Affiliation:
1. Department of Biochemistry, Biological Processes Technology Institute, Center for Biodegradation Research & Informatics,1
2. Department of Microbiology,2 and
3. Department of Soil, Water and Climate,3 University of Minnesota, St. Paul, Minnesota 55108, and
4. Department of Soil and Environmental Sciences, University of California, Riverside, California 925214
Abstract
ABSTRACT
Pseudomonas
sp. strain ADP contains the genes,
atzA
, -
B
, and -
C
, that encode three enzymes which metabolize atrazine to cyanuric acid. Atrazine-catabolizing pure cultures isolated from around the world contain genes homologous to
atzA
, -
B
, and -
C
. The present study was conducted to determine whether the same genes are present in an atrazine-catabolizing bacterial consortium and how the genes and metabolism are subdivided among member species. The consortium contained four or more bacterial species, but two members,
Clavibacter michiganese
ATZ1 and
Pseudomonas
sp. strain CN1, collectively mineralized atrazine.
C. michiganese
ATZ1 released chloride from atrazine, produced hydroxyatrazine, and contained a homolog to the
atzA
gene that encoded atrazine chlorohydrolase.
C. michiganese
ATZ1 stoichiometrically metabolized hydroxyatrazine to
N
-ethylammelide and contained genes homologous to
atzB
and
atzC
, suggesting that either a functional AtzB or -C catalyzed
N
-isopropylamine release from hydroxyatrazine.
C. michiganese
ATZ1 grew on isopropylamine as its sole carbon and nitrogen source, explaining the ability of the consortium to use atrazine as the sole carbon and nitrogen source. A second consortium member,
Pseudomonas
sp. strain CN1, metabolized the
N
-ethylammelide produced by
C. michiganese
ATZ1 to transiently form cyanuric acid, a reaction catalyzed by AtzC. A gene homologous to the
atzC
gene of
Pseudomonas
sp. strain ADP was present, as demonstrated by Southern hybridization and PCR.
Pseudomonas
sp. strain CN1, but not
C. michiganese
, metabolized cyanuric acid. The consortium metabolized atrazine faster than did
C. michiganese
individually. Additionally, the consortium metabolized a much broader set of triazine ring compounds than did previously described pure cultures in which the
atzABC
genes had been identified. These data begin to elucidate the genetic and metabolic bases of catabolism by multimember consortia.
Publisher
American Society for Microbiology
Subject
Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology
Cited by
149 articles.
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