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Team:KULeuven/Modelling/Vanillin Production
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[2] J.B. Andersen et al., “New Unstable Variants of Green Fluorescent Protein for Studies of Transient Gene Expression in Bacteria,” Applied and Environmental Microbiology, vol. 64, Jun. 1998, pp. 2240–2246 | [2] J.B. Andersen et al., “New Unstable Variants of Green Fluorescent Protein for Studies of Transient Gene Expression in Bacteria,” Applied and Environmental Microbiology, vol. 64, Jun. 1998, pp. 2240–2246 | ||
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| + | [3] K. Nath et al., “Protein degradation in Escherichia Coli,” The Journal of Biological Chemistry, vol. 246, Nov. 1971, pp. 6956-6967 | ||
Revision as of 08:53, 9 September 2009
Contents |
Vanillin Production
overview
The vanillin synthesis consists of a five step process starting from tyrosine. By locking both the transcription of the Sam 8 and COMT enzyme we prevent vanillin synthesis without the presence of RIBOKEY. E. coli controls its own tyrosine production which is an non essential amino acid. However,should this be insufficient, we can always add extra tyrosine. The production process will be tested in two steps. First, from tyrosine to ferulic acid; then from ferrulic acid to vanillin. Because we want the production of vanillin proportional to the amount of input key, it is essential that the regulated enzymes that catalyse the production of (intracellular) vanillin degrade as fast as possible. As proteins are normally very stable in the intracellular environment the SAM8 and COMT where labelled with a LVA-tag, which insures relatively fast half times.
Models
| Name | Value | Comments | Reference |
|---|---|---|---|
| Degradation Rates | |||
| dmRNA | 2.3105E-3 s-1 | [1] | |
| dSam8 | 2.8881E-4 s-1 | Fast degradation through to LVA tag | [2] |
| dSam5 | 1.9254E-5 s-1 | [3] | |
| dCOMT | 2.8881E-4 s-1 | Fast degradation through to LVA tag | [2] |
| dFcs | 1.9254E-5 s-1 | [3] | |
| dEch | 1.9254E-5 s-1 | [3] | |
| dVanillin | 8.6643E-6 s-1 | Equivalent degradation dilution rate of vanillin | [4] |
| Transcription Rates | |||
| ktrans | 0.00848 s-1 | estimate | [4] |
| Key Lock Parameters | |||
| kunlock | 0.00237 s-1 | Rate of unlocking the RIBOLOCK through key | [6] |
| klock | 0.00416 s-1 | Rate of locking of unlocked RIBOLOCK-Key complex. | [3] |
| kopen | 7.5 s-1 | Rate of unlocking RIBOLOCK when no key is present (LEAK). | [3] |
| kclose | 500 s-1 | Rate of locking of leaked RIBOLOCK. | [3] |
Simulation
Because COMT and SAM8 are regulated by the amount of mRNA key its worthy to investigate the change of COMT and SAM8 production in function of the input amount of mRNA key. Because Sam8 and COMT are located behind the same lock they are both translated at the same rate, therefore only the concentration of COMT is shown.
The following figure shows that the steady state level of vanillin concentration is (non linearly) regulated by the amount of mRNA input key.
References
[1] J.A. Bernstein et al., “Global analysis of mRNA decay and abundance in Escherichia coli at single-gene resolution using two-color fluorescent DNA microarrays,” Proceedings of the National Academy of Sciences of the United States of America, vol. 99, Jul. 2002, pp. 9697–9702
[2] J.B. Andersen et al., “New Unstable Variants of Green Fluorescent Protein for Studies of Transient Gene Expression in Bacteria,” Applied and Environmental Microbiology, vol. 64, Jun. 1998, pp. 2240–2246
[3] K. Nath et al., “Protein degradation in Escherichia Coli,” The Journal of Biological Chemistry, vol. 246, Nov. 1971, pp. 6956-6967
