Zhang Yong, Liu Wei, Xu Chunping, Huang Wei, He Peixin
School of Food and Biological Engineering, Zhengzhou University of Light Industry, Zhengzhou, China.
College of Food and Biological Engineering, Zhengzhou University of Light Industry, Zhengzhou, Henan, China; Collaborative Innovation Center of Food Production and Safety, Zhengzhou, Henan, China.
Int J Med Mushrooms. 2017;19(5):395-403. doi: 10.1615/IntJMedMushrooms.v19.i5.20.
In this study, a high yield of crude polysaccharide (16.73 ± 0.756%) was extracted from the spent mushroom substrate of Lentinus edodes using a hot alkali extraction method. Two groups of polysaccharides (designated as LSMS-1 and LSMS-2) were obtained from the crude extract by size exclusion chromatography (SEC), and their molecular characteristics were examined by a multiangle laser-light scattering (MALLS) and refractive index detector system. The weight-average molar masses of LSMS-1 and LSMS-2 were determined to be 6.842 × 106 and 2.154 × 106 g/mol, respectively. The SEC/MALLS analysis revealed that the molecular shapes of LSMS-1 and LSMS-2 were sphere-like forms in aqueous solution. Carbohydrate composition analysis using chromatography--mass spectrometry revealed that they were both acid heteropolysaccharides. LSMS-1 comprised mainly glucose and galacturonic acid, whereas LSMS-2 mainly consisted of xylose and glucuronic acid. Fourier transform infrared spectral analysis of the purified fractions revealed typical characteristic polysaccharide groups. In addition, MTT assays with refined polysaccharide doses of 25, 50, 100, 200, and 400 µg/mL suggested that both of the polysaccharide fractions exhibited antiproliferative activity against 6 tested human tumor cell lines in a concentration-dependent manner, and LSMS-2 had better anticancer capacity in vitro than LSMS-1. The inhibition ratio of LSMS-2 against A549 human lung cancer cells, the SGC7901 gastric cancer cell line, MCF-7 breast cancer cells, the U937 histiocytic lymphoma cell line, and the MG-63 human osteosarcoma cell line reached 43.55%, 29.97%, 19.63%, 18.24%, and 17.93%, respectively, at a concentration of 400 µg/mL.
在本研究中,采用热碱提取法从香菇废弃菌糠中提取出高产率的粗多糖(16.73±0.756%)。通过尺寸排阻色谱(SEC)从粗提物中获得了两组多糖(分别命名为LSMS-1和LSMS-2),并采用多角度激光散射(MALLS)和折射率检测系统对其分子特性进行了检测。测定LSMS-1和LSMS-2的重均摩尔质量分别为6.842×10⁶和2.154×10⁶ g/mol。SEC/MALLS分析表明,LSMS-1和LSMS-2在水溶液中的分子形状为球状。采用色谱-质谱联用技术进行的碳水化合物组成分析表明,它们均为酸性杂多糖。LSMS-1主要由葡萄糖和半乳糖醛酸组成,而LSMS-2主要由木糖和葡萄糖醛酸组成。对纯化组分的傅里叶变换红外光谱分析揭示了典型的多糖基团特征。此外,用25、50、100、200和400 µg/mL的精制多糖剂量进行的MTT试验表明,这两种多糖组分均对6种受试人肿瘤细胞系具有浓度依赖性的抗增殖活性,且LSMS-2在体外的抗癌能力优于LSMS-1。在浓度为400 µg/mL时,LSMS-2对A549人肺癌细胞、SGC7901胃癌细胞系、MCF-7乳腺癌细胞、U937组织细胞淋巴瘤细胞系和MG-63人骨肉瘤细胞系的抑制率分别达到43.55%、29.97%、19.63%、18.24%和17.93%。