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Optimization of the Purification Methods for Recovery of Recombinant Growth Hormone from Paralichthys olivaceus 被引量:2

Optimization of the Purification Methods for Recovery of Recombinant Growth Hormone from Paralichthys olivaceus
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摘要 This study aimed to optimize the purification of recombinant growth hormone from Paralichthys olivaceus. Recombinant flounder growth hormone (r-fGH) was expressed by Escherichia coli in form of inclusion body or as soluble protein under different inducing conditions. The inclusion body was renatured using two recovery methods, i.e., dilution and dialysis. Thereafter, the refolded protein was purified by Glutathione Sepharase 4B affinity chromatography and r-fGH was obtained by cleavage of thrombin. For soluble products, r-fGH was directly purified from the lysates by Glutathione Sepharase 4B affinity chromatography. ELISA-receptor assay demonstrated that despite its low receptor binding activity, the r-fGH purified from refolded inclusion body had a higher yield (2.605 mg L^-1) than that from soluble protein (1.964 mg L^-l). Of the tested recovery methods, addition of renaturing buffer (pH 8.5) into denatured inclusion body yielded the best recovery rate (17.9%). This work provided an optimized purification method for high recovery of r-fGH, thus contributing to the application of r-fGH to aquaculture. This study aimed to optimize the purification of recombinant growth hormone from Paralichthys olivaceus. Recombinant flounder growth hormone (r-fGH) was expressed by Escherichia coli in form of inclusion body or as soluble protein under different inducing conditions. The inclusion body was renatured using two recovery methods, i.e., dilution and dialysis. Thereafter, the refolded protein was purified by Glutathione Sepharase 4B affinity chromatography and r-fGH was obtained by cleavage of thrombin. For soluble products, r-fGH was directly purified from the lysates by Glutathione Sepharase 4B affinity chromatography. ELISA-receptor assay demonstrated that despite its low receptor binding activity, the r-fGH purified from refolded inclusion body had a higher yield (2.605 mgL-1) than that from soluble protein (1.964 mgL-1). Of the tested recovery methods, addition of renaturing buffer (pH 8.5) into denatured inclusion body yielded the best recovery rate (17.9%). This work provided an optimized purification method for high recovery of r-fGH, thus contributing to the application of r-fGH to aquaculture.
出处 《Journal of Ocean University of China》 SCIE CAS 2013年第1期169-174,共6页 中国海洋大学学报(英文版)
基金 supported by the National Natural Science Foundation of China (No.30901111) the China Agriculture Research System (CARS-50) the key Project of Chinese Ministry of Education (No.108083)
关键词 Paralichthys olivaceus growth hormone fusion expression PURIFICATION receptor binding activity 重组人生长激素 纯化方法 优化 牙鲆 可溶性蛋白质 包涵体纯化 大肠杆菌表达 受体结合活性
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