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. 2002 Jun;184(11):2951–2962. doi: 10.1128/JB.184.11.2951-2962.2002

TABLE 2.

Quantitation of cell length and FtsZ rings after MinC/DicB-mediated filamentationa

Plasmid Time (min) R cells
R+ cells
R + R+ cells
% (n) Avg length (range) (μm) % (n) Avg length (range) (μm) L/R (μm) Avg length (range) (μm) L/R (μm)
pJE44 [PBAD::dicB] 10 20 (9) 6.7 (3.2-20.0) 80 (36) 13.4 (4.4-33.5) 5.5 12.0 (3.2-33.5) 6.1
60 7 (2) 21.9 (8.0-35.8) 93 (25) 15.1 (4.2-49.8) 4.9 15.6 (4.2-49.8) 5.4
120 35 (9) 39.0 (4.2-66.3) 65 (17) 30.3 (2.6-70.8) 16.1 33.3 (2.6-70.8) 27.1
180 30 (17) 51.4 (3.5-98.4) 70 (39) 11.0 (2.5-97.6) 8.6 23.3 (2.5-98.4) 26.0
pBAD33 (vector) 0 16 (14) 2.5 (1.9-3.5) 84 (72) 3.5 (1.9-15.9) 2.7 3.4 (1.9-15.9) 3.1
180 22 (13) 2.5 (1.8-3.8) 78 (47) 2.8 (1.9-4.5) 2.7 2.7 (1.8-4.5) 3.4
a

Cells of strain PB147(λDR120) [ΔminDE(Plac::gfp-ftsZ)] harboring the indicated plasmid or vector were treated and analyzed as described in the text. Parameters were calculated separately for cells without fluorescent ring structures (R cells), cells with one or more rings (R+ cells), and all cells combined (R + R+ cells). n, number of cells examined. Any visible accumulation of fluorescence resembling a ring was counted as one.