Part:BBa_K4030007
J23101-OmpA-arab-TT
Profile
Name: J23101-OmpA-arab-TT
Base Pairs: 3611bp
Origin: E. coli, synthetic
Properties: Arabinose expression system
Usage and Biology
Dental caries is a common disease. It not only directly affects human oral health, but also often causes adverse symptoms in other parts of the body. Global disease statistics in 2016 show that the incidence of dental caries in the population is ranking second among common diseases. Studies have shown that the formation of dental plaque is the result of the joint action of a variety of bacteria, including Streptococcus mutans, Lactobacillus, Actinomycetes, etc. Phage lyase ClyR (combined from different bacteriophage lytic enzymes) has a broad bactericidal spectrum, especially the only one reported to be extremely strong against Streptococcus mutans and Streptococcus mulberry. The enzyme is promising to kill these two kinds of streptococci are the main cause of dental caries.
Construct design
Arab is connected with OpmA and this sequence is inserted into plasmid pUC57_mini (Figure 2 and 3).
The profiles of every basic part are as follows:
BBa_K4030001
Name: arab
Base Pairs: 1479bp
Origin: Bacillus pumilus
Properties: Secreting arabinosidase to hydrolyze polysaccharides into monosaccharides.
Usage and Biology
BBa_K4030001 is a coding sequence of arab, which is an enzyme used to hydrolyze arabinose from arabinoxylans, a carbohydrate that appears normally in foods.
BBa_K4030000
Name: OmpA
Base Pairs: 63bp
Origin: Escherichia coli
Properties: Outer membrane protein A
Usage and Biology
Outer membrane protein A (OmpA) is a major protein in the Escherichia coli outer membrane.
Experimental approach
Group 1 Plasmid puc57-kan-mini-J23101-OmpA-araB-TT (Plasmid A) was transformed to E. coli Nissle 1917 by electroporation. We tried to monitor the concentration of the reducing sugar arabinose and thus access the activity of AraB. The concentration of reducing sugar was determined by the DNS kit and the A540 were recorded accordingly.
Sequence and Features
- 10INCOMPATIBLE WITH RFC[10]Illegal EcoRI site found at 745
- 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 745
Illegal NheI site found at 7
Illegal NheI site found at 30 - 21INCOMPATIBLE WITH RFC[21]Illegal EcoRI site found at 745
- 23INCOMPATIBLE WITH RFC[23]Illegal EcoRI site found at 745
- 25INCOMPATIBLE WITH RFC[25]Illegal EcoRI site found at 745
- 1000COMPATIBLE WITH RFC[1000]
None |