Synergistic effects of drought stress and photoperiods on phenology and secondary metabolism of Silybum marianum

Appl Biochem Biotechnol. 2014 Sep;174(2):693-707. doi: 10.1007/s12010-014-1098-5. Epub 2014 Aug 3.

Abstract

Silybum marianum is an important medicinal plant of the family Asteraceae, well known for its set of bioactive isomeric mixture of secondary metabolites "silymarin", primarily acting as a hepato-protective agent. Abiotic stress augments plant secondary metabolism in different plant tissues to withstand harsh environmental fluctuations. In the current study, our aim was to induce drought stress in vitro on S. marianum under the influence of different photoperiod treatments to study the effects, with respect to variations in secondary metabolic profile and plant growth and development. S. marianum was extremely vulnerable to different levels of mannitol-induced drought stress. Water deficiency inhibited root induction completely and retarded plant growth was observed; however, phytochemical analysis revealed enhanced accumulation of total phenolic content (TPC), total flavonoid content (TFC), and total protein content along with several antioxidative enzymes. Secondary metabolic content was positively regulated with increasing degree of drought stress. A dependent correlation of seed germination frequency at mild drought stress and antioxidative activities was established with 2 weeks dark + 2 weeks 16/8 h photoperiod treatment, respectively, whereas a positive correlation existed for TPC and TFC when 4 weeks 16/8 h photoperiod treatment was applied. The effects of drought stress are discussed in relation to phenology, seed germination frequency, biomass build up, antioxidative potential, and secondary metabolites accumulation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Droughts*
  • Germination
  • Peroxidases / metabolism
  • Photoperiod*
  • Silybum marianum / enzymology
  • Silybum marianum / metabolism*
  • Silybum marianum / physiology
  • Stress, Physiological*
  • Superoxide Dismutase / metabolism

Substances

  • Peroxidases
  • Superoxide Dismutase