K. Azhakanandam et al., HEMOGLOBIN (ERYTHROGEN(TM))-ENHANCED MITOTIC DIVISION AND PLANT-REGENERATION FROM CULTURED RICE PROTOPLASTS (ORYZA-SATIVA L.), Enzyme and microbial technology, 21(8), 1997, pp. 572-577
Supplementation of culture medium with hemoglobin solution (Erythrogen
(TM)) promoted mitotic division, cell colony formation, and plant rege
neration from rice (Oryza sativa L. cv. Taipei 309) protoplasts. The m
ean (+/- s.e.m., n = 5) final protoplast plating efficiency (FPE) at 2
8 days following exposure to 1:50 (v:v) Erythrogen(TM) (0.55 +/- 0.06%
) was significantly greater (P < 0.01) than in untreated controls (0.2
6 +/- 0.02%). A similar, but less pronounced effect (P < 0.01) also oc
curred with 1:100 (v:v) (PE 0.53 +/- 0.04%) and 1:500 (v:v) (PE 0.46 /- 0.05%) Erythrogen(TM), respectively. In contrast, there was no corr
esponding increase in plating efficiency with Erythrogen(TM) at 1:1,00
0 (v:v). These beneficial effects were sustained throughout culture. T
his leads to a 44% increase (P < 0.01) in protoplast-derived calli pro
ducing shoots compared to controls. Cytological analyses confirmed the
diploid status of plants regenerated from Erythrogen(TM)-treated and
control protoplasts. (C) 1997 Elsevier Science Inc.