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化州柚查尔酮合成酶基因克隆与序列分析

Cloning and sequence analyzing of chalcone synthase gene in Citrus grandis'tomenxosa'

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利用CTAB-LiCl法提取高质量的化州柚总RNA,采用RT-PCR技术克隆查尔酮合成酶基因,获得广东道地药材化橘红资源化州柚的查尔酮合成酶基因.该基因编码区全长1176bp,编码391个氨基酸残基,与同样来源于柑橘属的查尔酮合成酶基因同源性高达98%.CTAB-LiCl法能提取高质量的化州柚总RNA,可以用于后续基因克隆和分析;克隆获得的查尔酮合成酶具有编码区,与同属植物相同基因具有高度序列同源性.
To clone chalcone synthase ( CHS) gene from the Citrus grandis tomentosa, which was the genuine medicinal materials from Guangdong province, CTAB-LiCl treatment was used to extract RNA from Citrus grandis tomentosa' and RT-PCR was used to clone the CHS gene at the same time. The CHS gene included the open reading frame( ORF) , and it was consisted of 1173bp nucleic acid, encoded 391 amino acid residues. Compared with other CHS genes from citrus plant, it was found that they shared a sequence homology more than 98% at the nucleic acid level. Result showed that CTAB-LiCl treatment could extract high quality RNA from Citrus grandis tomentosa'. The cloned CHS gene from Citrus grandis tomentosa' had the open reading frame and shared a high sequence homology with other Citrus plant.

文海涛、赵红英、肖凤霞、林励

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广州中医药大学中药学院,广州,510006

化州柚 查尔酮合成酶 基因克隆

国家发改委高技专项

2003-26

2011

生物学杂志
合肥市科学技术协会

生物学杂志

CSTPCDCSCD
影响因子:0.554
ISSN:2095-1736
年,卷(期):2011.28(1)
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