Complexation of metals by phytosiderophores revealed by CE-ESI-MS and CE-ICP-MS

被引:34
|
作者
Dell'mour, Madeleine
Koellensperger, Gunda
Quirino, Joselito P. [2 ]
Haddad, Paul R. [2 ]
Stanetty, Christian
Oburger, Eva [3 ]
Puschenreiter, Markus [3 ]
Hann, Stephan [1 ]
机构
[1] Univ Nat Resources & Appl Life Sci, Dept Chem, BOKU Vienna, A-1190 Vienna, Austria
[2] Univ Tasmania, Sch Chem, Australian Ctr Res Separat Sci, Hobart, Tas, Australia
[3] Univ Nat Resources & Appl Life Sci, Dept Forest & Soil Sci, A-1190 Vienna, Austria
基金
奥地利科学基金会;
关键词
CE-ESI-MS; CE-ICP-MS; Metal complexation; Phytosiderophores; Rhizosphere; PLASMA-MASS SPECTROMETRY; CAPILLARY-ELECTROPHORESIS; MUGINEIC ACID; IRON ACQUISITION; HUMIC-ACID; CHROMATOGRAPHY; SPECIATION; NICKEL; SEPARATION; STABILITY;
D O I
10.1002/elps.200900635
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
CE-ESI-MS and CE-ICP-MS were implemented for studying three phytosiderophores (mugineic acid, epi-mugineic acid and deoxymugineic acid) and their metal complexes Free ligands and ferric complexes were analyzed using the first methodology, while six free metals (Co(II), Cu(II), Fe(III), Mn(II), Ni(II) and Zn(II)) together with the corresponding complexes were investigated by the latter technique. CE separation was realized at a voltage of +25 kV employing a BGE containing 20 mM ammonium bicarbonate at pH 7 2 Both techniques revealed limits of detection in the high nM to low mu M range Standard additions to hydroponic samples of H. distichon, cv. Bodega (spring barley) showed regression coefficients for the metal-ligand complexes ranging from 0 984 to 0 999 Additionally, results of a competitivity study allowed the determination of relative metal-phytosiderophore complex stability constants of deoxymugineic/mugineic acid.
引用
收藏
页码:1201 / 1207
页数:7
相关论文
共 50 条
  • [1] Speciation of Aluminum by CE-ESI-MS and CE-ICP-MS
    Nakamoto, Daisuke
    Tanaka, Miho
    BUNSEKI KAGAKU, 2014, 63 (05) : 383 - 390
  • [2] Application of CE-ICP-MS and CE-ESI-MS in metalloproteomics:: challenges, developments, and limitations
    Prange, A
    Pröfrock, D
    ANALYTICAL AND BIOANALYTICAL CHEMISTRY, 2005, 383 (03) : 372 - 389
  • [3] Application of CE-ICP-MS and CE-ESI-MS/MS for identification of Zn-binding ligands in Goji berries extracts
    Ruzik, Lena
    Kwiatkowski, Piotr
    TALANTA, 2018, 183 : 102 - 107
  • [4] CE-ESI-MS shows potential
    不详
    TRAC-TRENDS IN ANALYTICAL CHEMISTRY, 2008, 27 (09) : VII - VII
  • [5] CE-ICP-MS for studying interactions between metals and biomolecules
    Yin, Xue-Bo
    Li, Yan
    Yan, Xiu-Ping
    TRAC-TRENDS IN ANALYTICAL CHEMISTRY, 2008, 27 (06) : 554 - 565
  • [6] Development of a sheathless CE-ESI-MS interface
    Hirayama, Akiyoshi
    Abe, Hiroshi
    Yamaguchi, Nozomi
    Tabata, Sho
    Tomita, Masaru
    Soga, Tomoyoshi
    ELECTROPHORESIS, 2018, 39 (11) : 1382 - 1389
  • [7] Direct analysis of reduced and oxidized glutathione by CE-ESI-MS/MS
    Assuncao, Nilson Antonio
    Soare, Chrislaine Oliveira
    Dominque, Olivia
    Stevanil, Cassius Vinicius
    Becharal, Etelvino Jose Henriques
    FREE RADICAL BIOLOGY AND MEDICINE, 2007, 43 : S13 - S13
  • [8] Peptide characterization by CE-ESI-MS with orthogonal spray
    Serwe, M
    Ross, G
    CHROMATOGRAPHIA, 1999, 49 (Suppl 1) : S73 - S77
  • [9] Peptide characterization by CE-ESI-MS with orthogonal spray
    M. Serwe
    G. Ross
    Chromatographia, 1999, 49 : S73 - S77
  • [10] CE-ICP-MS: Advantages and improvements in selenium speciation
    Michalke, B
    SPECTROSCOPY, 2000, 15 (04) : 30 - +