Difference between revisions of "Part:BBa K3114004"
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===Design===
 
===Design===
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When designing this part and the rest of our collection, we were interested in creating parts that could be used in Golden Gate assembly right out of the distribution kit without the need to first domesticate the parts by cloning them into a Golden Gate entry vector. As such, these parts are not compatible with the iGEM Type IIS RFC[1000] assembly standard because we included the BsaI restriction site and MoClo standard fusion site in the part’s sequence.
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When designing this part and the rest of our collection, we were interested in creating parts that could be used in Golden Gate assembly right out of the distribution kit without the need to first domesticate them in a Golden Gate entry vector. As such, these parts are not compatible with the iGEM Type IIS RFC[1000] assembly standard because we included the BsaI restriction site and MoClo standard fusion site in the part’s sequence.
 
   
 
   
 
As per the MoClo standard, the 5’ signal peptide fusion sequence included in this part is AATG, and the 5’ signal peptide fusion sequence is AGGT.
 
As per the MoClo standard, the 5’ signal peptide fusion sequence included in this part is AATG, and the 5’ signal peptide fusion sequence is AGGT.

Revision as of 20:18, 18 October 2019


YcbK signal peptide (secretion tag)


Usage and Biology

The YcbK signal peptide is a 30-amino acid sequence which targets fused proteins to the Tat secretion pathway in E. coli. In this pathway, proteins are fully or partially folded before secretion to the periplasm. The signal peptide is cleavage site has not been experimentally determined.

Translocation of recombinant proteins to the periplasm can be an effective strategy for increasing protein yield by mitigating inclusion body formation and for simplifying purification procedures in E. coli (Sørensen and Mortensen, 2005). Many different signal peptide sequences have been characterized in literature. However, there are multiple factors that influence the ability of a particular signal peptide to target the recombinant protein of interest to the periplasm (Freudl, 2018). The optimal signal peptide candidate must therefore be determined experimentally. As such, iGEM Calgary sought to create a set of signal peptide parts so that teams may test multiple candidates in their genetic constructs to obtain optimal secretion. The parts were designed to be Golden Gate-compatible based on the MoClo standard for ease in creating the genetic constructs required to screen for the optimal candidate (Weber et al., 2011). They are also compatible with the BioBrick RFC[10] standard.

This signal peptide sequence originates from the uncharacterized YcbK protein in E. coli (Tullman-Ercek et al., 2007). Other signal peptides in this collection include:


Design

When designing this part and the rest of our collection, we were interested in creating parts that could be used in Golden Gate assembly right out of the distribution kit without the need to first domesticate them in a Golden Gate entry vector. As such, these parts are not compatible with the iGEM Type IIS RFC[1000] assembly standard because we included the BsaI restriction site and MoClo standard fusion site in the part’s sequence.

As per the MoClo standard, the 5’ signal peptide fusion sequence included in this part is AATG, and the 5’ signal peptide fusion sequence is AGGT.

Figure 1. Fusion sites used in the MoClo standard for Golden Gate assembly (Weber et al., 2011).

This part includes a start codon. A Gly-Gly spacer sequence was added to the end of the signal peptide sequence in order to ensure that the fused protein of interest will be in-frame following Golden Gate assembly.

This sequence has been codon optimized for high expression in E. coli.

Characterization

Each of the signal peptides in this collection was fused to the water-soluble chlorophyll binding protein 6GIX in a genetic circuit under the control of a T7 inducible promoter.

Figure 2. iGEM Calgary's genetic construct scheme. Each construct consists of a T7 inducible promoter, a strong RBS, one of six signal peptides, the water-soluble chlorophyll binding protein 6GIX with a 6X His tag, and a bidirectional terminator.


The graph below represents the concentration of 6GIX isolated from the periplasm of for each culture. The results suggest that the DsbA, MalE, PhoA, and TorA signal peptides are our most effective candidates for localization of 6GIX to the periplasmic space. Concentrations were determined using spectrophotometry.

Figure 3. Relative concentration of 6GIX protein obtained by performing a periplasmic isolation after secretion using various fused signal peptides. 50 ml cultures were grown to OD600=0.4 then induced with 100 mM IPTG for 8 hours at 37°C before the periplasmic isolation was performed. Genetic constructs for 6GIX without a fused signal peptide and the empty vector were used as controls. Values were obtained by spectrophotometric determination of protein concentration, and represent the mean of two replicates.


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
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI site found at 1
    Illegal BsaI.rc site found at 106


References

Freudl, R. (2018, March 29). Signal peptides for recombinant protein secretion in bacterial expression systems. Microbial Cell Factories. BioMed Central Ltd. https://doi.org/10.1186/s12934-018-0901-3

Sørensen, H. P., & Mortensen, K. K. (2005). Advanced genetic strategies for recombinant protein expression in Escherichia coli. Journal of Biotechnology, 115(2), 113–128. https://doi.org/10.1016/j.jbiotec.2004.08.004

Tullman-Ercek, D., Delisa, M. P., Kawarasaki, Y., Iranpour, P., Ribnicky, B., Palmer, T., & Georgiou, G. (2007). Export Pathway Selectivity of Escherichia coli Twin Arginine Translocation Signal Peptides. https://doi.org/10.1074/jbc.M610507200

Weber, E., Engler, C., Gruetzner, R., Werner, S., & Marillonnet, S. (2011). A modular cloning system for standardized assembly of multigene constructs. PLoS ONE, 6(2). https://doi.org/10.1371/journal.pone.0016765