| Literature DB >> 32507181 |
Rong Lan1, Ye Li2, Rong Shen3, Ran Yu4, Lihua Jing5, Shuangsheng Guo6.
Abstract
Chondroitin sulfate (CS) has attracted widespread attention because of its numerous pharmacological activities. Low-molecular-weight chondroitin sulfates (LMWCSs) derived from the degradation of CS are reported to have better biological properties than whole CS. In this study, to obtain LMWCSs with high antioxidant activity, we depolymerized CS using complex enzymes, namely, chondroitinase ABC I (ChSase ABC I) and ChSase ABC II. The conditions of the complex enzyme hydrolysis (CEH) were optimized, and the structures and antioxidant activities of CS and LMWCSs were investigated. The results showed that the CEH conditions enhanced the antioxidant activities of the products as compared to CS. The basic structures of the LMWCSs and sulfate groups were well preserved after hydrolysis. Therefore, CEH provides an efficient and safe strategy to obtain LMWCSs, which can be used in antioxidant drugs, healthy foods, and cosmetics.Entities:
Keywords: 1,1-diphenyl-2-picrylhydrazyl (PubChem CID: 74358); 3-(4,5-dimethylthiazol-2-yl)- 5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium (MTS, PubChem CID: 2762693); Deuterium oxide (PubChem CID: 24602); Ethanol (PubChem CID: 702); Ferrous sulfate (PubChem CID: 24393); Glucuronic acid (PubChem CID: 94715); Hydrogen peroxide (PubChem CID: 784); N-acetylgalactosamine (PubChem CID: 35717); Sodium dihydrogen phosphate (PubChem CID: 23672064); Trimethylolaminomethane (Tris, PubChem CID: 6503); antioxidant activities; complex enzyme hydrolysis; low-molecular-weight chondroitin sulfate
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Year: 2020 PMID: 32507181 DOI: 10.1016/j.carbpol.2020.116302
Source DB: PubMed Journal: Carbohydr Polym ISSN: 0144-8617 Impact factor: 9.381