Difference between revisions of "Part:BBa K649300:Experience"
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To characterize this part, we constructed the composite part(BBa_K649301). <br> | To characterize this part, we constructed the composite part(BBa_K649301). <br> | ||
| − | Because arginase is constitutively expressed, the expression level of urea in E. coli transformed with BBa_K649301 was higher than mock ''E. coli''. | + | |
| + | Because arginase is constitutively expressed, the expression level of urea in ''E. coli'' transformed with BBa_K649301 was higher than mock ''E. coli''. | ||
[[Image:MG1655_3K3_rocF.png|thumb|right|400px|Urea concentration in growth media 1 hour after IPTG induction.<br /> | [[Image:MG1655_3K3_rocF.png|thumb|right|400px|Urea concentration in growth media 1 hour after IPTG induction.<br /> | ||
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'''[Discussion]'''<br> | '''[Discussion]'''<br> | ||
In MG1655(argR +), addition of Trc promoter-rocF led to more production of urea compared to the bare backbone pSB3K3 as expected. These results show that insertion of rocF resulted in arginase production as expected, therefore completing the urea cycle in E.coli. | In MG1655(argR +), addition of Trc promoter-rocF led to more production of urea compared to the bare backbone pSB3K3 as expected. These results show that insertion of rocF resulted in arginase production as expected, therefore completing the urea cycle in E.coli. | ||
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===User Reviews=== | ===User Reviews=== | ||
Revision as of 12:07, 28 October 2011
This experience page is provided so that any user may enter their experience using this part.
Please enter
how you used this part and how it worked out.
Applications of BBa_K649300
To characterize this part, we constructed the composite part(BBa_K649301).
Because arginase is constitutively expressed, the expression level of urea in E. coli transformed with BBa_K649301 was higher than mock E. coli.
[Sample]
E.coli strains used in this study
-
MG1655
Plasmid transformed into E.coli in this study
| Designation | Parental vector | Introduced sequence(s) | Part No. |
|---|---|---|---|
| mock | pSB3K3 | PlacIQ | - |
| rocF | pSB3K3 | Ptrc-rocF | BBa_K649301 |
[Method]
Preparation of samples for urea concentration assay
- A single colony of cells transformed with engineered plasmids (mock, Ptrc-rocF or Ptrc-rocF-Arg box) was inoculated into 3 mL of LB with kanamycin and grown to saturation at 37℃
- The saturated culture was diluted 50-fold, grown till the log phase (OD600 = 0.5).
- The culture was induced with 1 mM IPTG at 37 ℃ for 1 hour.
- 1.5 mL of culture was centrifuged at 9,000 rpm for 1 minute and the supernatant fluid was used as a sample for urea concentration assay.
Urea concentration assay
- 10 µL of the supernatant fluid from each sample, 10 µL blank(LB),and 10 µL standard (10 mg/dL urea LB) were transferred to wells of clear bottom 96-well plates.
- 200 µL working reagent for coloring reaction from DIUR-500 -QuantiChrom™ Urea Assay Kit was added and the wells were taped lightly to mix.
- The mixture was incubated for 20 minutes at room temperature.
-
Optical density at 450 nm was read and urea concentration (mg/dL) of the sample was calculated as
ODSAMPLE, ODBLANK and ODSTANDARD are OD450 values of sample, standard and blank, respectively.
Each sample was assayed in triplicate and the averatge of three values were calculataed.
[Discussion]
In MG1655(argR +), addition of Trc promoter-rocF led to more production of urea compared to the bare backbone pSB3K3 as expected. These results show that insertion of rocF resulted in arginase production as expected, therefore completing the urea cycle in E.coli.
User Reviews
UNIQ652eaeed88ea15b2-partinfo-00000000-QINU UNIQ652eaeed88ea15b2-partinfo-00000001-QINU