A 90-kilobase conjugative chromosomal element coding for biphenyl and salicylate catabolism in Pseudomonas putida KF715

Citation
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
Citations number
40
Categorie Soggetti
Microbiology
Journal title
JOURNAL OF BACTERIOLOGY
ISSN journal
00219193 → ACNP
Volume
182
Issue
7
Year of publication
2000
Pages
1949 - 1955
Database
ISI
SICI code
0021-9193(200004)182:7<1949:A9CCEC>2.0.ZU;2-0
Abstract
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.