In vitro propagation of Salvia sclarea L. by meta-Topolin, and assessment of genetic stability and secondary metabolite profiling of micropropagated plants

ERİŞEN S., KURT GÜR G., SERVİ H.

Industrial Crops and Products, cilt.157, 2020 (SCI-Expanded) identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 157
  • Basım Tarihi: 2020
  • Doi Numarası: 10.1016/j.indcrop.2020.112892
  • Dergi Adı: Industrial Crops and Products
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Academic Search Premier, Aerospace Database, Biotechnology Research Abstracts, CAB Abstracts, Communication Abstracts, Compendex, Food Science & Technology Abstracts, Geobase, INSPEC, Metadex, Veterinary Science Database
  • Anahtar Kelimeler: Clary sage, Cytokinins, Micropropagation, Somaclonal variation
  • İstanbul Yeni Yüzyıl Üniversitesi Adresli: Evet

Özet

The influence of meta-Topolin (mT) on micropropagation of Salvia sclarea L. (clary sage) was compared with N6-benzylaminopurine (BAP), kinetin (KIN) and thidiazuron (TDZ). mT was superior over all other cytokinin for not only shoot regeneration but also rooting. The highest shoot number (4.9 shoots/explants) was noted on nodal segments cultured on Murashige and Skoog (MS) medium including 2.0 mg/L mT and 0.2 mg/L indole-3-acetic acid (IAA). The regenerated shoots derived from mT including medium were rooted successfully on MS medium having 1.0 mg/L 1-naphthaleneacetic acid (NAA). Plantlets were successfully acclimatised (100%) and exhibited vigorous development in the greenhouse. The genetic stability of the propagated plants was assessed by start codon targeted polymorphism (SCoT) primers. A total variability of 3.13% was noted in the regenerants that revealed a high rated of genetic stability among the micropropagated plants. In addition, the secondary metabolite profiling of micropropagated plants was evaluated with gas chromatography-mass spectrometry (GC–MS). Although the hexane extracts of plants were dominated by n-alkanes, cytokinins added in the culture media altered their secondary metabolite contents. The protocol described here is a rapid and reliable micropropagation protocol for large-scale production of clonally stable clary sage plants for commercial purposes.