Department of Botany and Plant Physiology, CCS Haryana Agricultural University, Hisar-125004, Haryana.
*Corresponding author, E-mail: profdatta@hau.ernet.in
Two genotypes of pigeon pea (Cajanus cajan L. Millsp.), salt tolerant Manak, (H77–216) and salt sensitive ICPL 88039 were subjected to treatment solutions with distilled water (C), H2O2 (100 μM; H), Glutathione, GSH (500 μM; G), H2O2 (100 μM) + GSH (500 μM) superimposed with S0B0 (DW), S0B10 (0 mM NaCl + 10 mM B as Na2B4O7.10H2O, S100 + B0 (100 mM NaCl + 0 mM B) and S100B10 (100 mM NaCl + 10 mM B) at the seedling stage in a BOD incubator at 27 ± 10C in dark for 96 h. Proteins from coleoptiles and radicles were resolved by SDS-PAGE. In tolerant cultivar Manak two proteins of molecular weight 67.6 and 81.1 kDa disappeared in S0B10 C, however 67.6 kDa reappeared with S0B10 H and S0B10 H +G treatments. Similarly two bands of 51.2 and 87.0 kDa disappeared due to S100 treatment but only 51.2 kDa reappeared with S100B0H and S100B0 H +G treatments. Likewise in radicle of Manak a 66.6 kDa protein disappeared with S0B10 C but same protein reappeared with H2O2, Glutathione, H2O2 + GSH treatments. Even S100B10 C treatment repressed 79.8 kDa protein in ICPL 88039 but got recovered with H2O2, Glutathione and H2O2 + GSH treatments. These observations accord credence to step-up regulation of protein synthetic machinery in pigeonpea by H2O2 and glutathione under salt-B toxicity conditions.
Boron, glutathione, H2O2, pigeonpea, proteins, regulation, salt, toxicity