Difference between revisions of "Part:BBa K3598051"

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===Demonstration===
 
===Demonstration===
  
[[File:T--BEIJING 4ELEVEN--1._Lark20201024-223452.png|600px|thumb|center|Figure 1. Part demonstration]]
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[[File:T--BEIJING 4ELEVEN--1._Lark20201024-223452.png|400px|thumb|center|Figure 1. Part demonstration]]
  
 
The AOX1-Human cathelicidin LL-37 is a composite part consisting of an AOX1 promoter, a Human cathelicidin LL-37 sequence, and an AOX1 terminator. It is designed for the expression of our AMP tredicapeptide. We inserted the sequence of the system onto vector pPIC9K and transferred the resulting plasmid into Pichia pastoris inoculated on BMMY culture, then added 5% methanol every day to induce its expression.  
 
The AOX1-Human cathelicidin LL-37 is a composite part consisting of an AOX1 promoter, a Human cathelicidin LL-37 sequence, and an AOX1 terminator. It is designed for the expression of our AMP tredicapeptide. We inserted the sequence of the system onto vector pPIC9K and transferred the resulting plasmid into Pichia pastoris inoculated on BMMY culture, then added 5% methanol every day to induce its expression.  

Revision as of 14:34, 27 October 2020


AOX1 Promoter_α factor secretion signal_Human CathelicidinLL-37_AOX 1 Terminator

The circuit we transformed into Pichia Pastoris to produce AMP Humancathelicidin-37.

Demonstration

Figure 1. Part demonstration

The AOX1-Human cathelicidin LL-37 is a composite part consisting of an AOX1 promoter, a Human cathelicidin LL-37 sequence, and an AOX1 terminator. It is designed for the expression of our AMP tredicapeptide. We inserted the sequence of the system onto vector pPIC9K and transferred the resulting plasmid into Pichia pastoris inoculated on BMMY culture, then added 5% methanol every day to induce its expression.

We tested the antimicrobial potency of Human cathelicidin LL-37 as fermentation product of our Pichia pastoris by adding its solution to plates inoculated with P. acnes and E. coli MG1655. It can be inferred from the results that the fermentation product's effect of killing E. coli MG1655 and P. acnes are not significant. Only a certain amount of bacteria within contact of the products were eliminated and the inhibition zones are quite unclear due to low volume of AMPs dissolved in solutions.

Figure 2. Plate verification of Human cathelicidin LL-37 on P. acnes
Figure 3. Plate verification of Human cathelicidin LL-37 on E. coli

Then, we verified Human cathelicidin LL-37's ability as a fermentation product to kill E. coli MG1655 and P. acnes by adding its solution to liquid culture inoculated with the two bacteria. We set the AMP concentration gradient as 2.5% and 25% in verification with E. coli and 25% with P. acnes because 2.5% proved in prior verification to be too low a concentration for the effects to be significant, and measured the OD600 of the bacteria. The results show that the fermentation product is effective in killing E. coli MG1655 and P. acnes.

Figure 5. OD600 verification of 25% fermentation broth Human cathelicidin LL-37 on E. coli
Figure 6. OD600 verification of 20% fermentation broth Human cathelicidin LL-37 on P.acnes

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NotI site found at 1335
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BamHI site found at 937
    Illegal XhoI site found at 1191
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal AgeI site found at 1401
  • 1000
    COMPATIBLE WITH RFC[1000]