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Identification of a new phospholipase D in Carica papaya latex
Authors:Abdelkafi Slim  Abousalham Abdelkarim  Fendri Imen  Ogata Hiroyuki  Barouh Nathalie  Fouquet Benjamin  Scheirlinckx Frantz  Villeneuve Pierre  Carrière Frédéric
Affiliation:CNRS, Aix-Marseille Université, Enzymologie Interfaciale et Physiologie de la Lipolyse, Marseille, France. slim.abdelkafi@enis.rnu.tn
Abstract:Phospholipase D (PLD) is a lipolytic enzyme involved in signal transduction, vesicle trafficking and membrane metabolism. It catalyzes the hydrolysis and transphosphatidylation of glycerophospholipids at the terminal phosphodiester bond. The presence of a PLD in the latex of Carica papaya (CpPLD1) was demonstrated by transphosphatidylation of phosphatidylcholine (PtdCho) in the presence of 2% ethanol. Although the protein could not be purified to homogeneity due to its presence in high molecular mass aggregates, a protein band was separated by SDS-PAGE after SDS/chloroform-methanol/TCA-acetone extraction of the latex insoluble fraction. This material was digested with trypsin and the amino acid sequences of the tryptic peptides were determined by micro-LC/ESI/MS/MS. These sequences were used to identify a partial cDNA (723 bp) from expressed sequence tags (ESTs) of C. papaya. Based upon EST sequences, a full-length gene was identified in the genome of C. papaya, with an open reading frame of 2424 bp encoding a protein of 808 amino acid residues, with a theoretical molecular mass of 92.05 kDa. From sequence analysis, CpPLD1 was identified as a PLD belonging to the plant phosphatidylcholine phosphatidohydrolase family.
Keywords:CpPLD1, Carica papaya phospholipase   D1, phospholipase D   EST, expressed sequence tag   EtOH, ethanol   MS, mass spectrometry   ORF, open reading frame   PA, phosphatidic acid   PEtOH, phosphatidylethanol   PLD, PtdCho, phosphatidylcholine   SDS-PAGE, sodium dodecyl sulfate-polyacrylamide gel   TBS, tris buffer saline   TLC, thin-layer chromatography
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