4.6 Article

Acceleration of the Dehydrogenation of D-Glucose to 2-Keto-D-gluconate in Aqueous Amino Acid via Hydrated Stacked Clay Nanosheets

Journal

LANGMUIR
Volume 38, Issue 19, Pages 6076-6085

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.langmuir.2c00387

Keywords

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Funding

  1. JSPS KAKENHI [20K05661]
  2. Grants-in-Aid for Scientific Research [20K05661] Funding Source: KAKEN

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The study developed an artificial bifunctional glucose/gluconic acid dehydrogenase using naturally abundant resources, L-aspartic acid and montmorillonite. This enzyme can mimic natural enzymatic functions and perform low-cost reactions that convert glucose to 2-keto-D-gluconate.
The assembly of discrete active species to form periodical nanostructures is essential in realizing low-cost artificial enzymes that mimic natural enzymatic functions in extraordinary bio(chemo)selective reactions. In this study, we developed artificial bifunctional glucose/gluconic acid dehydrogenase from naturally abundant resources: L-aspartic acid (Asp) and montmorillonite (a subgroup of smectite natural clay minerals). beta-D-Glucose (Glc) was dehydrogenated to 2-keto-D-gluconate (2-KGA) at 25 and 30 degrees C in an aqueous acidic solution (pH = 3, 4, and 5). The reaction involved sequential steps that yielded D-gluconic acid (GA) as an intermediate. The second step of the dehydrogenation (GA to 2-KGA) occurred at a higher rate than the first (Glc to GA), which is comparable to the natural process. A negatively charged carboxylate in Asp was required for the dehydrogenation, which donates an electron pair (COO:(-)) to the hydroxyl group bonded to the C(1)-position of Glc. The acidic sites in clay served as coenzymatic sites (electron acceptor), promoting the Glc dehydrogenation as the Glc reduced by Asp approached the clay coenzymatic sites. The active coenzymatic structures were developed in 48 h (induction period) through the rearrangement of the adsorbed Asp and Glc molecules on montmorillonite in water (intermediate structure). The spontaneous assembling of the intermediate structures facilitated the one-pot dehydrogenation of Glc to 2-KGA via periodic hydrated stacked layers comprising clay nanosheets, Asp, and Glc. The facile synthetic route proposed here is inexpensive and would be beneficial without using both GDH and GADH enzymes bound to a cell membrane.

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