“…After cocultivation, calluses (about 3 mm in diameter) were cultured on MP medium containing 200 mg l -1 timentin for 7 days for callus recovery and suppression of Agrobacterium growth. MS salts and vitamins, 30 g l -1 maltose, 5.0 mg l -1 2,4-D, 1.0 mg l -1 6-BA, 4.0 g l -1 phytagel MS7 MS basic salt and vitamins, 30 g l -1 Maltose, 7.0 mg l -1 2,4-D, 4.0 g l -1 phytagel NB7 N6 basic salt, 1 9 vitamin B stock A , 30 g l -1 Maltose, 500 mg l -1 CH, 500 mg l -1 L-proline, 7.0 mg l -1 2,4-D, 4.0 g l -1 phytagel MP MS5:1 medium with 2.0 g l -1 L-proline REG MS basic medium with 0.2 mg l -1 NAA, 0.5 mg l -1 GA, 1.0 mg l -1 6-BA, 30 g l -1 maltose, 4.0 g l -1 phytagel SM1 MP medium with 200 mg l -1 timentin and 50 mg l -1 hyg B SM2 MP medium with 200 mg l -1 timentin and 100 mg l -1 hyg B 1/2TM 1/2 MS based medium with 200 mg l -1 timentin and 50 mg l -1 hyg B A 1 9 vitamin B stock was composed of 9.9 mg l -1 thiamine, 9.5 mg l -1 pyridoxine hydrochloride, 4.5 mg l -1 nicotinic acid (Zhang et al 2013) Plant Cell Rep Selection and regeneration of putative transgenic plants After recovery, calluses were transferred to the first selection medium (SM1) containing 50 mg l -1 hyg B (Roche Diagnostics GmbH, Germany). Two weeks later, calluses with vigorous growth were transferred to the second selection medium (SM2) containing 100 mg l -1 hyg B.…”