Difference between revisions of "Part:BBa K2262007"
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__NOTOC__ | __NOTOC__ | ||
<partinfo>BBa_K2262007 short</partinfo> | <partinfo>BBa_K2262007 short</partinfo> | ||
+ | |||
+ | <br> | ||
+ | <br> | ||
[[File:Composite part Sa-AFP2.png|800px|thumb|center|'''Figure 1.''' P<sub>T7</sub>+RBS+Sa-AFP2+terminator ]] | [[File:Composite part Sa-AFP2.png|800px|thumb|center|'''Figure 1.''' P<sub>T7</sub>+RBS+Sa-AFP2+terminator ]] | ||
+ | |||
+ | <br> | ||
+ | <br> | ||
<h1>'''Introduction'''</h1> | <h1>'''Introduction'''</h1> | ||
+ | | ||
+ | This peptide possesses antifungal activity sensitive to inorganic cations from the defensin family and was proved to have an anti-fungal function [1]. NCTU_Formosa used it to be one of a training data for forming the antifungal peptide scoring card. | ||
− | + | <br> | |
<h1>'''Experiment'''</h1> | <h1>'''Experiment'''</h1> | ||
+ | <br> | ||
+ | |||
<p style="padding:1px;font-size:16px"><b>1. Cloning </b></p> | <p style="padding:1px;font-size:16px"><b>1. Cloning </b></p> | ||
+ | | ||
+ | We put T7 promoter, RBS, and Sa-AFP2 together with pSB1C3 as a backbone. Then we conducted Taq PCR to check the size of the DNA sequence was right. The length of T7 promoter+RBS+Sa-AFP2 is around 234 b.p. Its PCR product is around 546 b.p. | ||
+ | <br> | ||
+ | [[File:Agarose gel Sa-AFP2.png|200px|thumb|center|'''Figure 2.''' P<sub>T7</sub> + RBS + Sa-AFP2 <br> | ||
+ | The DNA sequence length of P<sub>T7</sub> + RBS + Sa-AFP2 is around 200 ~ 250 b.p. The size of its PCR product should be close to 500 ~ 550 b.p.]] | ||
− | + | <br> | |
<p style="padding:1px;font-size:16px"><b>2. Expressing</b></p> | <p style="padding:1px;font-size:16px"><b>2. Expressing</b></p> | ||
+ | | ||
+ | Because Sa-AFP2 had not been expressed by <i>E. coli</i> before, it was a new challenge. The strain we chose to make Sa-AFP2 was <i>E. coli</i> Rosetta-gami strain, which forms the disulfide bonds in the cytoplasm to express the protein. To ensure the peptide was produced, after breaking the bacteria and boiling the lysate with sample buffer and β-mercaptoethanol mixture for 15 minutes, we run SDS-PAGE to check the mass of the peptide. The mass of Sa-AFP2 is around 5.6 kDa. | ||
+ | <br> | ||
+ | <br> | ||
+ | [[File:SDS Sa-AFP2.png|500px|thumb|center|'''Figure 3.'''The mass of Sa-AFP2 is around 5.7 kDa. The result shows that NO.2, No.3, No.5, and No.6 had made the peptide.]] | ||
− | + | <br> | |
+ | <br> | ||
<h1>'''Safety'''</h1> | <h1>'''Safety'''</h1> | ||
<p style="padding:1px;"> | <p style="padding:1px;"> | ||
− | We do the safety part which is the same as the Sa-AFP1. See more in | + | |
+ | We do the safety part which is the same as the Sa-AFP1. See more in | ||
<html><a href="https://parts.igem.org/wiki/index.php?title=Part:BBa_K2262005">BBa_K2262005</a></html>. | <html><a href="https://parts.igem.org/wiki/index.php?title=Part:BBa_K2262005">BBa_K2262005</a></html>. | ||
+ | |||
+ | <br> | ||
+ | <br> | ||
<h1>'''Reference'''</h1> | <h1>'''Reference'''</h1> | ||
− | Terras FR1; Torrekens S; Van Leuven F; Osborn RW; Vanderleyden J; Cammue BP; Broekaert WF. "A new family of basic cysteine-rich plant antifungal proteins from Brassicaceae species." FEBS Lett. 1993 Feb 1;316(3):233-40. | + | [1] Terras FR1; Torrekens S; Van Leuven F; Osborn RW; Vanderleyden J; Cammue BP; Broekaert WF. "A new family of basic cysteine-rich plant antifungal proteins from Brassicaceae species." FEBS Lett. 1993 Feb 1;316(3):233-40. |
<!-- Add more about the biology of this part here | <!-- Add more about the biology of this part here |
Latest revision as of 15:14, 7 December 2017
T7 Promoter+RBS+Sa-AFP2
Introduction
This peptide possesses antifungal activity sensitive to inorganic cations from the defensin family and was proved to have an anti-fungal function [1]. NCTU_Formosa used it to be one of a training data for forming the antifungal peptide scoring card.
Experiment
1. Cloning
We put T7 promoter, RBS, and Sa-AFP2 together with pSB1C3 as a backbone. Then we conducted Taq PCR to check the size of the DNA sequence was right. The length of T7 promoter+RBS+Sa-AFP2 is around 234 b.p. Its PCR product is around 546 b.p.
2. Expressing
Because Sa-AFP2 had not been expressed by E. coli before, it was a new challenge. The strain we chose to make Sa-AFP2 was E. coli Rosetta-gami strain, which forms the disulfide bonds in the cytoplasm to express the protein. To ensure the peptide was produced, after breaking the bacteria and boiling the lysate with sample buffer and β-mercaptoethanol mixture for 15 minutes, we run SDS-PAGE to check the mass of the peptide. The mass of Sa-AFP2 is around 5.6 kDa.
Safety
We do the safety part which is the same as the Sa-AFP1. See more in
BBa_K2262005.
Reference
[1] Terras FR1; Torrekens S; Van Leuven F; Osborn RW; Vanderleyden J; Cammue BP; Broekaert WF. "A new family of basic cysteine-rich plant antifungal proteins from Brassicaceae species." FEBS Lett. 1993 Feb 1;316(3):233-40.
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]