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Team:Uppsala-Sweden/rna
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==The Constructs== | ==The Constructs== | ||
<h3>Constructs for antisense RNA</h3> | <h3>Constructs for antisense RNA</h3> | ||
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| + | The purpose of the antisense-RNA's is to inhibit the translation of two of the subunits in the PDC. We choose to inhibit the E1 and the E2 subunit because inhibition of the E1 subunit blocks the reaction from initializing while inhibition of the E2 would prevent the active complexes from forming due to it's function as a scaffold protein. Inhibition of the E3 subunit could cause unwanted build up of intermediates and therefore we choose not to aim at it. | ||
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| + | According MING-DE DENG and JOHN R. COLEMAN in "Ethanol Synthesis by Genetic Engineering in Cyanobacteria", the production of ethanol is only one percent of what could be espected from the enzyme activities measured. They further in the discussion propose that this is due to low substrate levels (pyruvate) or low substrate levels caused by low carbon flux [in the glycolysis] due to competition from other pathways in the organism. | ||
| + | We further know that the inhibition of the PDC causes high levels of pyruvate in many organisms. If indeed the limiting factor for the synthesis of ethanol is the pyruvate level then inhibtion of the PDC should do the job, provided an increase of the carbon flux through the glycolysis is the result. | ||
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| + | The antisense-RNA's is designed to be complementary to the transcribed mRNA's using Sfold. We have designed 12 antisense-RNA's that have different length and are aiming at the ribosome binding site in the beginning of the mRNA transcript and also a bit downstream where we had a high probability for a exposed segment of the mRNA. | ||
Revision as of 11:49, 20 October 2009
The Constructs
Constructs for antisense RNA
The purpose of the antisense-RNA's is to inhibit the translation of two of the subunits in the PDC. We choose to inhibit the E1 and the E2 subunit because inhibition of the E1 subunit blocks the reaction from initializing while inhibition of the E2 would prevent the active complexes from forming due to it's function as a scaffold protein. Inhibition of the E3 subunit could cause unwanted build up of intermediates and therefore we choose not to aim at it.
According MING-DE DENG and JOHN R. COLEMAN in "Ethanol Synthesis by Genetic Engineering in Cyanobacteria", the production of ethanol is only one percent of what could be espected from the enzyme activities measured. They further in the discussion propose that this is due to low substrate levels (pyruvate) or low substrate levels caused by low carbon flux [in the glycolysis] due to competition from other pathways in the organism.
We further know that the inhibition of the PDC causes high levels of pyruvate in many organisms. If indeed the limiting factor for the synthesis of ethanol is the pyruvate level then inhibtion of the PDC should do the job, provided an increase of the carbon flux through the glycolysis is the result.
The antisense-RNA's is designed to be complementary to the transcribed mRNA's using Sfold. We have designed 12 antisense-RNA's that have different length and are aiming at the ribosome binding site in the beginning of the mRNA transcript and also a bit downstream where we had a high probability for a exposed segment of the mRNA.
