Difference between revisions of "Part:BBa K1022110"

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'''For Other peptides and their characterization please visit [http://2013.igem.org/Team:TU-Delft/PeptideCharacterization Peptide characterization] on TU Delft iGEM13 Wiki'''
 
'''For Other peptides and their characterization please visit [http://2013.igem.org/Team:TU-Delft/PeptideCharacterization Peptide characterization] on TU Delft iGEM13 Wiki'''
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'''Comparison with two peptides:'''
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The fact that for none of the peptides a MIC could be determined for ''E. coli'' (>150µM) further confirms the expected selectivity towards Gram-positives which is observed in the following graph(Figure 2):
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[[Image:Coli high conc TUD.jpg|frame|600px|center]]
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Figure 2: MICs of Maximim-H5, Signiferin and Magainin on ''E. coli''
  
 
==Peptide Production==
 
==Peptide Production==

Revision as of 13:00, 3 October 2013

PT7: RBS: Maximin H5: His 6

This bio-brick contains the promoter pT7 followed by Maximin H5 peptide with a His-6 tag.

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]

Characterization

For more info, visit [http://2013.igem.org/Team:TU-Delft/PeptideCharacterization TU Delft iGEM13 Wiki]

Peptide Characterization:

An important part of the project TU Delft iGEM13 is inhibition of growth or killing of bacteria with the use of antimicrobial peptides (AMPs). In order to get an idea of the toxicity of our peptides we conducted several minimal inhibiting concentration (MIC) experiments. These MIC measurements where done on E. coli, B. subtilis and S. delphini, with the first as representative of our Gram-negative expression host, the second for the Gram-positive targets and the last for our specific target.

MIC determination:

The MIC of Maximin H5 on S. delphini, B. subtilis and E. coli were done according to the protocol described [http://2013.igem.org/Team:TU-Delft/PeptideCharacterization here]. Maximin H5 did not give a measurable reduction in growth below 40µM (Figure 1), making us decide not to proceed testing, as modeling showed it was not possible to reach these concentrations through expression in E.coli.


Figure2 Maximin TUD.jpg

Figure 1: MIC of Maximin H5 on S. delphini


For Other peptides and their characterization please visit [http://2013.igem.org/Team:TU-Delft/PeptideCharacterization Peptide characterization] on TU Delft iGEM13 Wiki

Comparison with two peptides:

The fact that for none of the peptides a MIC could be determined for E. coli (>150µM) further confirms the expected selectivity towards Gram-positives which is observed in the following graph(Figure 2):

Coli high conc TUD.jpg

Figure 2: MICs of Maximim-H5, Signiferin and Magainin on E. coli

Peptide Production

For more info about the production of the peptide Maximin H5, visit [http://2013.igem.org/Team:TU-Delft/Peptides#SUMO Peptide production] on TU Delft iGEM13 Wiki.

Also check the construct used for the peptide production BBa_K1022101 and more characterization.