Allen850413 (Talk | contribs) |
|||
(39 intermediate revisions by 3 users not shown) | |||
Line 92: | Line 92: | ||
<a href="https://2018.igem.org/Team:CCU_Taiwan/Medal"><li class="list" id="home3">Medals</li></a> | <a href="https://2018.igem.org/Team:CCU_Taiwan/Medal"><li class="list" id="home3">Medals</li></a> | ||
<a href="https://2018.igem.org/Team:CCU_Taiwan/Judge"><li class="list" id="home4">For Judges</li></a> | <a href="https://2018.igem.org/Team:CCU_Taiwan/Judge"><li class="list" id="home4">For Judges</li></a> | ||
+ | <a href="https://2018.igem.org/Team:CCU_Taiwan/Achievements"><li class="list" id="home5">Achievements</li></a> | ||
</ul> | </ul> | ||
</li> | </li> | ||
Line 130: | Line 131: | ||
<a href="https://2018.igem.org/Team:CCU_Taiwan/Entrepreneurship"><li class="list" id="human_practice3">Entrepreneurship</li></a> | <a href="https://2018.igem.org/Team:CCU_Taiwan/Entrepreneurship"><li class="list" id="human_practice3">Entrepreneurship</li></a> | ||
<a href="https://2018.igem.org/Team:CCU_Taiwan/engaging_experts"><li class="list" id="human_practice4">Engaging Experts</li></a> | <a href="https://2018.igem.org/Team:CCU_Taiwan/engaging_experts"><li class="list" id="human_practice4">Engaging Experts</li></a> | ||
− | <a href="https://2018.igem.org/Team:CCU_Taiwan/ | + | <a href="https://2018.igem.org/Team:CCU_Taiwan/Integrate"><li class="list" id="human_practice5">Integrated HP</li></a> |
</ul> | </ul> | ||
</li> | </li> | ||
Line 147: | Line 148: | ||
</header> | </header> | ||
+ | <div class="indicator"> | ||
+ | <div class="pointerDrylab" id="1"><a href="#ca1">UV-Vis</a></div> | ||
+ | <div class="pointerDrylab" id="2"><a href="#ca2">NMR</a></div> | ||
+ | <div class="pointerDrylab" id="2"><a href="#ca3">TGA</a></div> | ||
+ | </div> | ||
<div class="backgroundDrylab"> | <div class="backgroundDrylab"> | ||
Line 153: | Line 159: | ||
<div class="content"> | <div class="content"> | ||
<br><br> | <br><br> | ||
− | <p class="description">  We analyzed the lignin-like polymer we produced to confirm | + | <p class="description">  We analyzed the lignin-like polymer we produced to confirm our experiment is successful. We started from analyzing the content and structure by UV-visible spectroscopy. Second, we used NMR spectroscopy and Mass Spectroscopy to analyze information about the molecular structure and molecular weight. In the last stage, Thermogravimetric analysis is used to analyze the melting or decomposition point of our product. After completed these analysis above, we have a deeper understanding of the lignin-like polymer we made. These data also help us improve, or even discuss the application of our products.</p> |
<br><br> | <br><br> | ||
− | <p class="first">Reaction experiment</p><br> | + | <p class="first">Reaction experiment</p><br> <br> |
− | <p class="description">   | + | <p class="second" id="ca1">Ultraviolet–visible spectroscopy, UV-Vis</p> |
− | + | ||
− | + | <p class="description">  Ultraviolet–visible spectroscopy (UV–Vis) refers to absorption spectroscopy or reflectance spectroscopy in the ultraviolet-visible spectral region.The absorption or reflectance in the visible range directly affects the perceived color of the chemicals involved.The wavelengths of absorption peaks can be correlated with the types of bonds in a given molecule and are valuable in determining the functional groups within a molecule.</p> | |
+ | |||
+ | <p class="description">   Data revealed difference between samples with only coniferyl alcohol and samples with Laccase and Peroxidase. The absorption peak shifted to the left, comparing with simulation from study (P. J. Salazar-Valencia et al. 2005), the wavelength of β-O-4 linkage absorption peak is shorter. This results are similar to the results of the study, we believe our product contain β-O-4 linkage.</p> | ||
+ | |||
+ | <br> | ||
+ | <div id="Analysis1" class="polaroid" style="display:inline-block"> | ||
<img src="https://static.igem.org/mediawiki/2018/2/20/T--CCU_Taiwan--CCUUVvisible1.jpg" width="100%"> | <img src="https://static.igem.org/mediawiki/2018/2/20/T--CCU_Taiwan--CCUUVvisible1.jpg" width="100%"> | ||
<div class="container"> | <div class="container"> | ||
Line 165: | Line 176: | ||
</div> | </div> | ||
</div> | </div> | ||
− | + | <div id="Analysis2" class="polaroid" style="display:inline-block"> | |
<img src="https://static.igem.org/mediawiki/2018/d/de/T--CCU_Taiwan--CCUlinkage.jpg" width="100%"> | <img src="https://static.igem.org/mediawiki/2018/d/de/T--CCU_Taiwan--CCUlinkage.jpg" width="100%"> | ||
<div class="container"> | <div class="container"> | ||
Line 171: | Line 182: | ||
</p> | </p> | ||
</div> | </div> | ||
− | </div> | + | </div><br><br> |
− | + | <ol> | |
− | < | + | <li>This UV/Vis diagram shows the range from 230um to 300um of peaks. Peaks of Laccase only and peaks of peroxidase & laccase are very similar.</li> |
+ | <li>Compare with coniferyl alcohol (reactant) and laccase (product), we can obviously find out the the reactant peak at 270um has shift to 250um. </li> | ||
+ | </ol> | ||
+ | </p> | ||
+ | <p class="description"> | ||
+ |   This result greatly proves our enzymes have reaction with coniferyl alcohol. | ||
+ | Combine our prediction and dimer structure, we determine that the peak at 250um is beta-O-4 bond. | ||
+ | |||
+ | </p> | ||
+ | <br> <br> <br> | ||
+ | |||
+ | <p class="second" id="ca2">Nuclear Magnetic Resonance Spectroscopy, NMR</p> | ||
+ | |||
+ | <div class="row"> | ||
+ | <div id="halftext3"><p class="description">  Nuclear Magnetic Resonance (NMR) is based on quantum magnetic properties at the atomic scale. The method of NMR observation of atoms is to place the sample under a large external magnetic field.Using such a process, molecular science research, such as molecular structure, dynamics, etc., can be performed.</p><br> | ||
+ | |||
+ | <p class="description"> | ||
+ |   In the NMR experiment, we measured the commercial lignin, coniferyl alcohol, and the products we made.<br><br> | ||
+ |   We first predict the form of the bonds between each monomer. Then, we dissolve the coniferyl alcohol in ethanol and measured NMR to obtain the 1H-NMR chart. Some of the peak did changed but others didn't, we find the most suitable bond to form of the product.<br><br> | ||
+ |   Our peaks were not very obvious to examination since the concentration of our product is too low, we couldn't get the correct and proper structural analysis, but, there are still some small peaks which similar to lignin, we think it could prove that it successfully form structures which similar to lignin. That may explained our reaction indirectly. | ||
+ | The successful reaction of the enzymes. | ||
+ | </p></div> | ||
<div id="Analysis3" class="polaroid" style="display:inline-block"> | <div id="Analysis3" class="polaroid" style="display:inline-block"> | ||
<img src="https://static.igem.org/mediawiki/2018/f/f6/T--CCU_Taiwan--CCUGshift.jpg" width="100%"> | <img src="https://static.igem.org/mediawiki/2018/f/f6/T--CCU_Taiwan--CCUGshift.jpg" width="100%"> | ||
Line 181: | Line 213: | ||
</div> | </div> | ||
</div> | </div> | ||
− | <div | + | </div> |
− | + | <br><br> | |
− | + | ||
− | + | ||
− | + | <div id="Analysis4" class="polaroid" style="display:inline-block"> | |
<img src="https://static.igem.org/mediawiki/2018/4/4d/T--CCU_Taiwan--CCUconuferylNMR.png" width="100%"> | <img src="https://static.igem.org/mediawiki/2018/4/4d/T--CCU_Taiwan--CCUconuferylNMR.png" width="100%"> | ||
<div class="container"> | <div class="container"> | ||
<p>Figure4: NMR Spectrum of coniferyl alcohol</p> | <p>Figure4: NMR Spectrum of coniferyl alcohol</p> | ||
</div> | </div> | ||
− | </div> | + | </div><br><br> |
<div id="Analysis5" class="polaroid" style="display:inline-block"> | <div id="Analysis5" class="polaroid" style="display:inline-block"> | ||
Line 205: | Line 235: | ||
<p>Figure6: NMR Spectrum of Laccase-involved reaction product</p> | <p>Figure6: NMR Spectrum of Laccase-involved reaction product</p> | ||
</div> | </div> | ||
− | </div> | + | </div><br><br> |
<div id="Analysis7" class="polaroid" style="display:inline-block"> | <div id="Analysis7" class="polaroid" style="display:inline-block"> | ||
Line 212: | Line 242: | ||
<p>Figure7: NMR Spectrum of Laccase & Peroxidase-involved reaction product</p> | <p>Figure7: NMR Spectrum of Laccase & Peroxidase-involved reaction product</p> | ||
</div> | </div> | ||
− | </div><br><br> | + | </div> |
+ | <br><br><br> | ||
+ | <p class="second" id="ca3">Thermogravimetric analysis, TGA</p> | ||
+ | <p class="description">  Thermogravimetric analysis (TGA) is a method of thermal analysis in which the mass of a sample is measured over time as the temperature changes. A TGA can be used for materials characterization through analysis of characteristic decomposition patterns. It is an especially useful technique for the study of polymeric materials.</p> | ||
+ | <br><br> | ||
+ | <div id="Analysis8" class="polaroid" style="display:inline-block"> | ||
+ | <img src="https://static.igem.org/mediawiki/2018/8/82/T--CCU_Taiwan--JOE_TGApicture.png" width="100%"> | ||
+ | <div class="container"> | ||
+ | <p>Figure8: TGA chart for measuring the weight loss</p> | ||
+ | </div> | ||
+ | </div> | ||
+ | <br><br> | ||
+ | <p class="description"> | ||
+ |   According to the chart, there is a tendency of pyrolysis at 150~160 °C; peroxidase+laccase has a pyrolysis reaction at 340~400 °C; laccase has a pyrolysis reaction at 420~480 °C.<br><br> | ||
+ | <ol> | ||
+ | <li>The boiling point of coniferyl alcohol is 163~165°C. Compared with the TGA chart, there is a trend change in the range of 150~160°C. That's the temperature causes the structure to pyrolysis, the slope inclined.</li><br> | ||
+ | <li>The product is similar to lignin and has a pyrolysis interval at 200-400 °C.</li><br> | ||
+ | <li>The product of laccase and the product of peroxidase+laccase have different phase transition temperatures, which can prove that the products are not the same, also indirectly proves that we have a successful reaction, we can also find out that peroxidase does have interactions with the reactants.</li> | ||
+ | </ol> | ||
+ | </p> | ||
+ | |||
+ | |||
+ | <br><br> | ||
+ | |||
+ | |||
+ | |||
+ | |||
+ | <br><br> | ||
<p class="second">Reference</p> | <p class="second">Reference</p> | ||
<p class="description"> P. J. Salazar-Valencia, S. T. P´erez-Merchancano, and L. E. Bol´ıvar-Marin´ez. (2005). Optical Properties in Biopolymers: Lignin Fragments. Brazilian Journal of Physics, vol. 36, no. 3B. | <p class="description"> P. J. Salazar-Valencia, S. T. P´erez-Merchancano, and L. E. Bol´ıvar-Marin´ez. (2005). Optical Properties in Biopolymers: Lignin Fragments. Brazilian Journal of Physics, vol. 36, no. 3B. | ||
Line 219: | Line 276: | ||
<br> | <br> | ||
− | + | <br> | |
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
</div> | </div> | ||
</div> | </div> |
Latest revision as of 08:50, 1 December 2018
ANALYSIS
We analyzed the lignin-like polymer we produced to confirm our experiment is successful. We started from analyzing the content and structure by UV-visible spectroscopy. Second, we used NMR spectroscopy and Mass Spectroscopy to analyze information about the molecular structure and molecular weight. In the last stage, Thermogravimetric analysis is used to analyze the melting or decomposition point of our product. After completed these analysis above, we have a deeper understanding of the lignin-like polymer we made. These data also help us improve, or even discuss the application of our products.
Reaction experiment
Ultraviolet–visible spectroscopy, UV-Vis
Ultraviolet–visible spectroscopy (UV–Vis) refers to absorption spectroscopy or reflectance spectroscopy in the ultraviolet-visible spectral region.The absorption or reflectance in the visible range directly affects the perceived color of the chemicals involved.The wavelengths of absorption peaks can be correlated with the types of bonds in a given molecule and are valuable in determining the functional groups within a molecule.
Data revealed difference between samples with only coniferyl alcohol and samples with Laccase and Peroxidase. The absorption peak shifted to the left, comparing with simulation from study (P. J. Salazar-Valencia et al. 2005), the wavelength of β-O-4 linkage absorption peak is shorter. This results are similar to the results of the study, we believe our product contain β-O-4 linkage.
Figure1: UV-Visible spectrum of products
Figure2: Simulation of the electronic or ultraviolet spectra for the 3 Coniferyl Alcohol units, with β-O-4 and β-5 linkages. (P. J. Salazar-Valencia et al. 2005)
- This UV/Vis diagram shows the range from 230um to 300um of peaks. Peaks of Laccase only and peaks of peroxidase & laccase are very similar.
- Compare with coniferyl alcohol (reactant) and laccase (product), we can obviously find out the the reactant peak at 270um has shift to 250um.
This result greatly proves our enzymes have reaction with coniferyl alcohol. Combine our prediction and dimer structure, we determine that the peak at 250um is beta-O-4 bond.
Nuclear Magnetic Resonance Spectroscopy, NMR
Nuclear Magnetic Resonance (NMR) is based on quantum magnetic properties at the atomic scale. The method of NMR observation of atoms is to place the sample under a large external magnetic field.Using such a process, molecular science research, such as molecular structure, dynamics, etc., can be performed.
In the NMR experiment, we measured the commercial lignin, coniferyl alcohol, and the products we made.
We first predict the form of the bonds between each monomer. Then, we dissolve the coniferyl alcohol in ethanol and measured NMR to obtain the 1H-NMR chart. Some of the peak did changed but others didn't, we find the most suitable bond to form of the product.
Our peaks were not very obvious to examination since the concentration of our product is too low, we couldn't get the correct and proper structural analysis, but, there are still some small peaks which similar to lignin, we think it could prove that it successfully form structures which similar to lignin. That may explained our reaction indirectly.
The successful reaction of the enzymes.
Figure3: Chemical shift of coniferyl alcohol
Figure4: NMR Spectrum of coniferyl alcohol
Figure5: NMR Spectrum of commercial dealkaline lignin
Figure6: NMR Spectrum of Laccase-involved reaction product
Figure7: NMR Spectrum of Laccase & Peroxidase-involved reaction product
Thermogravimetric analysis, TGA
Thermogravimetric analysis (TGA) is a method of thermal analysis in which the mass of a sample is measured over time as the temperature changes. A TGA can be used for materials characterization through analysis of characteristic decomposition patterns. It is an especially useful technique for the study of polymeric materials.
Figure8: TGA chart for measuring the weight loss
According to the chart, there is a tendency of pyrolysis at 150~160 °C; peroxidase+laccase has a pyrolysis reaction at 340~400 °C; laccase has a pyrolysis reaction at 420~480 °C.
- The boiling point of coniferyl alcohol is 163~165°C. Compared with the TGA chart, there is a trend change in the range of 150~160°C. That's the temperature causes the structure to pyrolysis, the slope inclined.
- The product is similar to lignin and has a pyrolysis interval at 200-400 °C.
- The product of laccase and the product of peroxidase+laccase have different phase transition temperatures, which can prove that the products are not the same, also indirectly proves that we have a successful reaction, we can also find out that peroxidase does have interactions with the reactants.
Reference
P. J. Salazar-Valencia, S. T. P´erez-Merchancano, and L. E. Bol´ıvar-Marin´ez. (2005). Optical Properties in Biopolymers: Lignin Fragments. Brazilian Journal of Physics, vol. 36, no. 3B.