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Cloning and characterization of hemerythrin gene from Sipuncula Phascolosoma esculenta

机译:七叶草(Sipuncula Phascolosoma esculenta)的菊红素基因的克隆与鉴定

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摘要

Hemerythrin is a non-heme respiratory protein involved in oxygen storage and transport in invertebrates. In the present study, the hemerythrin cDNA was cloned from Phascolosoma esculenta (denoted as PeHr) by PCR and rapid amplification of cDNA ends approaches. The full-length PeHr consisted of 770 bp containing of a 5′-terminal untranslated region (UTR) of 83 bp, a 3′-terminal UTR of 327 bp, and a coding domain sequence of 360 bp encoding a polypeptide of 120 amino acids with estimated molecular mass of 13.6 kDa and theoretical isoelectric point of 5.78. The expression profiles of PeHr were evaluated by real-time RT-PCR under blood loss stress. The expression level of PeHr was significantly up-regulated from 45 to 48 h, then slightly recovered to its original level. The coding sequence of the PeHr was cloned and expressed in Escherichia coli BL21 (DE3) for antibodies preparation. Western blotting analysis conformed that the generated antibodies could specifically identify not only recombinant product, but also native protein from the total protein extraction. Our results indicated that PeHr might be involved into haemocytes regeneration, and its function roles should be further investigated by the generated antibodies.
机译:Hemerythrin是一种非血红素呼吸蛋白,参与无脊椎动物的氧气存储和运输。在本研究中,通过PCR从嗜血杆菌(Phascolosoma esculenta)(称为PeHr)中克隆了hemerythrin cDNA,并快速扩增了cDNA末端。全长PeHr由770 bp的5'端非翻译区(UTR)的83 bp,3'端的UTR 327 bp的组成和360 bp的编码域序列组成,编码120个氨基酸估计分子量为13.6 kDa,理论等电点为5.78。在失血压力下,通过实时RT-PCR评估了PeHr的表达谱。 PeHr的表达水平从45h显着上调至48h,然后略微恢复至原始水平。克隆PeHr的编码序列并在大肠杆菌BL21(DE3)中表达以制备抗体。 Western印迹分析证实,所产生的抗体不仅可以特异性地鉴定重组产物,而且可以从总蛋白提取物中特异性鉴定天然蛋白。我们的结果表明,PeHr可能参与了血细胞的再生,其功能作用应通过产生的抗体进一步研究。

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