Characterization of mannitol-2-dehydrogenase in Saccharina japonica: evidence for a new polyol-specific long-chain dehydrogenases/reductase

PLoS One. 2014 May 15;9(5):e97935. doi: 10.1371/journal.pone.0097935. eCollection 2014.

Abstract

Mannitol plays a crucial role in brown algae, acting as carbon storage, organic osmolytes and antioxidant. Transcriptomic analysis of Saccharina japonica revealed that the relative genes involved in the mannitol cycle are existent. Full-length sequence of mannitol-2-dehydrogenase (M2DH) gene was obtained, with one open reading frame of 2,007 bp which encodes 668 amino acids. Cis-regulatory elements for response to methyl jasmonic acid, light and drought existed in the 5'-upstream region. Phylogenetic analysis indicated that SjM2DH has an ancient prokaryotic origin, and is probably acquired by horizontal gene transfer event. Multiple alignment and spatial structure prediction displayed a series of conserved functional residues, motifs and domains, which favored that SjM2DH belongs to the polyol-specific long-chain dehydrogenases/reductase (PSLDR) family. Expressional profiles of SjM2DH in the juvenile sporophytes showed that it was influenced by saline, oxidative and desiccative factors. SjM2DH was over-expressed in Escherichia coli, and the cell-free extracts with recombinant SjM2DH displayed high activity on D-fructose reduction reaction. The analysis on SjM2DH gene structure and biochemical parameters reached a consensus that activity of SjM2DH is NADH-dependent and metal ion-independent. The characterization of SjM2DH showed that M2DH is a new member of PSLDR family and play an important role in mannitol metabolism in S. japonica.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Catalytic Domain
  • Fructose / chemistry
  • Gene Expression Regulation, Enzymologic
  • Hydrogen Peroxide / pharmacology
  • Laminaria / enzymology*
  • Mannitol Dehydrogenases / biosynthesis
  • Mannitol Dehydrogenases / chemistry
  • Mannitol Dehydrogenases / genetics*
  • Models, Molecular
  • Molecular Sequence Data
  • Oxidation-Reduction
  • Phylogeny
  • Protein Structure, Secondary
  • Salinity
  • Structural Homology, Protein
  • Substrate Specificity
  • Transcription, Genetic

Substances

  • Fructose
  • Hydrogen Peroxide
  • Mannitol Dehydrogenases

Grants and funding

This research was supported by the National High Tech 863 Project (2012AA10A406), Shandong Agriculture Breeding Engineering Biological Resources Innovation of Research Project, National Key Technology Research & Development Program (2013BAB01B01), and Ocean Public Welfare Scientific Research Project (201405040). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.