4.6 Article

Laboratory In-Situ Production of Autochthonous and Allochthonous Fluorescent Organic Matter by Freshwater Bacteria

期刊

MICROORGANISMS
卷 9, 期 8, 页码 -

出版社

MDPI
DOI: 10.3390/microorganisms9081623

关键词

fluorescent organic matter; autochthonous; allochthonous; excitation emission matrix fluorescence spectroscopy; environmental microbiology

资金

  1. Natural Environmental Research Council (NERC) [NE/K007572/1, NE/R003106/1]
  2. Chelsea Technologies Ltd. [NE/K007572/1]
  3. Engineering & Physical Sciences Research Council (EPSRC) [NE/R003106/1]
  4. Department of Science and Technology (DST) as part of an India-UK Water Quality Programme award [NE/R003106/1]
  5. NERC [NE/R003106/1] Funding Source: UKRI

向作者/读者索取更多资源

This study investigates the origin and range of fluorescent organic matter (FOM) produced by environmentally sourced freshwater bacteria, challenging the binary classification of FOM as either autochthonous or allochthonous. The study demonstrates that FOM processing and production occur along a dynamic continuum, with both in-situ production by microbial processes and transportation into aquatic systems from external sources. Additionally, fluorescence intensity data for environmental bacteria isolate monocultures are presented for the first time, allowing for the assessment of the relative contribution of different bacteria to the autochthonous FOM pool.
This work investigates the origin and range of fluorescent organic matter (FOM) produced in-situ by environmentally sourced freshwater bacteria. Aquatic FOM is an essential component in global carbon cycling and is generally classified as either autochthonous, produced in-situ via microbial processes, or allochthonous, transported into aquatic systems from external sources. We have demonstrated that, within laboratory model systems, environmentally sourced mixed microbial communities and bacterial isolates can produce and/or export FOM associated with both autochthonous and allochthonous material. This study focuses on fluorescence peak B, T, M, C and C+, exploring (1) the cellular nature of FOM produced, (2) FOM exported as extracellular material into the water column and (3) the impact of physical cell lysis on FOM signature. For the laboratory model systems studied, Peak T fluorescence is retained within bacterial cells (>68%), while Peak C fluorescence is mainly observed as extracellular material (>80%). Peak M is identified as both cellular and extracellular FOM, produced by all isolated freshwater microorganisms investigated. The origin of Peak C+ is postulated to originate from functional metabolites associated with specific microorganisms, seen specifically within the Pseudomonas sp. monoculture here. This work challenges the binary classification of FOM as either allochthonous or autochthonous, suggesting that FOM processing and production occurs along a dynamic continuum. Within this study, fluorescence intensity data for the environmental bacteria isolate monocultures are presented as enumeration corrected data, for the first time providing quantitative fluorescence data per bacterial colony forming unit (cfu). From this, we are able to assess the relative contribution of different bacteria to the autochthonous FOM pool and if this material is cellular or extracellular.

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