TY - JOUR
T1 - Transformation of the herbicide 2,6-dichlorobenzonitrile to the persistent metabolite 2,6-dichlorobenzamide (BAM) by soil bacteria known to harbour nitrile hydratase or nitrilase
AU - Holtze, Maria Sommer
AU - Sørensen, Jan
AU - Hansen, Hans Christian B.
AU - Aamand, Jens
N1 - Funding Information:
This work was supported by the Immunalyse Project (Grant no. 9901188, The Danish Technical Research Council) and the RECETO research school (The Danish Research Council).
PY - 2006/12
Y1 - 2006/12
N2 - In soil the herbicide 2,6-dichlorobenzonitrile (dichlobenil) is degraded to the persistent metabolite 2,6-dichlorobenzamide (BAM) which has been detected in 19% of samples taken from Danish groundwater. We tested if common soil bacteria harbouring nitrile-degrading enzymes, nitrile hydratases or nitrilases, were able to degrade dichlobenil in vitro. We showed that several strains degraded dichlobenil stoichiometrically to BAM in 1.5-6.0 days; formation of the amide intermediate thus showed nitrile hydratase rather than nitrilase activity, which would result in formation of 2,6-dichlorobenzoic acid. The non-halogenated analogue benzonitrile was also degraded, but here the benzamide intermediate accumulated only transiently showing nitrile hydratase followed by amidase activity. We conclude that a potential for dichlobenil degradation to BAM is found commonly in soil bacteria, whereas further degradation of the BAM intermediate could not be demonstrated.
AB - In soil the herbicide 2,6-dichlorobenzonitrile (dichlobenil) is degraded to the persistent metabolite 2,6-dichlorobenzamide (BAM) which has been detected in 19% of samples taken from Danish groundwater. We tested if common soil bacteria harbouring nitrile-degrading enzymes, nitrile hydratases or nitrilases, were able to degrade dichlobenil in vitro. We showed that several strains degraded dichlobenil stoichiometrically to BAM in 1.5-6.0 days; formation of the amide intermediate thus showed nitrile hydratase rather than nitrilase activity, which would result in formation of 2,6-dichlorobenzoic acid. The non-halogenated analogue benzonitrile was also degraded, but here the benzamide intermediate accumulated only transiently showing nitrile hydratase followed by amidase activity. We conclude that a potential for dichlobenil degradation to BAM is found commonly in soil bacteria, whereas further degradation of the BAM intermediate could not be demonstrated.
KW - Amidase
KW - BAM
KW - Dichlobenil
KW - Nitrilase
KW - Nitrile hydratase
UR - http://www.scopus.com/inward/record.url?scp=33750535621&partnerID=8YFLogxK
U2 - 10.1007/s10532-005-9021-y
DO - 10.1007/s10532-005-9021-y
M3 - Article
SN - 0923-9820
VL - 17
SP - 503
EP - 510
JO - Biodegradation
JF - Biodegradation
IS - 6
ER -