# Abbreviations: CM – cytoplasmic membrane,

OM – outer membrane, C – cytoplasm, P – periplasm Figure 2 Unmasked β-galactosidase activity as indicator of cell lysis of Congo Red non-binding derivatives of the colR -deficient strain. The data present percentage of β-galactosidase activity, measured from non-permeabilized cells against the total β-galactosidase activity determined from permeabilized bacteria. Results for P. putida PaW85 (wt), colR-deficient strain (colR), and for different transposon insertion derivatives of the colR mutant are shown. Bacteria were grown for 24 hours on solid 0.2% glucose M9 minimal medium containing 1 mM phenol. Data (mean ± standard deviation) of at least three independent determinations are presented. MG-132 concentration Inspection of identified genes (Table 2) revealed that in accordance with our previous results [25], disruption of the

oprB1 (PP1019) gene did eliminate the lysis. Knockouts of sugar transport genes located Selleckchem Lorlatinib upstream of oprB1, i.e., gtsA (PP1015), gtsB (PP1016), and gtsD (PP1018) also suppressed the lysis phenotype of the colR mutant. In addition to sugar transport genes, lysis was also suppressed by inactivation of the two-component system CbrA-CbrB, which is known to regulate several catabolic pathways and the cellular ratio of carbon to Methane monooxygenase nitrogen [39, 40]. The death of the colR mutant was also Selleckchem ACY-1215 prevented by the knockout of a sigma factor SigX, which regulates expression of major outer membrane protein OprF in Pseudomonas aeruginosa and Pseudomonas fluorescens [41]. Consistent with that, inactivation of oprF also suppressed lysis of the colR mutant. It is noteworthy that the disruption

of the SecA and SecB components of the general Sec protein secretion pathway also eliminated the lysis (Table 2). The isolation of a secA-knockout in our screen was particularly surprising because SecA has been shown essential not only for Sec pathway but also for the viability of bacteria [42]. Sequencing of two independently identified secA mutants revealed that they both possessed minitransposon insertion at the very end of the secA gene – between 37 and 38 nt from the stop codon (Table 2). Therefore, these mutants most probably coded for a truncated SecA protein lacking the last 12-13 amino acids.