“…The embryo axes were put, within the next twenty minutes after cotyledon dissection, in groups of four onto Whatman filter papers, which were afterward transferred to sterile glass tubes (diameter 3 cm, height 13.5 cm) containing fourteen milliliters of Heller’s mineral medium [ 29 ]. Eight culture conditions were used: +S, embryo axes cultured in vitro on Heller’s medium supplemented with 60 mM sucrose [ 17 , 27 , 28 , 29 , 30 , 32 , 33 , 34 , 38 ], +G, 120 mM glucose, and +F, 120 mM fructose [ 34 ], and −S, embryo axes cultured in vitro on Heller’s medium without sucrose (−Sn, non-inoculated cultured without sucrose and −Si, inoculated cultured without sucrose). Furthermore, axes before being transferred to glass tubes with Heller’s medium were not inoculated (the control, i.e.…”