Molecular cloning, recombinant expression, and antifungal functional characterization of the lipid transfer protein from Panax ginseng

Biotechnol Lett. 2016 Jul;38(7):1229-35. doi: 10.1007/s10529-016-2100-9. Epub 2016 Apr 6.

Abstract

Objectives: To establish an efficient expression system for a fusion protein GST-pgLTP (Lipid Transfer Protein) and to test its antifungal activity.

Results: The nucleotide sequence of LTP gene was obtained from Panax ginseng using RT-PCR. The ORF of the cDNA is 363 bp, codING for a protein OF 120 amino acids with a calculated MW of 12.09 kDa. The pgLTP gene with a His6-tag at the C-terminus was cloned into the pGEX-6p1 vector to generate a GST-fusion pgLTP protein construct that was expressed in Escherichia coli Rosetta. Following purification by Ni-NTA, the fusion protein exhibited antifungal activity against five fungi found in ginseng.

Conclusion: The fusion protein GST-pgLTP has activity against a broad spectrum of phytopathogenic fungi, and can potentially be adapted for production to combat fungal diseases that affect P. ginseng.

Keywords: Antifungal activity; Lipid transfer proteins; Panax ginseng; Protein expression and purification.

MeSH terms

  • Amino Acid Sequence
  • Antifungal Agents / chemistry
  • Antifungal Agents / classification
  • Antifungal Agents / metabolism
  • Carrier Proteins / chemistry
  • Carrier Proteins / classification
  • Carrier Proteins / genetics
  • Carrier Proteins / metabolism*
  • Cloning, Molecular
  • DNA, Complementary
  • Microbial Sensitivity Tests
  • Molecular Sequence Data
  • Panax / metabolism*
  • Plant Proteins / chemistry
  • Plant Proteins / classification
  • Plant Proteins / genetics
  • Plant Proteins / metabolism*
  • Recombinant Proteins / chemistry
  • Recombinant Proteins / classification
  • Recombinant Proteins / genetics
  • Recombinant Proteins / metabolism*

Substances

  • Antifungal Agents
  • Carrier Proteins
  • DNA, Complementary
  • Plant Proteins
  • Recombinant Proteins
  • lipid transfer protein