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. 2016 Jul 13;7:1098. doi: 10.3389/fmicb.2016.01098

Table 3.

Evaluation of K. oxytoca M5a1 biofilm formation in the presence of indigenous expressed QQ-proteins.

QQ protein (plasmid) Biofilm thickness [μm] P-value Volume [μm3/ μm2] P-value Biofilm structure
none (wild type) 41 ± 5 22 ± 3 Compact 3D-biofilm with wavy structures
MBP (pMAL-c2X) 44 ± 4 23 ± 4 Compact 3D-biofilm with wavy structures
QQ-2 (pRS611) 10 ± 1 <0.0001 3 ± 1 <0.0001 Reduced cell adhesion
QQ-3 (pRS612) 22 ± 2 <0.0001 16 ± 4 <0.0127 Compact monolayer without wavy structures
QQ-4 (pRS613) 17 ± 2 <0.0001 9 ± 2 <0.0001 Compact monolayer without wavy structures
QQ-5 (pRS614) 19 ± 3 <0.0001 11 ± 3 <0.0002 Compact monolayer without wavy structures
QQ-6 (pRS615) 19 ± 2 <0.0001 12 ± 2 <0.0001 Compact monolayer without wavy structures
QQ-7 (pRS616) 19 ± 2 <0.0001 13 ± 3 <0.0006 Compact monolayer with few but multi-layered cell aggregates
QQ-8 (pRS617) 12 ± 1 <0.0001 6 ± 2 <0.0001 Reduced cell adhesion
QQ-9 (pRS618) 25 ± 3 <0.0001 13 ± 2 <0.0003 Compact monolayer without wavy structures
QQ-12 (pRS621) 22 ± 1 <0.0001 17 ± 3 <0.0148 Several layers of cells with areas without cell adhesion

Flow cells were inoculated with 1.35 × 108 cells of K. oxytoca M5a1 expressing MBP-QQ-ORFs from plasmids. After 1 h, flow cells were flowed for 72 h at 30°C with 20 mL/h GC medium containing 30 μM IPTG. Biofilms were analyzed after 72 h in at least three biological replicates, each with two technical replicates (see Materials and Methods). Average values are depicted with ± standard deviations. Average thickness and volume of MBP control and QQ biofilms are significantly different (p < 0.02, unpaired t-tests).