Plant glucosinolate biosynthesis and breakdown pathways shape the rhizosphere bacterial/archaeal community

Plant Cell Environ. 2024 Jun;47(6):2127-2145. doi: 10.1111/pce.14870. Epub 2024 Feb 28.

Abstract

Rhizosphere microbial community assembly results from microbe-microbe-plant interactions mediated by small molecules of plant and microbial origin. Studies with Arabidopsis thaliana have indicated a critical role of glucosinolates in shaping the root and/or rhizosphere microbial community, likely through breakdown products produced by plant or microbial myrosinases inside or outside of the root. Plant nitrile-specifier proteins (NSPs) promote the formation of nitriles at the expense of isothiocyanates upon glucosinolate hydrolysis with unknown consequences for microbial colonisation of roots and rhizosphere. Here, we generated the A. thaliana triple mutant nsp134 devoid of nitrile formation in root homogenates. Using this line and mutants lacking aliphatic or indole glucosinolate biosynthesis pathways or both, we found bacterial/archaeal alpha-diversity of the rhizosphere to be affected only by the ability to produce aliphatic glucosinolates. In contrast, bacterial/archaeal community composition depended on functional root NSPs as well as on pathways of aliphatic and indole glucosinolate biosynthesis. Effects of NSP deficiency were strikingly distinct from those of impaired glucosinolate biosynthesis. Our results demonstrate that rhizosphere microbial community assembly depends on functional pathways of both glucosinolate biosynthesis and breakdown in support of the hypothesis that glucosinolate hydrolysis by myrosinases and NSPs happens before secretion of products to the rhizosphere.

Keywords: Arabidopsis; below‐ground; community composition; diversity; microbiota; nitrile; specialised metabolism.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Arabidopsis Proteins / genetics
  • Arabidopsis Proteins / metabolism
  • Arabidopsis* / genetics
  • Arabidopsis* / metabolism
  • Arabidopsis* / microbiology
  • Archaea* / genetics
  • Archaea* / metabolism
  • Bacteria* / genetics
  • Bacteria* / metabolism
  • Glucosinolates* / biosynthesis
  • Glucosinolates* / metabolism
  • Mutation
  • Nitriles / metabolism
  • Plant Roots* / metabolism
  • Plant Roots* / microbiology
  • Rhizosphere*

Substances

  • Glucosinolates
  • Arabidopsis Proteins
  • Nitriles