TY - JOUR
T1 - From biomolecules to biogeochemistry
T2 - Exploring the interaction of an indigenous bacterium with gold
AU - Sanyal, Santonu K.
AU - Pukala, Tara
AU - Mittal, Parul
AU - Reith, Frank
AU - Brugger, Joël
AU - Etschmann, Barbara
AU - Shuster, Jeremiah
N1 - Funding Information:
Proteomic analysis and electron microscopy analysis were performed at the Adelaide Proteomics Centre and Adelaide Microscopy, respectively, at the University of Adelaide. This research was funded by the Australian Research Council grant ( ARC-FT100150200 ) awarded to the late Frank Reith (c/o JS). The support Frank provided to his research group and colleagues was inspiration to pursue this study and see it to fruition despite his lamentable absence. Therefore, this story is dedicated inrespect to him and his passion for gold geomicrobiology research – we miss you, Frank.
Funding Information:
Proteomic analysis and electron microscopy analysis were performed at the Adelaide Proteomics Centre and Adelaide Microscopy, respectively, at the University of Adelaide. This research was funded by the Australian Research Council grant (ARC-FT100150200) awarded to the late Frank Reith (c/o JS). The support Frank provided to his research group and colleagues was inspiration to pursue this study and see it to fruition despite his lamentable absence. Therefore, this story is dedicated inrespect to him and his passion for gold geomicrobiology research – we miss you, Frank.
Publisher Copyright:
© 2023 The Author(s)
PY - 2023/10
Y1 - 2023/10
N2 - Specialised microbial communities colonise the surface of gold particles in soils/sediments, and catalyse gold dissolution and re-precipitation, thereby contributing to the environmental mobility and toxicity of this ‘inert’ precious metal. We assessed the proteomic and physiological response of Serratia proteamaculans, the first metabolically active bacterium enriched and isolated directly from natural gold particles, when exposed to toxic levels of soluble Au3+ (10 μM). The results were compared to a metal-free blank, and to cultures exposed to similarly toxic levels of soluble Cu2+ (0.1 mM); Cu was chosen for comparison because it is closely associated with Au in nature due to similar geochemical properties. A total of 273 proteins were detected from the cells that experienced the oxidative effects of soluble Au, of which 139 (51%) were upregulated with either sole expression (31%) or had synthesis levels greater than the Au-free control (20%). The majority (54%) of upregulated proteins were functionally different from up-regulated proteins in the bacteria-copper treatment. These proteins were related to broad functions involving metabolism and biogenesis, followed by cellular process and signalling, indicating significant specificity for Au. This proteomic study revealed that the bacterium upregulates the synthesis of various proteins related to oxidative stress response (e.g., Monothiol-Glutaredoxin, Thiol Peroxidase, etc.) and cellular damage repair, which leads to the formation of metallic gold nanoparticles less toxic than ionic gold. Therefore, indigenous bacteria may mediate the toxicity of Au through two different yet simultaneous processes: i) repairing cellular components by replenishing damaged proteins and ii) neutralising reactive oxygen species (ROS) by up-regulating the synthesis of antioxidants. By connecting the fields of molecular bacteriology and environmental biogeochemistry, this study is the first step towards the development of biotechnologies based on indigenous bacteria applied to gold bio-recovery and bioremediation of contaminated environments.
AB - Specialised microbial communities colonise the surface of gold particles in soils/sediments, and catalyse gold dissolution and re-precipitation, thereby contributing to the environmental mobility and toxicity of this ‘inert’ precious metal. We assessed the proteomic and physiological response of Serratia proteamaculans, the first metabolically active bacterium enriched and isolated directly from natural gold particles, when exposed to toxic levels of soluble Au3+ (10 μM). The results were compared to a metal-free blank, and to cultures exposed to similarly toxic levels of soluble Cu2+ (0.1 mM); Cu was chosen for comparison because it is closely associated with Au in nature due to similar geochemical properties. A total of 273 proteins were detected from the cells that experienced the oxidative effects of soluble Au, of which 139 (51%) were upregulated with either sole expression (31%) or had synthesis levels greater than the Au-free control (20%). The majority (54%) of upregulated proteins were functionally different from up-regulated proteins in the bacteria-copper treatment. These proteins were related to broad functions involving metabolism and biogenesis, followed by cellular process and signalling, indicating significant specificity for Au. This proteomic study revealed that the bacterium upregulates the synthesis of various proteins related to oxidative stress response (e.g., Monothiol-Glutaredoxin, Thiol Peroxidase, etc.) and cellular damage repair, which leads to the formation of metallic gold nanoparticles less toxic than ionic gold. Therefore, indigenous bacteria may mediate the toxicity of Au through two different yet simultaneous processes: i) repairing cellular components by replenishing damaged proteins and ii) neutralising reactive oxygen species (ROS) by up-regulating the synthesis of antioxidants. By connecting the fields of molecular bacteriology and environmental biogeochemistry, this study is the first step towards the development of biotechnologies based on indigenous bacteria applied to gold bio-recovery and bioremediation of contaminated environments.
KW - Biogeochemistry
KW - Copper
KW - Gold
KW - Gold-associated proteins
KW - Microbe-mineral interaction
KW - Serratia proteamaculans
UR - http://www.scopus.com/inward/record.url?scp=85168779956&partnerID=8YFLogxK
U2 - 10.1016/j.chemosphere.2023.139657
DO - 10.1016/j.chemosphere.2023.139657
M3 - Article
C2 - 37543229
AN - SCOPUS:85168779956
SN - 0045-6535
VL - 339
JO - Chemosphere
JF - Chemosphere
M1 - 139657
ER -