中国医药科学
中國醫藥科學
중국의약과학
CHINA MEDICINE AND PHARMACY
2014年
23期
74-76,210
,共4页
孙鹏珍%刘月%王大可%李爱欣%王淑敏
孫鵬珍%劉月%王大可%李愛訢%王淑敏
손붕진%류월%왕대가%리애흔%왕숙민
裂褶菌%多糖%蛋白质%含量测定
裂褶菌%多糖%蛋白質%含量測定
렬습균%다당%단백질%함량측정
Schizophyllumcommune%Polysaccharide%Protein%Content determination
目的:建立裂褶菌子实体中多糖、蛋白质含量的测定方法。方法采用分光光度法测定多糖和总蛋白含量,检测波长分别为479nm和595nm。结果多糖浓度在0.012~0.040mg/mL范围内具有良好的线性关系,回归方程为Y=23.0753X-0.1733,r=0.9998,子实体多糖含量为7.26%;蛋白浓度在0.0078~0.0321mg/mL范围内具有良好的线性关系,回归方程为Y=20.0830X+0.1451,r=0.9997,子实体总蛋白含量为0.2631%。结论本研究建立的方法简便、快速、准确,重复性好,为裂褶菌子实体多糖和蛋白质含量的测定提供了依据。
目的:建立裂褶菌子實體中多糖、蛋白質含量的測定方法。方法採用分光光度法測定多糖和總蛋白含量,檢測波長分彆為479nm和595nm。結果多糖濃度在0.012~0.040mg/mL範圍內具有良好的線性關繫,迴歸方程為Y=23.0753X-0.1733,r=0.9998,子實體多糖含量為7.26%;蛋白濃度在0.0078~0.0321mg/mL範圍內具有良好的線性關繫,迴歸方程為Y=20.0830X+0.1451,r=0.9997,子實體總蛋白含量為0.2631%。結論本研究建立的方法簡便、快速、準確,重複性好,為裂褶菌子實體多糖和蛋白質含量的測定提供瞭依據。
목적:건립렬습균자실체중다당、단백질함량적측정방법。방법채용분광광도법측정다당화총단백함량,검측파장분별위479nm화595nm。결과다당농도재0.012~0.040mg/mL범위내구유량호적선성관계,회귀방정위Y=23.0753X-0.1733,r=0.9998,자실체다당함량위7.26%;단백농도재0.0078~0.0321mg/mL범위내구유량호적선성관계,회귀방정위Y=20.0830X+0.1451,r=0.9997,자실체총단백함량위0.2631%。결론본연구건립적방법간편、쾌속、준학,중복성호,위렬습균자실체다당화단백질함량적측정제공료의거。
Objective Set up Schizophyllumcommune sporophore polysaccharide and protein content determination method. Methods Use spectrophotometry to determine polysaccharide and protein content, detection wavelength is 479nm and 595nm. Results Polysaccharide concentration possesses good linear relationship between 0.012-0.010mg/mL, regression equation is Y=23.0753X-0.1733, r=0.9998, sporophore polysaccharide content is 7.26%; protein concentration possesses good linear relationship between 0.0078-0.0321mg/mL, regression equation is Y=20.0830X+0.1451, r=0.9997, sporophore total protein is 0.2631%. Conclusion The method set up by the research is simple, fast, accurate and has good repeatability which provides basis for Schizophyllumcommune sporophore polysaccharide and protein content determination.