TY - JOUR
T1 - Elemental Sulfur Formation by Sulfuricurvum kujiense Is Mediated by Extracellular Organic Compounds
AU - Cron, Brandi
AU - Henri, Pauline
AU - Chan, Clara S.
AU - Macalady, Jennifer L.
AU - Cosmidis, Julie
N1 - Funding Information:
This work was supported by grants from the National Science Foundation to JM (EAR-1252128) and CC (EAR-1251918). Support for this study was furthermore provided by the Penn State Department of Geosciences through startup funding to JC. BC was supported by the Penn State Department of Geosciences Distinguished Postdoctoral Fellowship. TOC measurements were performed using seed funding from the Penn State Energy and Environmental Sustainability Laboratories (EESL).
Funding Information:
Edward Dudley at the Penn State E. coli reference center is thanked for providing the E. coli strain. We thank Chrissie Nims and Max Wetherington (Penn State University) for their help with Raman analyses, and TJ (Tawanda) Zimudzi (Penn State University) for his help with FTIR measurements. Karol Confer at the Water Quality Laboratory (Energy and Environmental Sustainability Laboratories) is thanked for performing TOC measurements. We thank Professor Chris House and Zhidan Zhang (Penn State University) for assistance with S. kujiense strain culture experiments. Sulfur K-edge XANES analyses were performed on beamline 4?3 of the Stanford Synchrotron Radiation Lightsource (SSRL, Stanford, CA) with the assistance of Matthew Latimer and Erik Nelson. Use of the SSRL, SLAC National Accelerator Laboratory, is supported by the U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences under Contract No. DE-AC02-76SF00515. The SSRL Structural Molecular Biology Program is supported by the DOE Office of Biological and Environmental Research, and by the National Institutes of Health, National Institute of General Medical Sciences. The contents of this publication are solely the responsibility of the authors and do not necessarily represent the official views of NIGMS or NIH. We thank Jian Wang for providing support on STXM beamline SM of the Canadian Light Source (CLS, Saskatoon, Canada). CLS is supported by the Canada Foundation for Innovation, Natural Sciences and Engineering Research Council of Canada, the University of Saskatchewan, the Government of Saskatchewan, Western Economic Diversification Canada, the National Research Council Canada, and the Canadian Institutes of Health Research. Funding. This work was supported by grants from the National Science Foundation to JM (EAR-1252128) and CC (EAR-1251918). Support for this study was furthermore provided by the Penn State Department of Geosciences through startup funding to JC. BC was supported by the Penn State Department of Geosciences Distinguished Postdoctoral Fellowship. TOC measurements were performed using seed funding from the Penn State Energy and Environmental Sustainability Laboratories (EESL).
Publisher Copyright:
© Copyright © 2019 Cron, Henri, Chan, Macalady and Cosmidis.
PY - 2019/11/27
Y1 - 2019/11/27
N2 - Elemental sulfur [S(0)] is a central and ecologically important intermediate in the sulfur cycle, which can be used by a wide diversity of microorganisms that gain energy from its oxidation, reduction, or disproportionation. S(0) is formed by oxidation of reduced sulfur species, which can be chemically or microbially mediated. A variety of sulfur-oxidizing bacteria can biomineralize S(0), either intracellularly or extracellularly. The details and mechanisms of extracellular S(0) formation by bacteria have been in particular understudied so far. An important question in this respect is how extracellular S(0) minerals can be formed and remain stable in the environment outside of their thermodynamic stability domain. It was recently discovered that S(0) minerals could be formed and stabilized by oxidizing sulfide in the presence of dissolved organic compounds, a process called S(0) organomineralization. S(0) particles formed through this mechanism possess specific signatures such as morphologies that differ from that of their inorganically precipitated counterparts, encapsulation within an organic envelope, and metastable crystal structures (presence of the monoclinic β- and γ-S8 allotropes). Here, we investigated S(0) formation by the chemolithoautotrophic sulfur-oxidizing and nitrate-reducing bacterium Sulfuricurvum kujiense (Epsilonproteobacteria). We performed a thorough characterization of the S(0) minerals produced extracellularly in cultures of this microorganism, and showed that they present all the specific signatures (morphology, association with organics, and crystal structures) of organomineralized S(0). Using “spent medium” experiments, we furthermore demonstrated that soluble extracellular compounds produced by S. kujiense are necessary to form and stabilize S(0) minerals outside of the cells. This study provides the first experimental evidence of the importance of organomineralization in microbial S(0) formation. The prevalence of organomineralization in extracellular S(0) precipitation by other sulfur bacteria remains to be investigated, and the biological role of this mechanism is still unclear. However, we propose that sulfur-oxidizing bacteria could use soluble organics to stabilize stores of bioavailable S(0) outside the cells.
AB - Elemental sulfur [S(0)] is a central and ecologically important intermediate in the sulfur cycle, which can be used by a wide diversity of microorganisms that gain energy from its oxidation, reduction, or disproportionation. S(0) is formed by oxidation of reduced sulfur species, which can be chemically or microbially mediated. A variety of sulfur-oxidizing bacteria can biomineralize S(0), either intracellularly or extracellularly. The details and mechanisms of extracellular S(0) formation by bacteria have been in particular understudied so far. An important question in this respect is how extracellular S(0) minerals can be formed and remain stable in the environment outside of their thermodynamic stability domain. It was recently discovered that S(0) minerals could be formed and stabilized by oxidizing sulfide in the presence of dissolved organic compounds, a process called S(0) organomineralization. S(0) particles formed through this mechanism possess specific signatures such as morphologies that differ from that of their inorganically precipitated counterparts, encapsulation within an organic envelope, and metastable crystal structures (presence of the monoclinic β- and γ-S8 allotropes). Here, we investigated S(0) formation by the chemolithoautotrophic sulfur-oxidizing and nitrate-reducing bacterium Sulfuricurvum kujiense (Epsilonproteobacteria). We performed a thorough characterization of the S(0) minerals produced extracellularly in cultures of this microorganism, and showed that they present all the specific signatures (morphology, association with organics, and crystal structures) of organomineralized S(0). Using “spent medium” experiments, we furthermore demonstrated that soluble extracellular compounds produced by S. kujiense are necessary to form and stabilize S(0) minerals outside of the cells. This study provides the first experimental evidence of the importance of organomineralization in microbial S(0) formation. The prevalence of organomineralization in extracellular S(0) precipitation by other sulfur bacteria remains to be investigated, and the biological role of this mechanism is still unclear. However, we propose that sulfur-oxidizing bacteria could use soluble organics to stabilize stores of bioavailable S(0) outside the cells.
UR - http://www.scopus.com/inward/record.url?scp=85076707630&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85076707630&partnerID=8YFLogxK
U2 - 10.3389/fmicb.2019.02710
DO - 10.3389/fmicb.2019.02710
M3 - Article
C2 - 31827465
AN - SCOPUS:85076707630
SN - 1664-302X
VL - 10
JO - Frontiers in Microbiology
JF - Frontiers in Microbiology
M1 - 2710
ER -