AI Article Synopsis

  • The study focuses on var. chinensis, a plant known for its pharmaceutical and ornamental uses, by analyzing primary and secondary metabolites in different in vitro tissues (callus, adventitious roots, and shoots) using advanced chromatography techniques.
  • The researchers optimized in vitro culture methods using hormonal treatments on bulbs to promote growth and metabolite production, with specific concentrations found to be most effective.
  • Results indicated that shoots and roots cultivated in a particular nutrient medium yielded the highest levels of metabolites, suggesting that this method could be beneficial for mass-producing valuable compounds from the plant.

Article Abstract

var. chinensis is a perennial monocot plant that is well known for its pharmaceutical and ornamental uses. This study aimed to understand the changes in the primary and secondary metabolites in different in vitro tissues of (callus, adventitious root, and shoot) using high-performance liquid chromatography and gas chromatography time-of-flight mass spectrometry. In addition, to optimize the most efficient in vitro culture methods for primary and secondary metabolite production, bulbs were used as explants and cultivated in Murashige and Skoog (MS) medium containing different hormones at various concentrations. In addition, the present study found suitable hormonal concentrations for callus, adventitious root, and shoot induction and analyzed the primary and secondary metabolites. The MS medium supplemented with 1.0 mg L dicamba, 3.0 mg L indole-3-butyric acid (IBA), and 3.0 mg L 6-benzylaminopurine (BAP) was the most efficient media for callus, adventitious root, and shoot induction in . The tissue induced in this medium was subjected to primary (amines, amino acids, organic acids, sugars, and sugar alcohols) and secondary metabolite (galantamine and phenolic acids) analysis. The shoots and roots showed the highest amounts of metabolites. This study showed that bulb in vitro culture can be an efficient micropropagation method for and the production of primary and secondary metabolites, offering implications for the mass production of primary and secondary metabolite compounds from tissues generated in vitro.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11154942PMC
http://dx.doi.org/10.1021/acsomega.4c01735DOI Listing

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