Difference between revisions of "Team:British Columbia/Project/S-Layer/Laccases"

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                         Clean-up kit(Macherey-Nagel).</p>
 
                         Clean-up kit(Macherey-Nagel).</p>
 
                     <h3>Cloning of laccase enzyme into rsaA plasmid in <i>C. crescentus</i></h3>
 
                     <h3>Cloning of laccase enzyme into rsaA plasmid in <i>C. crescentus</i></h3>
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<p> The small laccase (sLAC) gene from <i>Amycolatopsis sp.</i> 75iv2 ATCC 39116 was amplified using the following primers: sLAC_pSB1C3_F (5'-TCCgaattcgcggccgcttctagATGCAGGGCACGACCCGG) and sLAC_pSB1C3_R (5'-TCCtactagtagcggccgctgcagTCAGTGTTCGTGGACACC) to clone the construct in pSB1C3. The amplicon was digested with EcoRI and PstI, PCR purified and ligated into a pSB1C3, which was also digested EcoRI and PstI and gel purified. Site-directed mutagenesis (SDM) was done to remove any forbidden cut-sites using a protocol outlined in Nobebook section and the following primers:SDM_sLAC_F (5'-GTACGCCGAGAAGATTTCCGACGAGCTGTAC) and SDM_sLAC_R(5'-GTACAGCTCGTCGGAAATCTTCTCGGCGTAC). After the mutation was sequence confirmed, the selected region of laccase gene was amplified to add the BglII and PstI using following the primers: 5'-5’-GTTTCTTCAGATCTACGACCCGGCGGATCACG and 5'-GTTTCTTCCTGCAGAGACACCGGCCGGCATCGT . The sLAC amplicon was digested with BglII and PstI restriction enzymes, PCR purified and ligated into a p4A723 RsaA plasmid conferring chloramphenicol (CM) resistance. The ligation mix was transformed into chemically competent DH5alpha E. coli cells and transformed cells were plated onto LB + CM (12.5 µg/mL). Insertion of sLAC into p4A723 was preliminarily confirmed by colony PCR of selected transformants, using the aforementioned primers for sLAC, and checking for appropriately sized bands (850 bp). The selected colonies were sent for Sanger sequencing using the IRAT forward primer for confirmation.
+
<p> The small laccase (sLAC) gene from <i>Amycolatopsis sp.</i> 75iv2 ATCC 39116 was amplified using the following primers: sLAC_pSB1C3_F (5'-TCCgaattcgcggccgcttctagATGCAGGGCACGACCCGG) and sLAC_pSB1C3_R (5'-TCCtactagtagcggccgctgcagTCAGTGTTCGTGGACACC) to clone the construct in pSB1C3. The amplicon was digested with EcoRI and PstI, PCR purified and ligated into a pSB1C3, which was also digested EcoRI and PstI and gel purified. Site-directed mutagenesis (SDM) was done to remove any forbidden cut-sites using a protocol outlined in Nobebook section and the following primers:SDM_sLAC_F (5'-GTACGCCGAGAAGATTTCCGACGAGCTGTAC) and SDM_sLAC_R(5'-GTACAGCTCGTCGGAAATCTTCTCGGCGTAC). After the mutation was sequence confirmed, the selected region of laccase gene was amplified to add the BglII and PstI using following the primers: 5'-GTTTCTTCAGATCTACGACCCGGCGGATCACG and 5'-GTTTCTTCCTGCAGAGACACCGGCCGGCATCGT . The sLAC amplicon was digested with BglII and PstI restriction enzymes, PCR purified and ligated into a p4A723 RsaA plasmid conferring chloramphenicol (CM) resistance. The ligation mix was transformed into chemically competent DH5alpha E. coli cells and transformed cells were plated onto LB + CM (12.5 µg/mL). Insertion of sLAC into p4A723 was preliminarily confirmed by colony PCR of selected transformants, using the aforementioned primers for sLAC, and checking for appropriately sized bands (850 bp). The selected colonies were sent for Sanger sequencing using the IRAT_F(5'CGGAGCCGCCAGAACGGTCAGGCCGACATTCAC)  for confirmation.
 
After sequence confirmation, the isolated construct DNA were electroporated into electrocompetent C.crescentus with an RsaA Amber mutation and colonies were grown on a PYE-CM plate. One colony was selected and streaked onto a fresh plate, which would be used for all future assays.
 
After sequence confirmation, the isolated construct DNA were electroporated into electrocompetent C.crescentus with an RsaA Amber mutation and colonies were grown on a PYE-CM plate. One colony was selected and streaked onto a fresh plate, which would be used for all future assays.
  

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Laccases

Laccase
S-Layer Engineering

Abstract

"Lorem ipsum dolor sit amet, consectetur adipiscing elit, sed do eiusmod tempor incididunt ut labore et dolore magna aliqua. Ut enim ad minim veniam, quis nostrud exercitation ullamco laboris nisi ut aliquip ex ea commodo consequat. Duis aute irure dolor in reprehenderit in voluptate velit esse cillum dolore eu fugiat nulla pariatur. Excepteur sint occaecat cupidatat non proident, sunt in culpa qui officia deserunt mollit anim id est laborum."

Key Achievements

  • Cloned small laccases(sLac) in p4A723 plasmid containing rsaA protein and transformed into C. crescentus for the display on cell surface.
  • Determined toxic copper concentrations for C. crescentus

    • Introduction

    Current pretreatment and hydrolysis approaches to biomass depolymerization involve thermochemical methods that apply alkaline chemicals, in addition to high heat and pressure (Chundawat S. 2011). These methods enhance the fractionation of lignin and hemicellulose from the plant cell wall, thereby allowing enzymes access to the cellulosic fraction for downstream processing. Although these methods are effective, their high cost to industries and to the environment requires that alternative methods to remove the more recalcitrant components of lignocellulosic biomass, are erected. We intend to produce a system that minimally relies on external thermochemical treatments to make the cellulosic component of biomass available for valuable-chemical production. To achieve this, we attempted to engineer surface layer expression of a small laccase derived from Amycolatopsis sp. 75iv2 shown to act on and degrade lignin (Majumdar S. 2014), in Caulobacter crescentus.

    Laccases belong to a superfamily of enzymes called multicopper oxidases (MCO), and are expressed by several rot-fungi and soil bacteria (Sirim D. 2011). As an MCO, they catalyze the one-electron oxidation of substrates through associated four-electron reductions of molecular oxygen to water, using four copper ions coordinated in designated copper centers (Jones Solomon E. 2015, Kunamneni A. 2007). Their broad phenolic and polyphenolic substrate specificity allows for direct transformation of lignin, or removal of toxic phenols that arise during lignocellulosic biomass pre-treatment (Kunamneni A. 2007).

    Design

    WE MUST ADD THIS SECTION :)

    Methods

    All Caulobacter cultures were grown in PYE media supplemented with 2 μg/ml chloramphenicol unless stated otherwise. All plasmid DNA extractions were performed with QIAprep Spin Miniprep Kit (Qiagen). DNA purification from gels or PCR mixtures were done with NucleoSpin® Gel and PCR Clean-up kit(Macherey-Nagel).

    Cloning of laccase enzyme into rsaA plasmid in C. crescentus

    The small laccase (sLAC) gene from Amycolatopsis sp. 75iv2 ATCC 39116 was amplified using the following primers: sLAC_pSB1C3_F (5'-TCCgaattcgcggccgcttctagATGCAGGGCACGACCCGG) and sLAC_pSB1C3_R (5'-TCCtactagtagcggccgctgcagTCAGTGTTCGTGGACACC) to clone the construct in pSB1C3. The amplicon was digested with EcoRI and PstI, PCR purified and ligated into a pSB1C3, which was also digested EcoRI and PstI and gel purified. Site-directed mutagenesis (SDM) was done to remove any forbidden cut-sites using a protocol outlined in Nobebook section and the following primers:SDM_sLAC_F (5'-GTACGCCGAGAAGATTTCCGACGAGCTGTAC) and SDM_sLAC_R(5'-GTACAGCTCGTCGGAAATCTTCTCGGCGTAC). After the mutation was sequence confirmed, the selected region of laccase gene was amplified to add the BglII and PstI using following the primers: 5'-GTTTCTTCAGATCTACGACCCGGCGGATCACG and 5'-GTTTCTTCCTGCAGAGACACCGGCCGGCATCGT . The sLAC amplicon was digested with BglII and PstI restriction enzymes, PCR purified and ligated into a p4A723 RsaA plasmid conferring chloramphenicol (CM) resistance. The ligation mix was transformed into chemically competent DH5alpha E. coli cells and transformed cells were plated onto LB + CM (12.5 µg/mL). Insertion of sLAC into p4A723 was preliminarily confirmed by colony PCR of selected transformants, using the aforementioned primers for sLAC, and checking for appropriately sized bands (850 bp). The selected colonies were sent for Sanger sequencing using the IRAT_F(5'CGGAGCCGCCAGAACGGTCAGGCCGACATTCAC) for confirmation. After sequence confirmation, the isolated construct DNA were electroporated into electrocompetent C.crescentus with an RsaA Amber mutation and colonies were grown on a PYE-CM plate. One colony was selected and streaked onto a fresh plate, which would be used for all future assays.

    Results

    Conclusion

    References

      Chundawat S, Beckham G, Himmel M, Dale B. 2011. Deconstruction of Lignocellulosic Biomass to Fuels and Chemicals. Annual Review of Chemical and Biomolecular Engineering 2:121-145.
      Sirim D, Wagner F, Wang L, Schmid R, Pleiss J. 2011. The Laccase Engineering Database: a classification and analysis system for laccases and related multicopper oxidases. Database 2011:bar006.
      3. Jones Solomon E. 2015. Electron transfer and reaction mechanism of laccases. Cell. Mol. Life Sci. 72:869-883.
      4. Reiss R, Ihssen J, Richter M, Eichhorn E, Schilling B, Thöny-Meyer L. 2013. Laccase versus Laccase-Like Multi-Copper Oxidase: A Comparative Study of Similar Enzymes with Diverse Substrate Spectra. PLoS ONE 8:e65633.
      5. Kunamneni A, Ballesteros A, Plou FJ, Alcalde M. 2007. Fungal laccase – a versatile enzyme for biotechnological applications, p 233-245. In Mendez-Vilas A (ed). Communicating current research and educational topics and trends in applied microbiology. FORMATEX, Badajoz.
      6. Majumdar S, Lukk T, Solbiati J, Bauer S, Nair S, Cronan J, Gerlt J. 2014. Roles of Small Laccases from Streptomyces in Lignin Degradation. Biochemistry 53:4047-4058.
      7. More S, Malini S. 2011. Isolation, Purification, and Characterization of Fungal Laccase from Pleurotus sp. Enzyme Research 2011:1-7.

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