Isolate D47 has previously been shown to degrade a range of urea-based herb
icides. The DNA encoding the16 S rRNA gene of this strain was amplified by
polymerase chain reaction (PCR) and sequenced. Database similarity searches
indicated the gene was similar to those present in Arthrobacter species. T
he 16S rRNA gene sequence was compared to eight full-length sequences that
have been obtained from related strains in this cluster by both distance an
d parsimony methods. The analyses confirmed the inferred relationship betwe
en D47 and Arthrobacter oxydans-type strains within the Arthrobacter globif
ormis group. Biochemical tests confirmed this result. Studies with C-14-car
bonyl-labelled diuron indicated that D47 hydrolysed the urea side chain at
the carbonyl group. Loss of the parent compound was accompanied by an equal
accumulation of 3,4-dichloroaniline and loss of [C-14]-CO2. Cell-free extr
acts of D47 indicated a broad temperature optimum for degradative activity
between 15 degreesC and 30 degreesC. a broad pH optimum of 5.5-8.0 and a de
cline in activity with increasing salt concentration beyond 50 mM. This inf
ormation sets the basic characteristics of the strain and the enzyme for cl
oning and expression of the gene(s) encoding this activity in a heterologou
s host.