Molecular cloning of a phospholipase D gene from Aspergillus nidulans and characterization of its deletion mutants

FEMS Microbiol Lett. 2003 Jul 29;224(2):231-7. doi: 10.1016/S0378-1097(03)00440-3.

Abstract

We cloned a gene pldA encoding a protein containing phospholipase D (PLD) motifs from a filamentous fungus Aspergillus nidulans. The deduced protein product of pldA consists of 833 amino acids and contains four conserved regions of a PLD gene family. Deletion mutants of pldA grew and formed conidia in a normal manner. Although PLD and transphosphatidylation activities against phosphatidylcholine of the mutant cell extract did not change, the Ca(2+)-dependent PLD activity against phosphatidylethanolamine was significantly reduced, but not in the wild-type cell extract. This activity was markedly enhanced by high osmotic growth conditions in the wild-type cells, and pldA of A. nidulans likely encodes a Ca(2+)-dependent phosphatidylethanolamine-hydrolyzing PLD.

MeSH terms

  • Aspergillus nidulans / enzymology*
  • Aspergillus nidulans / genetics*
  • Aspergillus nidulans / growth & development
  • Calcium / metabolism
  • Cloning, Molecular
  • Culture Media
  • Gene Deletion
  • Hydrolysis
  • Mutagenesis
  • Phospholipase D / genetics*
  • Phospholipase D / metabolism*
  • Phospholipids / metabolism
  • Phylogeny

Substances

  • Culture Media
  • Phospholipids
  • Phospholipase D
  • Calcium