Distinct biotite-weathering activities of Arthrobacter pascens F74 under different contact conditions.
glucose dehydrogenase activity
interaction between biotite and bacterium
mineral-weathering bacterium
weathering mechanisms
Journal
Journal of basic microbiology
ISSN: 1521-4028
Titre abrégé: J Basic Microbiol
Pays: Germany
ID NLM: 8503885
Informations de publication
Date de publication:
Apr 2020
Apr 2020
Historique:
received:
14
09
2019
revised:
02
12
2019
accepted:
03
12
2019
pubmed:
17
12
2019
medline:
9
10
2020
entrez:
17
12
2019
Statut:
ppublish
Résumé
Bacteria play important roles in mineral weathering and soil formation. However, little is known regarding the interactions between biotite and Arthrobacter strains. In this study, the mineral-mineral activities of the Arthrobacter pascens F74 isolated from a weathered rock surface were evaluated for its weathering behavior under direct contact and no contact with biotite. No contact was obtained by using dialysis bags. When directly in contact with biotite, Al and Fe concentrations increased by 9- to 47-fold compared with the controls in the presence of strain F74. Furthermore, strain F74 increased mobilized Al by 106% to 175% and Fe by 29% to 123% under direct contact than under no contact conditions. During biotite dissolution, significantly higher cell numbers and lower pH in the culture medium were observed in the presence of strain F74 under direct contact conditions than under no contact conditions. Significantly higher gluconic acid concentration and glucose dehydrogenase activity were found under direct contact conditions than under no contact and no biotite conditions. Scanning electron microscopy analysis showed cell adhesion on the biotite surface. These results demonstrated that strain F74 behaved differently with respect to biotite-weathering effectiveness and mechanisms under different contact conditions. The results also suggested that direct contact between biotite and strain F74 was important for the production of gluconic acid, cell adhesion on the mineral surface, and the mineral dissolution of the strain.
Identifiants
pubmed: 31840843
doi: 10.1002/jobm.201900518
doi:
Substances chimiques
Aluminum Silicates
0
Ferrous Compounds
0
Gluconates
0
Minerals
0
biotite
1302-27-8
Aluminum
CPD4NFA903
Iron
E1UOL152H7
Glucose 1-Dehydrogenase
EC 1.1.1.47
gluconic acid
R4R8J0Q44B
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
362-371Subventions
Organisme : National Natural Science Foundation of China
ID : 41473075
Organisme : Postgraduate Research & Practice Innovation Program of Jiangsu Province
ID : KYCX17-0654
Informations de copyright
© 2019 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
Références
White AF, Brantley SL. Chemical weathering rates of silicate minerals: an overview. In: White AF, Brantley SL, editors. Chemical weathering rates of silicate minerals. Washington, DC: Mineralogical Society of America; 1995. p. 1-22.
Shirokova LS, Bénézeth P, Pokrovsky OS, Gerard E, Bénédicte M, Alfredsson H. Effect of the heterotrophic bacterium Pseudomonas reactans on olivine dissolution kinetics and implications for CO2 storage in basalts. Geochim Cosmochim Acta. 2012;80:30-50.
Schulz S, Brankatschk R, Dümig A, Kögel-Knabner I, Schloter M, Zeyer J. The role of microorganisms at different stages of ecosystem development for soil formation. Biogeosciences. 2013;10:3983-96.
Miot J, Benzerara K, Kappler A. Investigating microbe-mineral interactions: recent advances in X-ray and electron microscopy and redox-sensitive methods. Ann Rev Earth Planetary Sci. 2014;42:271-89.
Barker WW, Welch SA, Chu S, Banfield JF. Experimental observations of the effects of bacteria on aluminosilicate weathering. Am Mineral. 1998;83:1551-63.
Huang J, Sheng XF, Xi J, He LY, Huang Z, Wang Q, et al. Depth-related changes in community structure of culturable mineral weathering bacteria and in weathering patterns caused by them along two contrasting soil profiles. Appl Environ Microbiol. 2014;80:29-42.
Zavarzina DG, Chistyakova NI, Shapkin AV, Savenko AV, Zhilina TN, Kevbrin VV, et al. Oxidative biotransformation of biotite and glauconite by alkaliphilic anaerobes: the effect of Fe oxidation on the weathering of phyllosilicates. Chem Geol. 2016;439:98-109.
Wang Q, Gao S, Ma X, Mao X, He L, Sheng X. Distinct mineral weathering effectiveness and metabolic activity between mineral-weathering bacteria Burkholderia metallica F22 and Burkholderia phytofirmans G34. Chem Geol. 2018;489:38-45.
Uroz S, Calvaruso C, Turpault MP, Frey-Klett P. Mineral weathering by bacteria: ecology, actors and mechanisms. Trends Microbiol. 2009;17:378-87.
Chen W, Luo L, He LY, Wang Q, Sheng XF. Distinct mineral weathering behaviors of the novel mineral-weathering strains Rhizobium yantingense H66 and Rhizobium etli CFN42. Appl Environ Microbiol. 2016;82:4090-99.
Perez A, Rossano S, Trcera N, Huguenot D, Fourdrin C, Verney-Carron A, et al. Bioalteration of synthetic Fe(III)-, Fe(II)-bearing basaltic glasses and Fe-free glass in the presence of the heterotrophic bacteria strain Pseudomonas aeruginosa: impact of siderophores. Geochim Cosmochim Acta. 2016;188:147-62.
Wightman PG, Fein JB. The effect of bacterial cell wall adsorption on mineral solubilities. Chem Geol. 2004;212:247-54.
Ahmed E, Holmström SJM. Microbe-mineral interactions: the impact of surface attachment on mineral weathering and element selectivity by microorganisms. Chem Geol. 2015;403:13-23.
Brown GE Jr, Foster AL, Ostergren JD. Mineral surfaces and bioavailability of heavy metals: a molecular-scale perspective. Proc Natl Acad Sci U S A. 1999;96:3388-95.
Bennett PC, Rogers JR, Choi WJ, Hiebert FK. Silicates, silicate weathering, and microbial ecology. Geomicrobiol J. 2001;18:3-19.
Cheng C, Wang Q, He L, Sheng X. Change in mineral weathering behaviors of a bacterium Chitinophaga jiangningensis JN53 under different nutrition conditions. J Basic Microbiol. 2017;57:293-301.
Collignon C, Uroz S, Turpault M-P, Frey-Klett P. Seasons differently impact the structure of mineral weathering bacterial communities in beech and spruce stands. Soil Biol Biochem. 2011;43:2012-22.
Calvaruso C, Turpault M-P, Frey-Klett P, Uroz S, Pierret MC, Tosheva Z, et al. Increase of apatite dissolution rate by Scots pine roots associated or not with Burkholderia glathei PML1(12)Rp in open-system flow microcosms. Geochim Cosmochim Acta. 2013;106:287-306.
Wang Q, Cheng C, He L, Huang Z, Sheng X. Characterization of depth-related changes in bacterial communities involved in mineral weathering along a mineral-rich soil profile. Geomicrobiol J. 2014;31:431-44.
Frey B, Rieder SR, Brunner I, Plotze M, Koetzsch S, Lapanje A, et al. Weathering-associated bacteria from the Damma glacier forefield: physiological capabilities and impact on granite dissolution. Appl Environ Microbiol. 2010;76:4788-96.
Becerra-Castro C, Kidd P, Kuffner M, Prieto-Fernández Á, Hann S, Monterroso C, et al. Bacterially induced weathering of ultramafic rock and its implications for phytoextraction. Appl Environ Microbiol. 2013;79:5094-103.
Wang Q, Wang R, He L, Sheng X. Location-related differences in weathering behaviors and populations of culturable rock-weathering bacteria along a hillside of a rock mountain. Microb Ecol. 2017;73:838-49.
Sheng XF, Zhao F, He LY, Qiu G, Chen L. Isolation and characterization of silicate mineral-solubilizing Bacillus globisporus Q12 from the surfaces of weathered feldspar. Can J Microbiol. 2008;54:1064-8.
Uroz S, Turpault M-P, van Scholl L, Palin B, Frey-Klett P. Long term impact of mineral amendment on the distribution of the mineral weathering associated bacterial communities from the beech Scleroderma citrinum ectomycorrhizosphere. Soil Biol Biochem. 2011;43:2275-82.
Wu LL, Jacobson AD, Hausner M. Characterization of elemental release during microbe-granite interactions at T = 28°C. Geochim Cosmochim Acta. 2008;72:1076-95.
Zhao F, Qiu G, Huang Z, He LY, Sheng X. Characterization of Rhizobium sp. Q32 isolated from weathered rocks and its role in silicate mineral weathering. Geomicrobiol J. 2013;30:616-22.
Karan G, Natarajan KA, Modak JM. Estimation of mineral-adhered biomass of Thiobacillus ferrooxidans by protein assay - some problems and remedies. Hydrometallurgy. 1996;42:169-75.
Holscher T, Gorisch H. Knockout and overexpression of pyrroloquinoline quinone biosynthetic genes in Gluconobacter oxydans 621H. J Bacteriol. 2006;188:7668-76.
Meyer M, Schweiger P, Deppenmeier U. Effects of membrane-bound glucose dehydrogenase overproduction on the respiratory chain of Gluconobacter oxydans. Appl Microbiol Biotechnol. 2013;97:3457-66.
Bradford MM. A rapid and simple method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem. 1976;72:248-54.
Balland C, Poszwa A, Leyval C, Mustin C. Dissolution rates of phyllosilicates as a function of bacterial metabolic diversity. Geochim Cosmochim Acta. 2010;74:5478-93.
Burghelea CI, Dontsova K, Zaharescu DG, Maier RM, Huxman T, Amistadi MK, et al. Trace element mobilization during incipient bioweathering of four rock types. Geochim Cosmochim Acta. 2018;234:98-114.
Meena VS, Maurya BR, Verma JP. Does a rhizospheric microorganism enhance K+ availability in agricultural soils? Microbiol Res. 2014;169:337-347.
Wang RR, Wang Q, He LY, Qiu G, Sheng XF. Isolation and the interaction between a mineral-weathering Rhizobium tropici Q34 and silicate minerals. World J Microbiol Biotechnol. 2015;31:747-53.
Hong H, Fang Q, Cheng L, Wang C, Churchman GJ. Microorganism-induced weathering of clay minerals in a hydromorphic soil. Geochim Cosmochim Acta. 2016;184:272-88.
Bennett PC, Hiebert FK, Choi WJ. Microbial colonization and weathering of silicates in a petroleum-contaminated groundwater. Chem Geol. 1996;132:45-53.