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Molecular‐level characterization of reactive and refractory dissolved natural organic nitrogen compounds by atmospheric pressure photoionization coupled to Fourier transform ion cyclotron resonance mass spectrometry
Author(s) -
Osborne Daniel M.,
Podgorski David C.,
Bronk Deborah A.,
Roberts Quinn,
Sipler Rachel E.,
Austin David,
Bays James S.,
Cooper William T.
Publication year - 2013
Publication title -
rapid communications in mass spectrometry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.528
H-Index - 136
eISSN - 1097-0231
pISSN - 0951-4198
DOI - 10.1002/rcm.6521
Subject(s) - chemistry , fourier transform ion cyclotron resonance , mass spectrometry , analytical chemistry (journal) , photoionization , mass spectrum , polyatomic ion , ion cyclotron resonance , ion , ionization , chromatography , organic chemistry , cyclotron
RATIONALE Dissolved organic nitrogen (DON) represents a significant fraction of the total dissolved nitrogen pool in most surface waters and serves as an important nitrogen source for phytoplankton and bacteria. As with other natural organic matter mixtures, ultrahigh resolution Fourier transform ion cyclotron resonance mass spectrometry (FTICRMS) is the only technique currently able to provide molecular composition information on DON. Although electrospray ionization (ESI) is the most commonly used ionization method, it is not very efficient at ionizing most DON components. METHODS Positive‐ and negative‐mode atmospheric pressure photoionization (APPI) coupled with ultrahigh resolution FTICRMS at 9.4 T were compared for determining the composition of DON before and after bioassays. Toluene was added as the APPI dopant to the solid‐phase DON extracts, producing a final sample that was 90% methanol and 10% toluene by volume. RESULTS Positive‐mode (+) APPI proved significantly more efficient at ionizing DON; 62% of the formulas that could be assigned in the positive‐ion spectrum contained at least one nitrogen atom vs. 31% in the negative‐ion spectrum. FTICR mass spectral data indicated that most of the refractory DON compounds (i.e. nonreactive during the 5 days of the incubation) had molecular compositions representative of lignin‐like molecules, while lipid‐like and protein‐like molecules comprised most of the small reactive component of the DON pool. CONCLUSIONS From these data we conclude that (+) APPI FTICRMS is a promising technique for describing the molecular composition of DON mixtures. The technique is particularly valuable in assessing the bioavailability of individual components of DON when combined with bioassays. Copyright © 2013 John Wiley & Sons, Ltd.