Difference between revisions of "Part:BBa K1993018"
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<partinfo>BBa_K1993018 short</partinfo> | <partinfo>BBa_K1993018 short</partinfo> | ||
| − | luciferase2 | + | Luciferase(firely Luciferase) |
| + | |||
| + | Luciferase is a generic term for the class of oxidative enzymes that produce bioluminescence, and is distinct from a photoprotein. A variety of organisms regulate their light production using different luciferases in a variety of light-emitting reactions. So, multiple luciferases had been found and used in biological researches. | ||
| + | We had constructed two kinds of luciferases. One of them was firely luciferase that is from Photinus pyralis[1]. | ||
| + | Unlike other fluorescent proteins, light excitation is not needed for luciferase bioluminescence, which means minimal autofluorescence and therefore virtually background-free fluorescence[2]. In other words, sinci luciferase reaction is a enzymatic reaction, light is emitted when luciferase acts on the appropriate luciferin substrate. Photon emission can be detected by light sensitive apparatus such as aluminometer or modified optical microscopes. This allows observation of biological processes[3]. | ||
| + | The chemical reaction catalyzed by firefly luciferase takes place in two steps: | ||
| + | • luciferin + ATP → luciferyl adenylate + PPi | ||
| + | • luciferyl adenylate + O2 → oxyluciferin + AMP + light | ||
| + | Light is produced because the reaction forms oxyluciferin in an electronically excited state. The reaction releases a photon of light as oxyluciferin goes back to the ground state. | ||
| + | <html> | ||
| + | <img src="https://static.igem.org/mediawiki/2016/c/ce/T--SYSU-MEDICINE--luciferase2-1.png" style="width:600px" ></a> | ||
| + | |||
| + | </html> | ||
| + | |||
| + | '''Figure 1 Mechanism for luciferase [4]''' | ||
| + | |||
| + | In biological research, luciferase is commonly used as a reporter to assess the transcriptional activity in cells that are transfected with a genetic construct containing the luciferase gene under the control of a promoter of interest[5]. But in our project, we used luciferase for another purpose: trace the cells non-invasively inside a live mouse using a sensitive charge-couple device camera. | ||
| + | Once we constructed the luciferase, we tested our plasmids inside a mouse. | ||
| + | |||
| + | ==References== | ||
| + | |||
| + | [1] Gould SJ, Subramani S (Nov 1988). "Firefly luciferase as a tool in molecular and cell biology". Analytical Biochemistry. 175 (1): 5–13. | ||
| + | |||
| + | [2] Williams TM, Burlein JE, Ogden S, Kricka LJ, Kant JA (Jan 1989). "Advantages of firefly luciferase as a reporter gene: application to the interleukin-2 gene promoter".Analytical Biochemistry. 176 (1): 28–32. | ||
| + | |||
| + | [3] "Introduction to Bioluminescence Assays". Promega Corporation. Retrieved2009-03-07. | ||
| + | |||
| + | [4] Baldwin TO (Mar 1996). "Firefly luciferase: the structure is known, but the mystery remains". Structure. 4 (3): 223–8 | ||
| + | |||
| + | [5]Fan F, Wood KV (Feb 2007). "Bioluminescent assays for high-throughput screening". ASSAY and Drug Development Technologies. 5 (1): 127–36. | ||
| − | |||
| − | |||
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Revision as of 04:44, 16 October 2016
Luciferase(Firefly Luciferase)
Luciferase(firely Luciferase)
Luciferase is a generic term for the class of oxidative enzymes that produce bioluminescence, and is distinct from a photoprotein. A variety of organisms regulate their light production using different luciferases in a variety of light-emitting reactions. So, multiple luciferases had been found and used in biological researches.
We had constructed two kinds of luciferases. One of them was firely luciferase that is from Photinus pyralis[1].
Unlike other fluorescent proteins, light excitation is not needed for luciferase bioluminescence, which means minimal autofluorescence and therefore virtually background-free fluorescence[2]. In other words, sinci luciferase reaction is a enzymatic reaction, light is emitted when luciferase acts on the appropriate luciferin substrate. Photon emission can be detected by light sensitive apparatus such as aluminometer or modified optical microscopes. This allows observation of biological processes[3].
The chemical reaction catalyzed by firefly luciferase takes place in two steps:
• luciferin + ATP → luciferyl adenylate + PPi
• luciferyl adenylate + O2 → oxyluciferin + AMP + light
Light is produced because the reaction forms oxyluciferin in an electronically excited state. The reaction releases a photon of light as oxyluciferin goes back to the ground state.
Figure 1 Mechanism for luciferase [4]
In biological research, luciferase is commonly used as a reporter to assess the transcriptional activity in cells that are transfected with a genetic construct containing the luciferase gene under the control of a promoter of interest[5]. But in our project, we used luciferase for another purpose: trace the cells non-invasively inside a live mouse using a sensitive charge-couple device camera. Once we constructed the luciferase, we tested our plasmids inside a mouse.
References
[1] Gould SJ, Subramani S (Nov 1988). "Firefly luciferase as a tool in molecular and cell biology". Analytical Biochemistry. 175 (1): 5–13.
[2] Williams TM, Burlein JE, Ogden S, Kricka LJ, Kant JA (Jan 1989). "Advantages of firefly luciferase as a reporter gene: application to the interleukin-2 gene promoter".Analytical Biochemistry. 176 (1): 28–32.
[3] "Introduction to Bioluminescence Assays". Promega Corporation. Retrieved2009-03-07.
[4] Baldwin TO (Mar 1996). "Firefly luciferase: the structure is known, but the mystery remains". Structure. 4 (3): 223–8
[5]Fan F, Wood KV (Feb 2007). "Bioluminescent assays for high-throughput screening". ASSAY and Drug Development Technologies. 5 (1): 127–36.
Sequence and Features
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- 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 808