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机构地区:[1]浙江育英职业技术学院生物技术系,浙江杭州310018 [2]浙江工商大学食品与生物工程学院,浙江杭州310018
出 处:《食品科学》2015年第8期61-66,共6页Food Science
基 金:浙江省教育科学规划研究课题(SCG348);国家自然科学基金青年科学基金项目(31101339)
摘 要:采用水提醇沉法,通过单因素试验和正交试验研究黄花菜粗多糖(crude polysaccharides from Hemerocallis citrina Baroni,CPH)的提取工艺,并利用Sevag法和H2O2氧化法提纯制备黄花菜精制多糖(deproteinized polysaccharides from Hemerocallis citrina Baroni,DPH),通过理化检验和紫外光谱、红外光谱、高效液相色谱分析,考察DPH的性质与结构,同时还研究DPH对铜绿假单胞菌、大肠杆菌、金黄色葡萄球菌、白假丝酵母、黑曲霉的抑制作用。正交试验结果表明,CPH最优提取条件为浸提温度75℃、浸提时间3 h、液固比20∶1(m L/g)、浸提2次。在此条件下,CPH提取率为28.36%。理化性质、光谱与色谱特征表明,DPH是一种具有α-型吡喃糖苷结构的水溶性杂多糖,是由L-鼠李糖、D-木糖、L-阿拉伯糖、D-甘露糖、D-葡萄糖和D-半乳糖组成,且可能是一种与蛋白质或多肽以共价键结合的糖复合物。抑菌实验结果表明,DPH对金黄色葡萄球菌、铜绿假单胞菌、大肠杆菌具有明显的抑制作用,相应的最小抑菌质量浓度分别为10、10、25 mg/m L。The extraction of crude polysaccharides from Hemerocallis citrina Baroni(CPH) by water extraction and alcohol precipitation was optimized using one-factor-at-a-time and orthogonal array methods. After CPH was deproteinized by Sevag method and decolorized by H2O2 oxidation method, the physicochemical properties and structure of the deproteinized polysaccharides from(DPH) were analyzed and characterized by UV spectrometry, infrared(IR) spectrometry and high performance liquid chromatography(HPLC). Meanwhile, the inhibitory activities of DPH against Pseudomonas aeruginosa, Escherichia coli, Staphylococcus aureus, Candida albicans and Aspergillus niger were investigated. The results showed that the optimal conditions for CPH extraction were determined as two extraction cycles with distilled water at a solvent/solid ratio of 20:1(m L/g) at 75 ℃ for 3 h. Under these conditions, the extraction yield of CPH was 28.36%. Meanwhile, DPH was water-soluble heteropolysaccharides which possessed the structure of α-pyranosides and consisted of L-rhamnose, D-xylose, L-arabinose, D-mannose, D-glucose and D-galactose. DPH was probably formed by conjugation of polysaccharides with proteins or polypeptides through peptide bonds. Furthermore, DPH had strong inhibitory activities against Staphylococcus aureus, Pseudomonas aeruginosa, and Escherichia coli, their corresponding minimum inhibitory concentrations(MICs) were 10, 10, and 25 mg/m L, respectively.
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