Abstract
Direct interspecies electron transfer (DIET) has been considered as a novel and highly efficient strategy in both natural anaerobic environments and artificial microbial fuel cells. A syntrophic model consisting of Geobacter metallireducens and Geobacter sulfurreducens was studied in this work. We conducted in vivo molecular mapping of the outer surface of the syntrophic community as the interface of nutrients and energy exchange. System for Analysis at the Liquid Vacuum Interface combined with time-of-flight secondary ion mass spectrometry was employed to capture the molecular distribution of syntrophic Geobacter communities in the living and hydrated state. Principal component analysis with selected peaks revealed that syntrophic Geobacter aggregates were well differentiated from other control samples, including syntrophic planktonic cells, pure cultured planktonic cells, and single population biofilms. Our in vivo imaging indicated that a unique molecular surface was formed. Specifically, aromatic amino acids, phosphatidylethanolamine components, and large water clusters were identified as key components that favored the DIET of syntrophic Geobacter aggregates. Moreover, the molecular changes in depths of the Geobacter aggregates were captured using dynamic depth profiling. Our findings shed new light on the interface components supporting electron transfer in syntrophic communities based on in vivo molecular imaging.
Original language | English |
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Pages (from-to) | 10402-10411 |
Number of pages | 10 |
Journal | Analytical Chemistry |
Volume | 92 |
Issue number | 15 |
DOIs | |
State | Published - Aug 4 2020 |
Funding
X.-Y.Y. is thankful for the support of the Pacific Northwest National Laboratory (PNNL) Earth and Biological Sciences Directorate (EBSD) mission seed Laboratory Directed Research and Development (LDRD). F.L. thanks the Yantai Institute of the Coastal Zone Research Chinese Academy of Sciences for funding from the National Natural Science Foundation of China (No. 91751112 and 41573071). The research was performed in the W. R. Wiley Environmental Molecular Sciences Laboratory (EMSL), a national scientific user facility via general user proposals 49694 and 50569. Microbial culture was conducted in the Biological Sciences Facility at PNNL. We are grateful to Prof. Derek Lovley for providing Geobacter metallireducens and Geobacter sulfurreducens strains. We thank Xiaofei Yu for technical assistance. W.W. is thankful for the support of the PNNL Alternate Sponsored Fellowship (ASF) and Graduate Fellowship from University of Chinese Academy of Sciences. PNNL is operated by Battelle for the DOE under Contract DE-AC05-76RL01830.