Difference between revisions of "Part:BBa K200006:Design"
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Revision as of 14:18, 1 September 2009
OtsB: Part 2 of 2 coding for trehalose producing enzymes
Sequence codes for trehalose phosphatase enzyme. This enzyme is the second of two required for the conversion of glucose to trehalose.
This enzyme catalyses the following reaction:
alpha,alpha-trehalose 6-phosphate + H2O -> alpha,alpha-trehalose + phosphate
Trehalose is a disaccharide formed from two glucose molecules. Throughout nature, trehalose is associated with resistance to dessication and cold shock [http://www.pnas.org/content/99/15/9727.full.pdf+html 1], and is naturally produced in Escherichia Coli. We hope that by upregulating the trehalose production pathways in E.coli we can increase trehalose concentrations within our cell, thereby conferring some resistance to protein degredation in our system. This would allow easy transport and storage of the final product.
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 455
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
PCR from Escherichia Coli BL21(DE3)
Primers Used:
Forward:
GCTCTAGATGACAGAACCGTTAACCG
Recomended Temperatures for PCR : 54.5C(without overhang) and 64.8C(with overhang)
Reverse:
GGACTAGTATTAGATACTACGACTAAACGAC
Recomended Temperatures for PCR : 54.7C(without overhang) and 64.2C(with overhang)
Biobrick Overhang shown in Bold
Source
Coding sequence isolated from e-coli
References
<biblio>#otsb1 pmid=12105274 </biblio>