow us to insert Biobricks into the ''Bacillus subtilis'' genome at the AmyE locus and as a 3-5 copy plasmid that will replicate autonomously in ''Bacillus''.
+We are using the [http://bioinfo.clontech.com/infusion/ In-Fusion™ PCR method from ClonTech] to create new Biobrick-compatible integrative and episomal vectors. These vectors will allow us to insert Biobricks into the ''Bacillus subtilis'' genome at the AmyE locus and as a 3-5 copy plasmid that will replicate autonomously in ''Bacillus''.
 {| class="wikitable" border="0" align="center"
@@ Line 34: / Line 39: @@
 '''ECE166''' : High-level constitutive expression of a Green Fluorescent Protein (with the promoter Pupp)
+[[Team:Cambridge/Bacillus_subtilis_transformation|Read more...]]
 [[Image: phototrans166.jpg | thumb | 300px | center | Observation with microscope (x20) : B.S. transformed with ECE166 ]]
@@ Line 43: / Line 50: @@
 [[Image: 153Amylase.jpg | thumb | 200px | left | IA751 transformed with ECE153 : SUCCESFUL TRANSFORMATION, no zone of clearing ]]
 [[Image: 112Amylase.jpg | thumb | 200px | center | IA751 transformed with ECE112 : SUCCESFUL TRANSFORMATION for 4 colonies out of 5, no zone of clearing ]]
+[[Team:Cambridge/Bacillus_subtilis_transformation|Read more...]]
+=='''B. subtilis Promoters Designed'''==
-=Testing ''B.subtilis'' promoters and RBSs=
+[http://partsregistry.org/cgi/partsdb/pgroup.cgi?pgroup=iGEM2008&group=Cambridge Biobricks submitted:]
-We are seeking to test the expression strength and response to inducers in several promoters in ''B.subtilis'', in combination with different Bacillus-specific ribosome binding sites.
-==''B. subtilis'' Promoter Testing with Beta-galactosidase Assay==
-We are aiming to characterize four different ''Bacillus subtilis'' promoters on the ECE112 backbone using the beta-galactosidase assay. Protocol for beta-galactosidase assay as described [http://openwetware.org/wiki/Beta-Galactosidase_Assay_(A_better_Miller) here]
-B. subtilis Promoters to be Tested:
 * Pupp - a strong constitutive ''Bacillus cereus'' promoter present on ''B. subtilis'' vector ECE166
+** [[Team:Cambridge/Bacillus_subtilis_transformation| Successfully expressed in an episomal vector...]]
 * Ppac - constitutive, present on ''B. subtilis'' vector ECE151
 * Pspac - IPTG inducible, present on ''B. subtilis'' vector ECE151
 * Pxyl - xylose inducible, present on ''B. subtilis'' vector ECE153
+[[Team:Cambridge/Signalling/Constructs| Read more about the constructs made...]]
+[[Team:Cambridge/Signalling/Primers| Read more about the primers used...]]
-Information about the ''B. subtilis'' vectors can be found [http://openwetware.org/wiki/IGEM:Cambridge/2008/Turing_Pattern_Formation/Vectors here]
+Information about the ''B. subtilis'' vectors can be found [[Team:Cambridge/Signalling/Vectors|here]].
-===The Schematic:===
-# PCR the 4 promoters out of the corresponding ''B.subtilis'' vectors using primers containing the standard biobrick restriction sites
-# Transform TOP10 with Biobrick I732007
-# Single colony PCR the transformed TOP10 cells and miniprep the colony containing I732007
-# Digest the promoter with EcoRI and SpeI
-# Digest I732007 plasmid with EcoRI and XbaI
-# Ligate the promoter to the I732007 backbone
-# Transform TOP10 cells with the new construct which should have Ampicillin resistance
-# Single colony PCR for successfully transformed cells and miniprep for more of new construct
-# Digest the new construct with EcoRI and BamHI
-# Digest ECE112 vector with EcoRI and BamHI
-# Dirty ligation of the promoter to ECE112 vector
-# Single colony PCR for the plasmid and miniprep
-# Transform ''B. subtilis'' with the plasmid which contains amyE for integration and lacZ for beta-galactosidase assay
-# Perform beta- galatosidase assay!
-=Links=
-* Chris French's [http://openwetware.org/wiki/Cfrench:BacTrans1 protocol on transforming B. subtilis]
-* We have last year's protocol; not sure if it's trustworthy, need to compare with online resources
-* [[IGEM:Cambridge/2008/Turing_Pattern_Formation/BCSG_Transformation_Protocol|Protocol from BCSG catalog]]
-** used in Cornell bacteriology course, probably should start here
-[http://www.sciencedirect.com/science?_ob=ArticleURL&_udi=B6T30-3VCK5Y0-3&_user=1495569&_rdoc=1&_fmt=&_orig=search&_sort=d&view=c&_acct=C000053194&_version=1&_urlVersion=0&_userid=1495569&md5=847137ffc5cf267e12b5625aaadecb0e B. Subtilis Transformation Protcol - Electroporation]
-[http://aem.highwire.org/cgi/content/abstract/71/12/8818 Bongers et al. … of a Subtilin-Regulated Expression System in Bacillus subtilis: Strict Control of Gene Expression …. Applied and Environmental Microbiology (2005)]
-* SURE: handy expression system for B. subtilis
-* What about feedback/regulation effects of subtilin on the cell
-[http://lib.bioinfo.pl/pmid:18261893 Expression and characterization of aiiA gene from Bacillus subtilis BS-1.]
-* (Some strains of) Bacillus subtilis produces a gene called aiiA that degrades AHL molecules from gram-negative bacteria
-* this is biobricked
-== Links to Cambridge 2007 Wiki ==
-*[http://www.ccbi.cam.ac.uk/iGEM2007/index.php/Bacillus_subtilis_SynBio_chassis B. subtilis group]
-*[http://www.ccbi.cam.ac.uk/iGEM2007/index.php/Detailed_background_information_-_B._subtilis B. subtilis group: more info]
+<html>
+<div style="color: white; font: 2px;">x</div>
+      </div></div>
+      <b class="b4f"></b><b class="b3f"></b><b class="b2f"></b><b class="b1f"></b>
+  </td></tr></table></table>
+</html>
 __NOEDITSECTION__
 __NOTOC__