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Structural properties and antioxidant capacity of different aminated starch-phenolic acid conjugates.
An, Feng-Kun; Li, Meng-Yun; Luo, Hai-Lu; Liu, Xing-Long; Fu, Zhen; Ren, Min-Hong.
Afiliação
  • An FK; Institute of Light Industry and Food Engineering, Guangxi University, Nanning, China; Key Laboratory of Deep Processing and Safety Control for Specialty Agricultural Products in Guangxi Universities, Guangxi University, Nanning, China.
  • Li MY; Institute of Light Industry and Food Engineering, Guangxi University, Nanning, China; Key Laboratory of Deep Processing and Safety Control for Specialty Agricultural Products in Guangxi Universities, Guangxi University, Nanning, China.
  • Luo HL; Institute of Light Industry and Food Engineering, Guangxi University, Nanning, China; Key Laboratory of Deep Processing and Safety Control for Specialty Agricultural Products in Guangxi Universities, Guangxi University, Nanning, China.
  • Liu XL; Institute of Light Industry and Food Engineering, Guangxi University, Nanning, China; Key Laboratory of Deep Processing and Safety Control for Specialty Agricultural Products in Guangxi Universities, Guangxi University, Nanning, China.
  • Fu Z; Institute of Light Industry and Food Engineering, Guangxi University, Nanning, China; Key Laboratory of Deep Processing and Safety Control for Specialty Agricultural Products in Guangxi Universities, Guangxi University, Nanning, China. Electronic address: fuzhen13@gxu.edu.cn.
  • Ren MH; Guangxi Vocational & Technical Institute of Industry, Nanning 530001, China.
Food Chem ; 460(Pt 2): 140592, 2024 Dec 01.
Article em En | MEDLINE | ID: mdl-39067431
ABSTRACT
Different aminated starch (AS) [EEAS (introducing ethylenediamine into starch using cross-linking-etherification-amination method (CEA)), EPAS (introducing o-phenylenediamine using CEA), OEAS (introducing ethylenediamine using cross-linking-oxidation-amination method (COA)), and OPAS (introducing o-phenylenediamine using COA)] were synthesized. The AS-phenolic acids [gallic acid (GA), syringic acid (SA), and vanillic acid (VA)] conjugates were prepared by laccase-catalyzed reaction. The grafting efficiency of EEAS on GA, SA, and VA was 36.59%, 69.71%, and 68.85%, respectively. SA reduced the maximum depolymerization rate of EEAS. The relative crystallinity of EEAS and EPAS grafted phenolic acid increased, and their particles showed severe breakage in appearance. OEAS-phenolic acid conjugates lost its granular structure and behaved as flakes and lumps, while the surface of OPAS-phenolic acid conjugates remained smooth after grafting phenolic acid. GA increased the DPPH· scavenging efficiency of EEAS from 16.12% to 79.92%. The increased antioxidant capacity of the conjugates suggested that AS-phenolic acids conjugates have high potential for applications.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Amido / Hidroxibenzoatos / Antioxidantes Idioma: En Revista: Food Chem / Food chem / Food chemistry Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China País de publicação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Amido / Hidroxibenzoatos / Antioxidantes Idioma: En Revista: Food Chem / Food chem / Food chemistry Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China País de publicação: Reino Unido