Copper mobilisation from Cu sulphide minerals by methanobactin: Effect of pH, oxygen and natural organic matter.

Cu sulphide dissolution aerobic methane oxidation chalkophore ligand-promoted dissolution methanobactin microbial Cu acquisition

Journal

Geobiology
ISSN: 1472-4669
Titre abrégé: Geobiology
Pays: England
ID NLM: 101185472

Informations de publication

Date de publication:
09 2022
Historique:
revised: 03 05 2022
received: 30 11 2021
accepted: 24 05 2022
pubmed: 19 6 2022
medline: 20 8 2022
entrez: 18 6 2022
Statut: ppublish

Résumé

Aerobic methane oxidation (MOx) depends critically on the availability of copper (Cu) as a crucial component of the metal centre of particulate methane monooxygenase, one of the main enzymes involved in MOx. Some methanotrophs have developed Cu acquisition strategies, in which they exude Cu-binding ligands termed chalkophores under conditions of low Cu availability. A well-characterised chalkophore is methanobactin (mb), exuded by the microaerophilic methanotroph Methylosinus trichosporium OB3b. Aerobic methanotrophs generally reside close to environmental oxic-anoxic interfaces, where the formation of Cu sulphide phases can aggravate the limitation of bioavailable Cu due to their low solubility. The reactivity of chalkophores towards such Cu sulphide mineral phases has not yet been investigated. In this study, a combination of dissolution experiments and equilibrium modelling was used to examine the dissolution and solubility of bulk and nanoparticulate Cu sulphide minerals in the presence of mb as influenced by pH, oxygen and natural organic matter. In general, we show that mb is effective at increasing the dissolved Cu concentrations in the presence of a variety of Cu sulphide phases that may potentially limit Cu bioavailability. More Cu was mobilised per mole of mb from Cu sulphide nanoparticles compared with well-crystalline bulk covellite (CuS). In general, the efficacy of mb at mobilising Cu from Cu sulphides is pH-dependent. At lower pH, e.g. pH 5, mb was ineffective at solubilizing Cu. The presence of mb increased dissolved Cu concentrations between pH 7 and 8.5, where the solubility of all Cu sulphides is generally low, both in the presence and absence of oxygen. These results suggest that chalkophore-promoted Cu mobilisation from sulphide phases is an effective extracellular mechanism for increasing dissolved Cu concentrations at oxic-anoxic interfaces, particularly in the neutral to slightly alkaline pH range. This suggests that aerobic methanotrophs may be able to fulfil their Cu requirements via the exudation of mb in natural environments where the bioavailability of Cu is constrained by very stable Cu sulphide phases.

Identifiants

pubmed: 35716154
doi: 10.1111/gbi.12505
pmc: PMC9544142
doi:

Substances chimiques

Imidazoles 0
Minerals 0
Oligopeptides 0
Sulfides 0
methanobactin 0
Copper 789U1901C5
Oxygen S88TT14065

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

690-706

Informations de copyright

© 2022 The Authors. Geobiology published by John Wiley & Sons Ltd.

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Auteurs

Danielle D Rushworth (DD)

Centre for Microbiology and Environmental Systems Science, University of Vienna, Vienna, Austria.

Iso Christl (I)

Soil Chemistry, Institute of Biogeochemistry and Pollutant Dynamics, ETH, Zurich, Switzerland.

Naresh Kumar (N)

Soil Chemistry and Chemical Soil Quality, Environmental Sciences, Wageningen University, Wageningen, The Netherlands.

Kevin Hoffmann (K)

Soil Chemistry, Institute of Biogeochemistry and Pollutant Dynamics, ETH, Zurich, Switzerland.

Ruben Kretzschmar (R)

Soil Chemistry, Institute of Biogeochemistry and Pollutant Dynamics, ETH, Zurich, Switzerland.

Moritz F Lehmann (MF)

Department of Environmental Geosciences, University of Basel, Basel, Switzerland.

Walter D C Schenkeveld (WDC)

Soil Chemistry and Chemical Soil Quality, Environmental Sciences, Wageningen University, Wageningen, The Netherlands.

Stephan M Kraemer (SM)

Centre for Microbiology and Environmental Systems Science, University of Vienna, Vienna, Austria.

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Classifications MeSH