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SBC001产生的低聚葡萄糖的生产优化、结构分析及其益生元和抗炎作用

Production Optimization, Structural Analysis, and Prebiotic- and Anti-Inflammatory Effects of Gluco-Oligosaccharides Produced by SBC001.

作者信息

Kim Minhui, Jang Jae-Kweon, Park Young-Seo

机构信息

Department of Food Science and Biotechnology, Gachon University, Gyeonggi-do 13120, Korea.

Food Nutrition Major, School of Food, Chungkang College of Cultural Industries, Icheon 17390, Korea.

出版信息

Microorganisms. 2021 Jan 19;9(1):200. doi: 10.3390/microorganisms9010200.

DOI:10.3390/microorganisms9010200
PMID:33477973
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7835818/
Abstract

SBC001, isolated from chive, produces glucansucrase and synthesizes oligosaccharides through its enzymatic activity. This study was conducted to optimize oligosaccharide production using response surface methodology, analyze the structure of purified oligosaccharides, and investigate the prebiotic effect on 24 bacterial and yeast strains and the anti-inflammatory activity using RAW 264.7 macrophage cells. The optimal conditions for oligosaccharide production were a culture temperature of 30 °C and sucrose and maltose concentrations of 9.6% and 7.4%, respectively. Based on H-NMR spectroscopic study, the oligosaccharides were identified as gluco-oligosaccharides that consisted of 23.63% α-1,4 glycosidic linkages and 76.37% α-1,6 glycosidic linkages with an average molecular weight of 1137 Da. The oligosaccharides promoted the growth of bacterial and yeast strains, including , , , , , and . When lipopolysaccharide-stimulated RAW 264.7 cells were treated with the oligosaccharides, the production of nitric oxide was decreased; the expression of inducible nitric oxide synthase, tumor necrosis factor-α, interleukin (IL)-1β, IL-6, and IL-10 was suppressed; and the nuclear factor-kappa B signaling pathway was inhibited. In conclusion, the gluco-oligosaccharides obtained from SBC001 exhibited a prebiotic effect on six bacterial and yeast strains and anti-inflammatory activity in RAW 264.7 macrophage cells.

摘要

从细香葱中分离得到的SBC001可产生葡聚糖蔗糖酶,并通过其酶活性合成低聚糖。本研究采用响应面法优化低聚糖的生产,分析纯化后低聚糖的结构,并研究其对24种细菌和酵母菌株的益生元效应以及使用RAW 264.7巨噬细胞的抗炎活性。低聚糖生产的最佳条件是培养温度30℃,蔗糖和麦芽糖浓度分别为9.6%和7.4%。基于核磁共振氢谱研究,这些低聚糖被鉴定为葡萄糖低聚糖,其由23.63%的α-1,4糖苷键和76.37%的α-1,6糖苷键组成,平均分子量为1137 Da。这些低聚糖促进了包括[此处原文缺失具体菌株名称]等细菌和酵母菌株的生长。当用这些低聚糖处理脂多糖刺激的RAW 264.7细胞时,一氧化氮的产生减少;诱导型一氧化氮合酶、肿瘤坏死因子-α、白细胞介素(IL)-1β、IL-6和IL-10的表达受到抑制;核因子-κB信号通路被抑制。总之,从SBC001获得的葡萄糖低聚糖对六种细菌和酵母菌株表现出益生元效应,并在RAW 264.7巨噬细胞中具有抗炎活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/784b/7835818/cc5fe8412152/microorganisms-09-00200-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/784b/7835818/9a58e039ca97/microorganisms-09-00200-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/784b/7835818/9fb2007e1ee0/microorganisms-09-00200-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/784b/7835818/aaa99d043c45/microorganisms-09-00200-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/784b/7835818/4091ac37eb81/microorganisms-09-00200-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/784b/7835818/316cf925b3c2/microorganisms-09-00200-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/784b/7835818/02fc401683ea/microorganisms-09-00200-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/784b/7835818/ee15e1467221/microorganisms-09-00200-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/784b/7835818/cc5fe8412152/microorganisms-09-00200-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/784b/7835818/9a58e039ca97/microorganisms-09-00200-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/784b/7835818/9fb2007e1ee0/microorganisms-09-00200-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/784b/7835818/aaa99d043c45/microorganisms-09-00200-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/784b/7835818/4091ac37eb81/microorganisms-09-00200-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/784b/7835818/316cf925b3c2/microorganisms-09-00200-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/784b/7835818/02fc401683ea/microorganisms-09-00200-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/784b/7835818/ee15e1467221/microorganisms-09-00200-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/784b/7835818/cc5fe8412152/microorganisms-09-00200-g008.jpg

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