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Team:SDU-Denmark/Project/BioBricks
From 2012.igem.org
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| - | <h2>Primary | + | <h2>Primary Nucleaic Acid Sequence </h2> |
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The <b<SST</b> gene sequence can be found through the <a href="http://partsregistry.org/wiki/index.php?title=Part:BBa_K899000"><b>link</b></a> by clicking on 'Get selected sequences'. | The <b<SST</b> gene sequence can be found through the <a href="http://partsregistry.org/wiki/index.php?title=Part:BBa_K899000"><b>link</b></a> by clicking on 'Get selected sequences'. | ||
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| - | <h2>Description of | + | <h2>Description of Function </h2> |
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<b>Sucrose:sucrose fructosyltransferase </b> (SST) is one out of two necessary enzymes to produce inulin. The function of SST is to make a tri-saccharide with sucrose as substrate. Two molecules of sucrose is transformed to either 1-kestose or neokestose which is a precursor to inulin. </br></br> | <b>Sucrose:sucrose fructosyltransferase </b> (SST) is one out of two necessary enzymes to produce inulin. The function of SST is to make a tri-saccharide with sucrose as substrate. Two molecules of sucrose is transformed to either 1-kestose or neokestose which is a precursor to inulin. </br></br> | ||
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<h2>Authorship </h2> | <h2>Authorship </h2> | ||
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| - | The original idea for the project is built entirely on the thoughts and ideas of the team's ten participants. All theoretical text and hypotheses about the project is likewise done by the iGEM team. | + | The original idea for the project is built entirely on the thoughts and ideas of the team's ten participants. All theoretical text and hypotheses about the project is likewise done by the iGEM team.</br></br> |
| - | + | It is known that both plants and bacteria can produce fructosyltransferase but with a different degree of polymerizing of inulin. The plants need two enzymes and the bacteria only one. Our idea is based on introducing the two plant enzymes into bacteria with none. </br> | |
| - | + | No other has so far tried to construct a bacteria like ours and therefore all documentation on this subject on our wiki page is made by ourselves. | |
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</br></br> | </br></br> | ||
| - | <h2>Safety | + | <h2>Safety Notes </h2> |
<p> | <p> | ||
| - | See our kill-switch system and considerations on avoiding horizontal gene transfer under <a href="https://2012.igem.org/Team:SDU-Denmark/labwork/Constructs">Constructs</a> | + | See our kill-switch system and considerations on avoiding horizontal gene transfer under <a href="https://2012.igem.org/Team:SDU-Denmark/labwork/Constructs">Constructs</a>. |
</br></br> | </br></br> | ||
| - | <h2> | + | <h2>Acknowledgement of Sources and References </h2> |
<p> | <p> | ||
The original coding genes that are uploaded on Partsregistry is built on scientific articles which can be found at the following links under references.</br> | The original coding genes that are uploaded on Partsregistry is built on scientific articles which can be found at the following links under references.</br> | ||
Latest revision as of 02:38, 27 September 2012
BioBricks
See our submitted BioBricks and composite parts
Primary Nucleaic Acid Sequence
The
Sucrose:sucrose fructosyltransferase (SST) is one out of two necessary enzymes to produce inulin. The function of SST is to make a tri-saccharide with sucrose as substrate. Two molecules of sucrose is transformed to either 1-kestose or neokestose which is a precursor to inulin.
Fructan:Fructan fructosyltransferase (FFT) is the next necessary enzyme in inulin production. This enzyme has the ability to polymerize the tri-saccharide SST made and elongate the chain with fructose molecules.
Both enzymes is from the glycosyltransferase family and are originally expressed in some plants.
The original idea for the project is built entirely on the thoughts and ideas of the team's ten participants. All theoretical text and hypotheses about the project is likewise done by the iGEM team.
It is known that both plants and bacteria can produce fructosyltransferase but with a different degree of polymerizing of inulin. The plants need two enzymes and the bacteria only one. Our idea is based on introducing the two plant enzymes into bacteria with none.
No other has so far tried to construct a bacteria like ours and therefore all documentation on this subject on our wiki page is made by ourselves.
See our kill-switch system and considerations on avoiding horizontal gene transfer under Constructs.
The original coding genes that are uploaded on Partsregistry is built on scientific articles which can be found at the following links under references.
For the FFT:http://partsregistry.org/Part:BBa_K899001:Design
For the SST:http://partsregistry.org/Part:BBa_K899000:Design
Description of Function
Authorship
Safety Notes
Acknowledgement of Sources and References
