In vitro propagation and cell cultures of memory tonic herb Evolvulus alsinoides: a best source for elicited production of scopoletin

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• 作者：Vikas Bandu Naikawadi ; Mahendra Laxman Ahire…
• 关键词：Cell culture ; Dementia ; Elicitors ; Evolvulus alsinoides ; In vitro propagation ; Memory power ; Scopoletin
• 刊名：Applied Microbiology and Biotechnology
• 出版年：2016
• 出版时间：April 2016
• 年：2016
• 卷：100
• 期：8
• 页码：3463-3476
• 全文大小：679 KB
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• 作者单位：Vikas Bandu Naikawadi (1) (2)
  Mahendra Laxman Ahire (1) (3)
  Anindita Lahiri (1)
  Tukaram Dayaram Nikam (1)
  
  1. Department of Botany, Savitribai Phule Pune University, Pune, 411 007, Maharashtra, India
  2. Department of Botany, Chandmal Tarachand Bora College, Shirur (Ghodnadi), Tal. Shirur 412 210, Dist., Pune, Maharashtra, India
  3. Department of Botany, Yashwantrao Chavan Institute of Science, Satara, 415 001, Maharashtra, India
  
• 刊物类别：Chemistry and Materials Science
• 刊物主题：Chemistry
  Biotechnology
  Microbiology
  Microbial Genetics and Genomics
  
• 出版者：Springer Berlin / Heidelberg
• ISSN：1432-0614

文摘

Evolvulus alsinoides L. is used for preparation of ‘Shankhapushpi’, an important popular ayurvedic drug that contributes considerably to the improvement of memory power. The improvement is attributed to the presence of furanocoumarin scopoletin, a metabolite with a wide range of biological activities. This report describes, for the first time, an in vitro culture system for propagation and enhanced production of scopoletin. Different concentrations of auxins and cytokinins individually and in combination were used in Murashige and Skoog (MS) medium to induce shoot regeneration in cotyledonary nodal explants and callus formation in leaf explants. The best response was achieved in MS medium fortified with 5.0 μM 6-benzyladenine (BA) in which 96 % of cultures produced 7.6 ± 0.6 shoots per explant. Regenerated shoots were rooted on MS medium with 5.0 μM indole-3-acetic acid (IAA). Plantlets were successfully acclimatized and established in soil. MS medium fortified with 10 μM BA + 5.0 μM IAA showed maximum growth and accumulation of scopoletin in cell cultures. Cell cultures could be maintained over 24 months. The influences of auxins, cytokinins, organic acids, amino acids, and fungal-derived elicitors on production of scopoletin were studied. Presence of either l-arginine, sodium pyruvate, or yeast extract highly promoted scopoletin production as compared with control and achieved 75.02-, 72.13-, and 57.98-fold higher accumulation, respectively. The results presented herein have laid solid foundation for large-scale production of scopoletin and further investigation of its purification and utilization as a novel pharmaceutical drug.