Difference between revisions of "Part:BBa K4119005"
| Line 3: | Line 3: | ||
<partinfo>BBa_K4119005 short</partinfo> | <partinfo>BBa_K4119005 short</partinfo> | ||
| − | + | Pvgb is an oxygen-dissolving regulated promoter from Vitreoscilla. We have done its expression effect in C. tyrobutyricum before, which proves that it can express bs2 fluorescent protein in different amounts under different oxygen concentrations of C. tyrobutyricum. On the premise that the expression of perR gene can affect the growth of C. tyrobutyricum, We hope that pvgb promoter can be connected with perR gene by Gibson assembly method, and perR gene can be expressed in different degrees by pvgb promoter and the conditions of controlling different oxygen concentrations, so that C. tyrobutyricum has higher oxygen adaptability. | |
| + | |||
| + | |||
| + | ===Results=== | ||
| + | The growth profiles of the Engineered strains under different contents of oxygen | ||
| + | After the experimental strain was activated by TGA plate medium, the single colony was selected and incubated at 37 °C in TGA liquid medium until the OD600 was about 1.0 as seed solution, and transferred to a 50 mL volume centrifuge tube containing 15 mL TGA medium according to the 5% volume specific inoculation amount, and placed in 37 °C 0r, 50 r, 100 r cultivate for 80 h respectively for growth detection. | ||
<html lang="en"> | <html lang="en"> | ||
| Line 18: | Line 23: | ||
</body> | </body> | ||
</html> | </html> | ||
| + | |||
| + | Ecpects | ||
| + | In subsequent experiments, we will further test the effect of dynamic regulation of perR by Pvgb on the growth of C. tyrobutyricum, and we expect to achieve better growth than wild bacteria in both microoxygen and aerobic conditions. | ||
| + | |||
| + | |||
<!-- --> | <!-- --> | ||
<span class='h3bb'>Sequence and Features</span> | <span class='h3bb'>Sequence and Features</span> | ||
Revision as of 14:23, 12 October 2022
Pvgb-perR-Cpa fdx terminator
Pvgb is an oxygen-dissolving regulated promoter from Vitreoscilla. We have done its expression effect in C. tyrobutyricum before, which proves that it can express bs2 fluorescent protein in different amounts under different oxygen concentrations of C. tyrobutyricum. On the premise that the expression of perR gene can affect the growth of C. tyrobutyricum, We hope that pvgb promoter can be connected with perR gene by Gibson assembly method, and perR gene can be expressed in different degrees by pvgb promoter and the conditions of controlling different oxygen concentrations, so that C. tyrobutyricum has higher oxygen adaptability.
Results
The growth profiles of the Engineered strains under different contents of oxygen After the experimental strain was activated by TGA plate medium, the single colony was selected and incubated at 37 °C in TGA liquid medium until the OD600 was about 1.0 as seed solution, and transferred to a 50 mL volume centrifuge tube containing 15 mL TGA medium according to the 5% volume specific inoculation amount, and placed in 37 °C 0r, 50 r, 100 r cultivate for 80 h respectively for growth detection.
Results:
Ecpects In subsequent experiments, we will further test the effect of dynamic regulation of perR by Pvgb on the growth of C. tyrobutyricum, and we expect to achieve better growth than wild bacteria in both microoxygen and aerobic conditions.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]