Heat stress-induced reactive oxygen species participate in the regulation of HSP expression, hyphal branching and ganoderic acid biosynthesis in Ganoderma lucidum

Microbiol Res. 2018 Apr:209:43-54. doi: 10.1016/j.micres.2018.02.006. Epub 2018 Feb 19.

Abstract

Heat stress (HS) is an important environmental factor that affects the growth and metabolism of edible fungi, but the molecular mechanism of the heat stress response (HSR) remains unclear. We previously reported that HS treatment increased the length between two hyphal branches and induced the accumulation of ganoderic acid biosynthesis and the gene expression of heat shock proteins (HSPs) in Ganoderma lucidum. In this study, we found that HS induced a significant increase in the cytosolic ROS concentration, and exogenously added ROS scavengers NAC, VC and NADPH oxidase (Nox) inhibitor DPI reduce the cytosolic ROS accumulation in G. lucidum. In addition, the phenomena of the increased gene expression and increased length between the two hyphal branches and the accumulation of GA biosynthesis induced by HS were mitigated. Furthermore, we investigated the effects of HS on Nox-silenced strains (NoxABi-10, NoxABi-11 and NoxRi-4, NoxRi-7) and found that the level of ROS concentration was lower than that in wild-type (WT) strains treated with HS. Additionally, Nox silenced strains reduced the HS-induced increase in HSP expression, the length between two hyphal branches and GA biosynthesis compared with the WT strain. These data indicate that HS-induced ROS participate in the regulation of HSP expression, hyphal branching and ganoderic acid biosynthesis in G. lucidum. In addition, these findings identified potential pathways linking ROS networks to HSR, physiological and metabolic processes in fungi and provide a valuable reference for studying the role of ROS in HSR, mycelium growth and secondary metabolites.

Keywords: Ganoderma lucidum; Heat stress; Reactive oxygen species.

MeSH terms

  • Acetates / pharmacology
  • Antioxidants / metabolism
  • Cyclopentanes / pharmacology
  • Heat-Shock Proteins / genetics
  • Heat-Shock Proteins / metabolism*
  • Heat-Shock Response / physiology*
  • Hydrogen Peroxide / metabolism
  • Hyphae / growth & development*
  • NADPH Oxidases / metabolism
  • Oxidation-Reduction
  • Oxidative Stress
  • Oxylipins / pharmacology
  • Reishi / metabolism*
  • Triterpenes / metabolism*

Substances

  • Acetates
  • Antioxidants
  • Cyclopentanes
  • Heat-Shock Proteins
  • Oxylipins
  • Triterpenes
  • ganoderic acid
  • methyl jasmonate
  • Hydrogen Peroxide
  • NADPH Oxidases