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Cascade/Parallel Biocatalysis via Multi-enzyme Encapsulation on Metal-Organic Materials for Rapid and Sustainable Biomass Degradation.
Li, Qiaobin; Pan, Yanxiong; Li, Hui; Lenertz, Mary; Reed, Kailyn; Jordahl, Drew; Bjerke, Taylor; Ugrinov, Angel; Chen, Bingcan; Yang, Zhongyu.
Afiliação
  • Li Q; Department of Chemistry and Biochemistry, North Dakota State University, Fargo, North Dakota 58102, United States.
  • Pan Y; Department of Chemistry and Biochemistry, North Dakota State University, Fargo, North Dakota 58102, United States.
  • Li H; Department of Plant Sciences, North Dakota State University, Fargo, North Dakota 58102, United States.
  • Lenertz M; Department of Chemistry and Biochemistry, North Dakota State University, Fargo, North Dakota 58102, United States.
  • Reed K; Department of Chemistry and Biochemistry, North Dakota State University, Fargo, North Dakota 58102, United States.
  • Jordahl D; Department of Chemistry and Biochemistry, North Dakota State University, Fargo, North Dakota 58102, United States.
  • Bjerke T; Sheyenne High School, West Fargo, North Dakota 58078, United States.
  • Ugrinov A; Department of Chemistry and Biochemistry, North Dakota State University, Fargo, North Dakota 58102, United States.
  • Chen B; Department of Plant Sciences, 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 ; 13(36): 43085-43093, 2021 Sep 15.
Article em En | MEDLINE | ID: mdl-34478257
ABSTRACT
Multiple-enzyme cooperation simultaneously is an effective approach to biomass conversion and biodegradation. The challenge, however, lies in the interference of the involved enzymes with each other, especially when a protease is needed, and thus, the difficulty in reusing the enzymes; while extracting/synthesizing new enzymes costs energy and negative impact on the environment. Here, we present a unique approach to immobilize multiple enzymes, including a protease, on a metal-organic material (MOM) via co-precipitation in order to enhance the reusability and sustainability. We prove our strategy on the degradation of starch-containing polysaccharides (require two enzymes to degrade) and food proteins (require a protease to digest) before the quantification of total dietary fiber. As compared to the widely adopted "official" method, which requires the sequential addition of three enzymes under different conditions (pH/temperature), the three enzymes can be simultaneously immobilized on the surface of our MOM crystals to allow for contact with the large substrates (starch), while MOMs offer sufficient protection to the enzymes so that the reusability and long-term storage are improved. Furthermore, the same biodegradation can be carried out without adjusting the reaction condition, further reducing the reaction time. Remarkably, the simultaneous presence of all enzymes enhances the reaction efficiency by a factor of ∼3 as compared to the official method. To our best knowledge, this is the first experimental demonstration of using aqueous-phase co-precipitation to immobilize multiple enzymes for large-substrate biocatalysis. The significantly enhanced efficiency can potentially impact the food industry by reducing the labor requirement and enhancing enzyme cost efficiency, leading to reduced food cost. The reduced energy cost of extracting enzymes and adjusting reaction conditions minimize the negative impact on the environment. The strategy to prevent protease damage in a multi-enzyme system can be adapted to other biocatalytic reactions involving proteases.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Peptídeo Hidrolases / Glucana 1,4-alfa-Glucosidase / Biomassa / Enzimas Imobilizadas / Estruturas Metalorgânicas / Amilases Tipo de estudo: Prognostic_studies Idioma: En Revista: ACS Appl Mater Interfaces Assunto da revista: BIOTECNOLOGIA / ENGENHARIA BIOMEDICA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Peptídeo Hidrolases / Glucana 1,4-alfa-Glucosidase / Biomassa / Enzimas Imobilizadas / Estruturas Metalorgânicas / Amilases Tipo de estudo: Prognostic_studies Idioma: En Revista: ACS Appl Mater Interfaces Assunto da revista: BIOTECNOLOGIA / ENGENHARIA BIOMEDICA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos