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来自黄粉虫的新型抗冻蛋白AFP72的克隆与表达

Cloning and expression of a novel antifreeze protein AFP72 from the beetle Tenebrio molitor.

作者信息

Yan Qing-Hua, Yang Li, Wang Qing, Zhang Hui-Rong, Shao Qiang

机构信息

Department of Life Science and Technology, Xinxiang Medical University, Xinxiang Henan 453003, P.R. China.

出版信息

Mol Biol (Mosk). 2012 Jul-Aug;46(4):576-83.

Abstract

A novel antifreeze protein AFP72 cDNA (GenBbank accession No. AY929389) was obtained by RT-PCR from Tenebrio molitor. The 216 bp fragment encodes a protein of 72 amino acid residues. Sequence analysis revealed that the cDNA displays a high degree of homology with T. molitor antifreeze proteins, ranging up to 90.78%. Recombinant plasmids pMAL-p2X-afp72 and pMAL-c2X-afp72 were transferred into E. coil TBI to induce a MBP fusion protein by IPTG. The target fusion protein was released from the periplasm and cytoplasm by the cold osmotic shock procedure and sonication respectively. The content of the fusion protein came up to 38.9 and 41.5% of the total dissolved protein, respectively. The fusion protein was purified through an amylose affinity column, and incised by factor Xa. Molecular sieve chromatography was used to achieve a high state of purity of the target protein. The purified target protein displayed a single band in SDS-PAGE. The fusion protein was shown to increase resistance to low temperatures in bacteria. This finding could help in further investigations of the properties and function of antifreeze proteins.

摘要

通过逆转录聚合酶链反应(RT-PCR)从黄粉虫中获得了一种新型抗冻蛋白AFP72的互补DNA(cDNA)(基因银行登录号:AY929389)。这个216碱基对的片段编码一个由72个氨基酸残基组成的蛋白质。序列分析表明,该cDNA与黄粉虫抗冻蛋白具有高度同源性,同源性高达90.78%。重组质粒pMAL-p2X-afp72和pMAL-c2X-afp72被转入大肠杆菌TBI中,通过异丙基-β-D-硫代半乳糖苷(IPTG)诱导产生麦芽糖结合蛋白(MBP)融合蛋白。分别通过冷渗透休克法和超声处理从周质和细胞质中释放目标融合蛋白。融合蛋白的含量分别达到总溶解蛋白的38.9%和41.5%。融合蛋白通过直链淀粉亲和柱进行纯化,并用Xa因子切割。采用分子筛色谱法使目标蛋白达到高纯度状态。纯化后的目标蛋白在十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)中显示为单一条带。结果表明,融合蛋白可增强细菌对低温的抗性。这一发现有助于进一步研究抗冻蛋白的性质和功能。

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