Difference between revisions of "Part:BBa K3409013"

(Usage and Biology)
(Usage and Biology)
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===Usage and Biology===
 
===Usage and Biology===
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Microcin PDI (Proximity Dependent Inhibition) which was first identified in 2009 and requires close physical proximity between the producer and susceptible strains. MccPDI has a narrow spectrum and can kill several strains of E. coli: multidrug resistant E. coli, enterotoxigenic E. coli expressing F5 (K99) and F4 (K88) fimbriae, enterohemorrhagic E. coli O157:H7 and O26, as well as commensal strains such as E. coli K12. It has also been shown that Shigella is sensitive to MccPDI. It recognizes specific Outer Membrane Protein F motifs on the target and leads to lethal membrane damage. The MccPDI gene cluster was initially identified in the strain E. coli 25 plasmid. It is a locus of approximately 4.8kb and is composed of 5 genes which are each necessary for the appropriate expression, activity and secretion of microcin PDI:
  
 
[[File: Native MccPDI Cluster.png|border|700px]]
 
[[File: Native MccPDI Cluster.png|border|700px]]
 +
 +
MccPDI gene cluster originally found in E. coli 25 is not constitutive and is controlled by the EnvZ/OmpR Two Component System (TCS). In fact, knockout mutants of the TCS did not show a PDI+ phenotype. EnvZ is an osmotic sensor which upregulates the phosphorylation of OmpR (a transcription factor) which binds to the promoter region upstream of McpM, McpI and McpA. It was shown that the production of MccPDI was higher in M9 medium compared to LB medium. Furthermore, mcpD and mcpB are under the influence of another transcriptional regulation.
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 +
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For this construction, the expression of MccPDI is constitutive. It contains the native coding sequences of each one of the 5 genes and we replaced the rest with promoters, ribosome binding sites (RBS) and terminators contained in the iGEM Registry of Standard Biological Parts.
  
 
===Bibliography===
 
===Bibliography===

Revision as of 08:42, 19 October 2020


Microcin PDI gene cluster

Contains all the elements necessary to constitutively express the entire Microcin PDI gene cluster to produce and secrete the antimicrobial peptide Microcin PDI: mcpM: coding for microcin PDI, mcpI: coding for the immunity protein, mcpA: coding for the activator protein, mcpD and mcpB coding for the secreting proteins. mcpM, mcpI, mcpA are under the control of the same promoter and the sequence is organized as follows: a promoter (BBa_J23111), an RBS (BBa_J61127), the CDS for McpM-His (BBa_K3409003), an RBS (BBa_J61130), the CDS for McpI (BBa_K3409004), an RBS (BBa_J61118), the CDS for McpA (BBa_K3409005) and a double forward terminator (BBa_B0015). mcpD and mcpB are under the control of another promoter and the sequence is organized as follows: a promoter (BBa_J23118), an RBS (BBa_J61118), the CDS for McpD, (BBa_K3409006), an RBS (BBa_J1109), the CDS for McpB (BBa_K3409007) and a double terminator (BBa_B0015).

Usage and Biology

Microcin PDI (Proximity Dependent Inhibition) which was first identified in 2009 and requires close physical proximity between the producer and susceptible strains. MccPDI has a narrow spectrum and can kill several strains of E. coli: multidrug resistant E. coli, enterotoxigenic E. coli expressing F5 (K99) and F4 (K88) fimbriae, enterohemorrhagic E. coli O157:H7 and O26, as well as commensal strains such as E. coli K12. It has also been shown that Shigella is sensitive to MccPDI. It recognizes specific Outer Membrane Protein F motifs on the target and leads to lethal membrane damage. The MccPDI gene cluster was initially identified in the strain E. coli 25 plasmid. It is a locus of approximately 4.8kb and is composed of 5 genes which are each necessary for the appropriate expression, activity and secretion of microcin PDI:

Native MccPDI Cluster.png

MccPDI gene cluster originally found in E. coli 25 is not constitutive and is controlled by the EnvZ/OmpR Two Component System (TCS). In fact, knockout mutants of the TCS did not show a PDI+ phenotype. EnvZ is an osmotic sensor which upregulates the phosphorylation of OmpR (a transcription factor) which binds to the promoter region upstream of McpM, McpI and McpA. It was shown that the production of MccPDI was higher in M9 medium compared to LB medium. Furthermore, mcpD and mcpB are under the influence of another transcriptional regulation.


For this construction, the expression of MccPDI is constitutive. It contains the native coding sequences of each one of the 5 genes and we replaced the rest with promoters, ribosome binding sites (RBS) and terminators contained in the iGEM Registry of Standard Biological Parts.

Bibliography

Characterization of a novel microcin that kills enterohemorrhagic escherichia coli O157:H7 and O26. Applied and Environmental Microbiology, 78(18), 6592–6599. https://doi.org/10.1128/AEM.01067-12

Lu, S. Y., Graça, T., Avillan, J. J., Zhao, Z., & Call, D. R. (2019). Microcin PDI inhibits antibioticresistant strains of Escherichia coli and Shigella through a mechanism of membrane disruption and protection by homotrimer self-immunity. Applied and Environmental Microbiology, 85(11), 1–18. https://doi.org/10.1128/AEM.00371-19

Sawant, A. A., Casavant, N. C., Call, D. R., & Besser, T. E. (2011). Proximity-dependent inhibition in Escherichia coli isolates from cattle. Applied and Environmental Microbiology, 77(7), 2345–2351. https://doi.org/10.1128/AEM.03150-09

Zhao, Z., Orfe, L. H., Liu, J., Lu, S. Y., Besser, T. E., & Call, D. R. (2017). Microcin PDI regulation and proteolytic cleavage are unique among known microcins. Scientific Reports, 7(February), 1–14. https://doi.org/10.1038/srep42529


Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 7
    Illegal NheI site found at 30
    Illegal NheI site found at 1498
    Illegal NheI site found at 1521
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]