F. Bolognese et al., Activation and inactivation of Pseudomonas stutzeri methylbenzene catabolism pathways mediated by a transposable element, APPL ENVIR, 65(5), 1999, pp. 1876-1882
The arrangement of the genes involved in o-xylene, m-xylene, and p-xylene c
atabolism was investigated in three Pseudomonas stutzeri strains: the wild-
type strain OX1, which is able to grow on o-xylene but not on the meta and
para isomers; the mutant M1, which grows on m-xylene and p-xylene but is un
able to utilize the ortho isomer; and the revertant R1, which can utilize a
ll the three isomers of xylene, A 3-kb insertion sequence (IS) termed ISPs1
, which inactivates the m-xylene and p-xylene catabolic pathway in P. stutz
eri OX1 and the o-xylene catabolic genes in P. stutzeri M1, was detected. N
o IS was detected in the corresponding catabolic regions of the P, stutzeri
R1 genome. ISPs1 is present in several copies in the genomes of the three
strains. It is flanked by 24-bp imperfect inverted repeats, causes the dire
ct duplication of 8 bp in the target DNA, and seems to be related to the IS
L3 family.