1‐Alkyl‐1 <i>H</i> ‐Benzimidazolium Sulfonates as Non‐Competitive Inhibitors of Polyphenol Oxidase

Polyphenol oxidase (PPO) has been the subject of many inhibition studies due to its presence in many species, causing enzymatic browning in fruits and vegetables, and its pigmentation role in mammalian species. In the present study, the inhibitory properties of twelve 1-alkyl-1H-benzimidazolium sulfonates and two 1-alkyl-1H-benzimidazolium iodides on PPO activity have been investigated. The PPO enzyme was purified from banana using Sepharose 4B-tyrosine-p-aminobenzoic acid affinity gel chromatography. The effects of 14 different synthesized benzimidazole derivatives on the PPO enzyme were investigated, and they were found to significantly inhibit the enzyme in question. When ADME predictions were examined, it was seen that all compounds that include methylbenzenesulfonate structure showed good pharmacokinetic properties; only compounds 3a and 3b, which contain iodide, violated the Ghose rules. These compounds, which were effective at low concentrations, may serve as promising lead molecules for the development of PPO inhibitors with potential applications in food preservation, cosmetic formulations, and pharmaceutical research, pending further in vivo and formulation-based studies.

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Publication Details

Journal
Biotechnology and Applied Biochemistry
Published
2026-02-15
DOI
https://doi.org/10.1002/bab.70145
Primary Topic
Enzyme-mediated dye degradation
Type
article
Field-Weighted Citation Impact
0.00

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article

1‐Alkyl‐1 H ‐Benzimidazolium Sulfonates as Non‐Competitive Inhibitors of Polyphenol Oxidase

Adem Ergün, Harun Uslu, Mert Olgun Karataş, Bünyamin Göktaş et al.
Biotechnology and Applied Biochemistry
Enzyme-mediated dye degradation
article

1‐Alkyl‐1 H ‐Benzimidazolium Sulfonates as Non‐Competitive Inhibitors of Polyphenol Oxidase

Adem Ergün, Harun Uslu, Mert Olgun Karataş, Bünyamin Göktaş, Oktay Arslan, Nahit Gencer, Kübra Çikrikci
article en

Abstract

Polyphenol oxidase (PPO) has been the subject of many inhibition studies due to its presence in many species, causing enzymatic browning in fruits and vegetables, and its pigmentation role in mammalian species. In the present study, the inhibitory properties of twelve 1-alkyl-1H-benzimidazolium sulfonates and two 1-alkyl-1H-benzimidazolium iodides on PPO activity have been investigated. The PPO enzyme was purified from banana using Sepharose 4B-tyrosine-p-aminobenzoic acid affinity gel chromatography. The effects of 14 different synthesized benzimidazole derivatives on the PPO enzyme were investigated, and they were found to significantly inhibit the enzyme in question. When ADME predictions were examined, it was seen that all compounds that include methylbenzenesulfonate structure showed good pharmacokinetic properties; only compounds 3a and 3b, which contain iodide, violated the Ghose rules. These compounds, which were effective at low concentrations, may serve as promising lead molecules for the development of PPO inhibitors with potential applications in food preservation, cosmetic formulations, and pharmaceutical research, pending further in vivo and formulation-based studies.

Biotechnology and Applied Biochemistry
Balıkesir University (TR), Fırat University (TR), Inonu University (TR)
Balikesir Üniversitesi
Zero hunger
Openalex Percentile: Top 53%
Enzyme-mediated dye degradation
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