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cDNA and Genomic DNA Clonings of Chalcone Synthase from Pueraria lobata

机译:葛根查尔酮合酶的cDNA和基因组DNA克隆

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Four cDNAs encoding chalcone synthase (CHS), the key enzyme in flavonoid biosynthesis, were isolated from Pueraria lobata cells challenged with yeast extract elicitor using bean CHS cDNA as a probe. The longest clone contained a complete open reading frame of 1170 bp which would predict a protein of about 43kDa. The others were not full-length clones. Using isolated cDNA as a probe, Southern blot hybridization of genomic DNA fragments revealed the presence of multiple CHS genes in the P. lobata. genome. We cloned and sequenccd one CHS genomic clone, gCHS14, whose 5' untranslated region showed homology with the bean CHS gene CHS15 and included the several reported sequences characteristic of stress response.
机译:以豆类CHS cDNA为探针,从酵母提取激发子激发的野葛细胞中分离出了四种编码类黄酮生物合成关键酶查耳酮合酶(CHS)的cDNA。最长的克隆包含一个1170 bp的完整开放阅读框,可以预测约43kDa的蛋白质。其他不是全长克隆。使用分离的cDNA作为探针,基因组DNA片段的Southern印迹杂交揭示了球状假单胞菌中存在多个CHS基因。基因组。我们克隆并测序了一个CHS基因组克隆gCHS14,其5'非翻译区显示出与豆类CHS基因CHS15的同源性,并包括几个报道的胁迫响应特征序列。

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