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Magnetic Multienzyme@Metal-Organic Material for Sustainable Biodegradation of Insoluble Biomass.
Lenertz, Mary; Li, Qiaobin; Armstrong, Zoe; Scheiwiller, Allison; Ni, Gigi; Wang, Jien; Feng, Li; MacRae, Austin; Yang, Zhongyu.
Afiliación
  • Lenertz M; Department of Chemistry and Biochemistry, North Dakota State University, Fargo, North Dakota 58102, United States.
  • Li Q; Department of Chemistry and Biochemistry, North Dakota State University, Fargo, North Dakota 58102, United States.
  • Armstrong Z; Department of Chemistry and Biochemistry, North Dakota State University, Fargo, North Dakota 58102, United States.
  • Scheiwiller A; Department of Chemistry and Biochemistry, North Dakota State University, Fargo, North Dakota 58102, United States.
  • Ni G; Department of Chemistry and Chemical Biology, Harvard University, Boston, Massachusetts 02138, United States.
  • Wang J; California State University, San Marcos, San Marcos, California 92096, United States.
  • Feng L; Department of Chemistry and Biochemistry, North Dakota State University, Fargo, North Dakota 58102, United States.
  • MacRae A; Department of Chemistry and Biochemistry, North Dakota State University, Fargo, North Dakota 58102, United States.
  • Yang Z; Department of Chemistry and Biochemistry, North Dakota State University, Fargo, North Dakota 58102, United States.
ACS Appl Mater Interfaces ; 16(9): 11617-11626, 2024 Mar 06.
Article en En | MEDLINE | ID: mdl-38410049
ABSTRACT
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 [ACS Appl. Mater. Interfaces 2021, 13, 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 [ACS Appl. Mater. Interfaces 2020, 12, 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 Ca2+, 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.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Celulosa / Enzimas Inmovilizadas Idioma: En Revista: ACS Appl Mater Interfaces Asunto de la revista: BIOTECNOLOGIA / ENGENHARIA BIOMEDICA Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Celulosa / Enzimas Inmovilizadas Idioma: En Revista: ACS Appl Mater Interfaces Asunto de la revista: BIOTECNOLOGIA / ENGENHARIA BIOMEDICA Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos
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