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首页> 外文期刊>Journal of Traditional Chinese Medical Sciences >Improving the accumulation of 18 α-and 18 β-glycyrrhizins by over-expressing GuHMGR, GuSQS1, and GuBAS genes in Glycyrrhiza uralensis
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Improving the accumulation of 18 α-and 18 β-glycyrrhizins by over-expressing GuHMGR, GuSQS1, and GuBAS genes in Glycyrrhiza uralensis

机译:通过过度表达 GuHMGR 提高18 α-和18 β-甘草甜素的积累 uralgyural uralensis 中的 GuSQS 1和 GuBAS 基因

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摘要

Objective To study the influence of over-expression of three functional genes involved in GC biosynthetic pathway, GuHMGR , GuSQS 1, and GuBAS on GC production. Methods Three plant expression vectors were constructed and transformed into Agrobacterium tumefaciens EHA105, which were used to infect Glycyrrhiza uralensis hypocotyls explants. After induction, selection, differentiation, culture, and transplantation, 12, 15, and 5 regenerated plants over-expressing GuHMGR , GuSQS 1, and GuBAS , were obtained, respectively. Results RT-PCR analysis showed these transgenic regenerated G. uralensis plants had 2–6 copies of GuHMGR , GuSQS 1, or GuBAS. HPLC analysis showed the contents of 18 α - and 18 β -GC in all transgenic regenerated samples were both higher than that in the blank control. With the increase of copy numbers of GuHMGR , GuSQS 1, and GuBAS , the contents of 18 α - and 18 β -GC were both increased in most samples. The highest 18 α - and 18 β -GC contents in transgenic regenerated plants were about 3.05 times and 2.80 times higher than that in the blank control, respectively. Conclusion Over-expression of the GuHMGR , GuSQS 1, and GuBAS genes enhance the accumulation of 18 α - and 18 β -GC in the roots and rhizomes of G. uralensis . We hope this work can lay a foundation for the molecular breeding research of G. uralensis and improving the quality of the roots and rhizomes of G. uralensis cultivars.
机译:目的研究GC生物合成途径中涉及的三个功能基因GuHMGR,GuSQS 1和GuBAS的过表达对GC产生的影响。方法构建三种植物表达载体,并转化到根癌农杆菌EHA105中,用于感染甘草下胚轴外植体。诱导,选择,分化,培养和移植后,分别获得了过量表达GuHMGR,GuSQS 1和GuBAS的12、15和5个再生植物。结果RT-PCR分析显示,这些转基因的再生甘草植物具有2–6个GuHMGR,GuSQS 1或GuBAS拷贝。 HPLC分析显示,所有转基因再生样品中18α-和18β-GC的含量均高于空白对照。随着GuHMGR,GuSQS 1和GuBAS拷贝数的增加,大多数样品中18α-和18β-GC的含量均增加。转基因再生植株中最高的18α-和18β-GC含量分别比空白对照高3.05倍和2.80倍。结论GuHMGR,GuSQS 1和GuBAS基因的过表达增强了甘草根和根中18α-和18β-GC的积累。我们希望这项工作能够为G.uralensis的分子育种研究和提高G.uralensis品种的根和根茎质量奠定基础。

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