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Cleavage of phosphate from 5'-nucleotides: 5'NT/5PN activity

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Revision as of 16:57, 12 May 2026 by Hagi BucknWise (talk | contribs) (Created page with "{{BreadcrumbsNutrients}} * Page authors: PRIMO * Responsible curator: Hagen Buck-Wiese ---- __TOC__ <div class="model-box"> {| class="model-ib" style="float:right; margin-left:1em; margin-bottom:1em;" ! 5'-nucleotidase activity (5'NT) |- | '''Approach:''' radiolabelled ATP substrate assay |- | '''Context:''' incubation, lab |- | '''Spatial scale:''' point sample |- | '''Temporal scale:''' hours to da...")
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5'-nucleotidase activity (5'NT)
Approach: radiolabelled ATP substrate assay
Context: incubation, lab
Spatial scale: point sample
Temporal scale: hours to days
Units: mol ATP L-1 h-1
Community captured: heterotrophic bacteria
Co-measurements: cell abundance

Method Overview

5'-nucleotidase (5'NT, also called 5'-phosphonucleoside phosphohydrolase) cleaves phosphate from the 5' position of nucleotides such as ATP, ADP, and AMP. It represents a specific pathway for phosphorus regeneration from dissolved organic nucleotides, which are important components of dissolved organic phosphorus. Activity is measured by adding radiolabelled 32P- or 33P-labelled ATP at tracer concentrations to seawater samples incubated at in situ temperature. After incubation, the reaction is stopped and the phosphate liberated from 32/33P-ATP (free Pi) is separated from nucleotide-bound phosphate by ion-exchange chromatography or activated charcoal adsorption. The radioactivity in the Pi fraction reflects 5'NT activity[1].

Scale of measurement

Sampling of incubations run for hours to days.

Data generated

5'NT activity (mol ATP equivalents hydrolyzed L-1 h-1) at saturating substrate, representing the community's capacity to regenerate phosphate from dissolved nucleotides.

Units & currency

Units are mol ATP L-1 h-1. The currency is phosphorus.

Sample size

Typical samples are < 1 L in volume.

Repositories & databases

Limitations

Rates represent Vmax at saturating substrate; in situ rates depend on the ambient nucleotide concentration, which is typically in the low nM range and sub-saturating. The radiotracer method requires handling of 32P, a high-energy beta emitter.

Example Applications & Protocols

Classic examples

  • Ammerman & Azam (1985) Bacterial 5'-nucleotidase in aquatic ecosystems: a novel mechanism of phosphorus regeneration [1]

Recent applications

Common calculations/conversions

  • 5'NT activity (nmol Pi released L-1 h-1) = (cpmPi fraction / cpmtotal added) × [ATP added] / incubation time.

References

  1. 1.0 1.1 Ammerman, J. W., & Azam, F. (1985). Bacterial 5'-nucleotidase in aquatic ecosystems: a novel mechanism of phosphorus regeneration. Science, 227(4692), 1338–1340. https://doi.org/10.1126/science.227.4692.1338