Difference between revisions of "Part:BBa K4195154"
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__NOTOC__ | __NOTOC__ | ||
<partinfo>BBa_K4195154 short</partinfo> | <partinfo>BBa_K4195154 short</partinfo> | ||
+ | ===Biology=== | ||
+ | <b>NanoLuc</b><br/> | ||
+ | NanoLuc is a novel engineered luciferase enzyme that relies on the substrate furimazine to produce high intensity, glow-type luminescence. With high stability, small size and bright luminescence, it is an attractive luminescent reporter (''1''). | ||
− | + | [[File:T--XMU-China--NanoLuc.png|500px]] | |
+ | |||
+ | '''Fig. 1 The bioluminescent reaction catalyzed by NanoLuc® luciferase (''1'').''' | ||
+ | |||
+ | ===Usage and design=== | ||
+ | |||
+ | NanoLuc was selected for its good performance in enhancing the report signal. We add <partinfo>BBa_K3222000</partinfo>, <partinfo>BBa_K4195068</partinfo>, <partinfo>BBa_B0034</partinfo> and <partinfo>BBa_K731721</partinfo> to construct the expression system and obtained the composite <partinfo>BBa_K4195154</partinfo>, which are assembled on the expression vector pSB1C3 by standard assembly. The constructed plasmids were transformed into ''E. coli'' BL21(DE3), then the positive transformants were selected by chloramphenicol and confirmed by colony PCR and sequencing. | ||
+ | |||
+ | |||
+ | ===Characterization=== | ||
+ | |||
+ | ====1. ''In Vivo'' Verification==== | ||
+ | |||
+ | '''1) Agarose Gel Electrophoresis''' | ||
+ | |||
+ | After transferring the plasmid into BL21(DE3), colony PCR was used to certify the plasmid was correct. The expected result was obtained (981bp). | ||
+ | |||
+ | [[File:T--XMU-China--K4195154 (K4195154 pSB1C3, colony PCR).png|300px]] | ||
+ | |||
+ | '''Fig. 2 The result of colony PCR. Plasmid pSB1C3.''' | ||
+ | |||
+ | |||
+ | '''2) Bioluminescence measurement''' | ||
+ | |||
+ | Colonies harboring the correct plasmid were cultivated and induced. The expression behavior of NanoLuc is observed by measuring the bioluminescence as time progressed using microplate reader. | ||
+ | |||
+ | Results are documented in related pages: <partinfo>BBa_K4195141</partinfo>, <partinfo>BBa_K4195142</partinfo>, <partinfo>BBa_K4195143</partinfo>, <partinfo>BBa_K4195144</partinfo>, <partinfo>BBa_K4195145</partinfo>, <partinfo>BBa_K4195149</partinfo>, <partinfo>BBa_K4195150</partinfo>, <partinfo>BBa_K4195151</partinfo>. | ||
+ | |||
+ | ====2. ''In Vitro'' Verification==== | ||
+ | |||
+ | Plasmid was put into the cell-free system for expression. The expression behavior of NanoLuc is observed by measuring the bioluminescence as time progressed using microplate reader. | ||
+ | |||
+ | Results are documented in related pages: <partinfo>BBa_K4195146</partinfo>, <partinfo>BBa_K4195147</partinfo>, <partinfo>BBa_K4195148</partinfo>. | ||
+ | |||
+ | ===Reference=== | ||
+ | |||
+ | 1. C. G. England, E. B. Ehlerding, W. Cai, NanoLuc: A Small Luciferase Is Brightening Up the Field of Bioluminescence. ''Bioconjug Chem'' '''27''', 1175-1187 (2016). | ||
− | |||
− | |||
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Latest revision as of 06:25, 13 October 2022
T7-Nanoluc-T7t
Biology
NanoLuc
NanoLuc is a novel engineered luciferase enzyme that relies on the substrate furimazine to produce high intensity, glow-type luminescence. With high stability, small size and bright luminescence, it is an attractive luminescent reporter (1).
Fig. 1 The bioluminescent reaction catalyzed by NanoLuc® luciferase (1).
Usage and design
NanoLuc was selected for its good performance in enhancing the report signal. We add BBa_K3222000, BBa_K4195068, BBa_B0034 and BBa_K731721 to construct the expression system and obtained the composite BBa_K4195154, which are assembled on the expression vector pSB1C3 by standard assembly. The constructed plasmids were transformed into E. coli BL21(DE3), then the positive transformants were selected by chloramphenicol and confirmed by colony PCR and sequencing.
Characterization
1. In Vivo Verification
1) Agarose Gel Electrophoresis
After transferring the plasmid into BL21(DE3), colony PCR was used to certify the plasmid was correct. The expected result was obtained (981bp).
Fig. 2 The result of colony PCR. Plasmid pSB1C3.
2) Bioluminescence measurement
Colonies harboring the correct plasmid were cultivated and induced. The expression behavior of NanoLuc is observed by measuring the bioluminescence as time progressed using microplate reader.
Results are documented in related pages: BBa_K4195141, BBa_K4195142, BBa_K4195143, BBa_K4195144, BBa_K4195145, BBa_K4195149, BBa_K4195150, BBa_K4195151.
2. In Vitro Verification
Plasmid was put into the cell-free system for expression. The expression behavior of NanoLuc is observed by measuring the bioluminescence as time progressed using microplate reader.
Results are documented in related pages: BBa_K4195146, BBa_K4195147, BBa_K4195148.
Reference
1. C. G. England, E. B. Ehlerding, W. Cai, NanoLuc: A Small Luciferase Is Brightening Up the Field of Bioluminescence. Bioconjug Chem 27, 1175-1187 (2016).
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 619
- 21INCOMPATIBLE WITH RFC[21]Illegal XhoI site found at 38
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 141
- 1000COMPATIBLE WITH RFC[1000]