A Fructan Exohydrolase from Maize Degrades Both Inulin and Levan and Co-Exists with 1-Kestotriose in Maize

Int J Mol Sci. 2021 May 13;22(10):5149. doi: 10.3390/ijms22105149.

Abstract

Enzymes with fructan exohydrolase (FEH) activity are present not only in fructan-synthesizing species but also in non-fructan plants. This has led to speculation about their functions in non-fructan species. Here, a cell wall invertase-related Zm-6&1-FEH2 with no "classical" invertase motif was identified in maize. Following heterologous expression in Pichia pastoris and in Nicotiana benthamiana leaves, the enzyme activity of recombinant Zm-6&1-FEH2 displays substrate specificity with respect to inulin and levan. Subcellular localization showed Zm-6&1-FEH2 exclusively localized in the apoplast, and its expression profile was strongly dependent on plant development and in response to drought and abscisic acid. Furthermore, formation of 1-kestotriose, an oligofructan, was detected in vivo and in vitro and could be hydrolyzed by Zm-6&1-FEH2. In summary, these results support that Zm-6&1-FEH2 enzyme from maize can degrade both inulin-type and levan-type fructans, and the implications of the co-existence of Zm-6&1-FEH2 and 1-kestotriose are discussed.

Keywords: 1-kestotriose; Zea mays; fructan exohydrolase; inulin; levan.

MeSH terms

  • Fructans / metabolism*
  • Glycoside Hydrolases / genetics
  • Glycoside Hydrolases / metabolism*
  • Inulin / metabolism*
  • Nicotiana / genetics
  • Nicotiana / metabolism
  • Plant Leaves / genetics
  • Plant Leaves / growth & development
  • Plant Leaves / metabolism
  • Saccharomycetales / genetics
  • Saccharomycetales / metabolism
  • Trisaccharides / metabolism*
  • Zea mays / growth & development
  • Zea mays / metabolism*

Substances

  • Fructans
  • Trisaccharides
  • 1-kestose
  • Inulin
  • levan
  • Glycoside Hydrolases

Supplementary concepts

  • Komagataella pastoris