Identification of medicinal plant Schisandra chinensis using a potential DNA barcode ITS2
To test whether the internal transcribed spacer 2 (ITS2) region is an effective marker for using in authenticating of the <em>Schisandra chinensis</em> at the species and population levels, separately. And the results showed that the wild populations had higher percentage of individuals that had substitution of C→A at site 86-bp than the cultivated populations. At sites 10-bp, 37-bp, 42-bp and 235-bp, these bases of the <em>Schisandra sphenanthera</em> samples differed from that of <em>S. chinensis</em>. Two species showed higher levels of inter-specific divergence than intra-specific divergence within ITS2 sequences. However, 24 populations did not demonstrate much difference as inter-specific and intra-specific divergences were concerned. Both <em>S. chinensis</em> and <em>S. sphenanthera</em> showed monophyly at species level, yet the samples of different populations shown polyphyly at population level. ITS2 performed well when using BLAST1 method. ITS2 obtained 100% identification success rates at the species level for <em>S. chinensis</em>, with no ambiguous identification at the genus level for ITS2 alone. The ITS2 region could be used to identify <em>S. chinensis</em> and <em>S. sphenanthera</em> in the “Chinese Pharmacopoeia”. And it could also correctly distinguish 100% of species and 100% of genera from the 193 sequences of <em>S. chinensis</em>. Hence, the ITS2 is a powerful and efficient tool for species identification of <em>S. chinensis</em>.