Analysis of microbial communities developed on the fouling layers of a membrane-coupled anaerobic bioreactor applied to wastewater treatment

Bioresour Technol. 2011 Apr;102(7):4618-27. doi: 10.1016/j.biortech.2011.01.007. Epub 2011 Jan 14.

Abstract

The structure of the biofouling layers formed on a pilot-scale membrane-coupled upflow anaerobic sludge blanket bioreactor (UASB) used to treat urban wastewater was analyzed by scanning electron microscopy and electron-dispersive X-ray microanalysis. For comparison, control samples of the membranes were fed either UASB effluent or raw wastewater in a laboratory-scale experiment. Microbial diversity in the fouling materials was analyzed by temperature gradient gel electrophoresis (TGGE) combined with sequence analysis of partial 16S rRNA. Significant differences in structure of the Bacteria communities were observed amongst the different fouling layers analyzed in the UASB membranes, particularly following a chemical cleaning step (NaClO), while the Archaea communities retained more similarity in all samples. The main Bacteria populations identified were evolutively close to Firmicutes (42.3%) and Alphaproteobacteria (30.8%), while Archaea were mostly affiliated to the Methanosarcinales and Methanospirillaceae. Sphingomonadaceae-related bacteria and methanogenic Archaea were persistently found as components of biofouling, regardless of chemical cleaning.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anaerobiosis
  • Analysis of Variance
  • Archaea / genetics*
  • Bacteria / genetics*
  • Bacteria / ultrastructure
  • Base Sequence
  • Bioreactors / microbiology*
  • Cluster Analysis
  • DNA Fingerprinting
  • DNA Primers / genetics
  • Denaturing Gradient Gel Electrophoresis
  • Electron Probe Microanalysis
  • Membranes, Artificial*
  • Microscopy, Electron, Scanning
  • Molecular Sequence Data
  • Phylogeny
  • RNA, Ribosomal, 16S / genetics
  • Sequence Analysis, DNA
  • Waste Disposal, Fluid / methods*
  • Water Purification / methods*

Substances

  • DNA Primers
  • Membranes, Artificial
  • RNA, Ribosomal, 16S