A Gene Cluster for Biosynthesis of Mannosylerythritol Lipids Consisted of 4-O-β-D-Mannopyranosyl-(2R,3S)-Erythritol as the Sugar Moiety in a Basidiomycetous Yeast Pseudozyma tsukubaensis

PLoS One. 2016 Jun 21;11(6):e0157858. doi: 10.1371/journal.pone.0157858. eCollection 2016.

Abstract

Mannosylerythritol lipids (MELs) belong to the glycolipid biosurfactants and are produced by various fungi. The basidiomycetous yeast Pseudozyma tsukubaensis produces diastereomer type of MEL-B, which contains 4-O-β-D-mannopyranosyl-(2R,3S)-erythritol (R-form) as the sugar moiety. In this respect it differs from conventional type of MELs, which contain 4-O-β-D-mannopyranosyl-(2S,3R)-erythritol (S-form) as the sugar moiety. While the biosynthetic gene cluster for conventional type of MELs has been previously identified in Ustilago maydis and Pseudozyma antarctica, the genetic basis for MEL biosynthesis in P. tsukubaensis is unknown. Here, we identified a gene cluster involved in MEL biosynthesis in P. tsukubaensis. Among these genes, PtEMT1, which encodes erythritol/mannose transferase, had greater than 69% identity with homologs from strains in the genera Ustilago, Melanopsichium, Sporisorium and Pseudozyma. However, phylogenetic analysis placed PtEMT1p in a separate clade from the other proteins. To investigate the function of PtEMT1, we introduced the gene into a P. antarctica mutant strain, ΔPaEMT1, which lacks MEL biosynthesis ability owing to the deletion of PaEMT1. Using NMR spectroscopy, we identified the biosynthetic product as MEL-A with altered sugar conformation. These results indicate that PtEMT1p catalyzes the sugar conformation of MELs. This is the first report of a gene cluster for the biosynthesis of diastereomer type of MEL.

MeSH terms

  • Amino Acid Sequence
  • Biosynthetic Pathways / genetics*
  • Carbon-13 Magnetic Resonance Spectroscopy
  • Chromatography, Thin Layer
  • Erythritol / analogs & derivatives*
  • Erythritol / metabolism*
  • Fungal Proteins / chemistry
  • Fungal Proteins / genetics
  • Genes, Fungal*
  • Glycolipids / biosynthesis*
  • Glycolipids / chemistry
  • Mannosides / metabolism*
  • Multigene Family*
  • Phylogeny
  • Plasmids / metabolism
  • Proton Magnetic Resonance Spectroscopy
  • Sequence Alignment
  • Sequence Analysis, Protein
  • Sequence Homology, Amino Acid
  • Stereoisomerism
  • Ustilaginales

Substances

  • Fungal Proteins
  • Glycolipids
  • Mannosides
  • mannosylerythritol lipid
  • Erythritol

Grants and funding

This work has been supported by Japan Science and technology Agency (JST) under Adaptable and Seamless Technology Transfer Program through Target-driven R&D (AS2621413N). JST had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. Toyobo Co., Ltd. provided support in the form of salaries for authors SY and TK, but did not have any additional role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript. The specific roles of these authors are articulated in the ‘author contributions’ section.