首页 | 本学科首页   官方微博 | 高级检索  
   检索      

灵芝胞外多糖的分离纯化及生物活性
引用本文:李平作,章克昌.灵芝胞外多糖的分离纯化及生物活性[J].微生物学报,2000,40(2):217-220.
作者姓名:李平作  章克昌
作者单位:无锡轻工大学生物工程学院,无锡,214036
摘    要:目前,灵芝多糖的抗肿瘤及免疫活性已得到人们的广泛关注1]。灵芝子实体多糖和发酵过程中产生的胞内和胞外多糖已被国内外的研究者证实都是有效多糖2]。因此利用深层发酵来大规模地生产生物活性多糖是目前灵芝开发利用技术的热点。国内对灵芝培养基的组成、培养方法等已?..

关 键 词:灵芝    胞外多糖    分离和纯化    生物活性
文章编号:0001-6209(2000)02-0217-20
修稿时间:1998-10-13

ISOLATION, PURIFICATION AND BIOACTIVITIES OF EXOPOLY SACCHARIDES FROM FERMENTED BROTH OF GANODERMA LUCIDUM
Li Pingzuo,Zhang Kechang.ISOLATION, PURIFICATION AND BIOACTIVITIES OF EXOPOLY SACCHARIDES FROM FERMENTED BROTH OF GANODERMA LUCIDUM[J].Acta Microbiologica Sinica,2000,40(2):217-220.
Authors:Li Pingzuo  Zhang Kechang
Institution:Li Pingzuo ,Zhang Kechang ;(School of Biotechnology, Wuxi University of Light Industry, Wuxi 214036)
Abstract:The exopolysaccharides of Ganoderma lucidum(GLEP) extracted from the fermentation broth after removing protein by Sevage and protease digestion procedures, were applied to a column of DEAE-cellulose(OH- form), and eluted stepwise with distilled water, sodium hydrogen carbonate (0.1 mol/L, 0.3 mol/L, 0.5 mol/L successively) and 0.1 mol/L sodium hydroxide. Five fractions were obtained, and the main fraction was known as GLEP-I, furthermore subjected to chromatography on a column of SepharoseC1-6B, eluted at a flow rate of 30 mL/(cm2.h), the relative viscosity of sample solution of 1.5. Two fractions, GLEP-IFr1 and GLEP-IFr2 with a ratio of 3.8:1, were obtained. Molecular weight of GLEP-IFr1 and GLEP-IFr2 was estimated to be 38,000 and 22,000 Dalton respectively by Membrane Osmometer. The animal test showed that GLEP-IFr1 could inhibited the growth of Sarcoma 180 tumor in mice. The average inhibition ratio was 57.4% (i.p. 10 mg/kg for 10 days). The result of immunological activity showed that GLEP-IFr1 could significantly improve macrophage cytophagy.
Keywords:Ganoderma lucidum  Exopolysaccharides  Isolation and purification  Bioactivity
本文献已被 CNKI 维普 万方数据 等数据库收录!
点击此处可从《微生物学报》浏览原始摘要信息
点击此处可从《微生物学报》下载免费的PDF全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号