科技导报
科技導報
과기도보
SCIENCE & TECHNOLOGY REVIEW
2010年
4期
37-41
,共5页
朱丽萍%颜世敢%李雁冰%周百成
硃麗萍%顏世敢%李雁冰%週百成
주려평%안세감%리안빙%주백성
多管藻%藻胆蛋白%R-藻红蛋白%R-藻蓝蛋白%得率%纯度%硫酸铵沉淀
多管藻%藻膽蛋白%R-藻紅蛋白%R-藻藍蛋白%得率%純度%硫痠銨沉澱
다관조%조담단백%R-조홍단백%R-조람단백%득솔%순도%류산안침정
Polysiphonia urceolata%phycobiliprotein%R-phycoerythrin%R-phycocyanin%recovery%purity%ammonium sulfate precipitation
藻胆蛋白是一类用途广泛、市场前景广阔的天然色素蛋白,但分离纯化困难.粗提条件优化对最终获得的藻胆蛋白的得率和纯度影响较大.研究了硫酸铵饱和度、盐析次数、分级盐析对海洋红藻多管藻R-藻红蛋白(RPE)和R-藻蓝蛋白(RPC)提取得率和纯度的影响.结果表明,多管藻RPE和RPC的得率随硫酸铵饱和度的提高而增加.饱和度为60%时得率最高,分别为91.59%、97.98%.饱和度20%的硫酸铵仍能沉淀47.3%的RPE和24.8%的RPC.RPE的纯度随硫酸铵饱和度的提高而降低,但RPC纯度随硫酸铵饱和度的提高而增加,至饱和度为45%时纯度最高,之后随饱和度的提高而缓慢降低.饱和度<40%时,RPE/RPC得率比随硫酸铵饱和度提高而增加;饱和度>40%时,RPE/RPC得率比趋于稳定.硫酸铵盐析2次与盐析1次相比,RPE、RPC的得率降低,但纯度提高.二步法盐析比一步法盐析RPE、RPC的纯度分别提高122.42%、18.67%,但得率降低.因此硫酸铵盐析提取多管藻RPE、RPC时,以饱和度60%为宜,盐析2次,二步法盐析有利于藻胆蛋白纯度的提高,二步法盐析时初次使用的硫酸铵饱和度应<20%.藻胆蛋白盐析条件优化可为藻胆蛋白的进一步分离纯化奠定基础.
藻膽蛋白是一類用途廣汎、市場前景廣闊的天然色素蛋白,但分離純化睏難.粗提條件優化對最終穫得的藻膽蛋白的得率和純度影響較大.研究瞭硫痠銨飽和度、鹽析次數、分級鹽析對海洋紅藻多管藻R-藻紅蛋白(RPE)和R-藻藍蛋白(RPC)提取得率和純度的影響.結果錶明,多管藻RPE和RPC的得率隨硫痠銨飽和度的提高而增加.飽和度為60%時得率最高,分彆為91.59%、97.98%.飽和度20%的硫痠銨仍能沉澱47.3%的RPE和24.8%的RPC.RPE的純度隨硫痠銨飽和度的提高而降低,但RPC純度隨硫痠銨飽和度的提高而增加,至飽和度為45%時純度最高,之後隨飽和度的提高而緩慢降低.飽和度<40%時,RPE/RPC得率比隨硫痠銨飽和度提高而增加;飽和度>40%時,RPE/RPC得率比趨于穩定.硫痠銨鹽析2次與鹽析1次相比,RPE、RPC的得率降低,但純度提高.二步法鹽析比一步法鹽析RPE、RPC的純度分彆提高122.42%、18.67%,但得率降低.因此硫痠銨鹽析提取多管藻RPE、RPC時,以飽和度60%為宜,鹽析2次,二步法鹽析有利于藻膽蛋白純度的提高,二步法鹽析時初次使用的硫痠銨飽和度應<20%.藻膽蛋白鹽析條件優化可為藻膽蛋白的進一步分離純化奠定基礎.
조담단백시일류용도엄범、시장전경엄활적천연색소단백,단분리순화곤난.조제조건우화대최종획득적조담단백적득솔화순도영향교대.연구료류산안포화도、염석차수、분급염석대해양홍조다관조R-조홍단백(RPE)화R-조람단백(RPC)제취득솔화순도적영향.결과표명,다관조RPE화RPC적득솔수류산안포화도적제고이증가.포화도위60%시득솔최고,분별위91.59%、97.98%.포화도20%적류산안잉능침정47.3%적RPE화24.8%적RPC.RPE적순도수류산안포화도적제고이강저,단RPC순도수류산안포화도적제고이증가,지포화도위45%시순도최고,지후수포화도적제고이완만강저.포화도<40%시,RPE/RPC득솔비수류산안포화도제고이증가;포화도>40%시,RPE/RPC득솔비추우은정.류산안염석2차여염석1차상비,RPE、RPC적득솔강저,단순도제고.이보법염석비일보법염석RPE、RPC적순도분별제고122.42%、18.67%,단득솔강저.인차류산안염석제취다관조RPE、RPC시,이포화도60%위의,염석2차,이보법염석유리우조담단백순도적제고,이보법염석시초차사용적류산안포화도응<20%.조담단백염석조건우화가위조담단백적진일보분리순화전정기출.
Phycobiliproteins are a family of natural pigment proteins with wide applications and promising market prospects,but their extraction and purification is difficult.Extraction optimization plays an important role in the recovery and purification of the final phycobiliproteins.In this paper,ammonium sulfate saturation,precipitation frequency,ammonium sulfate fractionation are employed to extract R-phycoerythrin and R-phycocyanin from marine red alga Polysiphonia urceolata.The results show that the yields of RPE and RPC are increased with increasing ammonium sulfate saturation.At 60%saturation,their yields reach the highest,up to 91.59%and 97.98%,respectively.20%saturation could still precipitate 47.3%of RPE and 24.8%of RPC.The purity of RPE is decreased with increasing salt concentration.However,RPC purity is increased with increasing ammonium sulfate saturation,at 45%saturation,the purity reaches the highest,and then slowly decreases as the saturation further increases.During the saturation of 20%~40%,the recovery ratio of RPE and RPC increases with increasing salt concentration;at 40%.the ratio reaches the highest,then is stabilized above 40%.The twice ammonium sulfate precipitation is better than once for RPE and RPC extraction,their yields fall,but their purity is increased:Ammonium sulfate fractionation could significantly increase the purity of RPE and RPC,by 122.42%and 18.67%,as compared to one-step salting,but their yield is decreased significantly.So 60%saturation of ammonium sulfate is suitable for extraction of RPE and RPC from Polysiphonia urceolata,twice salting and two-step fractionation are good for purity increasing,but the first fractionation saturation of ammonium sulfate should be below 20%.This study can be a help for the phycobiliproteins purification.