Difference between revisions of "Part:BBa K3889131"
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and TE → is the terminator efficiency of the <partinfo>BBa_B0010</partinfo> | and TE → is the terminator efficiency of the <partinfo>BBa_B0010</partinfo> | ||
+ | |||
+ | ===Results=== | ||
+ | |||
+ | [[File:T--IISER-Tirupati India--Bsfield1.png|centre|900 px]]<br> | ||
+ | Fig. Field 1: | ||
+ | a. B.subtilis 168 with B0010 Terminator Check Cassette-green fluoresence at wavelength 498nm (under magnification 100X) | ||
+ | b. B.subtilis 168 with B0010 Terminator Check Cassette in bright field (under magnification 100X) | ||
+ | c. B.subtilis 168 with B0010 Terminator Check Cassette-red fluoresence at wavelength 587nm (under magnification 100X) | ||
+ | |||
+ | [[File:T--IISER-Tirupati India--Bsfield2.png|900 px]]<br> | ||
+ | Fig. Field 2: | ||
+ | a. B.subtilis 168 with B0010 Terminator Check Cassette-green fluoresence at wavelength 498nm (under magnification 100X) | ||
+ | b. B.subtilis 168 with B0010 Terminator Check Cassette in bright field(under magnification 100X) | ||
+ | c. B.subtilis 168 with B0010 Terminator Check Cassette-red fluoresenceat wavelength 587nm (under magnification 100X) | ||
+ | d. B.subtilis 168 with B0010 Terminator Check Cassette at wavelength 383nm (under magnification 100X) | ||
+ | |||
+ | Under a confocal microscope, we could observe the expression of sfGFP and mCherry and observe their differences in fluorescence intensities signifying that BBa_B0010 works in Bacillus subtilis. | ||
+ | |||
<!-- Add more about the biology of this part here | <!-- Add more about the biology of this part here |
Latest revision as of 00:28, 22 October 2021
Bacillus subtilis BBa_B0010 terminator check cassette
BBa_B0010 Terminator check cassette for use in Bacillus subtilis.
Fig 1. Spacer replaced from BBa_K3889130 by BBa_B0010
Formulae for terminator efficiency [1]:
where
mCherry0 → mCherry produced by device without terminator
sfGFP0 → sfGFP produced by device without terminator
Using the device (BBa_K3889130) without any changes, TEDevice can be calculated which gives the expression of mCherry in absence of a terminator.
where
mCherry → mCherry produced by the device with terminator
sfGFP → sfGFP produced by the device with terminator
and TE → is the terminator efficiency of the BBa_B0010
Results
Fig. Field 1: a. B.subtilis 168 with B0010 Terminator Check Cassette-green fluoresence at wavelength 498nm (under magnification 100X) b. B.subtilis 168 with B0010 Terminator Check Cassette in bright field (under magnification 100X) c. B.subtilis 168 with B0010 Terminator Check Cassette-red fluoresence at wavelength 587nm (under magnification 100X)
Fig. Field 2:
a. B.subtilis 168 with B0010 Terminator Check Cassette-green fluoresence at wavelength 498nm (under magnification 100X)
b. B.subtilis 168 with B0010 Terminator Check Cassette in bright field(under magnification 100X)
c. B.subtilis 168 with B0010 Terminator Check Cassette-red fluoresenceat wavelength 587nm (under magnification 100X)
d. B.subtilis 168 with B0010 Terminator Check Cassette at wavelength 383nm (under magnification 100X)
Under a confocal microscope, we could observe the expression of sfGFP and mCherry and observe their differences in fluorescence intensities signifying that BBa_B0010 works in Bacillus subtilis.
Sequence and Features
- 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.rc site found at 121
References
1. Gale, G. A. R., Wang, B., & McCormick, A. J. (2021). Evaluation and Comparison of the Efficiency of Transcription Terminators in Different Cyanobacterial Species. Frontiers in Microbiology, 11. https://doi.org/10.3389/fmicb.2020.624011