Difference between revisions of "Part:BBa K2088000"
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[[Image:E.coli_with_C23O_gene_and_Control_before_catechol_treating.jpg|thumb|500px|left|Figure1:There is a plate with each three streaks of three different colonies, "J23100 + B30034 + C23O + dT" and "J23100 + C23O(with native RBS) + dT" are colonies transformed with C23O coding gene, while pbaC is the control without C23O gene. Before dripping catechol solution onto the conlonies, the three streaks showed the same color colonies.]] | [[Image:E.coli_with_C23O_gene_and_Control_before_catechol_treating.jpg|thumb|500px|left|Figure1:There is a plate with each three streaks of three different colonies, "J23100 + B30034 + C23O + dT" and "J23100 + C23O(with native RBS) + dT" are colonies transformed with C23O coding gene, while pbaC is the control without C23O gene. Before dripping catechol solution onto the conlonies, the three streaks showed the same color colonies.]] | ||
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Figure2 shows the plate after dripping catechol solution(0.2mol/L) | Figure2 shows the plate after dripping catechol solution(0.2mol/L) |
Revision as of 08:27, 18 October 2016
catechol 2,3-dioxygenase gene
This basic part is catechol 2,3-dioxygenase gene from Sphingobium sp. YBL2. It converts catechol by meta-cleavage to the bright yellow product 2-hydroxymuconate semialdehyde. In our project, it plays a great role of degrading catechol, which is one of the main metabolites in 3-phenoxybenzoate degradation.
We teseted this basic part by constrcuting two devices:
- 1.Constitutive promoter (BBa_J23100) + its native rbs + C23O + double terminator (BBa_B0015).
- 2.Constitutive promoter (BBa_J23100) + BBa_B0034 + C23O + double terminator (BBa_B0015).
We made plate streaking for three E.coli with different plasmids.
Figure1 shows the plate before dripping catechol solution.
Figure2 shows the plate after dripping catechol solution(0.2mol/L)
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI site found at 804