Regeneration of Plants from Cell Suspensions Frozen at −20, −70 and −196°C

Cell suspensions of carrot, Datura, tobacco and soybean subjected to ?20°C, ?70°C and ?196°C in the presence of a suitable cryoprotective agent, and stored for various lengths of time have been revived. After revival these cells divided to form callus masses. Direct immersion in liquid nitrogen invariably killed the cells, whereas cooling at the rate of 1 or 2°C/min, or pre-freezing briefly at ?20 and ?70°C, followed by freezing at ?196°C retained the viability. Depending on the plant species up to 70% of the cell clumps could withstand ultra-cooling. Tobacco and Datura cell suspensions were more sensitive to cold treatment than were those of carrot. Actively growing cell suspensions containing small cell-clumps revived rapidly, while filtered cell-suspensions of free cells only occasionally survived. Calli of tobacco and carrot obtained from frozen suspensions have been regenerated into plants.     

Pollen—embryogenesis and chromosomal variability in anther culture of Brassica hirta Moench （Sinapis alba L）

The anther cultures of Brassica hirta underwent pollenembryogenesis and callusing,which showed a wide range of chromosome numbers varying from 9 (n=12) to a highly polyploid.For embryogenesis,pretreatment of floral buds in 0.4 M sucrose solution for 72 hrs at 4℃ was superior to freshly cultured anthers.Culture temperature of 30℃ for 14 days before maintenance of cultures at 25℃ was significantly beneficial for embryo yield in comparison to cultures continuously incubated at 25℃.Dark treatment during culture was more effective for pollen-embryo yield.     

Effect of inter-cropping bell-pepper with ginger on plant parasitic nematode populations and crop yields

During 1994 studies were undertaken to improve ginger (Zingiber officinale Roscoe) yield against the nematodes Pratylenchus penetrans, Meloidogyne incognita, Helicotylenchus dihystera and Tylenchorhynchus mashhoodi in Himachal Pradesh (HP) (India) by inter-cropping bell-pepper (Capsicum annum L) in eight different sequences (treatments). Inter-cropping of “one rhizome of ginger x one plant of bell-pepper” gave the highest ginger yield (600 g per rhizome). This treatment was completely free from P. penetrans and M. incognita. All treatments with bell-pepper plants equal to or higher in number to that of ginger rhizomes had higher ginger yields than treatments with ginger alone or with fewer bell-pepper plants. In the former, populations of P. penetrans and M. incognita were lower than in the latter treatments. The yield of ginger varied irrespective of population densities of H. dihystera and T. mashhoodi, indicating that P. penetrans and M. incognita are the major nematode problems of ginger in HP. Bell-pepper was a non-host to P. penetrans and non-preferred host to M. incognita. This helped to improve ginger yields by making the rhizosphere unfavourable for the development and multiplication of the major ginger nematode pests.     

Overcoming Self-incompatibility through the Use of Lectins and Sugars in Petunia and Eruca

Treatment of stigma with a lectin (Con A/PHA) before pollinationwas effective in overcoming self-incompatibility in Petuniahybrida, a gametophytic self-incompatible system, and Erucasativa, a sporophytic self-incompatible system. Treatment ofpollen with glucose/N-acetyl-D-galactosamine (tested only withPetunia) was also effective. These results suggest the involvementof pollen lectins and specific sugar components of the pistilin self-incompatibility recognition. Petunia hybrida, Eruca sativa, self-incompatibility, pollen recognition, lectins     

In vitro Propagation of Red Cabbage (Brassica oleracea L. var. capitata)

By manipulation of various growth regulators and physical conditions,plants have been regenerated from excised roots, stem segments,cotyledons, leaves, and callus cultures of red cabbage (Brassicaoleracea var. capitata) grown under in vitro conditions. Shootbuds were induced on isolated root segments (1 cm long) culturedon Murashige and Skoog's medium and the frequency of bud formationwas greatly enhanced by the addition of kinetin (0.5 part 10^–6).Callus obtained from the seeds, cotyledons, and hypocotyl segmentscultured on a medium fortified with 2,4-D (1 part 10^–6),kinetin (0.1 part 10^–6), and coconut milk (10%, v/v) hasbeen repeatedly subcultured. The callus is slow growing, andon transference to a kinetin (2 parts 10^–6) and IAA (2parts 10^–6) medium underwent morphogenesis to give riseto plants. The significance of the propagation of red cabbageby in vitro culture is pointed out.     

Growth and Morphogenesis in Tissue Cultures of Anagallis arvensis

Morphogenesis has been induced in excised organs and callus tissue cultures obtained from various parts of the seedling and mature plants of pimpernel (Anagallis arvensis). Vigorously growing cell cultures capable of being periodically subcultured have been established in liquid as well as on the agar-solidified Murashige and Skoog's medium supplemented with 2,4-D (0.1 mg/1) + kinetin (0.1 mg/l) + coconut milk (10%). The callus tissue obtained from excised hypocotyl segments is white, soft, friable and fast growing, and has been subcultured over a period of two years without showing any sign of decline in growth. The optimum conditions for growth are at pH 5.9, temperature 27°C, and with 4% sucrose as the carbon source. Under appropriate nutritional supply these cultures can be manipulated to induce rhizogenesis in the suspension cultures, and buds and “embryo-like” structures on agar-solidified media. The excised leaves, hypocotyl and stem segments regenerate buds. Of the cytokinins used, 6-(y,y-dimethylallylamino)-purine proved to be the best for the number of cultures producing buds, as well as for the number of buds per culture. Anatomical studies revealed that buds arise from the epidermal and subepidermal layers of leaves and hypocotyl; these buds form shoots which eventually develop into plantlets.