Subscribe to RSS
DOI: 10.1055/s-2003-41108
Genetic Characterization of the Three Medicinal Echinacea Species using RAPD Analysis
Publication History
Received: December 27, 2002
Accepted: March 8, 2003
Publication Date:
04 August 2003 (online)
Abstract
The three medicinal species of the Echinacea genus, E. angustifolia DC., E. pallida (Nutt.) Nutt. and E. purpurea (L.) Moench were distinguished using the RAPD (random amplified polymorphic DNA) technique. Species-specific markers were identified from amplicons obtained with four of the twenty 10-mer primers contained in the Operon RAPD kit A. In particular, one marker was identified for E. angustifolia (OPA 20, 1800 pb) and E. pallida (OPA 10, 600 pb) and three markers for E. purpurea (OPA 11 : 1250 pb; OPA 17 : 750, 1800 pb). Genetic distance analysis indicated a high degree of difference among the three species with a relative lower difference between E. angustifolia and E. pallida.
References
- 1 Percival S S. Use of Echinacea in medicine. Biochemical Pharmacology. 2000; 60 155-8
- 2 Mazza G, Cotrell T. Volatile components of roots, stems, leaves and flowers of Echinacea species. Journal of Agricultural and Food Chemistry. 1999; 47 3081-5
- 3 Sloley B D, Urichuk L J, Tywin C, Coutts R T, Pang P K, Shan J J. Comparison of chemical components and antioxidants capacity of different Echinacea species. Journal of Pharmacy and Pharmacology. 2001; 53 849-57
- 4 Perry N B, Burgess E J, Glennie V L. Echinacea standardization: analytical methods for phenolic compounds and typical levels in medicinal species. Journal of Agricultural and Food Chemistry. 2001; 49 1702-6
- 5 Speroni E, Govoni P, Guizzardi S, Renzulli C, Guerra M C. Anti-inflammatory and cicatrizing activity of Echinacea pallida Nutt. root extract. Journal of Ethnopharmacology. 2002; 79 265-72
- 6 Bauer R, Khan I A, Wagner H. TLC and HPLC analysis of Echinacea pallida and E. angustifolia roots. Planta Medica. 1988; 54 426-30
- 7 Williams J G, Kubelik A R, Livak K J, Rafalski J A, Tingey S V. DNA polymorphisms amplified by arbitrary primers are useful as genetic markers. Nucleic Acids Research. 1990; 18 6531-5
- 8 Zhang Kalin Y B, Leung H W, Yeung H W, Wong Ricky N S. Differentiation of Lycium barbarum from its Related Lycium Species using Random Amplified Polymorphic DNA. Planta Medica. 2001; 67 379-81
- 9 Cheng K T, Su C H, Chang H C, Huang J Y. Differentiation of genuines and counterfeits of Cordyceps species using random amplified polymorphic DNA. Planta Medica. 1998; 64 451-3
- 10 Zhang Y B, Ngan F N, Wang Z T, Ng T B, But P PH, Shaw P C, Wang J. Random primed polymerase chain reaction differentiates Codonopsis pilosula from different localities. Planta Medica. 1999; 65 157-60
- 11 Cheng K T, Tsay H S, Chen C F, Chou T W. Determination of the components in a Chinese prescription, Yu-Ping-Feng San, by RAPD analysis. Planta Medica. 1998; 64 563-5
- 12 Nadeau J H, Bedigian H G, Bouchard G, Denial T, Kosowsky M, Norberg R, Pugh S, Sargeant E, Turner R, Paigen B. Multilocus markers for mouse genome analysis: PCR amplification based on single primers of arbitrary nucleotide sequence. Mammalian genome. 1992; 3 55-64
-
13 McClelland M, Welsh J. DNA fingerprinting using arbitrarily primed DNA. In Dieffenbach CW and Dveksler GS, editors
Dieffenbach-Dveksler: PCR Primer: a laboratory manual . United States of America; Cold Spring Harbor Laboratory Press 1995: 203-11 - 14 Nei M, Li W H. Mathematical model for studying genetic variation in terms of restriction endonucleases. Proceedings of Natural Academy of Sciences U S A. 1979; 76 5269-73
Dr. Paola Nieri
Dipartimento di Psichiatria, Neurobiologia, Farmacologia e Biotecnologie
via Bonanno n°6
56126 Pisa
Italy
Phone: +39-050-24092
Fax: +39-050-503534
Email: paola.nieri@farm.unipi.it