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Appl. Environ. Microbiol., Apr 1997, 1326-1331, Vol 63, No. 4
J Dunbar, S White and L Forney
The effect of enrichment bias on the diversity of
2,4-dichlorophenoxyacetate (2,4-D)-degrading (2,4-D(sup+)) bacteria
recovered from soil was evaluated by comparing the diversity of isolates
obtained by direct plating to the diversity of isolates obtained from 85
liquid batch cultures. By the two methods, a total of 159 isolates were
purified from 1 g of soil and divided into populations based on repeated
extragenic palindromic sequence PCR (rep-PCR) genomic fingerprints.
Approximately 42% of the direct-plating isolates hybridized with the tfdA
and tfdB genes from Alcaligenes eutrophus JMP134(pJP4), 27% hybridized with
the tfdA and tfdB genes from Burkholderia sp. strain RASC, and 30%
hybridized with none of the probes. In contrast, the enrichment isolates
not only represented fewer populations than the isolates obtained by direct
plating but also exhibited, almost exclusively, a single hybridization
pattern with 2,4-D catabolic gene probes. Approximately 98% of the
enrichment isolates possessed pJP4-type tfdA and tfdB genes, whereas
isolates containing RASC-type tfdA and tfdB genes were obtained from only 2
of the 85 enrichment cultures. The skewed occurrence of the pJP4-type genes
among the isolates obtained by enrichment suggests that the competitive
fitness of 2,4-D(sup+) populations during growth with 2,4-D may be
influenced either by specific tfd alleles or by genetic factors linked to
these alleles. Moreover, the results indicate that evaluation of the
diversity and distribution of catabolic pathways in nature can be highly
distorted by the use of enrichment culture techniques.
Copyright © 1997, American Society for Microbiology
Genetic Diversity through the Looking Glass: Effect of Enrichment Bias
NSF Center for Microbial Ecology and Department of Microbiology, Michigan State University, East Lansing, Michigan, and Los Alamos National Laboratories, Los Alamos, New Mexico
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