Difference between revisions of "Part:BBa K5317018"
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===Theoretical Part Design=== | ===Theoretical Part Design=== | ||
+ | Placing the PknB kinase upstream of the reporter gene EGFP allows the visualization of localisation of PknB. | ||
+ | ===Sequence and Features=== | ||
+ | <partinfo>BBa_K5317018 SequenceAndFeatures</partinfo> | ||
+ | ===Cloning=== | ||
+ | PknB was synthesized and inserted by NEB HiFi Assembly into the pEGFP-C2 backbone plasmid (<span class="plainlinks">[https://parts.igem.org/Part:BBa_K3338020 K3338020]</span>) after its restriction enzyme digestion with SaIHI and BamHI, generating the PknB-eGFP cassette. | ||
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− | < | + | <head> |
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+ | <title>HTML Table Caption</title> | ||
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+ | </head> | ||
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+ | <body> | ||
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+ | <caption>Table1: Primers used to create matching overhangs of pknB amplicon to digested pEGFP-C2 backbone</caption> | ||
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+ | <table style="width:70%"> | ||
+ | |||
+ | <tr> | ||
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+ | <th>Primer name</th> | ||
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+ | <th>Sequence</th> | ||
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+ | </tr> | ||
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+ | <tr> | ||
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+ | <td>PknB_fw_1</td> | ||
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+ | <td>AGCTTCGAATTCTGCAGAatgataggtaaaataataaatgaacgatataaaattgtagataagcttgg</td> | ||
+ | |||
+ | </tr> | ||
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+ | <tr> | ||
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+ | <td>PknB_rev_2</td> | ||
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+ | <td>TCAGTTATCTAGATCCGGTGttatacatcatcatagctgacttctttttcagctacag</td> | ||
+ | |||
+ | </tr> | ||
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+ | </table> | ||
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+ | </body> | ||
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+ | </html> | ||
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+ | <html> | ||
+ | <center> | ||
+ | <img src="https://static.igem.wiki/teams/5317/pknb-egfp.png"width: 50%; height: 50%"> | ||
+ | </p> | ||
+ | </center> | ||
+ | </html> | ||
+ | Figure 1: Assembled vector map with pknB-EGFP integrated into the pEGFP-C2 backbone. | ||
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=References= | =References= |
Revision as of 18:07, 27 September 2024
CMV-EGFP-PknB
Usage and Biology
PknB is a eukaryote-like serine/threonine kinase in Staphylococcus aureus that plays an important role in the bacterial response to antibiotics, particularly beta-lactams, via its PASTA domain (Stehle et al.,2012). PknB is a membrane-localized protein consisting of an N-terminal cytosolic kinase domain, a central transmembrane segment and three C-terminal extracellular PASTA domains. The PASTA (penicillin-binding protein and serine/threonine kinase-associated) domain plays a critical role in the recognition and binding of beta-lactam antibiotics (Stehle et al.,2012). Upon binding these compounds, the PASTA domain initiates a signaling cascade by inducing autophosphorylation of the N-terminal kinase domain. This activation leads to the initiation of downstream signaling pathways (Cheung et al.,2010). In S. aureus, this mechanism is critical for early detection of antibiotics and helps the bacteria adapt to antibiotic stress (Sauer et al.,2018).
The composite part includes the upstream positioned reporter gene EGFP (K3338006) to charactarize the PknB regarding it's cellular localization pre and post antibiotics stimulation.
Cloning
Theoretical Part Design
Placing the PknB kinase upstream of the reporter gene EGFP allows the visualization of localisation of PknB.
Sequence and Features
- 10INCOMPATIBLE WITH RFC[10]Illegal XbaI site found at 2596
Illegal SpeI site found at 3259
Illegal PstI site found at 2021 - 12INCOMPATIBLE WITH RFC[12]Illegal SpeI site found at 3259
Illegal PstI site found at 2021 - 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 2271
- 23INCOMPATIBLE WITH RFC[23]Illegal XbaI site found at 2596
Illegal SpeI site found at 3259
Illegal PstI site found at 2021 - 25INCOMPATIBLE WITH RFC[25]Illegal XbaI site found at 2596
Illegal SpeI site found at 3259
Illegal PstI site found at 2021 - 1000COMPATIBLE WITH RFC[1000]
Cloning
PknB was synthesized and inserted by NEB HiFi Assembly into the pEGFP-C2 backbone plasmid (K3338020) after its restriction enzyme digestion with SaIHI and BamHI, generating the PknB-eGFP cassette.
Primer name | Sequence |
---|---|
PknB_fw_1 | AGCTTCGAATTCTGCAGAatgataggtaaaataataaatgaacgatataaaattgtagataagcttgg |
PknB_rev_2 | TCAGTTATCTAGATCCGGTGttatacatcatcatagctgacttctttttcagctacag |
Figure 1: Assembled vector map with pknB-EGFP integrated into the pEGFP-C2 backbone.
References
Pensinger, D. A., Schaenzer, A. J., & Sauer, J. D. (2018). Do Shoot the Messenger: PASTA Kinases as Virulence Determinants and Antibiotic Targets. Trends in microbiology, 26(1), 56–69. https://doi.org/10.1016/j.tim.2017.06.010
Rakette S, Donat S, Ohlsen K, Stehle T (2012) Structural Analysis of Staphylococcus aureus Serine/Threonine Kinase PknB. PLOS ONE 7(6): e39136. https://doi.org/10.1371/journal.pone.0039136
Tamber, S., Schwartzman, J., & Cheung, A. L. (2010). Role of PknB kinase in antibiotic resistance and virulence in community-acquired methicillin-resistant Staphylococcus aureus strain USA300. Infection and immunity, 78(8), 3637–3646. https://doi.org/10.1128/IAI.00296-10