Zinc-histidine as nucleation centers for growth of ZnS nanocrystals

Biochem Biophys Res Commun. 2000 May 27;272(1):29-35. doi: 10.1006/bbrc.2000.2712.

Abstract

Histidine is a chelator of zinc, most notably in zinc-finger proteins (zinc coordinated by cysteine and histidine) and in hyperaccumulator plants. Sulfide incorporation into molecules containing metal-cysteinyl complexes has been shown to occur in vivo in certain yeasts, leading to enhanced metal tolerance. Demonstrated here for the first time is incorporation of sulfide into zinc-histidine, resulting in histidine-ZnS nanocrystals (NCs) having unique optical properties. Sulfide complexation occurred optimally at alkaline pH into zinc-(histidine)2 species, and UV/Vis absorption maxima were red-shifted as increasing sulfide addition occurred. Intermediate sulfide concentrations led to multiple, thermodynamically preferred NC species within a sample. Fluorescence of histidine-ZnS NCs was greater than ZnS prepared previously with cysteinyl peptides. Transmission electron microscopy and selected-area electron diffraction indicated hexagonal ZnS crystals having an average size of 4.2 nm. A photocatalytic application of histidine-ZnS NCs was shown by efficient degradation of p-nitrophenol and paraquat in the presence of UV irradiation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Binding Sites
  • Chelating Agents / chemistry
  • Crystallization
  • Histidine / chemistry
  • Hydrogen-Ion Concentration
  • Microscopy, Electron
  • Organometallic Compounds / chemistry
  • Oxidation-Reduction
  • Photochemistry
  • Spectrometry, Fluorescence
  • Spectrophotometry
  • Spectrophotometry, Ultraviolet
  • Sulfides / chemistry*
  • Zinc / chemistry*
  • Zinc Compounds / chemistry*

Substances

  • Chelating Agents
  • Organometallic Compounds
  • Sulfides
  • Zinc Compounds
  • zinc-histidine complex
  • Histidine
  • Zinc
  • zinc sulfide