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Title: | Bicomponent Coassembled Hydrogel as a Template for Selective Enzymatic Generation of DOPA |
Authors: | Biswas, Sagar Ghosh, Tapas Kumar Kori, Deepak K. Das, Apurba Kumar |
Keywords: | Amino acids;Biology;High resolution transmission electron microscopy;Scanning electron microscopy;Amphiphilic molecules;Bicomponents;Co-assemble;Diaminonaphthalene;Enzymatic generation;l-Tyrosine;Living organisms;Scanning electron microscopy image;Selective generation;Spectroscopic technique;Hydrogels;levodopa;monophenol monooxygenase;tyrosine;hydrogel;metabolism;oxidation reduction reaction;Hydrogels;Levodopa;Monophenol Monooxygenase;Oxidation-Reduction;Tyrosine |
Issue Date: | 2021 |
Publisher: | American Chemical Society |
Citation: | Biswas, S., Ghosh, T., Kori, D. K. K., & Das, A. K. (2021). Bicomponent coassembled hydrogel as a template for selective enzymatic generation of DOPA. Langmuir, 37(37), 10883-10889. doi:10.1021/acs.langmuir.1c00438 |
Abstract: | In living organisms, tyrosinase selectively produces l-DOPA from l-tyrosine. Here, a bicomponent hydrogel is used as a template for tyrosinase-catalyzed selective generation of l-DOPA from tyrosine. An amphiphilic molecule 1,5-diaminonaphthalene (DAN) coassembles with 1,3,5-benzenetricarboxylic acid (BTC) to form a self-supporting hydrogel. After alteration of complementary acids, DAN does not coassemble to form a hydrogel. The coassembly mechanism is investigated using spectroscopic techniques. The transmission electron microscopy and scanning electron microscopy images reveal the morphology details. The l-DOPA is kept from being oxidized when the hydrogel is used as a template. The enzymatically synthesized l-DOPA can also be separated from the mixture by easy tuning of the bicomponent coassembly. © 2021 American Chemical Society. All rights reserved. |
URI: | https://doi.org/10.1021/acs.langmuir.1c00438 https://dspace.iiti.ac.in/handle/123456789/8677 |
ISSN: | 0743-7463 |
Type of Material: | Journal Article |
Appears in Collections: | Department of Chemistry |
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