Optical density and cell counts from flow cytometry of Ruegeria pomeroyi laboratory cultures

dc.contributor.author Diaz, Julia
dc.contributor.author Duhamel, Solange
dc.contributor.author Adams, Jamee
dc.coverage.temporal 20210309 - 20210323 (UTC)
dc.date.accessioned 2023-06-12T20:00:19Z
dc.date.available 2023-06-12T20:00:19Z
dc.date.created 2023-06-09
dc.date.issued 2023-06-12
dc.description Dataset: Ruegeria pomeroyi OD and FCM
dc.description.abstract Optical density (OD) and cell counts from flow cytometry (FCM) of marine bacterium Ruegeria pomeroyi laboratory cultures. These data were collected as part of a study of "Dissolved organic phosphorus utilization by the marine bacterium Ruegeria pomeroyi DSS-3 reveals chain length-dependent polyphosphate degradation" (Adams et al., 2022). Study abstract: Dissolved organic phosphorus (DOP) is a critical nutritional resource for marine microbial communities. However, the relative bioavailability of different types of DOP, such as phosphomonoesters (P-O-C) and phosphoanhydrides (P-O-P), is poorly understood. Here we assess the utilization of these P sources by a representative bacterial copiotroph, Ruegeria pomeroyi DSS-3. All DOP sources supported equivalent growth by R. pomeroyi, and all DOP hydrolysis rates were upregulated under phosphorus depletion (-P). A long-chain polyphosphate (45polyP) showed the lowest hydrolysis rate of all DOP substrates tested, including tripolyphosphate (3polyP). Yet the upregulation of 45polyP hydrolysis under -P was greater than any other substrate analyzed. Proteomics revealed three common P acquisition enzymes potentially involved in polyphosphate utilization, including two alkaline phosphatases, PhoD and PhoX, and one 5'-nucleotidase (5’-NT). Results from DOP substrate competition experiments show that these enzymes likely have broad substrate specificities, including chain length-dependent reactivity toward polyphosphate. These results confirm that DOP, including polyP, are bioavailable nutritional P sources for R. pomeroyi, and possibly other marine heterotrophic bacteria. Furthermore, the chain-length dependent mechanisms, rates and regulation of polyP hydrolysis suggest that these processes may influence the composition of DOP and the overall recycling of nutrients within marine dissolved organic matter. For a complete list of measurements, refer to the full dataset description in the supplemental file 'Dataset_description.pdf'. The most current version of this dataset is available at: https://www.bco-dmo.org/dataset/897371
dc.description.sponsorship NSF Division of Ocean Sciences (NSF OCE) OCE-1736967, NSF Division of Ocean Sciences (NSF OCE) OCE-1737083, NSF Division of Ocean Sciences (NSF OCE) OCE-2001212, NSF Division of Ocean Sciences (NSF OCE) OCE-1948042
dc.identifier.citation Diaz, J., Duhamel, S., & Adams, J. (2023). Optical density and cell counts from flow cytometry of Ruegeria pomeroyi laboratory cultures (Version 1) [Data Set]. Biological and Chemical Oceanography Data Management Office (BCO-DMO). https://doi.org/10.26008/1912/bco-dmo.897371.1
dc.identifier.doi 10.26008/1912/bco-dmo.897371.1
dc.identifier.uri https://hdl.handle.net/1912/66351
dc.language.iso en_US
dc.publisher Biological and Chemical Oceanography Data Management Office (BCO-DMO). Contact: bco-dmo-data@whoi.edu
dc.relation.uri http://lod.bco-dmo.org/id/dataset/897371
dc.relation.uri https://doi.org/10.26008/1912/bco-dmo.897371.1
dc.rights Creative Commons Attribution 4.0
dc.rights.uri https://creativecommons.org/licenses/by/4.0/
dc.title Optical density and cell counts from flow cytometry of Ruegeria pomeroyi laboratory cultures
dc.type Dataset
dspace.entity.type Publication
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