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聚羟基烷酸酯酶降解动力学研究 被引量:4

KINETIC STUDY FOR ENZYMATIC DEGRADATION OF POLYHYDROXYALKANOATES
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摘要 研究了羟基丁酸 羟基戊酸共聚物 (PHBV)在脂肪酶中的降解行为 ,用滴定法测定降解速度并进行酶促反应动力学研究 .探讨了降解速度与酶浓度和底物浓度的数学关系和Michaelis Menten常数 ,从实验上和理论上证实了PHBV的物理形态和几何尺寸对酶降解过程的影响 。 The microbial polyesters have attracted attention as an biodegradable materials for a wide range of agricultural, marine and medical applications. It is important to investigate the biodegradation behavior and kinetics of the biodegradable reaction. Traditional Michaelis-Menten kinetics was originally derived for homogeneous reactions in which both the enzyme and the substrate are soluble. The enzymatic degradation of poly ( hydroxybutyrate-co-hydroxyvalerate) ( PHBV) is a heterogeneous reaction, because PHBV is an insoluble substrate, and the kinetic relation needs to be altered to fit it. In this paper, the kinetics of the enzymatic degradation behavior of PHBV was studied. It is well known that the enzymatic hydrolysis of water-insoluble film of PHB by depolymerases produces water-soluble products composed of monomers and dimers of R-3-hydroxybutyric acid. The rates of degradation were determined by the titrimetric methods, which are quantitative by directly measuring the acid groups formed as a result of ester bond hydrolysis. The degradation of PHA samples with different shapes and,morphology was studied. The kinetic analysis revealed that the degradation reaction exponentials of PHBV powder, solution-casting film and solution-casting-leaching porous film were different, which were inconsistent with classical enzymatic kinetics. The variations of kinetics curves depended on the concentration of enzyme and PHA. A heterogeneous kinetics treatment was derived to describe the relationship of degradation rates with enzyme concentrations and substrates. The influence of PHBV physical morphology on their degradation was also investigated. The results. show that the specific surface area and the shape of PHA samples effect the adsorption and combination of enzyme to substrates and finally conduce to the changes of enzymatic degradation process and the rate of degradation of PHBV.
出处 《高分子学报》 SCIE CAS CSCD 北大核心 2002年第6期760-763,共4页 Acta Polymerica Sinica
基金 国家自然科学基金重点项目 (基金号 5 9932 0 5 0 ) 广东省自然科学基金项目 (基金号 990 6 2 1) 广东省"十五"重大科技专项 (A30 2 0 2 0 2 0 2 )资助
关键词 聚羟基烷酸酯 酶降酯 动力学 滴定 脂肪酶 羟基丁酸-羟基戊酸共聚物 polyhydroxyalkanoates enzymatic degradation kinetics titrimetry
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  • 1张龙彬,朱光明,许硕贵,王金花,秦瑞丰.辐射交联聚己内酯的酶降解动力学研究[J].辐射研究与辐射工艺学报,2006,24(5):275-278. 被引量:2
  • 2杨智.组织工程化血管构架及构建环境相关研究与进展[J].中国组织工程研究与临床康复,2007,11(19):3829-3832. 被引量:3
  • 3Anton W J, Stephen R W, David I. Biological applications of fullerenes. Bioorg Med Chem, 1996, 4:767--779.
  • 4Tokuyama H, Yamago S, Nakamura E, et al. Photoinduced biochemical activity of fullerene carboxylic acid. J Am Chem Soc, 1993, 115: 7918--7919.
  • 5Yang X L, Fan C H, Zhu H S. Photo-induced cytotoxicity of malonic acid [C-60]fullerene derivatives and its mechanism. Toxicol In Vitro, 2002, 16:41-46.
  • 6Sijbesma R, Srdanov G, Wudl F, et al. Synthesis of a fullerene derivative for the inhibition of HIV enzymes. J Am Chem Soc, 1993, 115: 6510--6512.
  • 7Friedman S H, Ganapathi P S, Rubin Y, et al. Optimizing the binding of fullerene inhibitors of the HIV-1 protease through predicted increases in bydrophobic desolvation. J Med Chem, 1998, 41:2424--2429.
  • 8Nakamura E, Tokuyama H, Yamago S, et al. Biological activity of water-soluble fullerenes. Structural dependence of DNA cleavage, cytotoxicity, and enzyme inhibitory activities including HIV-protease inhibition. Bull Chem Soc Jpn, 1996, 69:2143--2151.
  • 9Dugan L L, Turetsky D M, Du C, et al. Carboxyfullerenes as neuroprotective agents. Proc Natl Acad Sci USA, 1997, 94:9434--9439.
  • 10Francesco G, Nazario M. Fullerene polymers: Synthesis and properties. Chem Rev, 2006, 106:5136--5190.

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