FEMS Microbiology Ecology · 2000 · 234 citations · 51 references
Life SciencesMicrobiologyMolecular BiologyEnvironmental MicrobiologyMicrobial EcologyMicrobial MetabolismEnvironmental MicrobiomesMicrobial BiogeochemistryMicrobial Community DynamicsMicrobial Community ProfilingMicrobial DiversityBacterial Community DynamicsBacterial Community EcologyBiostimulationGroundwater MicrobiologyMethanogenesisMethanotrophic BacteriaMethanotrophic Microbial CommunitiesMethanotrophy
Changes in bacterial diversity during the field experiment on biostimulation were monitored by denaturing gradient gel electrophoresis (DGGE) analysis of PCR-amplified 16S rDNA fragments. The results revealed that the bacterial community was disturbed after the start of treatment, continued to change for 45 days or 60 days and then formed a relatively stable community different from the original community structure. DGGE analysis of soluble methane monooxygenase (sMMO) hydroxylase gene fragments, mmoX, was performed to monitor the shifts in the numerically dominant sMMO-containing methanotrophs during the field experiment. Sequence analysis on the mmoX gene fragments from the DGGE bands implied that the biostimulation treatment caused a shift of potential dominant sMMO-containing methanotrophs from type I methanotrophs to type II methanotrophs.
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Gerard Muyzer, Ellen C. de Waal, André G. Uitterlinden · Applied and Environmental Microbiology · 1993 · 11.5K citations · Full text
‘Touchdown’ PCR to circumvent spurious priming during gene amplification
R.H. Don, Peter Cox, Brandon J. Wainwright et al. · Nucleic Acids Research · 1991 · 2.6K citations · Full text