Silica and secondary metabolites as chemophenetic markers for characterization of bamboo species in relation to genetic and morphometric analysis

Mol Biol Rep. 2021 May;48(5):4487-4495. doi: 10.1007/s11033-021-06469-9. Epub 2021 Jun 11.

Abstract

Bamboo is a non-timber forest product and one of the most important grass plants of industrial and domestic use. It is widely distributed in tropical countries including India, China and Southeast Asian countries with wide genetic diversity. The diversity in the available genotypes becomes an important resource for the selection and improvement of the plants for ecological and commercial use. This study investigates eight commercially and ecologically important bamboo species of six genera (Bambusa, Dendrocalamus, Thyrsostachys, Vietnamosasa, Cephalostachyum and Indocalamus) from India, Thailand and Laos. These were evaluated for genetic differences by molecular makers, chemo-morphological variation and ability of silicon accumulation. The genetic cluster analyses of eight RAPD primers revealed genetic similarities in the ranges of 24-55%. The total silica content varied from 18.34 to 40.08 ppm in leaves of different bamboo species. Chemical analysis of the silicon content by ICP-OES and secondary metabolite profiling on TLC depicted the prominent distinction among the species. The PCA analysis of quantitative morphological data grouped the species in two major clusters and found to correlate with chemical pattern and genetic similarity to some extent. This is the first report that summarizes species-specific variability of leaf silica content, secondary metabolites, and quantitative morphological data towards delineation of genetic phylogeny of bamboo species.

Keywords: Bamboo; ICP-OES; Molecular markers; Silica; TLC.

MeSH terms

  • Bambusa / chemistry
  • Bambusa / classification*
  • Bambusa / genetics*
  • Bambusa / metabolism
  • DNA Primers
  • Genotype
  • India
  • Laos
  • Phylogeny*
  • Plant Leaves / chemistry
  • Plant Leaves / metabolism
  • Polymorphism, Genetic*
  • Random Amplified Polymorphic DNA Technique / methods
  • Silicon Dioxide / metabolism*
  • Species Specificity
  • Thailand

Substances

  • DNA Primers
  • Silicon Dioxide