...
首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >Purification of R-phycoerythrin from Gracilaria lemaneiformis by centrifugal precipitation chromatography
【24h】

Purification of R-phycoerythrin from Gracilaria lemaneiformis by centrifugal precipitation chromatography

机译:通过离心沉淀色谱法从Gracilaria Lemaneificis纯化R-植物植物

获取原文
获取原文并翻译 | 示例
           

摘要

Centrifugal precipitation chromatography (CpC) is a powerful chromatographic technique invented in the year 2000 but so far very little applied. The method combines dialysis, counter-current and salting out processes. The separation rotor consists of two identical spiral channels separated by a dialysis membrane (6-8 K MW cut-off) in which the upper channel is eluted with an ammonium sulfate gradient and the lower channel with water, and the mixtures are separated according to their solubility in ammonium sulfate as a chromatographic technique. In the present study, the method was successfully applied for separation and purification of R-phycoerythrin (R-PE), a protein widely used as a fluorescent probe, from the red alga Gracilaria lemaneiformis. The separation was performed with the elution of ammonium sulfate from 50% to 0% in 21.5 h at a flow rate of 0.5 ml/min, while the lower channel was eluted with water at a flow rate of 0.05 ml/min after sample charge, and the column was rotated at 200 rpm. After a single run, the absorbance ratio A(565)/A(280) (a criterion for the purity of R-PE) was increased from 0.5 of the crude to 6.5. The purified R-PE exhibited a typical "three peaks" spectrum with absorbance maximum at 497, 538 and 565 nm. The Native-PAGE showed one single protein band and 20 kDa (subunits alpha and beta) and 30 kDa (subunit gamma) can be observed in SDS-PAGE analysis which were consistent with the (alpha beta)(6 gamma) subunit composition of R-PE. The results indicated that CpC is an efficient method to obtain protein with the high purity from a complex source.
机译:离心沉淀色谱(CPC)是2000年发明的强大色谱技术,但到目前为止申请甚微。该方法结合了透析,逆流和盐水过程。分离转子由两种相同的螺旋通道组成,其由透析膜(6-8k Mw截止)分开,其中上通道用硫酸铵梯度和下沟道洗脱,并且根据它们在硫酸铵中的溶解度作为色谱技术。在本研究中,该方法被成功地应用于R-Phycoerythrin(R-PE)的分离和纯化,来自红藻藻属植物的红藻类探针广泛用作荧光探针的蛋白质。在0.5ml / min的流速下,在21.5小时内从50%至0%的硫酸铵洗脱硫酸铵的分离,而在样品电荷后,用水以0.05ml / min的流速洗脱下沟道。并且柱子以200rpm旋转。在一次运行之后,吸光度比a(565)/ a(280)(R-PE的纯度的标准)从粗产至6.5的0.5增加。纯化的R-PE在497,538和565nm处表现出典型的“三峰”光谱,吸光度最大。在SDS-PAGE分析中,本地页面显示出一个单一蛋白质带和20kDA(亚基α和β)和30kDa(亚基γ),其与R的(αβ)(6γ)亚基组合物一致-PE。结果表明,CPC是从复杂源的高纯度获得蛋白质的有效方法。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号