4.6 Article

Determination of 15N/14N of Ammonium, Nitrite, Nitrate, Hydroxylamine, and Hydrazine Using Colorimetric Reagents and Matrix-Assisted Laser Desorption Ionization-Time-of-Flight Mass Spectrometry (MALDI-TOF MS)

Journal

APPLIED AND ENVIRONMENTAL MICROBIOLOGY
Volume 88, Issue 7, Pages -

Publisher

AMER SOC MICROBIOLOGY
DOI: 10.1128/aem.02416-21

Keywords

nitrogen cycle; nitrogen isotope; N-15 atom%; mass spectrometry; colorimetric reagent; MALDI-TOF MS

Funding

  1. JSPS KAKENHI [19K05805, 20H02290, 20H00641, 19H00776]
  2. Institute for Fermentation, Osaka (IFO)
  3. MnDRIVE Initiative of the University of Minnesota
  4. MEXT Project for promoting public utilization of advanced research infrastructure [JPMXS0430300121]
  5. Japan Public-Private Partnership Student Study Abroad Program
  6. National Institute of Technology and evaluation (NBRC) (Chiba, Japan)
  7. Grants-in-Aid for Scientific Research [19H00776, 20H02290, 20H00641, 19K05805] Funding Source: KAKEN

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The nitrogen cycle is an essential process that involves the conversion of nitrogenous compounds to different nitrogen species. The N-15 labeling approach is a powerful technique to study nitrogen transformation reactions in cultures. A simple and high-throughput mass spectrometry method was developed to determine the N-15 atoms percent of various nitrogen species in liquid samples.
In the nitrogen (N) cycle, nitrogenous compounds are chemically and biologically converted to various aqueous and gaseous N species. The N-15-labeling approach is a powerful culture-dependent technique to obtain insights into the complex nitrogen transformation reactions that occur in cultures. In the N-15-labeling approach, the fates of supplemented N-15- and/or unlabeled gaseous and aqueous compounds are tracked by mass spectrometry (MS) analysis, whereas MS analysis of aqueous N species requires laborious sample preparation steps and is performed using isotope-ratio mass spectrometry, which requires an expensive mass spectrometer. We developed a simple and high-throughput MS method for determining the N-15 atoms percent of NH4+, NO2-, NO3-, NH2OH, and N2H4, where liquid samples (<0.5 mL) were mixed with colorimetric reagents (naphthylethylenediamine for NO2-, indophenol for NH4+, and p-aminobenzaldehyde for N2H4), and the mass spectra of the formed N complex dyes were obtained by matrix-assisted laser desorption ionization-time-of-flight (MALDI-TOF) MS. NH2OH and NO3- were chemically converted to NO2- by iodine oxidation and copper/hydrazine reduction reaction, respectively, prior to the above colorimetric reaction. The intensity of the isotope peak (M + 1 or M + 2) increased when the N complex dye was formed by coupling with a N-15-labeled compound, and a linear relationship was found between the determined N-15/N-14 peak ratio and N-15 atom% for the tested N species. The developed method was applied to bacterial cultures to examine their N-transformation reactions, enabling us to observe the occurrence of NO2- oxidation and NO3- reduction in a hypoxic Nitrobacter winogradskyi culture. IMPORTANCE N-15/N-14 analysis for aqueous N species is a powerful tool for obtaining insights into the global N cycle, but the procedure is cumbersome and laborious. The combined use of colorimetric reagents and MALDI-TOF MS, designated color MALDI-TOF MS, enabled us to determine the N-15 atom% of common aqueous N species without laborious sample preparation and chromatographic separation steps; for instance, the N-15 atom% of NO2- can be determined from >1,000 liquid samples daily at <$1 (U.S.) per 384 samples for routine analysis. This convenient MS method is a powerful tool that will advance our ability to explore the N-transformation reactions that occur in various environments and biological samples. N-15/N-14 analysis for aqueous N species is a powerful tool for obtaining insights into the global N cycle, but the procedure is cumbersome and laborious. The combined use of colorimetric reagents and MALDI-TOF MS, designated color MALDI-TOF MS, enabled us to determine the N-15 atom% of common aqueous N species without laborious sample preparation and chromatographic separation steps; for instance, the N-15 atom% of NO2- can be determined from >1,000 liquid samples daily at <$1 (U.S.) per 384 samples for routine analysis.

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