Critical regions for the sweetness of brazzein

FEBS Lett. 2003 Jun 5;544(1-3):33-7. doi: 10.1016/s0014-5793(03)00383-1.

Abstract

Brazzein is a small, heat-stable, intensely sweet protein consisting of 54 amino acid residues. Based on the wild-type brazzein, 25 brazzein mutants have been produced to identify critical regions important for sweetness. To assess their sweetness, psychophysical experiments were carried out with 14 human subjects. First, the results suggest that residues 29-33 and 39-43, plus residue 36 between these stretches, as well as the C-terminus are involved in the sweetness of brazzein. Second, charge plays an important role in the interaction between brazzein and the sweet taste receptor.

MeSH terms

  • Amino Acid Sequence
  • Escherichia coli / metabolism
  • Fruit
  • Genes, Plant
  • Humans
  • Models, Molecular
  • Molecular Sequence Data
  • Mutagenesis, Site-Directed
  • Plant Proteins / chemistry*
  • Plant Proteins / metabolism*
  • Protein Structure, Tertiary
  • Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
  • Spectrophotometry
  • Taste
  • Ultraviolet Rays
  • Water / chemistry

Substances

  • Plant Proteins
  • brazzein protein, Pentadiplandra brazzeana
  • Water