首页> 美国卫生研究院文献>International Journal of Molecular Sciences >The Expression of Millettia pinnata Chalcone Isomerase in Saccharomyces cerevisiae Salt-Sensitive Mutants Enhances Salt-Tolerance
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The Expression of Millettia pinnata Chalcone Isomerase in Saccharomyces cerevisiae Salt-Sensitive Mutants Enhances Salt-Tolerance

机译:酿酒酵母盐敏感突变体中的山茱Cha查尔酮异构酶的表达增强了耐盐性。

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摘要

The present study demonstrates a new Millettia pinnata chalcone isomerase (MpCHI) whose transcription level in leaf was confirmed to be enhanced after being treated by seawater or NaCl (500 mM) via transcriptome sequencing and Real-Time Quantitative Reverse Transcription PCR (QRT-PCR) analyses. Its full length cDNA (666 bp) was obtained by 3′-end and 5′-end Rapid Amplification of cDNA Ends (RACE). The analysis via NCBI BLAST indicates that both aminoacid sequence and nucleotide sequence of the MpCHI clone share high homology with other leguminous CHIs (73%–86%). Evolutionarily, the phylogenic analysis further revealed that the MpCHI is a close relative of leguminous CHIs. The MpCHI protein consists of 221 aminoacid (23.64 KDa), whose peptide length, amino acid residues of substrate-binding site and reactive site are very similar to other leguminous CHIs reported previously. Two pYES2-MpCHI transformed salt-sensitive Saccharomyces cerevisiae mutants (Δnha1 and Δnhx1) showed improved salt-tolerance significantly compared to pYES2-vector transformed yeast mutants, suggesting the MpCHI or the flavonoid biosynthesis pathway could regulate the resistance to salt stress in M. pinnata.
机译:本研究证明了一种新的千层莲查尔酮异构酶(MpCHI),其通过转录组测序和实时定量逆转录PCR(QRT-PCR)经海水或NaCl(500 mM)处理后,确认其叶片中的转录水平得到了增强。分析。通过cDNA末端的3'端和5'端快速扩增(RACE)获得其全长cDNA(666 bp)。通过NCBI BLAST进行的分析表明,MpCHI克隆的氨基酸序列和核苷酸序列与其他豆类CHIs具有高度同源性(73%–86%)。在进化上,系统发育分析进一步表明,MpCHI是豆科CHI的近亲。 MpCHI蛋白由221个氨基酸(23.64 KDa)组成,其肽长,底物结合位点和反应位点的氨基酸残基与以前报道的其他豆科CHIs非常相似。与pYES2载体转化的酵母突变体相比,两个pYES2-MpCHI转化的盐敏感性酿酒酵母突变体(Δnha1和Δnhx1)表现出显着改善的耐盐性,表明MpCHI或类黄酮生物合成途径可以调节Pin.ata鼠对盐胁迫的抗性。 。

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