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A New Strategy to Produce a Defensin: Stable Production of Mutated NP-1 in Nitrate Reductase-Deficient Chlorella ellipsoidea

机译:产生防御素的新策略:在硝酸还原酶缺陷型小球藻中稳定产生突变的NP-1。

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摘要

Defensins are small cationic peptides that could be used as the potential substitute for antibiotics. However, there is no efficient method for producing defensins. In this study, we developed a new strategy to produce defensin in nitrate reductase (NR)-deficient C. ellipsoidea (nrm-4). We constructed a plant expression vector carrying mutated NP-1 gene (mNP-1), a mature α-defensin NP-1 gene from rabbit with an additional initiator codon in the 5′-terminus, in which the selection markers were NptII and NR genes. We transferred mNP-1 into nrm-4 using electroporation and obtained many transgenic lines with high efficiency under selection chemicals G418 and NaNO3. The mNP-1 was characterized using N-terminal sequencing after being isolated from transgenic lines. Excitingly, mNP-1 was produced at high levels (approximately 11.42 mg/l) even after 15 generations of continuous fermentation. In addition, mNP-1 had strong activity against Escherichia coli at 5 µg/ml. This research developed a new method for producing defensins using genetic engineering.
机译:防御素是小的阳离子肽,可以用作抗生素的潜在替代品。但是,没有生产防御素的有效方法。在这项研究中,我们开发了一种新的策略来在硝酸还原酶(NR)缺乏的椭圆形梭菌(nrm-4)中产生防御素。我们构建了一个携带突变的NP-1基因(mNP-1),来自兔的成熟α-防御素NP-1基因的植物表达载体,该基因在5'-末端带有一个附加的启动子密码子,其中的选择标记是NptII和NR基因。我们通过电穿孔将mNP-1转移到nrm-4中,并在选择化学品G418和NaNO3下高效获得了许多转基因品系。从转基因品系分离后,使用N端测序对mNP-1进行鉴定。令人兴奋的是,即使经过15代连续发酵,mNP-1的产量仍很高(约11.42 mg / l)。另外,mNP-1以5μg/ ml对大肠杆菌具有很强的活性。这项研究开发了一种利用基因工程生产防御素的新方法。

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