Functional expression of FIP-fve, a fungal immunomodulatory protein from the edible mushroom Flammulina velutipes in Pichia pastoris GS115

被引:22
|
作者
Lin, Jing-Wei [1 ,2 ]
Jia, Jia [2 ]
Shen, Yu-Hua [3 ]
Zhong, Ming [2 ]
Chen, Li-Jing [2 ]
Li, Hao-Ge [2 ]
Ma, Hui [2 ]
Guo, Zhi-Fu [2 ]
Qi, Ming-Fang [1 ]
Liu, Li-Xia [4 ]
Li, Tian-Lai [1 ]
机构
[1] Shenyang Agr Univ, Coll Hort, Shenyang 110866, Liaoning Provin, Peoples R China
[2] Shenyang Agr Univ, Coll Biol Sci & Technol, Shenyang 110866, Liaoning Provin, Peoples R China
[3] Chifeng Univ, Coll Life Sci, Chifeng 024000, Inner Mongolia, Peoples R China
[4] NE Normal Univ, Sch Life Sci, Changchun 130024, Jilin Province, Peoples R China
基金
中国国家自然科学基金;
关键词
Flammulina velutipes; Fungal immunomodulatory protein; Shake-flask; Recombinant proteins; Chromatography; LING ZHI-8 LZ-8; MOLECULAR-CLONING; GANODERMA-TSUGAE; PURIFICATION; PEPTIDE; CDNA; GTS;
D O I
10.1016/j.jbiotec.2013.09.013
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
FIP-fve is a bioactive protein isolated from the mushroom Flammulina velutipes, which belongs to the fungal immunomodulatory protein (FIP) family and demonstrates several kinds of biological activities including anti-allergy, anti-tumor and immunomodulation. In the current study, the FIP-fve gene was cloned and expressed in the yeast Pichia pastoris GS115, and its correctness was confirmed by SDS-PAGE and Western blot. Optimal expression of rFIP-fve was observed when the P. pastoris cells were cultured in 1% methanol for 96 h, which resulted in a yield of 258.2 mgl(-1). The rFIP-fve protein was subsequently purified via ammonium sulfate precipitation and Sephadex G-100 gel chromatography. In vitro bioactivity examination showed that rFIP-fve could agglutinate human red blood cells and stimulate the cell viability of murine splenocytes. The immunomodulatory capacity and anti-tumor activity of rFIP-fve were demonstrated by enhanced interleukin-2 secretion and interferon-gamma release from the murine lymphocytes, similar to the biological FIP-fve. In conclusion, the FIP-fve gene was functionally and effectively expressed in P. pastoris, and rFIP-fve displayed biological activities similar to those of native FIP-fve. These results indicated the potential use of rFIP-fve from P. pastoris as an effective and feasible source for therapeutic studies and medical applications. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:527 / 533
页数:7
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