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Boosting the Antioxidant Potential of Polymeric Proanthocyanidins in Litchi Pericarp via Biotransformation of Utilizing ILactobacillus/I Plantarum

Liu, Haocheng ; Tang, Yuqian ; Deng, Zhaowen ; Yang, Jiguo ; Gan, Dan

Foods, 2023-06, Vol.12 (12) [Periódico revisado por pares]

MDPI AG

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  • Título:
    Boosting the Antioxidant Potential of Polymeric Proanthocyanidins in Litchi Pericarp via Biotransformation of Utilizing ILactobacillus/I Plantarum
  • Autor: Liu, Haocheng ; Tang, Yuqian ; Deng, Zhaowen ; Yang, Jiguo ; Gan, Dan
  • Assuntos: Antioxidants
  • É parte de: Foods, 2023-06, Vol.12 (12)
  • Descrição: In order to enhance the efficient utilization of polymeric proanthocyanidins from litchi pericarp, a process for transforming litchis’ polymeric proanthocyanidins (LPPCs) by using Lactobacilli has been established for products with highly antioxidative properties. Lactobacillus plantarum was selected to enhance the transformation effect. The transformation rate of LPPCs reached 78.36%. The content of litchis’ oligomeric proanthocyanidins (LOPCs) in the products achieved 302.84 μg grape seed proanthocyanidins (GPS)/mg DW, while that of total phenols was 1077.93 gallic acid equivalents (GAE) μg/mg DW. Seven kinds of substances have been identified in the products by using the HPLC-QTOF-MS/MS method, among which 4-hydroxycinnamic acid, 3,4-dihydroxy-cinnamic acid, and proanthocyanidin A2 were major components. The in vitro antioxidative activity of the products after transformation was significantly (p < 0.05) higher than those of LOPCs and LPPCs. The scavenging activity of the transformed products for DPPH free radicals was 1.71 times that of LOPCs. The rate of inhibiting conjugated diene hydroperoxides (CD-POV) was 2.0 times that of LPPCs. The scavenging activity of the products for ABTS free radicals was 11.5 times that of LPPCs. The ORAC value of the products was 4.13 times that of LPPCs. In general, this study realizes the transformation of polymeric proanthocyanidins into high-activity small-molecule substances.
  • Editor: MDPI AG
  • Idioma: Inglês
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  • Realização: ABCD-USP USP   Logos de Redes Sociais: Freepik

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