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由刺槐豆胶经GH-26内切-β-1,4-甘露聚糖酶(ManB-1601)产生的β-甘露寡糖的结构表征及体外发酵

Structural Characterization and in Vitro Fermentation of β-Mannooligosaccharides Produced from Locust Bean Gum by GH-26 endo-β-1,4-Mannanase (ManB-1601).

作者信息

Srivastava Praveen Kumar, Panwar Deepesh, Prashanth K V Harish, Kapoor Mukesh

机构信息

Academy of Scientific and Innovative Research (AcSIR) , CSIR-CFTRI Campus, Mysuru-570 020, India.

出版信息

J Agric Food Chem. 2017 Apr 5;65(13):2827-2838. doi: 10.1021/acs.jafc.7b00123. Epub 2017 Mar 28.

Abstract

Size exclusion chromatography of β-mannooligosaccharides (β-MOS) mixtures, obtained from ManB-1601 hydrolysis of locust bean gum, resulted in separation of oligosaccharides with various degrees of polymerization (DP 2, 3, and 5). The oligosaccharides were structurally [ESI-MS, FTIR, XRD, TGA, and NMR (H and C)] and functionally (in vitro fermentation) characterized. DP2 oligosaccharide was composed of two species, (A) mannopyranose β-1,4 mannopyranose and (B) α-1,6-galactosyl-mannopyranose, while DP3 oligosaccharide showed the presence of only one species, i.e. α-d-galactosyl-β-d-mannobiose. ManB-1601 was capable of cleaving near the branch points in the substrate, resulting in oligosaccharides with galactose at the terminal position apart from attacking unsubstituted β-1,4-glycosidic linkages. DP2 and DP3 improved the growth of three out of seven species of Lactobacillus while DP5 resulted in poor growth of all Lactobacillus spp. under in vitro conditions. DP2, DP3, and DP5 were found to inhibit the growth of Escherichia coli, Listeria monocytogenes and Salmonella typhi.

摘要

对刺槐豆胶经ManB-1601水解得到的β-甘露寡糖(β-MOS)混合物进行尺寸排阻色谱分析,可分离出不同聚合度(DP 2、3和5)的寡糖。对这些寡糖进行了结构表征(采用电喷雾电离质谱、傅里叶变换红外光谱、X射线衍射、热重分析以及核磁共振氢谱和碳谱)和功能表征(体外发酵)。DP2寡糖由两种物质组成,即(A)吡喃甘露糖β-1,4-吡喃甘露糖和(B)α-1,6-半乳糖基-吡喃甘露糖,而DP3寡糖仅有一种物质,即α-d-半乳糖基-β-d-甘露二糖。ManB-1601能够在底物的分支点附近切割,除了攻击未取代的β-1,4-糖苷键外,还会产生末端带有半乳糖的寡糖。在体外条件下,DP2和DP3促进了7种乳酸杆菌中3种的生长,而DP5则导致所有乳酸杆菌属的生长不佳。DP2、DP3和DP5均能抑制大肠杆菌、单核细胞增生李斯特菌和伤寒沙门氏菌的生长。

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