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首页> 外文期刊>World Journal of Microbiology & Biotechnology >Establishment of a transgene expression system for the marine microalga Schizochytrium by 18S rDNA-targeted homologous recombination
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Establishment of a transgene expression system for the marine microalga Schizochytrium by 18S rDNA-targeted homologous recombination

机译:18S rDNA靶向同源重组技术构建海洋微藻裂殖壶菌转基因表达系统

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摘要

Schizochytrium is an established candidate for commercial production of long chain polyunsaturated fatty acids (PUFAs) that are important in human health and aquaculture. Genetic engineering technology has been applied successfully to increase the metabolites in many organisms. In order to use genetic engineering technology to enhance lipid accumulation in Schizochytrium for economically feasible PUFAs production, the transgene expression system should be established first. In the present study, we investigated a novel transgene expression system in Schizochytrium by 18S rDNA-targeted homologous recombination. The targeting vector pBS-18S-ZeoR contains a portion of 18S rDNA from Schizochytrium and the Zeocin resistance gene (Streptoalloteichus hindustanus bleomycin gene, Sh ble gene) expression cassette. This targeting vector was transformed into Schizochytrium by electroporation and the transformants were then selected on Zeocin-containing plates. The exogenous Sh ble gene has been incorporated into the genome of Schizochytrium according to PCR amplification. More importantly, the majority of the transformants showed similar biomass and total lipid to the wild type strain. Our results suggest that the 18S rDNA is a suitable recombination site and this system could be used to introduce new functional genes into Schizochytrium.
机译:裂殖壶菌是长链多不饱和脂肪酸(PUFA)的商业化生产的可靠候选者,对人类健康和水产养殖至关重要。基因工程技术已成功应用于增加许多生物体中的代谢产物。为了利用基因工程技术增强裂殖壶菌中脂质的积累,以经济可行地生产PUFA,应首先建立转基因表达系统。在本研究中,我们通过靶向18S rDNA的同源重组研究了裂殖壶菌属中的新型转基因表达系统。靶向载体pBS-18S-ZeoR包含来自裂殖壶菌的部分18S rDNA和Zeocin抗性基因(Streptoalloteichus hindustanus bleomycin基因,Sh ble基因)表达盒。通过电穿孔将该靶向载体转化为裂殖壶菌,然后在含Zeocin的平板上选择转化体。根据PCR扩增,已将外源Sh ble基因掺入到裂殖壶菌的基因组中。更重要的是,大多数转化体显示出与野生型菌株相似的生物量和总脂质。我们的结果表明18S rDNA是合适的重组位点,该系统可用于将新的功能基因引入裂殖壶菌。

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