Effect of bioaugmentation and biostimulation on sulfate-reducing column startup captured by functional gene profiling

FEMS Microbiol Ecol. 2012 Oct;82(1):135-47. doi: 10.1111/j.1574-6941.2012.01412.x. Epub 2012 Jun 13.

Abstract

Sulfate-reducing permeable reactive zones (SR-PRZs) depend upon a complex microbial community to utilize a lignocellulosic substrate and produce sulfides, which remediate mine drainage by binding heavy metals. To gain insight into the impact of the microbial community composition on the startup time and pseudo-steady-state performance, functional genes corresponding to cellulose-degrading (CD), fermentative, sulfate-reducing, and methanogenic microorganisms were characterized in columns simulating SR-PRZs using quantitative polymerase chain reaction (qPCR) and denaturing gradient gel electrophoresis (DGGE). Duplicate columns were bioaugmented with sulfate-reducing or CD bacteria or biostimulated with ethanol or carboxymethyl cellulose and compared with baseline dairy manure inoculum and uninoculated controls. Sulfate removal began after ~ 15 days for all columns and pseudo-steady state was achieved by Day 30. Despite similar performance, DGGE profiles of 16S rRNA gene and functional genes at pseudo-steady state were distinct among the column treatments, suggesting the potential to control ultimate microbial community composition via bioaugmentation and biostimulation. qPCR revealed enrichment of functional genes in all columns between the initial and pseudo-steady-state time points. This is the first functional gene-based study of CD, fermentative and sulfate-reducing bacteria and methanogenic archaea in a lignocellulose-based environment and provides new qualitative and quantitative insight into startup of a complex microbial system.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Archaea / genetics
  • Archaea / metabolism*
  • Biodegradation, Environmental
  • Carboxymethylcellulose Sodium / metabolism
  • Denaturing Gradient Gel Electrophoresis
  • Ethanol / metabolism
  • Manure / microbiology*
  • Methane / metabolism
  • Polymerase Chain Reaction
  • RNA, Ribosomal, 16S / genetics
  • Sulfates / metabolism*
  • Sulfur-Reducing Bacteria / genetics
  • Sulfur-Reducing Bacteria / metabolism*

Substances

  • Manure
  • RNA, Ribosomal, 16S
  • Sulfates
  • Ethanol
  • Carboxymethylcellulose Sodium
  • Methane