Preprints
https://doi.org/10.5194/egusphere-2026-5821
https://doi.org/10.5194/egusphere-2026-5821
07 Oct 2026
 | 07 Oct 2026
Status: this preprint is open for discussion and under review for Biogeosciences (BG).

Technical note: Assessing potential hydrolytic enzyme activities on frozen samples as a tool to bridge microbial rate measurements with omics analysis

Kai Ziervogel, James Lin, and Leo Windels

Abstract. Extracellular hydrolytic enzymes play a central role in marine carbon and nutrient cycling. Their activities are typically measured immediately after sample collection, limiting integration with omics analyses conducted on frozen samples. We assessed the effects of one month of storage at -20 °C and -80 °C on potential activities of leucine aminopeptidase (LAP), β-glucosidase (β-glu), N-acetyl-β-D-glucosaminidase (NAG), and alkaline phosphatase (AP) in estuarine and offshore samples from the Gulf of Maine. Activities of LAP, β-glu, and NAG were generally well preserved on frozen filters, particularly at -80 °C. In contrast, AP showed greater sensitivity to freezing, especially in offshore particle-associated samples. All enzymes exhibited greater activity losses in frozen whole water samples than on filters. These results demonstrate that frozen filters, particularly when stored at -80 °C, can preserve several ecologically relevant extracellular enzyme activities and provide a practical approach to link enzyme assays with omics measurements on the same samples.

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Kai Ziervogel, James Lin, and Leo Windels

Status: open (until 18 Nov 2026)

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Kai Ziervogel, James Lin, and Leo Windels
Kai Ziervogel, James Lin, and Leo Windels
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Short summary
Marine microbes drive ocean elemental cycling, yet linking microbial diversity with biogeochemical rate measurements remains a longstanding challenge. We show that extracellular enzyme activities can be preserved during frozen storage, particularly on particle-containing filters. The findings enable direct coupling of enzyme activity measurements with omics analyses on archived samples, strengthening links between microbial community composition, function, and ecosystem processes.
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