银杏
查尔酮合酶
裸子植物
生物
互补DNA
打开阅读框
基因
分子克隆
序列分析
同源(生物学)
遗传学
肽序列
分子生物学
生物化学
植物
基因表达
作者
Yongzhen Pang,Guoan Shen,Chenghong Liu,Xiaojun Liu,Feng Tan,Xiaofen Sun,Kexuan Tang
出处
期刊:Dna Sequence
日期:2004-01-01
卷期号:15 (4): 283-290
被引量:20
标识
DOI:10.1080/10425170412331283814
摘要
A chalcone synthase (CHS) gene was cloned from Ginkgo biloba for the first time and it was also the first cloned gene involved in flavonoids metabolic pathway in G. biloba. The full-length cDNA of G. biloba CHS (designated as Gbchs) was 1608bp with poly(A) tailing and it contained a 1173bp open reading frame (ORF) encoding a 391 amino acid protein. Gbchs was found to have extensive homology with those of other plant chs genes via multiple alignments. The active sites of the CoA binding, coumaroyl pocket and cyclization pocket in CHS protein of Medicago sativa were also found in GbCHS. Molecular modeling of GbCHS indicated that the three-dimensional structure of GbCHS strongly resembled that of M. sativa (MsCHS2), implying GbCHS may have similar functions with MsCHS2. Phylogenetic tree analysis revealed that GbCHS had closer relationship with CHSs from gymnosperm plants than from other plants. Gbchs is a useful tool to study the regulation of flavonoids metabolism in G. biloba.
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