Methods Media and growth conditions All C. crescentus strains were grown at 30°C in peptone yeast extract (PYE) media [38]. When appropriate, kanamycin (5 μg/ml liquid, 20 μg/ml solid), chloramphenicol

(0.5 μg/ml liquid or 1 μg/ml solid), tetracycline (1 μg/ml liquid or 2 μg/ml solid) and nalidixic acid (20 μg/ml) were used. Escherichia coli strains were grown at 37°C in Luria-Bertani (LB) medium [39] with kanamycin (50 μg/ml), chloramphenicol (20 μg/ml liquid or 30 μg/ml solid), ampicillin (50 μg/ml liquid or 100 μg/ml solid), or tetracycline (12 μg/ml liquid or 12 μg/ml solid). Transposon mutagenesis and selection of ΦCbKR mutants The plasmid pFD1 [40], carrying the mariner transposon and the transposase gene, https://www.selleckchem.com/products/selonsertib-gs-4997.html was introduced into C. crescentus strain CB15 (wild-type) by conjugation with E. coli strain YB2028 (SM10λpir (pFD1)). Cells from five independent conjugations were pooled and frozen at -80°C. Aliquots of cells were thawed, mixed with undiluted Caulobacter phage ΦCbK stock (~1010 pfu/ml), plated on PYE supplemented with kanamycin and nalidixic acid and incubated at 30°C for several days until KanR ΦCbKR colonies appeared. Screening mutants Visual screening Overnight cultures of all ΦCbKR mutants were observed with a 100× objective on a Nikon Optiphot-2 microscope.

Tucidinostat nmr Strains were qualitatively scored on three phenotypes: presence of rosettes, presence of stalks, and presence of motile swarmer cells. Phage resistance Strains were grown overnight, normalized to equal OD600 and diluted to 100, 10-4 and 10-5. Cell dilutions were mixed in equal volumes with ΦCbK (~1010 pfu/ml) or plain PYE. The mixture was incubated at room temp for 10 minutes, then 5 μl spots were

placed onto PYE plates. The plates were incubated at 30°C for 3–5 days. Relative resistance was determined by the number and size of colonies that appeared. Confirmation of transposon mutant phenotypes and identification of genes The kanamycin marker in strains of interest were transduced into C. crescentus strain CB15 with the phage ΦCr30, Cyclin-dependent kinase 3 using a standard transduction protocol [41]. KanR colonies were isolated and overnight liquid cultures were shown to have the same phenotype as the parent strain. Genomic DNA was isolated using a phenol/chloroform extraction method. Briefly, cells were grown overnight at 30°C in 3 ml PYE + kanamycin. The entire culture was pelleted by centrifugation, and resuspended in cold TE pH 7.5 to a final volume of 500 μl. Lysozyme (Sigma) and RNAse (TEW-7197 Amresco) were added to final concentrations of 1 mg/ml and 0.1 mg/ml respectively, and the mixture was incubated at 37°C for 30 min before adding 0.1 volumes of 10% w/v SDS. Proteinase K (Amresco) was added to a final concentration of 1 mg/ml. The solution was mixed gently and incubated at 50°C for 2 hours with occasional mixing.