TGG-2016v7n2 - page 17

Triticeae Genomics and Genetics 2016, Vol.7, No.02, 1
-
16
14
breeding programs (Sakha, Gimiza, and International
Research Centre of Agriculture).Wheat seeds were
surface sterilized by immersion in a mixture of ethanol
96% and H
2
O
2
(1:1) for 3 minutes, followed by
several washings with sterile distilled water. The
concentrations of NaCl were chosen after preliminary
experiments in which the seeds were subjected to
different concentrations of NaCl. Eight seeds were
sown per pot. Each pot contained 3.8 kg of garden
clay soil in three replicates. All pots were irrigated
with tap water for two weeks until full germination.
The seedlings were then irrigated by different
concentrations of NaCl solutions (0, 20, 50, 150 and
300 mM) after two weeks from sowing. In order to
maintain the osmotic potential, the soil moisture
content was kept near the field capacity using tap
water. Plants were left to grow in natural conditions
under these conditions until crop yield production.
Dry weight wasdeter mined at the end of the
experimental period yields of the different organs
(roots, stems, leaves and spikes). To determine the dry
matter yields of the different organs they were dried in
an oven at 80°C. Successive weighting was carried out
until the constant dry weight of each sample was
reached. Carbohydrates were determined by the
anthrone-sulfuric acids method (Fales, 1951). Free
amino acids, proline and a soluble protein contents
were measured according to Moore and Stein (1948),
Bates et al. (1973) and Lowry et al. (1951)
respectively.
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