Xu Feng, Cheng Shui-Yuan, Cheng Shu-Han, Wang Yan, Du He-Wei
College of Horticulture Science and Engineering, Shandong Agricultural University, Tai'an 271018, China.
Zhi Wu Sheng Li Yu Fen Zi Sheng Wu Xue Xue Bao. 2007 Aug;33(4):309-17.
Chalcone synthase (CHS) catalyses the first and key regulatory step of flavonoid biosynthetic pathway. A chalcone synthase gene was isolated from Ginkgo biloba leaves using the method of rapid amplification of the cDNA ends (RACE). The full-length cDNA, designated as GbCHS2, is 1,608 bp in length (GenBank accession No. DQ054841) and contains an open reading frame of 1,173 bp encoding a protein of 391 amino acids. Alignment of the predicted amino acid sequence of GbCHS2 has been shown to have high sequence similarity with GbCHS1. All the active sites and active site motifs in GbCHS1 protein were also found in GbCHS2. Correlation analysis between CHS activity and flavonoid accumulation during ginkgo leaf growth indicated that CHS might be the rate-limiting enzyme in the biosynthesis pathway of flavonoids in ginkgo leaves. Results of semi-quantitative RT-PCR analysis showed that flavonoid accumulation paralleled the transcription level of change in chs gene, suggesting chs gene as the specific key gene regulating flavonoid accumulation in ginkgo leaves.
查尔酮合酶(CHS)催化类黄酮生物合成途径的第一步和关键调控步骤。采用cDNA末端快速扩增(RACE)方法从银杏叶中分离出一个查尔酮合酶基因。该全长cDNA命名为GbCHS2,长度为1608 bp(GenBank登录号:DQ054841),包含一个1173 bp的开放阅读框,编码一个由391个氨基酸组成的蛋白质。已证明GbCHS2预测的氨基酸序列与GbCHS1具有高度的序列相似性。在GbCHS2中也发现了GbCHS1蛋白中的所有活性位点和活性位点基序。银杏叶生长过程中CHS活性与类黄酮积累的相关性分析表明,CHS可能是银杏叶类黄酮生物合成途径中的限速酶。半定量RT-PCR分析结果表明,类黄酮积累与chs基因转录水平变化平行,表明chs基因是调控银杏叶类黄酮积累的特定关键基因。