葛根异黄酮合成酶基因的克隆与特性研究

Junbo Gou, Changfu Li, Fangfang Chen, Zhaobo Li, Jia Li
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引用次数: 2

摘要

异黄酮是葛根的主要活性成分。异黄酮生产的第一步是由细胞色素P450酶IFS完成的。虽然已经从葛中分离出IFS基因,但迄今为止还没有发现其生物学功能。本研究以安徽朗溪葛根为材料,通过RT-PCR技术克隆了IFS基因,命名为PlIFS。该PlIFS包含一个开放阅读框(ORF),编码521个氨基酸残基。将扩增的PlIFS基因以酵母GAL1发散启动子为对照,克隆到pESC-TRP载体中。将构建的重组质粒命名为pESC-TRP-PlIFS,按照LiAc/ssDNA/PEG法将重组质粒转化为酿酒酵母WAT11。在酵母菌中表达的PlIFS能够催化利尿素生成大豆苷元,表明其具有IFS活性。基因表达谱分析显示,PlIFS在根中表达量最高,这与葛根中异黄酮的积累一致。
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Molecular Cloning and Characterization of Isoflavone Synthase Gene from Pueraria lobata
Isoflavones are the main active component of kudzu(Pueraria lobata).The first committed step in the production of isoflavones is performed by a cytochrome P450 enzyme,IFS.While IFS genes have been isolated from kudzu,no biological functions have been identified to date.We cloned an IFS gene via RT-PCR,named PlIFS,using kudzu collected from Langxi(Anhui,China)as plant material.The PlIFS contained an open reading frame(ORF)encoding 521 amino acid residues.The amplified PlIFS gene was cloned into pESC-TRP vector,with yeast GAL1 divergent promoters as the control.The constructed recombinant plasmid,named pESC-TRP-PlIFS,was transformed into Saccharomyces cerevisiae strain WAT11 according to the LiAc/ssDNA/PEG method.The PlIFS expressed in yeast was able to catalyze daidzein formation from liquiritigenin,indicating that it had IFS activity.Gene expression pattern analysis revealed that PlIFS was expressed in roots at the highest level,which was consistent with isoflavones accumulation in kudzu plantlets.
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