Composite

Part:BBa_K2449026

Designed by: Malte Skovsager Andersen   Group: iGEM17_SDU-Denmark   (2017-10-23)


cenA-hlyA and secretion system with hlyB and hlyD regulated by penI

Type 1 secretion system, secreting the to enzymes endoglucanase and exoglucanase.

IT WAS NOT POSSIBLE TO DETECT ANYTHING.


Congo Red agar plates

To assess our cellulose degradation strains of E. coli we performed a screening with Carboxymethyl cellulose (CMC) Congo red agar plates. Congo red binds to cellulose molecules, making i possible to visualise the breakdown of the Congo red bound cellulose. NO visible difference between the bacteria this brick and the controls, suggesting that the type 1 secretion system is not working as intended.

T--SDU-Denmark--Congo_Red.jpg

Figure 1E. coli cultures containing seven different BioBricks plated on a Congo red plate containing the water soluble cellulose derivative CMC. Cellobiose phosphorylase on pSB1C3 with LacI promoter

SDS-PAGE of secreation

Secretion of the cellulases, endoglucanase and exoglucanase, was examined on a SDS-PAGE, with samples taken from the media isolated from an overnight culture. From the SDS-PAGE at Figure Y3 it was not possible to identify any proteins at the expected mass of endoglucanase and exoglucanase (47 kDa and 51 kDA, respectively)

T--SDU-Denmark--SDS-page_cenA_and_cex.jpg

Figure 2. Coomassie stained SDS-PAGE wíth Media isolated from five E.coli strains,

Conclusion

This BioBrick does not work! It is not possible to se any expression of the proteins.



Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 2327
    Illegal NotI site found at 627
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BamHI site found at 2179
    Illegal BamHI site found at 3389
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal NgoMIV site found at 260
    Illegal NgoMIV site found at 633
    Illegal NgoMIV site found at 1135
    Illegal NgoMIV site found at 2219
    Illegal AgeI site found at 2315
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI.rc site found at 680
    Illegal SapI site found at 2027
    Illegal SapI.rc site found at 763


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