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To decrease the cost of in vitro conservation of banana cv. Karpura Chakkarakeli (AAB; Mysore sub-group) without any adverse effects on cultures, expensive components of medium such as sucrose and gelling agents, i.e. phytagel or agar (90% of the total cost of the medium), were replaced with inexpensive alternates such as market sugar and isabgol, respectively (Experiment 1). In general, no significant effects of isabgol and market sugar were observed on shoot (1.0–1.3 shoots/shoot explant) and root (1.5–2.0 roots/shoot explant) regeneration. Up to 12 months, 100% of cultures survived on isabgol-media, which was significantly higher than that on agar-media (79–83%) and on phytagel-media (51–57%). Isabgol-media with or without other constituents of medium were also tested for survival of banana cultures (Experiment 2); significant differences were observed for survival of cultures (20–100%). Slow growth of the cultures on isabgol-media was attributed to low availability of free water and consequently slower rate of transport of nutrients from isabgol matrix to the plantlets than that of other media tested, as evidenced by significantly lower relative matric potentials (0.801 and 0.804) of isabgol-media. In vitro conservation-derived plants grown in the field exhibited no significant morphological variations. The total cost of medium used for in vitro conservation of banana was decreased by 59% by using isabgol as an alternate gelling agent to agar and phytagel.
Sixteen representative accessions of proso millet [Panicum miliaceum] having distinct traits of agronomic importance were collected from altitudinal range of 510–2,695 m asl in the Central Himalayan Region (CHR) of India. Considerable diversity was found in morphophysiological traits viz., leaf length (16.80–32.00 cm), leaf width (1.7–2.1 cm), plant height (57.00–134.00 cm), days to 50 % flowering (34–54), days to 80 % maturity (111–144), and 1,000 seed weight (0.68–1.86 g). Collected accessions have been evaluated for a battery of biochemical parameters viz., chlorophyll, carotenoids, lipid peroxidation, cellular hydrogen peroxide, activity of nitrate reductase, lipoxygenase, catalase, peroxidase, superoxide dismutase along with super oxide free radical formation, glutathione (total, reduced, and oxidized), glutathione reductase, glutathione S-transferase, ascorbate (total, reduced, and oxidized), monodehydroascorbate reductase, and didehydroascorbate reductase. The sets of 12 genic- SSRs (simple sequence repeats), 54 ISSR (inter simple sequence repeats), and 40 SRAP (sequence related amplified polymorphism) markers were used to study the level of genetic diversity, and Nei’s gene diversity value of 0.20 was obtained with both ISSR and SRAP markers. SRAP markers showed higher average number of polymorphic bands, % polymorphism, polymorphic information content (PIC), and Shannon information index compared to ISSR markers; genic-SSRs showed no allelic variation. Cluster analysis shows close groupings of germplasm based on morpho-physiological traits as well as molecular markers. The diverse germplasm identified based on molecular markers with considerable diversity in morpho-physiological traits may be utilized for development of climate resilient cultivars.
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