生物加工过程
生物加工過程
생물가공과정
CHINESE JOURNAL OF BIOPROCESS ENGINEERING
2014年
2期
44-50
,共7页
李佳媚%孙润广%郭国赟%张智
李佳媚%孫潤廣%郭國赟%張智
리가미%손윤엄%곽국빈%장지
抗氧化%抗肿瘤%滑子菇%滑子菇多糖
抗氧化%抗腫瘤%滑子菇%滑子菇多糖
항양화%항종류%활자고%활자고다당
antioxidant%antitumor%Pholiota nameko%polysaccharide
为了研究滑子菇水提粗多糖(PNP)的体外生物活性,对滑子菇多糖的总还原力、清除,1二苯基苦苯肼自由基( DPPH·)和由Fe2+诱发的脂质过氧化反应的抑制作用进行研究,采用MTT比色法和胎盘蓝细胞计数检测对滑子菇水提粗多糖的体外抑制K562细胞生长作用进行了研究,采用流失细胞术对滑子菇多糖作用人白血病K562细胞后的细胞周期进行了研究。结果表明:滑子菇水提粗多糖PNP 具有一定的还原能力;在高质量浓度(800μg/mL)时具有接近于Vc清除DPPH·的能力,达.28%;PNP对Fe2+诱发的脂质过氧化反应具有一定的抑制作用,并且随着浓度的增加抑制作用逐渐增强,但总的增长趋势不大;MTT实验表明PNP对K562细胞的体外增长有抑制作用,在质量浓度为μg/mL和作用时间为 h时,可达到最高的抑制率.03%。流式细胞术对细胞周期的检测表明滑子菇多糖能够阻滞人白血病K562细胞于G1期。
為瞭研究滑子菇水提粗多糖(PNP)的體外生物活性,對滑子菇多糖的總還原力、清除,1二苯基苦苯肼自由基( DPPH·)和由Fe2+誘髮的脂質過氧化反應的抑製作用進行研究,採用MTT比色法和胎盤藍細胞計數檢測對滑子菇水提粗多糖的體外抑製K562細胞生長作用進行瞭研究,採用流失細胞術對滑子菇多糖作用人白血病K562細胞後的細胞週期進行瞭研究。結果錶明:滑子菇水提粗多糖PNP 具有一定的還原能力;在高質量濃度(800μg/mL)時具有接近于Vc清除DPPH·的能力,達.28%;PNP對Fe2+誘髮的脂質過氧化反應具有一定的抑製作用,併且隨著濃度的增加抑製作用逐漸增彊,但總的增長趨勢不大;MTT實驗錶明PNP對K562細胞的體外增長有抑製作用,在質量濃度為μg/mL和作用時間為 h時,可達到最高的抑製率.03%。流式細胞術對細胞週期的檢測錶明滑子菇多糖能夠阻滯人白血病K562細胞于G1期。
위료연구활자고수제조다당(PNP)적체외생물활성,대활자고다당적총환원력、청제,1이분기고분정자유기( DPPH·)화유Fe2+유발적지질과양화반응적억제작용진행연구,채용MTT비색법화태반람세포계수검측대활자고수제조다당적체외억제K562세포생장작용진행료연구,채용류실세포술대활자고다당작용인백혈병K562세포후적세포주기진행료연구。결과표명:활자고수제조다당PNP 구유일정적환원능력;재고질량농도(800μg/mL)시구유접근우Vc청제DPPH·적능력,체.28%;PNP대Fe2+유발적지질과양화반응구유일정적억제작용,병차수착농도적증가억제작용축점증강,단총적증장추세불대;MTT실험표명PNP대K562세포적체외증장유억제작용,재질량농도위μg/mL화작용시간위 h시,가체도최고적억제솔.03%。류식세포술대세포주기적검측표명활자고다당능구조체인백혈병K562세포우G1기。
Fungus polysaccharide had an important value of biological activity,Pholiota nameko was plant fungus of edible medicinal value. Water-extracted crude polysaccharides of Pholiota nameko, were investigated. Their antioxidant activity was studied by DPPH method, the lipid peroxidation by Fe2+method,the antitumor activity by MTT assay,and placenta blue cell count detection.The flow cytometer was used to study effects of PNP on K562 cell cycle.Experimental results showed that PNP had inhibitory ability and DPPH free radical scavenging capability similar to that of Vc on high concentration.PNP had actions on lipid peroxidation with the increasing of the concentration,the inhibitory effect increased.MTT assay showed that PNP inhibited the growth of K562 cells in vitro,exhibited dose-dependent and time-based effect,the highest inhibition rate is 35.03% when treated with PNP in 800 μg/mL for 48 h.In addition,the result of cell cycle analysis by flow cytometer showed that PNP could block the K562 cell in G1 phase.