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Evaluation of the Mass Spectral Analysis of Soil Inositol, Inositol Phosphates, and Related Compounds
Author(s) -
L'Annunziata Michael F.,
Fuller Wallace H.
Publication year - 1976
Publication title -
soil science society of america journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.836
H-Index - 168
eISSN - 1435-0661
pISSN - 0361-5995
DOI - 10.2136/sssaj1976.03615995004000050022x
Subject(s) - cyclitol , chemistry , inositol , mass spectrum , mass spectrometry , phosphate , ion , deuterium , hydrolysis , chromatography , organic chemistry , biochemistry , physics , receptor , quantum mechanics
The potential of mass spectrometry in the structure analysis of soil inositol, inositol phosphate carbon, and soil microbial metabolites was evaluated. Mass spectra of myo‐inositol (I) isolated from the organic phosphate fraction of a forest soil, quebrachitol (II), myo‐Inositol hexaacetate (III), d,l ‐epi‐inosose (IV), and of compounds I and II labeled with deuterium in the hydroxyl groups were determined. Intense fragment ion spectral peaks at mass/charge (m/e) 60, 73, and 102 were common to each of the natural occurring cyclitol structures studied. Structural variations of inositol were found to be identifiable by peak shifts from m/e 60, 73, and 102 to other m/e values as due to attached groups or to other carbon oxidation states. An exchange of the hydroxyl protons with deuterium permitted the determination of the number of hydroxyl groups on a given mass spectral ion fragment and supplied evidence for the presence of attached groups. Studies dealing with phosphated compounds in soils required a hydrolysis of the phosphate esters prior to the mass spectral analysis. The mass spectral analysis was found most useful for the identification of cyclitol structures in soil, microbial, and plant metabolism studies when the sample size is limited to microgram quantities.