From Retention Time to Functional Group Assignment: A Chemical Database-Driven Approach for High-Resolution Mass Data of Marine Dissolved Organic Matter.

rationaleThe high chemodiversity of marine dissolved organic matter (DOM) has challenged identification of singular DOM components. To infer chemical structure features of DOM with accurately determined molecular formulas, we assessed if empirically determined elution properties of stoichiometrically identical isomers obtained from a chemical database would predict features, such as the type and number of functional groups, in structurally unknown DOM isomers.

methodsDOM of different origin (North Sea, Southern Ocean) was analysed by LC-FT-MS using two different mass spectrometry methods. Chromatographic retention of DOM isomers was correlated with calculated retention properties of structurally known isomers in PubChem. A total of 7.7 million chemical identifiers were queried for their computed octanol-water coefficients (logP). The 50 most intense molecular formulas were queried for PubChem structure data files. The number and type of structural features was assigned to logP bins across the DOM elution window, to correlate the contribution of database-derived structure features to retention time of structurally unknown DOM isomers.

resultsThe intensity-weighted average of logP for C

conclusionsWe hypothesised DOM isomers belonging to comparatively older Southern Ocean water to elute earlier than young and less degraded molecules present in North Sea water. This hypothesis was verified based on three exemplarily selected molecular formulas cooccurring in all water samples. Our strategy circumvents issues of chimeric fragmentation spectra and furthermore adds retention time as a new physicochemical descriptor of DOM molecules.