Difference between revisions of "Lignin Monomers: Oxidation and Degradation"
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| − | ESR provides a basis for evaluating the radical formation of the monomers. Transient radicals, which are short lived and difficult to detect, are formed during the oxidation process (4). With the use of immobilized enzymes and ESR, these short lives radicals can be detected. Previous methods of detection are not able to detect these radicals because they couple quickly with other radicals in solution. Flowing substrate solution over immobilized enzyme allows for detection of these radicals on a sub millisecond time scale (4). This method termed immobilized enzyme ESR, or IE-ESR, uses a large amount of enzyme, but the enzyme can be reused (4). | + | ESR provides a basis for evaluating the radical formation of the monomers. Transient radicals, which are short lived and difficult to detect, are formed during the oxidation process (4). With the use of immobilized enzymes and ESR, these short lives radicals can be detected. Previous methods of detection are not able to detect these radicals because they couple quickly with other radicals in solution. Flowing substrate solution over immobilized enzyme allows for detection of these radicals on a sub millisecond time scale (4). This method termed immobilized enzyme ESR, or IE-ESR, uses a large amount of enzyme, but the enzyme can be reused (4). Multiple substrates can be ran over the immobilized enzyme as long as washes of the enzyme with buffer occurs between each new substrate. |
Revision as of 20:58, 12 May 2020
Abstract
The lignin polymer is synthesized via oxidative coupling of three basic monomers: p-coumaryl alcohol, coniferyl alcohol, and sinapyl alcohol. These three monomers each possess a phenol group that stabilizes the radical intermediate generated during the oxidation reaction. Although some literature exists showing the ESR spectra of these short-lived radical intermediates, we have revisited these intermediates using a combination of experimental techniques [HPLC and immobilized enzyme-ESR technique (IE-ESR)] and computational approaches [B3YLP/ESR-II and WINSIM]. Two radicals dimerize together to create lignan, which is biologically active and currently being tested for pharmacological properties. HPLC was used to study the oxidation of coniferyl alcohol, the monomeric lignan, and validate the formation of dimers. The mechanisms of this dimer formation were also studied to better understand the oxidative coupling of the lignin monomers.
Introduction
Lignin
Lignin is a large polymer structure in plant cell walls. The interest in lignin arose from the difficultly to isolate it from plants for products and structure determination (1). This difficult process has produced a vast amount of research to determine how lignin is formed, and procedures to isolate it from plants without modifications. The issue lies with the lignin-carbohydrate linkages that occur between lignin and polymeric carbohydrates (1). The difficulty associated with separating lignin from these carbohydrates and other matter of the plant makes trials on them difficult. Synthetic lignans are often used in research since the process of separating lignin is difficult and time consuming. The main purpose of lignin in plants is to assist water movement and distribution around the plant (1). This property makes its presence especially important in trees. In softwood trees, it makes up about 28% of the mass of the tree (1). It is the second most abundant polymer in the makeup of plants, cellulose being the first most abundant. There are three monomers of lignan: ferulic acid, p-coumaric acid, and sinapic acid. These are all characterized by a phenol group and a varying number of methoxy substituents occurring at the C-3 and C-5 position. There are alcohol forms of the monomers, which is what predominates in nature. These forms are coniferyl alcohol, p-coumaryl alcohol, and sinapyl alcohol.
Ferulic Acid
Coniferyl Alcohol
Sinapic Acid
Sinapyl Alcohol
p-coumaric Acid
p-coumaryl Alcohol
They differ from the acid forms by having an alcohol group opposed to a carboxylic acid group on their side chain. The monomers couple together as radicals after they have undergone a one electron and one hydrogen oxidation process. Radicals occur at the O-4, C-1, C-3, C-5, and C-β positions (1). By losing one electron and one hydrogen, a radical molecule is formed that is unstable. To gain stability, it undergoes oxidative coupling with another radical. This coupling can result in the formation of dimers, known as lignan, or polymers, known as lignin, but is more prevalent for a monomer to couple with a growing polymer (1). The reactivity of the radicals can be determined using radical densities. This can be completed using EPR and computational chemistry programs, such as Web M.O. and WINSIM. Using these programs can help pinpoint which position has a higher radical density, which allows determination of which position a radical is more likely to form. Previous research determined these radicals were more likely at the C-5 and C-β positions (3). The delocalization of the unpaired electron significantly effects its reactivity and product formation. The comparison of this delocalization and substituent makeup can be used to observe influences on the radical coupling reactions (3).
ESR provides a basis for evaluating the radical formation of the monomers. Transient radicals, which are short lived and difficult to detect, are formed during the oxidation process (4). With the use of immobilized enzymes and ESR, these short lives radicals can be detected. Previous methods of detection are not able to detect these radicals because they couple quickly with other radicals in solution. Flowing substrate solution over immobilized enzyme allows for detection of these radicals on a sub millisecond time scale (4). This method termed immobilized enzyme ESR, or IE-ESR, uses a large amount of enzyme, but the enzyme can be reused (4). Multiple substrates can be ran over the immobilized enzyme as long as washes of the enzyme with buffer occurs between each new substrate.
The structure of lignin was determined after isolating lignin and degrading it into pieces (1). By putting these pieces back together, the larger polymer structure was formulated. New methods, such as degradation, using thioacidolysis, are now being approached (2).
Lignan
Lignan is formed from the oxidative coupling of two lignin monomers. The dimers are often linked between the beta-carbons on the side chain of each monomer. Many of the dimers stated often in literature possess this linking structure. These dimers have biological activity, whereas the larger structure of lignin does not. This allows them to have potential healths benefits associated with them. Some of these benefits are anti-mubial, anti-inflammatory, and antioxidant. The relationship between allergies and lignan has also been studied. It might be related to having an anti-histamine effect on allergy symptoms.
Research is currently being done to study the relationship between cancer and lignan. Breast cancer has been studied the most, but other cancers such as prostate and ovarian are being researched. Currently there are no conclusions regarding those cancers, as the research is in beginning stages. Many studies are centered around whether consumption of flax seeds correlates to a reduction in the risk of breast cancer, as well as the mortality. The reason flax seeds are being researched is because they have the highest concentration of lignans. With breast cancer, it was found flax seed consumption did decrease the risk of breast cancer, as well as the mortality of breast cancer, in post-menopausal women. This is believed to be because the lignan acts as a competitive inhibitor to estrogen. Some lignans, such as matairesinol and lariciresinol, have structures similar to estrogen. This allows them to bind to the estrogen receptor on the cancer cell, therefore blocking estrogen from binding. This prevents further growth of the cancer.
Experimental Methods
Oxidation of Lignin Monomers
Beaker reactions with varying reaction conditions were completed to analyze the oxidation of each monomer. For each monomer, 100 mL of a 2 mM standard solution of the monomer (purchased from Sigma Aldrich) was made using 50/50 dioxane/pH 5 buffer. The pH 5 buffer was a phosphate-citrate buffer (purchased from Sigma Aldrich). Three reactions were then completed with varying concentrations of hydrogen peroxide in the presence of a constant HRP concentration in scintillation vials. The first reaction was composed of 5 mL of the 2 mM substrate, 10 μL of 0.5 M hydrogen peroxide (1 mM final concentration hydrogen peroxide) and 5 μL of HRP. The second reaction was composed of 5 mL of the 2 mM substrate, 5 μL of 0.5 M hydrogen peroxide (0.5 mM final concentration hydrogen peroxide) and 5 μL of HRP. The third reaction was composed of 5 mL of the 2 mM substrate, 5 μL of 0.5 M hydrogen peroxide (0.25 mM final concentration hydrogen peroxide) and 5 μL of HRP. These reactions were then analyzed on the HPLC for oxidation products of each monomer and compared.
Analysis of Monomer Oxidation
The reactions and the standards were analyzed on the HPLC using an acetonitrile (ACN) and water gradient for 25 minutes. The first 10 minutes were ran at 100% water, 10-20 minutes were ran at an 80% ACN/20% water gradient, and the remaining 5 minutes at 100% water.
Immobilization of Enzymes
An immobilization of peroxidase from horseradish (HRP) was completed using Affi-Gel® 10. This procedure is centered around the isolectric point of the enzyme. The immobilization was completed using a MOPS buffer (pH 7.0) and about 1 mL of Affi-Gel® 10 beads.
Setup of Enzyme Immobilization
Made 0.190 mM immobilized enzyme solution (abs 1.94) using a simple apparatus. A Poly-Prep® Chromatography Column (Bio-Rad Laboratories, Inc. product 731-1550) and 3-way stopcock (Bio-Rad Laboratories, Inc. product 732-8103) were used. The column was secured to a ring stand and the 3-way stopper was attached. A 5 mL lure-lock syringe was attached to the 3-way stopcock at a 90° angle. The initial HRP solution is a 5 mM solution of peroxidase from horseradish and MOPS buffer. About 1 mL of Affi-Gel® 10 beads were added to the column attached to the ring stand and washed with water. They were then washed with MOPS buffer. The peroxidase and buffer solution in the eppendorf tube was added to the column containing the Affi-Gel® 10 beads and mixed by inverting and flicking the bottom of the column. The column was sealed and placed on a LabQuake® for an hour.
Oxidation of Lignin Monomers Using Immobilized HRP
Beaker reactions with immobilized HRP
Beaker reactions were completed using the immobilized HRP and analyzed on the HPLC. The reactions had varying concentrations of hydrogen peroxide. A 2 mM standard was made for each monomer with a volume of 100 using 50/50 dioxane/pH 5 buffer. Before the immobilized HRP was used, it was rinsed twice with MOPS buffer. The first reaction was composed of 5 mL of substrate, 10 µL of 0.5 M hydrogen peroxide (1 mM final concentration hydrogen peroxide), and 50 µL of immobilized HRP. The second reaction was composed of 5 mL of substrate, 5 µL of 0.5 M hydrogen peroxide (0.5 mM final concentration hydrogen peroxide), and 50 µL of immobilized HRP. The third reaction was composed of 5 mL of substrate, 2.5 µL of 0.5 M hydrogen peroxide (0.25 mM final concentration hydrogen peroxide), and 50 µL of immobilized HRP. These reactions were then analyzed on the HPLC for possible oxidation products. The results were then compared to previously collected HPLC data using HRP, opposed to immobilized HRP.
Flat Cell Reactions with Immobilized Enzyme
A flat cell was loaded with glass wool, sand, and immobilized enzyme. Glass wool was lightly packed into the bottom neck of the flat cell. A small amount of sand was then mixed with nanopure water and added into the flat cell about 2 mm above the glass wool using a plastic 1 mL syringe. About 50 μL of immobilized enzyme is added on top of the glass wool and sand to fill most of the cavity of the flat cell. The pH 5 buffer was ran through the flat cell for about 10 minutes. A 1 mM ferulic acid, 1 mM hydrogen peroxide solution in 50/50 dioxane/pH 5 buffer was made. This solution was put in a 60 mL plastic syringe and flow controlled through the flat cell at 0.25 mL/minute, 0.5 mL/minute, 1 mL/minute, and 2 mL/minute. Flow was collected for each rate and analyzed on the HPLC. The same procedure was completed for p-coumaric acid.
EPR Analysis with Immobilized Enzyme
A flat cell was loaded with glass wool, sand, and immobilized enzyme using the procedure outlined above. A 10 mM ferulic acid solution in 50/50 dioxane/pH 7.4 buffer was made. Hydrogen peroxide was added to a concentration of 10 mM before EPR analysis. The solution was placed in a 60 mL plastic syringe and flow was controlled. Flow was analyzed at rates of 0.5 mL/minute, 1 mL/minute, and 2 mL/minute. The parameters for the program were modulation amplitude 0.5 G, sweep width 40.0 G, and center field at 3492.0 G.
Lignan Beaker Reactions
Beaker reactions of lignans were done with varying concentrations of hydrogen peroxide. Two lignan standards, (+)-pinoresinol and matiaresinol (purchased from Cayman Chemical, of 9.3 mM were created. A 2 mM coniferyl alcohol standard in 50/50 dioxane/pH 5 buffer was made. The first reaction was composed of 5 mL of substrate, 10 µL of 0.5 M hydrogen peroxide (1 mM final concentration hydrogen peroxide), and 5 µL of HRP. The second reaction was composed of 5 mL of substrate, 5 µL of 0.5 M hydrogen peroxide (0.5 mM final concentration hydrogen peroxide), and 5 µL of HRP. The third reaction was composed of 5 mL of substrate, 2.5 µL of 0.5 M hydrogen peroxide (0.25 mM final concentration hydrogen peroxide), and 5 µL of HRP. These reactions were then analyzed on the HPLC for lignan identification.
Lignin Degradation Using Alkaline Conditions
Lignin (purchased from Sigma Aldrich) was degraded in an alkaline solution of 100 mM NaOH. A solution of 50 grams of lignin and 10 mL of 100 mM NaOH were stirred on a stir plate for 24 hours. Samples of 10 µL of the mixture were extracted at 1 minute, 24 hours, and 48 hours after stirring and placed in 3 mL of pH 5 buffer. The samples were analyzed on the HPLC for degradation products.
Notes of Safety
Dioxane
Molecular Formula: C4H8O2
Molecular weight: 88.11 g/mol
Physical appearance: clear, colorless liquid
1,4-dioxane has the potential to be an eye, skin, and digestive tract irritant. To avoid contact, lab goggles, gloves, and protective clothing should be worn. In the case of exposure, eyes and skin should be flushed with water. If ingested, vomiting should not be induced and medical aid should be sought. Keep away from heat, sparks, and flame and use in a fume hood. Inhalation could induce breathing difficulties. It should be stored under nitrogen to less peroxide formation. If it is noticed that peroxide formation has occurred, do not open the container unless a professional. It has the potential to form explosive peroxides with prolonged exposure.
Sodium hydroxide
Molecular formula: NaOH
Molecular weight: 40 g/mol
Physical appearance: solid, white
Sodium hydroxide can cause eye, skin, and digestive tract burns. In the case of contact with sodium hydroxide, flush the eyes and skin with water for at least 15 minutes and seek medical attention. Vomiting should not be induced, but water can be drank. To mitigate these risks, lab safety googles, gloves, and protective clothing should be worn. Sodium hydroxide is hygroscopic so it must be stored in a tightly closed container. It is corrosive to material so caution is needed in case of a spill. Material should be disposed of in the proper disposal container.
Results
Lignin
HPLC Analysis
In figure 1, figure 2, and figure 3, beaker reactions of the oxidation of the three lignin monomers using H2O2 was completed. The same procedure was done using a 2 mM solution of the standard in 50/50 dioxane and pH 5 buffer. Dioxane was introduced into the reaction to assist with possible product formation solubility. Each reaction consisted of 5 mL of substrate, 5 μL of HRP, and a varying amount of 0.5 M H2O2 to reach final concentrations of 0.25 mM, 0.5 mM, and 1.0 mM. In figure 1 and figure 2, a standard is being consumed and producing oxidation products. These products could be dimers or small polymers. As the concentration of H2O2 increases, the more the standard is consumed and the more products formed. Since each reaction only differed by the concentration of the H2O2, each reaction can be compared. In figure 3 sinapic acid did not produce product peaks because the standard was never consumed. By changing the substrate to only being in pH 5 buffer, product peaks were seen.
In figure 4, figure 5, and figure 6, the same beaker reactions were completed as above using immobilized HRP in agarose beads. HPLC analysis was completed to ensure the enzyme was immobilized on the beads. Reactions were also completed to show reproducibility of previously collected HPLC data of the monomers. These reactions used 5 mL of substrate, 5 μL of HRPi, and a varying amount of 0.5 M H2O2 to reach final concentrations of 0.25 mM, 0.5 mM, and 1.0 mM. These figures showed the standard being decreased and oxidation products being formed. As the concentration of the H2O2 increased, more standard was consumed and more oxidation products were formed. Figure 6 is showing sinapic acid producing product peaks, but no peaks were shown in figure 3 with sinapic acid. This is because the substrate was changed to only be in pH 5 buffer opposed to 50/50 dioxane and pH 5 buffer.
To evaluate the use of the immobilized enzyme in a flat cell, samples of the waste were collected to ensure the immobilized enzyme was functioning in the flat cell. To do this, a flat cell was loaded with steel wool, sand, and agarose beads with HRPi. MOPS Buffer was then ran over the beads in the flat cell to wash them and ensure they were not dry. A substrate of 1 mM ferulic acid and 1 mM hydrogen peroxide in 50/50 dioxane/pH 5 buffer was then ran over the immobilized enzyme in the flat cell. The flow of the substrate was controlled using a syringe pump at 0.25 mL/min, 0.5 mL/min, 1 mL/min, and 2 mL/min. Samples of waste were then collected at each flow rate and analyzed on the HPLC. The results of ferulic acid are shown in figure 7. The same procedure was used for a substrate of 1 mM p-coumaric acid and 1 mM hydrogen peroxide in 50/50 dioxane/pH 5 buffer and is shown in figure 8.
EPR Analysis
Figure 9 shows previously collected EPR data of the oxidation of lignin monomers. In figure 10, figure 11, figure 12 and figure 13, preliminary ESR data is shown To complete preliminary ESR data collection using ferulic acid, a substrate of 1 mM ferulic acid in 50/50 dioxane/pH 5 buffer was made. The flat cell was then loaded with steel wool, sand, and immobilized enzyme. Buffer was ran over the immobilized enzyme for about an hour. The flat cell was then mounted in the ESR. Hydrogen peroxide was added to the substrate directly before flow was began so its concentration in solution was 1 mM. The substrate was then flowed through the flat cell in the ESR at a flow rate of 1 mL/min and a signal was collected. The flow of the substrate was then increased to 2 mL/min and a signal was collected. The flow of the substrate was then stopped, and no signal was apparent. This was done to ensure the signal being produced was a result of the oxidation of the monomers. If this was true, stopping the flow would stop the signal. The flow was then re-started with a flow rate of 2 mL/min, and the signal returned.
Computational analyses were completed of ESR experimental data of ferulic acid and coniferyl alcohol. A computational program called WINSIM was used to compare experimental data with simulated data. Simulating the experimental data allowed for the determination of coupling constants of the assumed radicals formed. This allowed determination of which radicals were more likely to form and potentially couple together.
Comparison of Ferulic Acid and Coniferyl Alcohol Using WebMO Calculations & WINSIM Simulation
| Position | Coniferyl Alcohol (G03) | Coniferyl Alcohol (sim-Burrkitt) Chemical ox | Coniferyl Alcohol (sim) g-shift -0.26, LS 22, LW 0.32 | Ferulic Acid (G03) | Ferulic Acid (sim-Burkitt) | Ferulic Acid (sim) g-shift: 1.46, LS: 80.9, LW: 0.34 |
| 10 (ortho to -OH) | 5.01 | 5.33 | 5.52 | 4.99 | 5.56 | 4.09 |
| 11 (meta to -OH) | 1.57 | 1.86 | 1.78 | 1.90 | 1.70 | 1.87 |
| 20 (ortho to -OCH3) | 2.56 | 1.16 | 1.18 | 2.46 | 1.53 | 0.55 |
| 19 (on alpha C | 2.49 | 2.32 | 3.08 | 2.71 | 2.64 | 2.62 |
| 18 (on beta C) | 6.0 | 5.50 | 7.16 | 5.87 | 5.28 | 5.39 |
| 17 (on gamma C | 1.29 | 3.92 | 3.97 | x | x | x |
| 21 (-OCH3) | 2.77 | 1.38 | 1.78 | 0.15 | 1.69 | 1.36 |
| 22 (-OCH3) | 0.15 | 1.38 | 1.78 | 2.54 | 1.69 | 1.36 |
| 23 (-OCH3) | 2.75 | 1.38 | 1.78 | 2.55 | 1.69 | 1.36 |
The above table shows the comparison of radical forms of coniferyl alcohol and ferulic acid. The table shows the experimental simulation values, previous collected values, and the WebMO calculation values. These values collected at this institution are on the figures below, the experimental simulation values are in bold and the WebMO 18 calculation values are in standard text.
| Coniferyl Alcohol Radical | Ferulic Acid Radical | |
Lignan
HPLC Analysis
Two dimers were used for analysis of the oxidation products of coniferyl alcohol. A 2mM standard of coniferyl alcohol in 50/50 dioxane and pH 5 buffer was used. A total of three reactions were done each with 5 mL of substrate, 5 μL of HRP, and a varying amount of 0.5 M H2O2 to reach final concentrations of 0.25 mM, 0.5 mM, and 1.0 mM in the reaction. These reactions were analyzed on the HPLC and compared with the dimer standards of 9.3 mM. By using the dimer standards, it was hoped they could be identified in the oxidation products of the monomers since both dimers are dimers of coniferyl alcohol. Comparing the dimer standards to the oxidation products of the coniferyl alcohol, the dimers could not be identified. It is possible there are other dimers present in the oxidation products, but not these dimers.
Discussion
With the use of HRP and H2O2, lignan monomers were able to be oxidized and analyzed on the HPLC using an acetonitrile and water gradient. Concentration dependent reactions were made so the substrate decreased linearly as the concentration of H2O2 within the reaction was increased. While the decrease of substrate was important, the products produced for each reaction were of interest. As the substrate was decreasing, or being consumed, the amount of products detected should increase. This was the case with the ferulic acid as well as the p-coumaric acid. For sinapic acid, this did not occur. The substrate was not consumed and products were not formed. Throughout each reaction, as the concentration of H2O2 was increased, the same, prominent substrate peak was present. The lack of products could be due to the double-methoxy substitutions on the phenol. Ferulic acid only posses one, and p-coumaric acid possess none. It is possible the two methoxy groups of sinapic acid restrict oxidation, therefore forming no products. These same results were observed when using both HRP and immobilized HRP (HRPi) in beaker reactions.
Flat cell reactions were completed using HRPi and H2O2 and analyzed on the HPLC to examine if oxidation products were being formed before analyzing the reactions using EPR. Products were produced meaning the HRPi was functioning and the reaction setup of the flat cell was adequate. Using the EPR for analysis, the coupling constants of the assumed radicals formed during the oxidation reaction were of interest. These constants could be determined using computational chemistry software, as well as simulations of the experimental data collected. Completing both of these analyses and comparing them showed radials were more likely to be formed at the C-5 and C-β positions than other positions on the molecule. These findings agreed with previous data collected by Russell, Forrester, Chesson, and Burkitt. The coupling constants of the assumed radials formed were of interest because they could be used as a way to predict how oxidative coupling occurs. The larger structure of lignin could be formed vs the dimers, known as lignan. By determining the coupling constants, the oxidative coupling process can be further studied to determine which structures are likely to couple together, and how they couple.
Lignan became of interest when analyzing oxidation products of the monomers on the HPLC. Their pathway of formation was of particular interest. The pathway was first approached using a process that started with the monomers and oxidized then. This was done because it was thought the radials formed during the oxidation reaction could potentially couple into dimers. Two lignans of coniferyl alcohol were chosen for analysis. By using these standards and comparing them to the beaker oxidation reactions of coniferyl alcohol in the presence of HRP and H2O2, these lignans could be identified in the oxidation products. This did not happen, but does not mean dimers did not exist in the products. The dimers chosen for analysis just were not present in the products. The pathway was then approached using a process that started with lignin, the larger structure, and attempted to break it down into dimers and monomers. This was done in an alkaline environment using NaOH. Results were inconclusive using this method, and stronger method development needs to be approached to determine the pathway of formation of the dimers from this angle.
Conclusion
Although some conclusions were made regarding the oxidation of lignin monomers, more research needs to be done to fully understand the oxidation process. Specifically, an analysis procedure needs to be determined for the products of the oxidation reaction. The oxidation reactions were successful, but no method was developed that allowed for successful analysis of the products of these reactions. Sinapic acid was also not oxidized, so a new approach needs to be done to oxidize this monomer and determine products of the reaction.
The EPR analysis of the monomers was successful as coupling constants were determined of the assumed radicals formed. This was only done with ferulic acid and coniferyl alcohol, so the other monomers need to be analyzed. It is likely they can be analyzed using the same method to determine these constants. It would be interesting to compare the acid and alcohol forms of the monomers for similarities in coupling constants. These constants can also then be compared among the monomers for similarities.
Little progress was made on the investigation into the pathway of formation of lignin. Two different approaches were used, but no conclusive results were developed for either of these. The degradation method presented the most promising results and literature is relatively abundant on the topic. More literature review should be done to determine a degradation method that can be completed and then analyzed on the HPLC. A successful method will assist with determining how lignan forms. This pathway can then be compared to the pathway of formation of lignin. Other lignans could also be researched to identify oxidation products of the monomers that could be dimers.
Future Directions
This current project did not reach any conclusions regarding the degradation of lignin. Although literature exists on this process, it was not able to duplicated in the lab. The next focus of this project involving lignin and lignan would be to determine the pathway that lignan forms. It was attempted to determine this pathway using a procedure that began with the monomers, but was unsuccessful in finding conclusive results. In response to these findings, it was decided to determine the pathway lignan forms by starting with the larger structure of lignin, and degrading it into monomers and dimers. More literature will need to be explored to determine a practical procedure to successfully degrade lignin and analyze it using HPLC. More lignan molecules could also be investigated using HPLC since a variety exist and are available for purchase from chemical companies. There are still many unknowns surrounding lignin and lignan and this project has the capability to be taken in many directions. The project will be taken over by Taylor Coffman with a focus on degradation methods as well as understanding the distinction between the lignin and lignan pathways of formation.
References
1. Introduction Dimmel Book
2. Chapter 2 Dimmel Book
3. Russel Paper
4. Brad Paper
Personal Reflection: Progress and Knowledge
Before I first started doing research with Stephanie Saey as a sophomore, I was under the impression you mixed compounds together and hoped for the best for research. My eyes were opened when I realized much more goes into research. In fact, more time is spent outside of the lab planning and analyzing than actually being in the lab. I learned method development is an important aspect of research. You need to go into the lab with a plan, and an alternate plan sometimes. My research experience before coming to Monmouth was so juvenile. I did science fair presentations on such silly things that I thought were so revolutionary and life changing at the time. I look back on my research here and think, I really did make the most out of my experience. I accomplished more than I ever thought I would, and I enjoyed my research here. Yes at times it was a pain, and I put it on the back burner, but I always had a passion for my research. I guess you could say I'm a lignin superfan now! I think greater growth, both as a student and as a researcher, occurred through my research failures. At first, failures felt like a slap in the face. But as my experience progressed, I realized these failures can be turned into successes. Failures mean you have successfully figured out something about your research doesn't work. It can guide you or direct you to the next step in your research. These "failures" pushed me to work harder and crave to find the explanation for different things I was interested in. I think being able to see this project grow from the start really cultivated my interest and love for this project. I have this curious and stubborn drive within me that continues to push me toward my goals and aspirations. The mentality I have leaving this research is completely opposite the mentality I had beginning it! Although there were some bumps along the way, I wouldn't change one thing! I have growth throughout this research, for the better, and have hopefully set it up well for the next person to take over. My experience here has been filled with my failures, but not once did I give up and lose sight at the finish.
Success is the ability to go from one failure to another with no loss of enthusiasm – Winston Churchill