Department of Chemistry and Biochemistry, North Dakota State University, Fargo, North Dakota 58102, United States.
Department of Chemistry and Chemical Biology, Harvard University, Boston, Massachusetts 02138, United States.
ACS Appl Mater Interfaces. 2024 Mar 6;16(9):11617-11626. doi: 10.1021/acsami.4c00651. Epub 2024 Feb 27.
Biodegradation of insoluble biomass such as cellulose via carbohydrase enzymes is an effective approach to break down plant cell walls and extract valuable materials therein. Yet, the high cost and poor reusability of enzymes are practical concerns. We recently proved that immobilizing multiple digestive enzymes on metal-organic materials (MOMs) allows enzymes to be reused via gravimetric separation, improving the cost efficiency of cereal biomass degradation [ , , 36, 43085-43093]. However, this strategy cannot be adapted for enzymes whose substrates or products are insoluble (e.g., cellulose crystals). Recently, we described an alternative approach based on magnetic metal-organic frameworks (MOFs) using model enzymes/substrates [ , , 37, 41794-41801]. Here, we aim to prove the effectiveness of combining these two strategies in cellulose degradation. We immobilized multiple carbohydrase enzymes that cooperate in cellulose degradation via cocrystallization with Ca, a carboxylate ligand (BDC) in the absence and presence of magnetic nanoparticles (MNPs). We then compared the separation efficiency and enzyme reusability of the resultant multienzyme@Ca-BDC and multienzyme@MNP-Ca-BDC composites via gravimetric and magnetic separation, respectively, and found that, although both composites were effective in cellulose degradation in the first round, the multienzyme@MNP-Ca-BDC composites displayed significantly enhanced reusability. This work provides the first experimental demonstration of using magnetic solid supports to immobilize multiple carbohydrase enzymes simultaneously and degrade cellulose and promotes green/sustainable chemistry in three ways: (1) reusing the enzymes saves energy/sources to prepare them, (2) the synthetic conditions are "green" without generating unwanted wastes, and (3) using our composites to degrade cellulose is the first step of extracting valuable materials from sustainable biomasses such as plants whose growth does not rely on nonregeneratable resources.
通过糖酶将不溶性生物质(如纤维素)生物降解是一种有效方法,可以破坏植物细胞壁并从中提取有价值的物质。然而,酶的高成本和较差的可重复使用性是实际关注的问题。我们最近证明,通过将多种消化酶固定在金属有机材料(MOM)上,可以通过重量分离使酶重复使用,从而提高谷物生物质降解的成本效益[,,36,43085-43093]。但是,这种策略不能适用于其底物或产物为不溶性的酶(例如纤维素晶体)。最近,我们使用模型酶/底物描述了一种基于磁性金属有机骨架(MOF)的替代方法[,,37,41794-41801]。在这里,我们旨在证明这两种策略在纤维素降解中的有效性。我们通过与 Ca 共晶化(Ca 是一种羧酸盐配体(BDC)),在不存在和存在磁性纳米颗粒(MNP)的情况下,将多种协同作用于纤维素降解的糖酶固定化。然后,我们通过重量和磁分离分别比较了所得多酶@Ca-BDC 和多酶@MNP-Ca-BDC 复合材料的分离效率和酶可重复使用性,发现尽管这两种复合材料在第一轮纤维素降解中都有效,但多酶@MNP-Ca-BDC 复合材料的可重复使用性明显提高。这项工作首次提供了使用磁性固体载体同时固定多种糖酶并降解纤维素的实验证明,并以三种方式促进了绿色/可持续化学:(1)重复使用酶可节省制备它们的能源/资源,(2)合成条件是“绿色的”,不会产生不需要的废物,(3)使用我们的复合材料降解纤维素是从植物等可持续生物质中提取有价值材料的第一步,植物的生长不依赖于不可再生资源。