Difference between revisions of "Part:BBa K4099008"
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<partinfo>BBa_K4099008 short</partinfo> | <partinfo>BBa_K4099008 short</partinfo> | ||
− | pIB165 | + | == Profile == |
+ | ==== Name: pIB165 ==== | ||
+ | ==== Base Pairs: 4139 bp ==== | ||
+ | ==== Origin: Escherichia coli, Addgene ==== | ||
+ | ==== Properties: A E. coli - Streptococci shuttle plasmid for gene expression. ==== | ||
+ | |||
+ | == Usage and Biology == | ||
+ | The plasmid pIB165 is a E. coli-Streptococci shuttle plasmid for gene expression in streptococci with P23 promoter. | ||
+ | |||
+ | == Experimental approach == | ||
+ | We extracted the pIB165 plasmid from E. coli for later electrotransformation. Its sequence map is shown in Figure 1. | ||
+ | [[File:T--Shanghai HS ID--BBa K4099008-Figure1.png|500px|thumb|center|Figure 1. DNA profile of the plasmid pIB165..]] | ||
+ | |||
+ | == Proof of function == | ||
+ | After we electrotransformed the plasmid pIB165 as the foreign DNA to test the transformation efficiency of our modified L. casei, it took several days to culture and finally saw the comparison results. As showing above, we can see that the modified L. casei (KO) has higher transformation efficiency with remarkably more colonies than the wild (Wild). | ||
+ | |||
+ | Transformation test result | ||
+ | [[File:T--Shanghai HS ID--BBa K4099000-Figure2.png|500px|thumb|center|Figure 2. Comparison between the wild L. casei (left) and modified L. casei (right, LSEI-2094 knocked out) in transformation..]] | ||
+ | Graph 1. Comparison between the wild L. casei and modified L. casei in transformation | ||
+ | |||
+ | [[File:T--Shanghai HS ID--BBa K4099000-Figure3.png|500px|thumb|center|Figure 3. Histogram comparison between wild strain and KO strain..]] | ||
+ | |||
+ | In addition, we measured OD600 of these strain groups which were pre-spreaded plates with different volumes of bacteria solutions so as to quantify the transformation results as showing above (Fig. 3). | ||
+ | In conclusion, it indicates that our modified L. casei has much higher efficiency of the foreign plasmid transformation than the wild and the modified L. casei has great potential to be used as the recombinant carrier in various areas. | ||
+ | |||
+ | |||
+ | |||
<!-- Add more about the biology of this part here | <!-- Add more about the biology of this part here |
Latest revision as of 07:24, 19 October 2021
pIB165
Profile
Name: pIB165
Base Pairs: 4139 bp
Origin: Escherichia coli, Addgene
Properties: A E. coli - Streptococci shuttle plasmid for gene expression.
Usage and Biology
The plasmid pIB165 is a E. coli-Streptococci shuttle plasmid for gene expression in streptococci with P23 promoter.
Experimental approach
We extracted the pIB165 plasmid from E. coli for later electrotransformation. Its sequence map is shown in Figure 1.
Proof of function
After we electrotransformed the plasmid pIB165 as the foreign DNA to test the transformation efficiency of our modified L. casei, it took several days to culture and finally saw the comparison results. As showing above, we can see that the modified L. casei (KO) has higher transformation efficiency with remarkably more colonies than the wild (Wild).
Transformation test result
Graph 1. Comparison between the wild L. casei and modified L. casei in transformation
In addition, we measured OD600 of these strain groups which were pre-spreaded plates with different volumes of bacteria solutions so as to quantify the transformation results as showing above (Fig. 3). In conclusion, it indicates that our modified L. casei has much higher efficiency of the foreign plasmid transformation than the wild and the modified L. casei has great potential to be used as the recombinant carrier in various areas.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 3991
- 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 4066
Illegal XhoI site found at 4072 - 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]