Purification of proanthocyanidins from nut seeds and study on its bactericidal mechanism against Streptococcus mutans

Author:

Lou Zaixiang12,Fan Xiaoyuan12,Liu Caihua1,Liao Yuemei1,Du Xiaojing2,Wang Hongxin2

Affiliation:

1. Guangxi Key Laboratory of Biology for Mango, Baise University , Baise 533000 , China

2. Center for Food Nutrition and Functional Food Engineering, School of Food Science and Technology, Jiangnan University , Wuxi 214122 Jiangsu , China

Abstract

Abstract Aim The aim of this study was to purify proanthocyanidins from areca nut seeds (P-AN) and to investigate the bactericidal activity and mechanism of the purified products against Streptococcus mutans. Methods and results Ultra-performance liquid chromatography tandem quadrupole time-of-flight mass spectrometry, Fourier transform infrared, Matrix-assisted laser desorption/ ionization time of flight mass spectrometry (MADLI-TOF-MS), and thiolysis experiment were used for P-AN chemical analysis. Time-kill analysis and glycolytic pH drop were used to evaluate the activity of S. mutans in vitro. Meanwhile, the investigation of the bacteriostatic mechanism included membrane protein, fluidity, permeability, and integrity tests. The results showed that P-AN was a kind of proanthocyanidin mainly composed of B-type proanthocyanidins and their polymers. Moreover, MADLI-TOF-MS and thiolysis experiments demonstrated that the degree of polymerization of P-AN was 13. The time-kill analysis showed that P-AN had strong bactericidal activity against S. mutans. P-AN at minimum inhibitory concentration (MIC) concentrations was able to induce S. mutans death, while complete lethality occurred at 2 MIC. Glycolysis test showed that P-AN significantly inhibited S. mutans acid production (P < .01). The morphological changes of S. mutans were observed by scanning electron microscopy and transmission electron microscopy experiments, which indicated that P-AN destroyed the cellular structure of S. mutans. At the same time, significant changes were observed in membrane proteins, fluidity, permeability, and integrity. Conclusion P-AN can effectively inhibit the activity of S. mutans. P-AN can reduce the erosion of the tooth surface by the acid of S. mutans. P-AN could break the structure of the cell membrane protein of S. mutans. P-AN could destroy the integrity of membrane, resulting in the death of S. mutans.

Funder

Guangxi Key Laboratory of Biology for Mango

National First-class Discipline Project of Food Science and Technology

Publisher

Oxford University Press (OUP)

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