Premium
Enrichment versus biofilm culture: a functional and phylogenetic comparison of polycyclic aromatic hydrocarbon‐degrading microbial communities
Author(s) -
Stach James E. M.,
Burns Richard G.
Publication year - 2002
Publication title -
environmental microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.954
H-Index - 188
eISSN - 1462-2920
pISSN - 1462-2912
DOI - 10.1046/j.1462-2920.2002.00283.x
Subject(s) - biology , cytophaga , bacteria , 16s ribosomal rna , enrichment culture , flavobacterium , biofilm , microbiology and biotechnology , proteobacteria , library , microbial population biology , phylogenetic diversity , ribosomal rna , botany , phylogenetic tree , gene , pseudomonas , genetics
Summary The effect that culture methods have on the diversity of degradative microbial communities is not well understood. We compared conventional batch enrichment with a biofilm culture method for the isolation of polycyclic aromatic hydrocarbon (PAH)‐degrading microbial communities from a PAH‐contaminated soil. The two methods were assessed by comparing: (i) the diversity of culturable bacteria; (ii) the diversity of PAH‐catabolic genes in isolated bacteria; (iii) the inter‐ and intraspecific diversity of active PAH‐catabolic gene classes; (iv) the diversity of bacteria present in 16S rRNA gene libraries generated from RNA extracted from the two communities and soil; and (v) the estimated diversity of active bacteria in the soil and culture systems. Single‐strand conformation polymorphism analysis showed that the biofilm culture yielded 36 bacterial and two fungal species compared with 12 bacterial species from the enrichment culture. Application of accumulation and non‐parametric estimators to clone libraries generated from 16S rRNA confirmed that the biofilm community contained greater diversity. Sequencing of clones showed that only species from the Proteobacteria were active in the enrichment culture, and that these species were expressing an identical nah Ac‐like naphthalene dioxygenase. 16S rRNA clones generated from the biofilm community indicated that species from the Cytophaga/Flavobacterium, high G+C bacteria and Proteobacteria were active at the time of sampling, expressing cnd A‐, nah Ac‐ and phn Ac‐like naphthalene dioxygenases. The diversity of active species in the biofilm culture system closely matched that in the PAH‐contaminated source soil. The results of this study showed that biofilm culture methods are more appropriate for the study of community‐level interactions in PAH‐degrading microbial communities. The study also indicated that cultivation of microbial communities on solid media might be the primary source of bias in the recovery of diverse species.