Final Scientific/Technical Report, DE-FG02-06ER64171, Integrated Nucleic Acid System for In-Field Monitoring of Microbial Community Dynamics and Metabolic Activity â Subproject to Co-PI Eric E. Roden | |
Eric E. Roden | |
关键词: ANL; CHEMISTRY; DNA; DYNAMICS; ELEMENTS; ETHANOL; EXPANSION; EXTRACTION; FEDERAL RADIATION COUNCIL; FUNCTIONALS; GENES; LIBRARIES; MOLECULAR BIOLOGY; MONITORING; NUCLEIC ACIDS; PURIFICATION; REACTORS; SEDIMENTS microbial; communities; ethanol; biostimulation; redox; metabolism; microarrays; | |
DOI : 10.2172/958308 RP-ID : DOE/ER/64171-1 Final Report PID : OSTI ID: 958308 Others : TRN: US201015%%1336 |
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学科分类:环境科学(综合) | |
美国|英语 | |
来源: SciTech Connect | |
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【 摘 要 】
This report summarizes research conducted in conjunction with a project entitled âIntegrated Nucleic Acid System for In-Field Monitoring of Microbial Community Dynamics and Metabolic Activityâ, which was funded through the Integrative Studies Element of the former NABIR Program (now the Environmental Remediation Sciences Program) within the Office of Biological and Environmental Research. Dr. Darrell Chandler (originally at Argonne National Laboratory, now with Akonni Biosystems) was the overall PI/PD for the project. The overall project goals were to (1) apply a model iron-reducer and sulfate-reducer microarray and instrumentation systems to sediment and groundwater samples from the Scheibe et al. FRC Area 2 field site, UMTRA sediments, and other DOE contaminated sites; (2) continue development and expansion of a 16S rRNA/rDNAÂŹ-targeted probe suite for microbial community dynamics as new sequences are obtained from DOE-relevant sites; and (3) address the fundamental molecular biology and analytical chemistry associated with the extraction, purification and analysis of functional genes and mRNA in environmental samples. Work on the UW subproject focused on conducting detailed batch and semicontinuous culture reactor experiments with uranium-contaminated FRC Area 2 sediment. The reactor experiments were designed to provide coherent geochemical and microbiological data in support of microarray analyses of microbial communities in Area 2 sediments undergoing biostimulation with ethanol. A total of four major experiments were conducted (one batch and three semicontinuous culture), three of which (the batch and two semicontinuous culture) provided samples for DNA microarray analysis. A variety of other molecular analyses (clone libraries, 16S PhyloChip, RT-PCR, and T-RFLP) were conducted on parallel samples from the various experiments in order to provide independent information on microbial community response to biostimulation.
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