Dissertation > Excellent graduate degree dissertation topics show
Studies on the Purification and Medical Function of Chondroitin Sulfate Isolated from Chinese Sturgeon
Author: XuChuanTun
Tutor: GuanRuiZhang
School: Jimei University
Course: Aquaculture
Keywords: shark sturgeon chondroitin sulfate isolation purification immunological competence
CLC: R96
Type: Master's thesis
Year: 2007
Downloads: 264
Quote: 1
Read: Download Dissertation
Abstract
|
Chondroitin sulfate was bioactive substance that isolated from various animals, mainly shark cartilage. Chondroitin sulfate has many physiological functions such as antiarthritis, blood fat adjustment, antioxidation, anticoagulation, immunity enhancement, and so on. To solve the problems due to the decrease of shark resources, the feasibility of extracting chondroitin sulfate from Chinese sturgeon cartilage was studied. The contents of chondroitin sulfate between shark and sturgeon cartilage were comparatively studied. We further studied the contents of wet cartilage and chondroitin sulfate among the different sizes and between head and back bond of sturgeon, a better technology for extracting chondroitin sulfate using alkali dilute-salt dilute-enzymolysis, and the physiological functions chondroitin sulfate on immunity of mouse experiment. The results showed:1. The contents of chondroitin sulfate between shark and sturgeon cartilage were not significantly (p>0.05) deferent. The purity of chondroitin sulfate isolated from sturgeon was significantly (p<0.05) higher than from shark. The contents of protein and nitrogen of chondroitin sulfate isolated from sturgeon cartilage were 2.66% and 3.04%respectively, both were highly significantly (p<0.01) lower than from shark cartilage.2. The contents of both head and backbone cartilage of medium size (5.91±0.25kg)of sturgeon were highly significantly (p<0.01) higher than small size (2.69±0.17kg) and big size(8.06±0.49kg) of sturgeon. The contents of chondroitin sulfate in unit weight of wet head cartilage of all sizes sturgeon were highly significantly (p<0.01) higher than those in unit weight of wet backbone cartilage. The content of chondroitin sulfate in unit weight of wet head cartilage highly significantly (p<0.01) decreased with the increase of sturgeon size, but that in unit weight of wet backbone cartilage was not significantly (p>0.05).3. In alkali dilute to extract the chondroitin sulfate from sturgeon cartilage, the density of alkali had a greatest effect, then the weight proportion, and the time, the best combination of extracting technique was: the 5% alkali concentration, the 1:6 weight proportion, and the time of 3 hours. In salt dilute to extract the chondroitin sulfate from sturgeon cartilage, the temperature had a greatest effect, then the salt concentration, and the time, the best combination was the 4% salt concentration, the temperature of 90, and the time of 20 minutes. In enzymeolysis, the enzyme concentration had greatest effect, then the temperature, and the time, the best combination was 0.4% enzyme concentration, the temperature of 52℃, and the time of 2.5 hours. The purity of chondroitin sulfate isolated by above best combination technique was significantly (p<0.05) higher than that by traditional technique, while the content of protein was significantly (p<0.05) lower.4. To study the immunity functions of chondroitin sulfate of sturgeon in mouse, three different dosages (2.5, 5.0, and 10.0 mg ml-1 ) of sturgeon chondroitin sulfate were adopted. Results showed that the medium dosage (5.0) of chondroitin sulfate significantly (p<0.05) enhanced the function of macrophage. All three dosages significantly (p<0.05)enhanced the thymus index of male mouse, while no significant (p>0.05) effect was found on the spleen index of male mouse, thymus and spleen index of female mouse, and the immunological function of mouse cell.
|
Related Dissertations
- Study on Protective Effects of Apple Polyphenol on Immune System Injury Caused by γ-Ray,S661.1
- Study on Wastewater Purification Effect of the Free Surface Wetland with Different Substrates and Plant Combination,X703
- Penicillium Expansum TS414 Lipase in Pichia Pastori: Expression, Purification and Enantioselective Esterification of (R, S)-naproxen,Q814
- Isolation & Characterization of a Cetochlor Degrading Strain Y3B-1 and Its Degrading Characteristics,X172
- Studies on Fermentation Optimization, Purification and Enzyme Characteristics of Lipase from Aspergillus Oryzae FS-1,TQ925.6
- Studies on Isolation, Purification and Chemical Structure for Polysaccharides from Camellia Chrysantha(Hu) Tuyama,S567.19
- Research of Glycosaminoglycan from Perna Virids Effect on Blood Lipid,R285.5
- Purification of Endogenous Proteases from (Litopenaeus Vannamei) Shrimp Head and Their Enzymology Properties,S985.21
- Study on the Preparation of the Low Molecular Weight Fuciodan from Sargassum Henslowianum (C.Agardh) and Anti-tumor Activity,TS254.9
- Under microaerobic conditions closed calcium carbide furnace exhaust COS gas adsorption purification,X781
- Studies on Extraction and Analysis of Fructooligosaccharides in Smallanthus Sonchifolius,TS255.1
- Optimization of Fermentation Conditions, Purification, Cloning and Expression of a Cold-active Lipase from Pseudomonas Sp.RT-1,TQ925
- Extraction, Purification and Antifungal Activity of Anthocyanins in Drop Fruits of Chinese Baberry,TQ914.1
- Preliminary Research on Characterization of Thermophilic Protease Pasey and Helicase Htc16,Q814
- Study on the Separation and Purification Way of Arctiin from Fructus Arctii and the Effect of Arctiin on the Growth of Mice C2C12 Cells,S853.7
- Purification of Human Respiratory Syncytial Virus Fusion Protein with Immunomagnetic Microsphere Technology,R373
- Isolation and Characterization of Carbendazim-Degrading Strains, Cloning and Expression of the mheI Gene,X172
- Isolation and Identification of Infectious Bronchitis Virus and Sequence Analysis of Its S1 Gene and N Gene,S852.65
- Isolationand Identification of Porcine Parvovirus and Parts of Its Biological Characteristics,S852.65
- Identification of Marine Sreptomyces Sp. GY-4 and Researches on Its Antimicrobial Substances,Q936
- Characterization of an Atrazine-Degrading Strain, Cloning of Key Degrading Related Genes and Construction of a Gene Cluster,X172
CLC: > Medicine, health > Pharmacy > Pharmacology
© 2012 www.DissertationTopic.Net Mobile
|