Team:GeorgiaState

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!align="center"|[https://igem.org/Team.cgi?year=2012&team_name=GeorgiaState Official Team Profile]
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===='''<font color="#0000FF">The 2012 Georgia State University iGEM Team strives to standardize the glyceraldehyde-3-phosphate dehydrogenase (pGAP) promoter shuttle vector to be used in the methylotrophic yeast ''Pichia pastoris''. Creating a standardized expression system within this eukaryotic organism allows the expression of a variety of proteins that can be used for many biological purposes. ''P. pastoris'', in comparison to the conventional recombinant host ''E. coli'', is an ideal choice for the expression of complex proteins due to its ability to perform post-translational modifications and provide a secretion system for these molecules. Modifying the pGAP vector to be used with the iGEM standard enables Georgia State and other teams to utilize ''P. pastoris'' as an expression host. In the future, we also plan to standardize the pPic9 shuttle vector to the iGEM standard.</font>'''====
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====<font color="#0000FF">'''''Agrobacterium tumefaciens'' is a gram-negative soil bacterium and the causative agent of Crown-Gall disease in both dicotyledon and monocotyledon plants. The tumors caused by Crown-Gall disease contain segments from the Tumor Inducing (Ti) Plasmid known as the TDNA, which completely integrate within the plant’s genome. The ability of the Ti plasmid to insert foreign DNA into a plant’s chromosome is used in the field of bio-engineering to manipulate plants to express desired traits. Modification of a gene of interest and insertion into the Ti Plasmid of ''A. tumefaciens'' allows exploitation of the natural ability of A. tumefaciens to transmit DNA. In genetic engineering, a binary vector system comprised of only a portion of the Ti plasmid is used because the entire Ti plasmid is over 250 kb, far too large to be easily manipulated. The binary vectors consist of small plasmids with a cloning site and a selectable marker between the left and right border of the TDNA. The aim of our project is to standardize a binary vector system within the parameters of the iGEM competition to be used for the expression of foreign proteins within plants'''</font>''' '''====
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            <h1 class="p3">Team GSU</h1>
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            <strong class="text-1">August 2, 14:35 AM</strong>
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            <p class="p4">The 2012 Georgia State University iGEM Team strives to standardize the glyceraldehyde-3-phosphate dehydrogenase (pGAP) promoter shuttle vector to be used in the methylotrophic yeast Pichia pastoris. Creating a standardized expression system within this eukaryotic organism allows the expression of a variety of proteins that can be used for many biological purposes. P. pastoris, in comparison to the conventional recombinant host E. coli, is an ideal choice for the expression of complex proteins due to its ability to perform post-translational modifications and provide a secretion system for these molecules. Modifying the pGAP vector to be used with the iGEM standard enables Georgia State and other teams to utilize P. pastoris as an expression host. In the future, we also plan to standardize the pPic9 shuttle vector to the iGEM standard.</p>
 +
            <p class="p4">Agrobacterium tumefaciens is a gram-negative soil bacterium and the causative agent of Crown-Gall disease in both dicotyledon and monocotyledon plants. The tumors caused by Crown-Gall disease contain segments from the Tumor Inducing (Ti) Plasmid known as the TDNA, which completely integrate within the plant's genome. The ability of the Ti plasmid to insert foreign DNA into a plant's chromosome is used in the field of bio-engineering to manipulate plants to express desired traits. Modification of a gene of interest and insertion into the Ti Plasmid of A. tumefaciens allows exploitation of the natural ability of A. tumefaciens to transmit DNA. In genetic engineering, a binary vector system comprised of only a portion of the Ti plasmid is used because the entire Ti plasmid is over 250 kb, far too large to be easily manipulated. The binary vectors consist of small plasmids with a cloning site and a selectable marker between the left and right border of the TDNA. The aim of our project is to standardize a binary vector system within the parameters of the iGEM competition to be used for the expression of foreign proteins within plants.</p>
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            <div class="date"> 07 <span> Sept </span> </div>
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                <p>Safety and Abstract due</p>
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            <div class="date">03<span>Oct</span></div>
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                <p>WIKI freeze and parts due</p>
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            <div class="date">12<span>Oct</span></div>
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                <p>East Regional Jamboree</p>
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            <div class="date">30<span>jun</span></div>
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                <p><a href="#" class="link-1">Lorem ipsum dolor.</a></p>
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                    Lorem ipsum dolor sit amet consectetuer adipiscing elit, sed diam nonummy nibh euismod tincidunt ut laoreet
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            <div class="date">26<span>jun</span></div>
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                <div class="extra-wrap">
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                <p><a href="#" class="link-1">sit consectetuer.</a></p>
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                    Ut wisi enim ad minim veniam quis nostrud exerci tation ullamcorper suscipit lobortis aliquip commodo consequat.
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            <div class="date">15<span>jun</span></div>
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                <p><a href="#" class="link-1">adipiscing elit.</a></p>
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          <div class="banner-1"><h2>We strive to make a difference in the <span class="clr-2">Synthetic Biology </span> world everyday through our <span class="clr-3">innovations </span> and
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<span class="clr-1">motivations.</span></h2></div>
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Revision as of 15:08, 3 October 2012

<!DOCTYPE html> Home

International

Genetically

Engineered

Machine

About Us

Team GSU

August 2, 14:35 AM

The 2012 Georgia State University iGEM Team strives to standardize the glyceraldehyde-3-phosphate dehydrogenase (pGAP) promoter shuttle vector to be used in the methylotrophic yeast Pichia pastoris. Creating a standardized expression system within this eukaryotic organism allows the expression of a variety of proteins that can be used for many biological purposes. P. pastoris, in comparison to the conventional recombinant host E. coli, is an ideal choice for the expression of complex proteins due to its ability to perform post-translational modifications and provide a secretion system for these molecules. Modifying the pGAP vector to be used with the iGEM standard enables Georgia State and other teams to utilize P. pastoris as an expression host. In the future, we also plan to standardize the pPic9 shuttle vector to the iGEM standard.

Agrobacterium tumefaciens is a gram-negative soil bacterium and the causative agent of Crown-Gall disease in both dicotyledon and monocotyledon plants. The tumors caused by Crown-Gall disease contain segments from the Tumor Inducing (Ti) Plasmid known as the TDNA, which completely integrate within the plant's genome. The ability of the Ti plasmid to insert foreign DNA into a plant's chromosome is used in the field of bio-engineering to manipulate plants to express desired traits. Modification of a gene of interest and insertion into the Ti Plasmid of A. tumefaciens allows exploitation of the natural ability of A. tumefaciens to transmit DNA. In genetic engineering, a binary vector system comprised of only a portion of the Ti plasmid is used because the entire Ti plasmid is over 250 kb, far too large to be easily manipulated. The binary vectors consist of small plasmids with a cloning site and a selectable marker between the left and right border of the TDNA. The aim of our project is to standardize a binary vector system within the parameters of the iGEM competition to be used for the expression of foreign proteins within plants.

Latest news
07 Sept

Safety and Abstract due

03Oct

WIKI freeze and parts due

12Oct

East Regional Jamboree

30jun

Lorem ipsum dolor.

Lorem ipsum dolor sit amet consectetuer adipiscing elit, sed diam nonummy nibh euismod tincidunt ut laoreet
26jun

sit consectetuer.

Ut wisi enim ad minim veniam quis nostrud exerci tation ullamcorper suscipit lobortis aliquip commodo consequat.
15jun

adipiscing elit.

Duis autem vel eum iriure dolor hendrerit vulputate velit esse molestie consequat, vel illum dolore eu feugiat.
Follow us

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