一种毛尖茶叶多糖MTP06的提取分离及其活性测定

本研究对一种毛尖茶叶多糖的结构与活性开展了研究。采用水提醇沉法提取毛尖茶叶粗多糖,经除蛋白后得到精制多糖(MP),以不同的柱层析方法对MP进行多次分离纯化,得到1个均一组分的毛尖茶叶多糖(Maojian Tea Polysaccharides No.06,MTP06)。采用1,1–二苯基–2–三硝基苯肼(1,1-diphenyl-2-picrylhydrazyl radical 2,2-diphenyl-1-(2,4,6-trinitrophenyl)hydrazyl,DPPH)自由基清除、小鼠免疫细胞RAW264.7增殖、吞噬能力和产生NO等试验方法对MTP06的活性进行研究。结果显示MTP06对0.1 mmol·L~(-1) DPPH溶液的自由基清除率为30.85%,对小鼠巨噬细胞RAW264.7的增殖、吞噬能力和产生NO的能力均有促进作用,与空白对照组间有显著差异(P0.01),且质量浓度为500 mg·L~(-1)时,活性最大。

Purification and Activity Determination of Polysaccharides MTP06 from Maojian Tea

To investigate the structure and activity of polysaccharides (MTP06), the polysaccharides were extracted and purified from Maojian tea. The refined Maojian tea polysaccharides (MP) were obtained after removing proteins. Different column chromatography methods were used for several times to purify the MP and an uniform polysaccharide named MTP06 was obtained. The effects of MTP06 on DPPH radical-scavenging activity, cell viability, engulfment capability and NO production of RAW264.7 macrophages were investigated . The results showed that the free radical scavenging rate of MTP06 to 0.1 mmol·L-1 DPPH solution was 30.85%. The highest viability, engulfment capability and NO production of RAW264.7 macrophages had been stimulated by MTP06 at 500 mg·L-1. The present results confirmed MTP06 can eliminate DPPH radicals and stimulate cell viabilities.