Dissertation > Excellent graduate degree dissertation topics show

Study on Laccase Catalyzed Oxidation of Phenolic Compounds in Non-Aqueous Media and Anti-Oxidation Activity of Its End Products

Author: GuoPan
Tutor: MaHuiLing
School: Northwest University of Science and Technology
Course: Conservation and Utilization of Wild Fauna and Flora
Keywords: Non-aqueous medium laccase phenolic polymerization enzyme kinetics antioxidant activity HPLC HPLC / MS
CLC: Q814
Type: Master's thesis
Year: 2011
Downloads: 52
Quote: 0
Read: Download Dissertation

Abstract


Modern enzymology reveals that. enzyme in non-aqueous medium show very high catalytic activity and has new properties, such as products in non-aqueous media with strong thermal stability, storage stability and three-dimensional structure of selectivity , etc. For the synthesis of functional polymers, the non-aqueous media is conducive to the formation of phenolic oligomers with more stable and enhanced oxidation ability than the monomer, which can help to improve the laccase stability in practical application and catalytic preparation of new functional compounds.In the study, 10 kinds of organic solvents with different water content were employed as reaction media to tests the activity of laccase catalyzed oxidation of phenolic compounds.. Stability and antioxidant activity, of end products were determinrd and, composition as well as structure were identified by HPLC,HPLC / MS analysis..Main results are as following:(1) For model substrates of caffeic acid and ferulic acid, optimum reaction condition for Trametes versicolor laccase were determined as: pH5.15 and pH4.85, temperatures 30℃, substrate concentration of 8mmol/L and 5mmol/L, enzyme concentration of 0.05U/mL and 0.025U/mL,respectively.(2) Different organic solvents with different fraction of water showed different role for laccase catalyzation. Enzyme activity were enhanced in either low volume fraction of hydrophilic solvent or high volume fraction of hydrophobic solvents. The most suitable reaction mediumof the laccase-catalyzed oxidations for caffeic acid and ferulic acid are 40% methanol, 92% hexane and 40% methanol, 92% isooctane.(3) The maximum absorption wavelength of laccase-catalyzed end-product for caffeic acid and ferulic acid were 388,408 nm. Oxidation products of caffeic acid are stable in the light relatively and have a stronger heat resistance; Oxidation products of ferulic acid are poor thermal stability and sensitivity to light, and should be stored in cool and dark condition.(4) Antioxidant activities of each substrate and their end product were valuated by through DPPH, FRAP and total reducing ability method. The results show that DPPH and FRAP method was consistent. The oxidation phenolic products generated in the hydrophobic medium owned relatively strong antioxidant activities, the maximum clearance rate could reach 85.4% and minimum IC50 is 0.049mmol / L, and reducing ability of phenolic substrate is much greater than the oxidation products. The antioxidant activity of caffeic acid and its Oxidation products was significantly stronger than that of ferulic acid, and it may be related to the number of phenolic hydroxyl groups and the degree of polymerization of a relationship.(5) Results of HPLC and HPLC/MS anslysis thowed that caffeic acid generated 4 oxidation products, three of them were identifies as dimer (C18H14O8), tetramer (C36H28O16) and not enterpreted polymer. Ferulic acid generated 2 oxidation products, dimmer (C20H18O8) and trimer (C30H26O12). Different reaction media has an important influence on the degree of polymerization and formation of products. 92% n-hexane and isooctane is conducive to oxidation of caffeic acid and ferulic acid in the formation of highly reactive oligomers.

Related Dissertations

  1. Study on the Pharmacokinetics of Xiaoaiping and Chlorogenic Acid in Rats and the Quality Standard of Xiaoaiping Preparations,R285
  2. Isolation Entophytes and Study on the Fermentation of Bacillus Subtilis tiD7 from Rehmannia,TQ461
  3. Mutagenesis of a Laccase Gene from Pleurotus eryngii in Vitro and Expression in Pichia Pastoris,TQ925
  4. Expression of a Laccase Gene from Lentinula Edodes in Pichia Pastoris and Degradation of Triarylmethane Dyes by Laccase in the Presence of Natural Mediators,TQ925
  5. Study on Extraction, Isolation and Antioxidant Activity of Lignans of Sesame Cake,TS229
  6. Isolation, Purification and Antioxidant Activity of Proteins from Chinese Yam,TS255.1
  7. Development of Detection Methods of Effective Biological Components from Tea by High Performance Liquid Chromatography and Their Applications in the Analysis of Fenghuang Oolong Tea,TS272.7
  8. Extraction Condition of Paeoniflorin from Paeonia Lactiflora,R284.2
  9. Technological Research on Preparation of High Activity Walnut Pulp by Ultrasonic-compound Enzyme Synergistic Method,TS255.6
  10. Preparation of Duck Egg White Peptide by Enzymatic Hydrolysis and the Evaluation of Its ACE Inhibition and Antioxidation,TS253.1
  11. Preparation and Antioxidant Activity of Phenylethanoid Glycosides from Cistanche Salsa,R284.2
  12. Injection with four commonly cefathiamidine Compatible Stability of transfusion,R942
  13. Amiodarone Hydrochloride Injection Compatible Stability of,R942
  14. Mezlocillin sodium infusion with four commonly Compatible Stability,R942
  15. Injection piperacillin sodium and tazobactam sodium content determination and compatible stability of visits,R927.2
  16. Acclimating, Screening and Degradation Characteristics of Pentachlorophenol-degrading Bacterium,R114
  17. Grisea MoIAP apoptosis inhibitory protein gene functional analysis and Bcl-2 spot on the water banana peanut pathogen Fusarium impact,S435.111.4
  18. Biodegradation Research of Nitrogen Heterocyclic Compounds in Simulating Soil by White Rot Fungi,X172
  19. Laccase catalyzed oxidation 17α- ethinyl estradiol experimental study,X50
  20. Preliminary Studies on Decolorization or Degradation of Triphenylmethane Dyes and Bamboo Alkali Lignin by Ligninolytic Enzymes,X703

CLC: > Biological Sciences > Bioengineering ( Biotechnology ) > Enzyme Engineering
© 2012 www.DissertationTopic.Net  Mobile