Tasso Mariana, Cordeiro Ana L, Salchert Katrin, Werner Carsten
Leibniz Institute of Polymer Research Dresden, Max Bergmann Center of Biomaterials Dresden, Hohe Strasse 6, 01069 Dresden, Germany.
Macromol Biosci. 2009 Sep 9;9(9):922-9. doi: 10.1002/mabi.200900005.
Enzymes cleaving the biopolymer adhesives of fouling organisms are attracting attention for the prevention of biofouling. We report a versatile and robust method to confine the serine protease Subtilisin A (or Subtilisin Carlsberg) to surfaces to be protected against biofouling. The approach consists of the covalent immobilization of the protease onto maleic anhydride copolymer thin film coatings. High-swelling poly(ethylene-alt-maleic anhydride) (PEMA) copolymer layers permitted significantly higher enzyme loadings and activities than compact poly(octadecene-alt-maleic anhydride) (POMA) films. Substantial fractions of the immobilized, active enzyme layers were found to be conserved upon storage in deionized water for several hours. Ongoing studies explore the potentialities of the developed bioactive coatings to reduce the adhesion of various fouling organisms.
用于切割污损生物的生物聚合物粘合剂的酶在防止生物污损方面正受到关注。我们报告了一种通用且稳健的方法,可将丝氨酸蛋白酶枯草杆菌蛋白酶A(或卡尔伯格枯草杆菌蛋白酶)固定在要防止生物污损的表面上。该方法包括将蛋白酶共价固定到马来酸酐共聚物薄膜涂层上。与致密的聚(十八烯-alt-马来酸酐)(POMA)薄膜相比,高溶胀性的聚(乙烯-alt-马来酸酐)(PEMA)共聚物层允许更高的酶负载量和活性。发现固定化的活性酶层的大部分在去离子水中储存数小时后仍能保持。正在进行的研究探索了所开发的生物活性涂层在减少各种污损生物附着方面的潜力。