A. Nishi et al., A 90-kilobase conjugative chromosomal element coding for biphenyl and salicylate catabolism in Pseudomonas putida KF715, J BACT, 182(7), 2000, pp. 1949-1955
The biphenyl and salicylate metabolic pathways in Pseudomonas putida KP715
are chromosomally encoded. The bph gene cluster coding for the conversion o
f biphenyl to benzoic acid and the sal gene cluster coding for the salicyla
te meta-pathway were obtained, from the KF715 genomic cosmid libraries. The
se two gene clusters were separated by 10-kb DNA and were highly prone to d
eletion when KF715 was grown in nutrient medium. Two types of deletions too
k place at the region including only the bph genes (ca. 40 kb) or at the re
gion including both the bph and sal genes (ca. 70 kb). A 90-kb, DNA region,
including both the bph and sal genes (termed the bph-sal element), was tra
nsferred by conjugation from KP715 to P. putida AC30. Such transconjugants
gained the ability to grow on biphenyl and salicylate as the sole sources o
f carbon. The bph and sal element was located on the chromosome of the reci
pient. The bph.-sal element in strain AC30 was also highly prone to deletio
n; however, it could be mobilized to the chromosome of P. putida KT2440 and
the two deletion mutants of KF715.