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. 2017 Nov 18;16(4):856–866. doi: 10.1111/pbi.12833

Table 3.

Mutation frequency determination of TALEN‐mediated lignin reduction lines under field conditions

Line Mutation frequency (%)a AcBr Lignin content (mg/g DW)b Lignin reduction (%) S/G molar ratioc
WT 0.0 241.8 ± 1.3 0.91
TC3 0.0 241.2 ± 4.2 0.2 0.89
CB3 70.0 200.6 ± 2.6* 17.0 n.a.
CB4 51.4 209.4 ± 5.3* 13.4 n.a.
CB5 69.9 215.5 ± 4.5* 10.9 0.80*
CB6 92.5 194.6 ± 6.1* 19.5 0.63*
CB7 68.1 194.1 ± 2.0* 19.7 0.71*
CB8 71.7 197.7 ± 5.9* 18.2 n.a.
CA4 80.0 198.9 ± 5.8* 17.7 n.a.
CA17 89.3 195.9 ± 4.3* 19.0 0.47*
B401 n.a. 219.0 ± 6.3* 9.4 n.a.

WT, wild‐type sugarcane; TC3, direct embryogenesis‐derived transgenic control with no mutation; CB3‐CB8, transgenic lines derived from biolistic transformation; CA4‐CA17, transgenic lines derived from Agrobacterium‐mediated transformation; B401, COMT RNAi line; DW, dry weight; n.a., not analyzed.

Values with asterisk in the same column indicate significant difference compared to WT (n = 3, < 0.05) as determined by t‐test.

a

Mutation frequency estimated by relative fluorescent quantitation based on capillary electrophoresis electropherogram. Mutation frequency (%) = (Sum of peak height of all mutant peaks over sum of peak height of all peaks including wild‐type peak) × 100.

b

Acetyl Bromide (AcBr) method was used to determine total lignin content.

c

Ratio of monolignol compositions of S (syringyl) and G (guaiacyl) subunits and expressed as mg/g DW.