Microbes produce nanobacteria-like structures, avoiding cell entombment

被引:167
作者
Bontognali, Tamaso R. R. [1 ]
Vasconcelos, Crisogono [1 ]
Warthmann, Rolf J. [1 ]
Dupraz, Christophe [2 ]
Bernasconi, Stefano M. [1 ]
McKenzie, Judith A. [1 ]
机构
[1] ETH, Inst Geol, CH-8092 Zurich, Switzerland
[2] Univ Connecticut, Ctr Integrat Geosci, Storrs, CT 06269 USA
关键词
nanobacteria; dolomite; biomineralization; microbial mats; stromatolites; microfossils;
D O I
10.1130/G24755A.1
中图分类号
P5 [地质学];
学科分类号
0709 ; 081803 ;
摘要
Microsedimentary structures referred to as nanobacteria-like particles were described from modern carbonate environments, where they form in close spatial association with sulfate-reducing bacteria (SRB). However, the exact mechanism of their formation, as well as their paleontological significance, remains controversial. Here we report on an investigation of microbe-mineral interactions in experimentally produced carbonate globules. The experiments were carried out under anoxic conditions at 30 degrees C with Desulfovibrio brasiliensis, a SRB known to mediate dolomite formation. We observed that extracellular polymeric substances (EPS) secreted by the microbial community play a key role in the mineralization process. Nanobacteria-like particles represent the early stage of carbonate nucleation within the EPS, which progressively evolve to larger globules displaying a grainy texture. We excluded the possibilities that these structures are fossils of nanobacteria, dissolution surfaces, or artifacts created during sample preparation. D. brasiliensis cells are predominantly located outside of the EPS aggregates where mineral growth takes place. As a result, they remain mobile and are rarely entombed within the mineral. This self-preservation behavior may not be limited to D. brasiliensis. Other microbes may produce, or may have produced during the geological past, biogenic minerals through a similar process. Mineralization within EPS explains why microbial relics are not necessarily present in biogenic carbonates.
引用
收藏
页码:663 / 666
页数:4
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