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. 2014 Sep 27;34(1):47–62. doi: 10.1007/s00299-014-1686-4

Table 5.

The effect of auxin transport inhibitor (10 µM TIBA) and anti-auxin (5 µM PCIB) tillers treatment on endogenous level of IAA and IBA in anthers of two DH lines of triticale (× Triticosecale Wittm.) with significantly different androgenic responsiveness (‘responsive’ DH28 and ‘recalcitrant’ DH19)

Treatment Days of treatment IAA (nmol g−1 DW) IBA (nmol g−1 DW)
DH19 DH28 DH19 DH28
Control* 30.5 ± 4.1 19.2 ± 0.8 0.38 ± 0.03 0.33 ± 0.01
 TIBA 3 41.1 ± 4.8 26.7 ± 3.1 0.31 ± 0.01 0.38 ± 0.04
21 14.6 ± 7.7 6.0 ± 0.2 2.1 ± 0.31 0.43 ± 0.02
 PCIB 3 14.1 ± 1.5 23.8 ± 2.8 0.96 ± 0.20 0.33 ± 0.04
21 27.7 ± 3.1 41.8 ± 6.0 0.53 ± 0.13 0.33 ± 0.01
 DMSO 3 19.1 ± 0.8 42.5 ± 4.0 1.02 ± 0.01 0.36 ± 0.01
21 46.6 ± 13.9 26.7 ± 8.5 0.40 ± 0.02 0.39 ± 0.01

DMSO (PCIB solvent) in 0.1 % concentration was used as additional control. All compounds were supplemented to Hogland’s medium at the start of cold tillers treatment (21 days at 4 °C) or 3 days before anthers isolation

Data are the means of 3 biological replications ±SE

Sample of anthers collected from several spikes with total fresh weight of 0.3 g was assumed to be one biological replication

TIBA 2,3,5-triiodobenzoic acid, PCIB p-chlorophenoxyisobutyric acid, DMSO dimethyl sulfoxide

* Anthers excised from tillers kept during the whole cold treatment (21 days) in Hoagland’s medium