Skip to main content
Figure 5 | Microbial Cell Factories

Figure 5

From: Development of an efficient conjugation-based genetic manipulation system for Pseudoalteromonas

Figure 5

Confirmation of in-frame deletion of bsmA in SM9913. (A) PCR detection of bsmA single crossover mutants using three primer pairs. M, DNA Marker III. PCR templates used are: 1–4, four independent colonies that can grow on the selective plate after mating. WT indicates SM9913 wild-type strain. NC indicates negative control ddH2O. (B) PCR confirmation of the mutants that underwent a second homologous recombination using the bsmA-wS and bsmA-wA primers. 1–2, two independent colonies after the second homologous recombination. WT indicates SM9913 wild type. NC indicates negative control ddH2O. (C) Biofilm formation of wild type SM9913 and ΔbsmA strains. Normalized biofilm formation (total biofilm/growth) in SWLB medium at 20°C after 1 d, 2 d, 3 d, and 4 d in 96-well plates. Data are the average of ten replicate wells from two independent cultures, and one standard deviation is shown. (D) Swimming motility of wild type SM9913 and ΔbsmA.

Back to article page