Mørch Y A, Donati I, Strand B L, Skjåk-Braek G
Department of Biotechnology, Norwegian University of Science and Technology, Trondheim, Norway.
Biomacromolecules. 2007 Sep;8(9):2809-14. doi: 10.1021/bm700502b. Epub 2007 Aug 15.
Through enzymatic modification, we are now able to manipulate the composition and sequential nanostructures of alginate, one of the most versatile gelling polymers found in nature. Here we report the application of a set of processive polymer-modifying epimerases for the preparation of novel alginates with highly improved functional properties essential for numerous applications as gel matrices. Gels of enzymatically engineered alginate were found to be more elastic and compact, less permeable, and extremely stable under physiological conditions, offering significant advantages over native alginates. As a result, this study shows that, by controlling alginate nanostructure, its macroscopic properties can be highly controlled. The ability to tailor alginate has a great impact on the wide use of this biomaterial in industry and medicine. More importantly, this adds more knowledge to the link between polymer nanostructure and macroscopic properties and may serve as a model system for other polymer-based materials.
通过酶促修饰,我们现在能够操控藻酸盐的组成和序列纳米结构,藻酸盐是自然界中最通用的凝胶聚合物之一。在此,我们报告了一组进行性聚合物修饰差向异构酶在制备新型藻酸盐方面的应用,这些新型藻酸盐具有高度改善的功能特性,对于作为凝胶基质的众多应用至关重要。发现经酶工程改造的藻酸盐凝胶更具弹性和致密性,渗透性更低,并且在生理条件下极其稳定,比天然藻酸盐具有显著优势。因此,这项研究表明,通过控制藻酸盐纳米结构,可以高度控制其宏观性质。定制藻酸盐的能力对这种生物材料在工业和医学中的广泛应用有很大影响。更重要的是,这为聚合物纳米结构与宏观性质之间的联系增添了更多知识,并可能作为其他基于聚合物的材料的模型系统。