华南理工大学学报(自然科学版) ›› 2009, Vol. 37 ›› Issue (6): 63-68.

• 生物工程 • 上一篇    下一篇

高良姜及其混淆品rDNA ITS序列的分析与鉴别

庞启华1  严萍1  赵树进2   

  1. 1. 华南理工大学 生物科学与工程学院, 广东 广州 510006;2. 广州军区 广州总医院, 广东 广州 510010
  • 收稿日期:2008-10-16 修回日期:2008-12-12 出版日期:2009-06-25 发布日期:2009-06-25
  • 通信作者: 赵树进(1958-),男,教授,博士生导师,主要从事生物制药研究.E-mail:gzzsjzhs@163.com E-mail:pqh_xin@yahoo.com.cn
  • 作者简介:庞启华(1968-),女,博士生,主要从事生物制药研究.
  • 基金资助:

    广东省自然科学基金资助项目(6104397)

Analysis and Identification of rDNA ITS Sequences of Alpinia officinarum Hance and Its Adulterants

Pang Qi-hua Yan Ping1  Zhao Shu-jin2   

  1. 1.School of Biological Science and Engineering, South China University of Technology, Guangzhou 510006, Guangdong, China; 2. General Hospital of Guangzhou Military Gommand, Guangzhou 510010, Guangdong, China
  • Received:2008-10-16 Revised:2008-12-12 Online:2009-06-25 Published:2009-06-25
  • Contact: 赵树进(1958-),男,教授,博士生导师,主要从事生物制药研究.E-mail:gzzsjzhs@163.com E-mail:pqh_xin@yahoo.com.cn
  • About author:庞启华(1968-),女,博士生,主要从事生物制药研究.
  • Supported by:

    广东省自然科学基金资助项目(6104397)

摘要: 用聚合酶链式反应(PCR)直接测序法测定和分析不同产地野生和农家品种的高良姜及其3种混淆品(山姜、华山姜和大高良姜)的核糖体DNA内转录间隔区(rDNAITS)序列,为高良姜种质资源研究和真伪鉴别提供分子数据.ITS序列分析结果表明:高良姜种内序列同源性达100%,测序结果中发现杂合位点,且广西样品杂合位点的两个碱基所占的比例与其它地方样品的不同.高良姜及其混淆品经测序、比对、排序得到的812bp序列中有61个变异位点,60个是信息位点,同源性达96.32%,其中ITS1和ITS2区中的11个位点在高良姜及其混淆品中差别明显,可以鉴别高良姜及其混淆品.同时发现,基于DNA序列的高良姜及其混淆品的系统分类结果与形态学的分类结果不完全一致,有待进一步研究探讨.

关键词: 高良姜, 混淆品, 核糖体DNA内转录间隔区, 序列分析, 鉴别

Abstract:

In order to provide molecular data for the germplasm resource study on Alpinia officinarum (A officina rum) Hance and to identify A. officinarum Hance from its adulterants, the rDNA internal transcribed spacer (ITS) sequences of A. officinarum Hance and its adulterants were determined and analyzed by means of polymerase chain reaction (PCR). Wild and cultivated A. officinarum Hance collected in different areas, and three adulterants including A. japonica (Thunb.), A. chinensis ( Retz. ) Rosc. and A. galanga ( L. ), were used as samples. The results of sequence analysis indicate that   the intraspecies sequence homology of A. officinarum Hance is up to 100% ;   there exist heterotic sites in all samples of A. officinarum Hance, and the proportion of the two bases in heterotic sites in the sample from Guangxi is different from that in other samples;   there are 61 variable sites (including 60 informative sites) in the 812bp sequences among A. officinarum Hance and its adulterants, with a homology of 96.32% ;   11 sites in the ITS1 and ITS2 regions can be used to identify A. officinarum Hance and its adulterants due to the great difference of the sites in different samples; and   some further researches should be performed because the classification results of A. officinarum Hance and its adulterants based on DNA sequences do not totally accord with those based on morphologic characteristics.

Key words: Alpinia officinarum Hance, adulterant, rDNA internal transcribed spacer, sequence analysis, identification