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One-step chromatographic procedure for purification of B-phycoerythrin from Porphyridium cruentum

机译:一步法从苦菜卟啉中纯化B-藻红蛋白

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B-phycoerythrin (B-PE) was separated and purified from microalga Porphyridium cruentum using one-step chromatographic method. Phycobiliproteins in P. cruentum was extracted by osmotic shock and initially purified by ultrafiltration. Further purification was carried out with a SOURCE 15Q exchange column and analytical grade B-PE was obtained with a purity ratio (A(545)/A(280)) of 5.1 and a yield of 68.5%. It showed a double absorption peaks at 545 nm and 565 nm and a shoulder peak at 498 nm, and displayed a fluorescence emission maximum at 580 nm. The analysis by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) showed a bulky band between 18 and 20 kDa which could be assigned to subunits alpha and beta and a low intensity band of 27 kDa assigned to gamma subunit. Our protocol provides attractive alternative to consider for the purification procedure to obtain analytical grade B-PE at commercial level. (C) 2016 Elsevier Inc. All rights reserved.
机译:使用一步色谱法从微藻克鲁氏卟啉菌中分离纯化B-藻红蛋白(B-PE)。通过渗透压休克提取苦瓜中的藻胆蛋白,并首先通过超滤纯化。用SOURCE 15Q交换柱进行进一步纯化,得到分析级B-PE,纯度比(A(545)/ A(280))为5.1,收率68.5%。其在545nm和565nm处显示双吸收峰,在498nm处显示肩峰,并且在580nm处显示最大荧光发射。通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)进行的分析显示,在18至20 kDa之间的大条带可以分配给α和β亚基,在27 kDa的低强度条带分配给γ亚基。我们的方案提供了诱人的替代方案,供您考虑以纯化方法获得商业级分析级B-PE。 (C)2016 Elsevier Inc.保留所有权利。

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