No abstract

Light emitting diodes (LEDs) are potential light sources for in vitro plant cultures. Here, axillary blackberry shoots were grown in MS medium with indole-3-butyric acid (1 mg L−1), naphthalene acetic acid (0.5 mg L−1), and sucrose supplementation (0–60 g L−1) and the cultures were incubated under four light treatments: three LED light treatments (blue + red light (2:1 spectral ratio), blue + red light (1:2), and cool + warm white light (1:1)) and a standard florescent tube white spectrum treatment. Sucrose was indispensable for rooting of blackberry microshoots. Sucrose concentrations up to 45 g L−1 increased total root length and root surface area under all light treatments. However, at this sucrose concentration, leaf area and vegetative growth were negatively affected. Plantlets grown in media containing 15–30 g L−1 of sucrose exhibited the highest leaf pigments, shoot length, and number of leaves. LED treatments increased leaf pigments as compared with florescent treatment. Plantlets grown under blue + red light (2:1) had the highest stoma aperture length and width, whereas cool + warm white light resulted in the lowest values. Among the LED treatments, blue + red light (2:1) resulted in the highest leaf area, chlorophyll and carotenoid contents, and vegetative growth, whereas fluorescent resulted in the lowest values. A combination of blue and red light at a 2:1 spectral ratio with 30 g L−1 of sucrose is recommended for the optimal in vitro rooting and vegetative growth of blackberry microshoots.

Bridelia stipularis (L.) Blume is a fruit-yielding climbing shrub native to Southern Asia and various parts of the plant have been used in traditional systems of medicines to treat a range of diseases. Proximate, mineral, phytochemical analysis of Bridelia stipularis fruit pericap and seeds were carried out in the present study to assess nutritional and phytochemical status. The pericarp and seeds were rich in carbohydrate (38.78 and 33.46 g/100 g dry mass), protein (8.94 and 44.40 g/100 g dry mass), fiber (3.86 and 2.83 g/100 g dry mass) and minerals, in addition to these, seeds also contain oil (9.10 g/ 100 g dry mass). Pericarp and seeds possess higher concentrations of phenolics (9.84-125.59 mg GAE/g dry mass), flavonoids (7.17-44.67 mg QE/g dry mass), tannins (11.79-17.71 mg TAE g dry mass) and lesser concentrations of antinutritive factors, such as phytate (0.06-0.26 g/100 g dry mass) and oxalate (0.23-0.46 g/100 g dry mass). The physicochemical characteristics and fatty acid profile revealed that B. stipularis seed oil could be used for edible purposes. The seed oil is abundant with linolenic acid (36.7 g/100 g of oil), oleic acid (23.39 g/100 g oil) and hence, it could be used in soap and detergents.

Red dragon fruit (Hylocereus polyrhizus) is an economic and promising fruit crop in arid and semi-arid regions with water shortage. An automated liquid culture system using bioreactors is a potential tool for micropropagation and large-scale production. In this study, axillary cladode multiplication of H. polyrhizus was assessed using cladode tips and cladode segments in gelled culture versus continuous immersion air-lift bioreactors (with or without a net). Axillary multiplication using cladode segments (6.4 cladodes per explant) was more effective than cladode tip explants (4.5 cladodes per explant) in gelled culture. Compared with gelled culture, continuous immersion bioreactors provided high axillary cladode multiplication (45.9 cladodes per explant) with a higher biomass and length of axillary cladodes. Inoculation of H. polyrhizus micropropagated plantlets with arbuscular mycorrhizal fungi (Gigaspora margarita and Gigaspora albida) significantly increased the vegetative growth during acclimatization. These findings will improve the large-scale propagation of dragon fruit.

Due to the limitations associated with shoot tip explants in the micropropagation of date palm, inflorescence explants are an ideal alternative. This chapter focuses on the protocol for the induction of callus from inflorescence tissue, establishment for proliferation of somatic embryos, germination, elongation, rooting, and acclimatization. Female inflorescences, 30-40 cm in length, cv. Shaishee, were used for culture initiation. After disinfection, the outer inflorescence cover (spathe) is cut open, and the spikelet explants, 1 cm long, are cultured on modified Murashige and Skoog (MS) medium containing 100 mg/L 2,4-D, 3 mg/L kinetin, and 3 mg/L 2ip and incubated at 25 ± 2 °C in the dark. Callus obtained after 6-8 months of culturing is transferred to the culture medium to induce somatic embryogenesis and plant regeneration. Well-developed regenerated shoots are cultured on MS medium containing 0.2 mg/L NAA for root induction and plantlets acclimatized in the greenhouse before transfer to the field.