Use of Nicotiana tabacum transplastomic plants engineered to express a His-tagged CP47 for the isolation of functional photosystem II core complexes

Plant Physiol Biochem. 2017 Feb:111:266-273. doi: 10.1016/j.plaphy.2016.12.009. Epub 2016 Dec 8.

Abstract

This work focuses on the development of a molecular tool for purification of Photosystem II (PSII) from Nicotiana tabacum (L.). To this end, the chloroplast psbB gene encoding the CP47 PSII subunit was replaced with an engineered version of the same gene containing a C-terminal His-tag. Molecular analyses assessed the effective integration of the recombinant gene and its expression. Despite not exhibiting any obvious phenotype, the transplastomic plants remained heteroplasmic even after three rounds of regeneration under antibiotic selection. However, the recombinant His-tagged CP47 protein associated in vivo to the other PSII subunits allowing the isolation of a functional PSII core complex, although with low yield of extraction. These results will open up possible perspectives for further spectroscopic and structural studies.

Keywords: Biolistic chloroplast transformation; CP47 His-tag; Photosystem II; Transplastomic tobacco plants.

MeSH terms

  • Blotting, Western
  • Electrophoresis, Polyacrylamide Gel
  • Genes, Plant
  • Genetic Engineering*
  • Genetic Vectors / metabolism
  • Light-Harvesting Protein Complexes / isolation & purification*
  • Light-Harvesting Protein Complexes / metabolism
  • Mutation / genetics
  • Nicotiana / genetics*
  • Nicotiana / metabolism*
  • Phenotype
  • Photosystem II Protein Complex / isolation & purification*
  • Photosystem II Protein Complex / metabolism
  • Plants, Genetically Modified
  • Plastids / metabolism*
  • Protein Subunits / metabolism
  • Recombinant Fusion Proteins / metabolism*
  • Spectrum Analysis

Substances

  • Light-Harvesting Protein Complexes
  • Photosystem II Protein Complex
  • Protein Subunits
  • Recombinant Fusion Proteins
  • photosystem II, chlorophyll-binding protein, CP-47