Team:Wisconsin-Madison/Parts

From 2009.igem.org

(Difference between revisions)
 
(18 intermediate revisions not shown)
Line 1: Line 1:
{{Wisconsin-Madison Template}}
{{Wisconsin-Madison Template}}
-
 
+
<center>
-
{|align="justify"
+
'''PARTS'''
-
|You can write a background of your team here.  Give us a background of your team, the members, etc.  Or tell us more about something of your choosing.
+
</center>
-
|[[Image:Example_logo.png|200px|right|frame]]
+
{| class="wikitable" border="0" align="center" width=300px
-
|-
+
|style="text-align:left" style="vertical-align:top"|
-
|
+
'''Basic Parts'''
-
''Tell us more about your project.  Give us background.  Use this is the abstract of your project.  Be descriptive but concise (1-2 paragraphs)''
+
* GSMT Gene
-
|[[Image:Team.png|right|frame|Your team picture]]
+
* SDMT Gene
-
|-
+
* ProU Promoter
-
|
+
* MetK Gene
-
|align="center"|[[Team:Wisconsin-Madison | Team Example]]
+
* NudF Gene
 +
* PhotoSystem Promoter
 +
'''Composite Parts'''
 +
* ProU Promoter : RBS + RFP + TERM
|}
|}
-
<!--- The Mission, Experiments --->
+
{| class="wikitable" border="0" align="center" width=750px
 +
|style="text-align:left" style="vertical-|
-
{| style="color:#1b2c8a;background-color:#0c6;" cellpadding="3" cellspacing="1" border="1" bordercolor="#fff" width="62%" align="center"
+
<center>
-
!align="center"|[[Team:Wisconsin-Madison|Home]]
+
'''Basic Parts'''
-
!align="center"|[[Team:Wisconsin-Madison/Team|The Team]]
+
</center>
-
!align="center"|[[Team:Wisconsin-Madison/Project|The Project]]
+
 
-
!align="center"|[[Team:Wisconsin-Madison/Parts|Parts Submitted to the Registry]]
+
<center>
-
!align="center"|[[Team:Wisconsin-Madison/Modeling|Modeling]]
+
'''GSMT Gene'''
-
!align="center"|[[Team:Wisconsin-Madison/Notebook|Notebook]]
+
</center>
-
|}
+
 
-
(''Or you can choose different headings. But you must have a team page, a project page, and a notebook page.'')
+
GSMT is a plasmid gene (854 bp) that codes for the enzyme that catalyze the first reaction in the salt tolerant pathway that we are interested. GSMT stands for Glycine Sarcosine N-Methyl Transferase. It catalyzes the conversion from glycine to sarcosine, using SAM as a methyl donor. In our project, we have this GSMT synthesized using MR. Gene. Naturally, this gene can be found in Galdieria sulphuraria, an extremephile that establishes high resistance to osmotic stress as well as acidic, thermal stresses and toxic metals. We PCR amplified gene GSMT with iGEM designated cutting sites and ribosome binding sites and biobricked it with pSB1A2.
 +
 
 +
<center>
 +
Modeling of [[Team:Wisconsin-Madison/GSMT%2BSDMT|GSMT and SDMT]]
 +
Found [http://partsregistry.org/Part:BBa_K220002 HERE] in Registry</center>
 +
 
 +
 
 +
<center>
 +
'''SDMT Gene'''
 +
</center>
 +
 
 +
SDMT is a plasmid gene (900 bp) that codes for the enzyme that catalyze the first reaction in the salt tolerant pathway that we are interested. This enzyme of this pathway is SDMT, which stands for Sarcosine Dimethylglycine Methyl Transferase. It catalyzes two steps of methylation, both that of sarcosine and dimethylglycine, to our final product, betaine, again using SAM as the methyl donor. The gene we used came from Galdieria sulphuraria, an extremephile that establishes high resistance to osmotic stress as well as acidic, thermal stresses and toxic metals. In our project, we really appreciate that Center for Eukaryotic Structural Genomics at University of Wisconsin-Madison graciously gave us the plasmid containing this gene. We PCR amplified gene SDMT with iGEM designated cutting sites and ribosome binding sites and biobricked it with pSB1A2.
 +
 
 +
<center>
 +
Modeling of [[Team:Wisconsin-Madison/SDMT|SDMT]]
 +
 
 +
Modeling of [[Team:Wisconsin-Madison/GSMT%2BSDMT|GSMT and SDMT]]
 +
Found [http://partsregistry.org/Part:BBa_K220000 HERE] in Registry</center>
 +
 
 +
 
 +
<center>
 +
'''ProU Promoter'''
 +
</center>
 +
 
 +
The ProU promoter (658 bp) was obtained from wild type K12 E. Coli Genomic DNA. Pro U controls transcription of the Pro U operon which contains three sub-units instrumental in bringing choline and proline into the cell. The promoter is most active during times of osmotic stress. We PCR amplified the gene proU with iGEM designated cutting sites and ribosome binding sites and biobricked it with pSB1A2.
 +
 
 +
<center>Found [http://partsregistry.org/Part:BBa_K220004 HERE] in Registry</center>
 +
 
 +
 
 +
<center>
 +
'''MetK Gene'''
 +
</center>
 +
 
 +
metK is a plasmid gene (1200 bp) that codes for the enzyme that catalyzes the reaction which produces a methyl donor which is used in the conversion of Glycine to Glycine betaine. The enzyme for this reaction is S-adenosyl-methionine (SAM) synthetase. S-adenosyl-methionine produced from Methionine and one ATP molecule in the presence of SAM synthetase. Three SAM molecules are used in the methylation of Glycine to Glycine betaine (trimethyl glycine). In our project Glycine betaine (an osmoprotectant) was synthesized in E. coli to increase salt tolerance. It was hypothesized that an over expression of metK would lead to an increased production of Glycine betaine.
 +
 
 +
<center>Found [http://partsregistry.org/Part:BBa_K220005 HERE] in Registry</center>
 +
 
 +
 
 +
<center>
 +
'''NudF Gene'''
 +
</center>
 +
 
 +
NudF is a plasmid gene (560 bp) that codes for the protein responsible for the enzymatic reaction in mevalonent pathway to form Dimethylallyl pyrophosphate (DMAPP). Specifically, in our project, we used it in the last step of mevalonate pathway to produce biofuels iso-pentenol. We PCR amplified gene nudF with iGEM designated cutting sites and ribosome binding sites and biobricked it with pSB1A2.  
 +
 
 +
<center>Found [http://partsregistry.org/Part:BBa_K220003 HERE] in Registry</center>
 +
 
 +
 
 +
<center>
 +
'''Composite Parts'''
 +
</center>
 +
<center>
 +
'''ProU Promoter : RBS + RFP + TERM'''
 +
</center>
-
===Note===
+
The ProU promoter (658 bp) was obtained from wild type K12 E. Coli Genomic DNA. Pro U controls transcription of the Pro U operon which contains three sub-units instrumental in bringing choline and proline into the cell. The promoter is most active during times of osmotic stress. Placing the proU promoter before the gene codes for red fluorescence protein with ribosomal binding site would enhance the level of red fluorescence expression under salt stress. We PCR amplified the gene proU with iGEM designated cutting sites and ribosome binding sites and biobricked it with pSB1A2.
-
If you choose to include a '''Parts Submitted to the Registry''' page, please list your parts here.  This is not necessary but it may be a nice list to keep track of.
+
<center>Found [http://partsregistry.org/Part:BBa_K220006 HERE] in Registry</center>

Latest revision as of 02:34, 21 October 2009


PARTS

Basic Parts

  • GSMT Gene
  • SDMT Gene
  • ProU Promoter
  • MetK Gene
  • NudF Gene
  • PhotoSystem Promoter

Composite Parts

  • ProU Promoter : RBS + RFP + TERM
Basic Parts

GSMT Gene

GSMT is a plasmid gene (854 bp) that codes for the enzyme that catalyze the first reaction in the salt tolerant pathway that we are interested. GSMT stands for Glycine Sarcosine N-Methyl Transferase. It catalyzes the conversion from glycine to sarcosine, using SAM as a methyl donor. In our project, we have this GSMT synthesized using MR. Gene. Naturally, this gene can be found in Galdieria sulphuraria, an extremephile that establishes high resistance to osmotic stress as well as acidic, thermal stresses and toxic metals. We PCR amplified gene GSMT with iGEM designated cutting sites and ribosome binding sites and biobricked it with pSB1A2.

Modeling of GSMT and SDMT

Found [http://partsregistry.org/Part:BBa_K220002 HERE] in Registry


SDMT Gene

SDMT is a plasmid gene (900 bp) that codes for the enzyme that catalyze the first reaction in the salt tolerant pathway that we are interested. This enzyme of this pathway is SDMT, which stands for Sarcosine Dimethylglycine Methyl Transferase. It catalyzes two steps of methylation, both that of sarcosine and dimethylglycine, to our final product, betaine, again using SAM as the methyl donor. The gene we used came from Galdieria sulphuraria, an extremephile that establishes high resistance to osmotic stress as well as acidic, thermal stresses and toxic metals. In our project, we really appreciate that Center for Eukaryotic Structural Genomics at University of Wisconsin-Madison graciously gave us the plasmid containing this gene. We PCR amplified gene SDMT with iGEM designated cutting sites and ribosome binding sites and biobricked it with pSB1A2.

Modeling of SDMT

Modeling of GSMT and SDMT

Found [http://partsregistry.org/Part:BBa_K220000 HERE] in Registry


ProU Promoter

The ProU promoter (658 bp) was obtained from wild type K12 E. Coli Genomic DNA. Pro U controls transcription of the Pro U operon which contains three sub-units instrumental in bringing choline and proline into the cell. The promoter is most active during times of osmotic stress. We PCR amplified the gene proU with iGEM designated cutting sites and ribosome binding sites and biobricked it with pSB1A2.

Found [http://partsregistry.org/Part:BBa_K220004 HERE] in Registry


MetK Gene

metK is a plasmid gene (1200 bp) that codes for the enzyme that catalyzes the reaction which produces a methyl donor which is used in the conversion of Glycine to Glycine betaine. The enzyme for this reaction is S-adenosyl-methionine (SAM) synthetase. S-adenosyl-methionine produced from Methionine and one ATP molecule in the presence of SAM synthetase. Three SAM molecules are used in the methylation of Glycine to Glycine betaine (trimethyl glycine). In our project Glycine betaine (an osmoprotectant) was synthesized in E. coli to increase salt tolerance. It was hypothesized that an over expression of metK would lead to an increased production of Glycine betaine.

Found [http://partsregistry.org/Part:BBa_K220005 HERE] in Registry


NudF Gene

NudF is a plasmid gene (560 bp) that codes for the protein responsible for the enzymatic reaction in mevalonent pathway to form Dimethylallyl pyrophosphate (DMAPP). Specifically, in our project, we used it in the last step of mevalonate pathway to produce biofuels iso-pentenol. We PCR amplified gene nudF with iGEM designated cutting sites and ribosome binding sites and biobricked it with pSB1A2.

Found [http://partsregistry.org/Part:BBa_K220003 HERE] in Registry


Composite Parts

ProU Promoter : RBS + RFP + TERM

The ProU promoter (658 bp) was obtained from wild type K12 E. Coli Genomic DNA. Pro U controls transcription of the Pro U operon which contains three sub-units instrumental in bringing choline and proline into the cell. The promoter is most active during times of osmotic stress. Placing the proU promoter before the gene codes for red fluorescence protein with ribosomal binding site would enhance the level of red fluorescence expression under salt stress. We PCR amplified the gene proU with iGEM designated cutting sites and ribosome binding sites and biobricked it with pSB1A2.

Found [http://partsregistry.org/Part:BBa_K220006 HERE] in Registry