Premium
Rhamnolipid‐Dependent Spreading Growth of Pseudomonas aeruginosa on a High‐Agar Medium: Marked Enhancement under CO 2 ‐Rich Anaerobic Conditions
Author(s) -
Nozawa Takashi,
Tanikawa Taichiro,
Hasegawa Hiroyuki,
Takahashi Chihiro,
Ando Yumi,
Matsushita Mitsugu,
Nakagawa Yoji,
Matsuyama Tohey
Publication year - 2007
Publication title -
microbiology and immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.664
H-Index - 70
eISSN - 1348-0421
pISSN - 0385-5600
DOI - 10.1111/j.1348-0421.2007.tb03959.x
Subject(s) - rhamnolipid , pseudomonas aeruginosa , surfactin , microbiology and biotechnology , mutant , biology , complementation , agar plate , agar , operon , bacillus subtilis , growth medium , bacterial growth , flagellum , strain (injury) , bacteria , biochemistry , gene , genetics , anatomy
Anaerobiosis of Pseudomonas aeruginosa in infected organs is now gaining attention as a unique physiological feature. After anaerobic cultivation of P. aeruginosa wild type strain PAO1 T, we noticed an unexpectedly expanding colony on a 1.5% agar medium. The basic factors involved in this spreading growth were investigated by growing the PAO1 T strain and its isogenic mutants on a Davis high‐agar minimal synthetic medium under various experimental conditions. The most promotive environment for this spreading growth was an O 2 ‐depleted 8% CO 2 condition. From mutational analysis of this spreading growth, flagella and type IV pili were shown to be ancillary factors for this bacterial activity. On the other hand, a rhamnolipid‐deficient rhlA mutant TR failed to exhibit spreading growth on a high‐agar medium. Complementation of the gene defect of the mutant TR with a plasmid carrying the rhlAB operon resulted in the restoration of the spreading growth. In addition, an external supply of rhamnolipid or other surfactants (surfactin from Bacillus subtilis or artificial product Tween 80) also restored the spreading growth of the mutant TR. Such activity of surfactants on bacterial spreading on a hard‐agar medium was unique to P. aeruginosa under CO 2 ‐rich anaerobic conditions.