Generator

Part:BBa_K3165048

Designed by: Mohit Das   Group: iGEM19_IISc-Bangalore   (2019-10-16)
Revision as of 13:53, 20 October 2019 by Mohitdas (Talk | contribs)

ccdB (L83S) under araBAD

The ccdB toxin mutated to a highly unstable state so as to be expressed by common laboratory bacterial strains under arabinose activation.

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BamHI site found at 120
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI site found at 396


Usage and Biology

Biology

Controller of Cell Division or Death B (ccdB) is the toxic component of the Eschereschia coli ccdAB anti-toxin toxin system. It is a globular, dimeric protein with 101 residues per protomer, involved in the maintenance of F plasmid in cells by a mechanism involving its binding to and the poisoning of DNA Gyrase which leads to the breaking of the double-stranded DNA in the bacteria. The L83S mutant of the wild type ccdB protein is being mutated at the 83rd amino acid residue position from Leucine to Serine in the core region of the protein.
Due to the core mutation in the wild type ccdB, the L83S mutant is highly unstable. This can be further verified by the data received from the Thermal Assay which confers it's melting point to be around ~ 420C and that it aggregates at a higher temperature.
We also used Top10 G (gryA) R462C which has a mutation in the Gyrase A at the 462th amino acid residue position i.e. change of arginine to cysteine which makes it resistant to recognition by ccdB (L83S).

Usage

This device can be for the production ccdB L83S in Top10 G (gryA) R462C strain of Eschereschia coli. Further, it can be used in Top10 PJAT strain with Gentamicin resistance for the production and to characterize it's effects on the bacterial population. The coding sequence of the ccdB L83S mutant protein is (BBa_K3165014) and under the promoter (BBa_K3165015)

Characterisation <h2>

IISc Bangalore 2019

Expression and characterisation

This part was incorporated in Top10 G (gryA) R462C which is one of the strain that can be used to produce ccdB L83S because of the mutation in GyraseA making the cells tolerant to it. The secondary culture (500mL) was induced with 1g of L-Arabinose and a total cell lysate was made by following the protein extraction protocol. Further, an uninduced sample was also separated as a control to check leaky transcription.

References

  1. Anusmita Sahoo, Shruti Khare, Sivasankar Devanarayanan, Pankaj C. Jain, and Raghavan Varadarajan
    "Residue proximity information and protein model discrimination using saturation-suppressor mutagenesis"
    doi: 10.7554/eLife.09532
  2. Bharat V.Adkar, Arti Tripathi, Anusmita Sahoo, Kanika Bajaj, Devrishi Goswami, Purbani Chakrabarti, Mohit K. Swarnkar, Rajesh S.Gokhale, Raghavan Varadarajan
    "Protein Model Discrimination Using Mutational Sensitivity Derived from Deep Sequencing"
    https://doi.org/10.1016/j.str.2011.11.021


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