Part:BBa_K2262005
T7 Promoter+RBS+Sa-AFP1
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-AFP1 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-AFP1 is234 b.p. Its PCR product is around 546 b.p.
2. Expressing
Because Sa-AFP1 had not been expressed by E. coli before, it was a new challenge. The strain we chose to make Sa-AFP1 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-AFP1 is around 5.7 kDa.
Safety
To make sure the lysate will not contain any living bacteria, we boiled the lysate for 15 minutes after sonicating the bacteria. The result of SDS-PAGE shows that the peptide still exists after boiling it. So, the only thing we need to know was that whether the lysate would have living bacteria after boiling. We put boiled lysate on an LB plate and cultured it at 37℃ for 16 hours. The result shows that there is no living E. coli after boiling it for 15 minutes.
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]
None |