引用本文:	夏长革,崔静,王中华,李成华,周君,李晔,张春丹,李太武,苏秀榕.南移养殖刺参(Apostichopus japonicus)原肌球蛋白基因的原核表达研究.海洋与湖沼,2013,44(1):205-208.

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*南移养殖刺参(Apostichopus japonicus)原肌球蛋白基因的原核表达研究*
夏长革^1,2, 崔静¹, 王中华¹, 李成华¹, 周君¹, 李晔¹, 张春丹¹, 李太武³, 苏秀榕¹
1.宁波大学海洋学院;2.长春市新立城水库管理局;3.宁波城市职业技术学院

摘要:

本研究克隆和表达了刺参原肌球蛋白(Tropomyosin, TRP)基因, 进一步研究刺参再生过程中重要分子的功能。结果表明, TRP基因序列总长为1203bp, 5′非翻译区为105bp, 3′非翻译区为240bp, 该序列包含一个855bp 的开放阅读框(open reading frame, ORF), 编码284 个氨基酸, 分子量为33.27kDa, 等电点为4.56。利用Escherichia coli对TRP进行了体外重组表达, 在1mmol/L IPTG和37℃条件下诱导, 能产生分子质量约为38kDa的重组蛋白, Western blot证明重组TRP与鼠抗刺参原肌球蛋白的多克隆抗体能特异性结合。

关键词: 刺参, 原肌球蛋白, 克隆与表达, 蛋白质印迹法

DOI：10.11693/hyhz201301030030

分类号:

基金项目:国家农业科技成果转化资金, 2007GB2C220359 号; 浙江省重大科技专项(优先主题)重大农业项目, 2008C02009-Ⅱ-2 号; 宁波市农业科技成果转化资金, 2007C30001 号

附件

PROKARYOTIC EXPRESSION OF TROPOMYOSIN GENE FROM SOUTH CULTURED SEA CUCUMBER APOSTICHOPUS JAPONICUS

XIA Chang-Ge^1,2, CUI Jing¹, WANG Zhong-Hua¹, LI Cheng-Hua¹, LI Cheng-Hua¹, LI Ye¹, ZHANG Chun-Dan¹, LI Tai-Wu³, SU Xiu-Rong¹

1.School of Marine Science, Ningbo University;2.Xinlicheng Reservoir Management Bureau in Changchun;3.Ningbo City College of Vocational Technology

Abstract:

Regeneration is a vital physiological process in Apostichopus japonicus, and was considered to a good model for organ and tissues culture in vitro. In order to further understand the function of some key molecules in this process, the tropomyosin gene of A. japonicus was cloned and expressed. The full-length of tropomyosin gene was 1203bp including a 105bp of 5′untranslated region (UTR), a 240bp of 3′UTR and a 855bp of open reading frame (ORF) encoding a polypeptide of 284 amino acids. The estimated molecular mass of tropomyosin gene is 33.27kDa, and the theoretical isoelectric point is 4.56. The recombinant pET-Trp protein was successfully expressed in E. coli. The recombinant protein pET-Trp had clearly visible band in 38kDa. The polyclonal antibody could specifically bind to the recombinant TRP by Western blot.

Key words: Apostichopus japonicus, Tropomyosin, Cloning and expression, Western blot