食品科学 ›› 2010, Vol. 31 ›› Issue (4): 139-142.doi: 10.7506/spkx1002-6300-201004032

• 分析检测 • 上一篇    下一篇

蛹虫草及其培养基中主要核苷类成分的分析比较

刘艳芳1 , 2,唐庆九2 ,* ,杨 焱2,张劲松2,郝瑞霞2,唐传红2,魏东芝1,史国平2   

  1. 1.华东理工大学 生物反应器工程国家重点实验室,鲁华生物技术研究所 2.农业部应用真菌资源与利用重点开放实验室,上海市食用菌工程技术研究中心,上海市农业遗传育种重点开放实验室,上海市农业科学院食用菌研究所
  • 收稿日期:2009-04-07 修回日期:2009-09-16 出版日期:2010-02-15 发布日期:2010-12-29
  • 通讯作者: 刘艳芳 E-mail:aliu-1980@163.com
  • 基金资助:

    “十一五”国家科技支撑计划项目(2006BAD06B08)

Comparative Analysis of Nucleotides between Fruiting Body of Cordyceps militaris (L. ex Fr.) Link and Cultured Medium

LIU Yan-fang1,2,TANG Qing-jiu2,*,YANG Yan2,ZHANG Jing-song2,HAO Rui-xia2,TANG Chuan-hong2,WEI Dong-zhi1,SHI Guo-ping2   

  1. 1. State Key Laboratory of Bioreactor Engineering, New World Institute of Biotechnology, East China University of Science and
    Technology, Shanghai 200237, China ;2. Key Laboratory of Applied Mycological Resources and Utilization, Ministry of
    Agriculture, Shanghai Research Center for Edible Fungi Biotechnology and Engineering, Key Laboratory of
    Agricultural Genetics and Breeding of Shanghai, Institute of Edible Fungi, Shanghai Academy of
    Agricultural Sciences, Shanghai 201106, China
  • Received:2009-04-07 Revised:2009-09-16 Online:2010-02-15 Published:2010-12-29
  • Contact: LIU Yan-fang E-mail:aliu-1980@163.com

摘要:

采用高效液相色谱法测定虫草中的核苷类成分,优化后的色谱条件为YMC-Polyamine 柱(250mm × 4.6mm,5μm);采用梯度洗脱,流动相:乙腈- 水(V/V):0~15min 为90:10,15~20min 为86.5:13.5,20~30min 为75:25,30~35min 为70:30;流速:1mL/min;柱温:30℃;检测波长:259nm;进样量:10μL。结果表明:胸腺嘧啶、虫草素、尿嘧啶、腺苷、腺嘌呤、尿苷、鸟嘌呤、次黄嘌呤均能得到较好分离,该方法稳定性好、精密度高、重现性好,适用于虫草中的核苷类成分的分析。经分析发现,蛹虫草子实体核苷类物质组成大致相似,但含量差异非常显著,同时发现蛹虫草培养基残基及固体发酵产物中虫草素含量较高,其他核苷类成分很少,因此认定蛹虫草培养基残基及固体发酵产物是非常优良的分离纯化虫草素的原料。

关键词: 蛹虫草, 高效液相色谱, 核苷, 虫草素, 固体发酵

Abstract:

A high performance liquid chromatographic (HPLC) method was developed for the determination of nucleotides. Meanwhile, a comparative analysis of nucleotides between fruiting body of Cordyceps militaris (L. ex Fr.) Link and cultured medium was conducted by the developed method. YMC-Polyamine column (5 μm, 250 mm × 4.6 mm) was used for the chromatographic separation. A mobile phase composed of acetonitrile and double distilled water at a flow rate of 1 mL/min was used for gradient elution and the elution program was as follows: acetonitrile/water (90:10, V/V) for 15 min → (86.5:13.5) for 20 min→(75:25) for 30 min → (70:30) for 35 min. Other chromatographic conditions were set as follows: column temperature 30 ℃, detection wavelength 259 nm, and injection volume 10 μL. Results showed that a good separation of thymine, cordycepin, uracil, adenosine, adenine, uridine, guanine and hypoxanthine was achieved. This method was stable, precise and reproducible and was successfully applied to the determination of nucleosides in commercial Cordyceps militaris (L. ex Fr.) Link samples. HPLC analysis revealed that a basic similarity of nucleotide kind was observed in various commercial samples of fruiting body of Cordyceps militaris (L. ex Fr.) Link. But the contents of nucleotides exhibited significant differences. A high content of cordycepin was found in cultured medium and solid fermentation products, but other nucleotides had a low content. These results demonstrate the excellence of cultured medium and solid fermentation products as a source of cordycepin.

Key words: Cordyceps sp., HPLC, nucleotides, cordycepin, solid fermentation products

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