Malairaj Sathuvan, Muthu Sakthivel, Gopal Venkatesh Babu, Perumal Palani, Ramasamy Rengasamy
Centre for Advanced Studies in Botany, University of Madras, Guindy Campus, Chennai 600 025, Tamilnadu, India.
Centre for Advanced Studies in Botany, University of Madras, Guindy Campus, Chennai 600 025, Tamilnadu, India.
J Chromatogr A. 2016 Jul 8;1454:120-6. doi: 10.1016/j.chroma.2016.05.063. Epub 2016 May 20.
R-Phycoerythrin is one of the phycobiliproteins widely found in seaweeds. In this study, we have shown to extract and purify R-Phycoerythrin from the south east cost Indian red seaweed Halymenia floresia. R-Phycoerythrin was extracted in 50mM phosphate buffer (pH 7.0). The preparative native PAGE purification was employed alternative to the chromatography and therefore can be scaled up efficiently. Both the yield and the purity of R-Phycoerythrin are very effective. The purified R-Phycoerythrin showed a single band on the examination by native PAGE electrophrosis. SDS-PAGE analysis showed five bands at 16kDa, 21kDa, 30kDa, 39kDa and 47kDa which corresponds to the α, β and γ', γ and αβ subunits. This preparative method for R-Phycoerythrin purification can offer a reference for R-Phycoerythrin purification from other marine red macro algae.
藻红蛋白是一种广泛存在于海藻中的藻胆蛋白。在本研究中,我们已证明可从印度东南部沿海的红色海藻弗洛雷斯海膜中提取和纯化藻红蛋白。藻红蛋白在50mM磷酸盐缓冲液(pH 7.0)中提取。采用制备型天然聚丙烯酰胺凝胶电泳纯化替代色谱法,因此可以有效地扩大规模。藻红蛋白的产量和纯度都非常高。纯化后的藻红蛋白在天然聚丙烯酰胺凝胶电泳检测中显示为单一条带。十二烷基硫酸钠-聚丙烯酰胺凝胶电泳分析显示在16kDa、21kDa、30kDa、39kDa和47kDa处有五条带,分别对应于α、β和γ'、γ以及αβ亚基。这种藻红蛋白纯化的制备方法可为从其他海洋红色大型藻类中纯化藻红蛋白提供参考。