different explants of crocus sativus l. such as corm, style, ovary, petal, anther and leaf were cultured on ls and ms media supplemented with naa and bap or 2,4-d plus bap at different combinations. shoot and corm induction occurred in addition to the formation of other organs. efficient plantlet regeneration with strong roots occurred at 1 mg 1-i of both naa and bap. an increase in 2,4-d level...

An in vitro mass propagation protocol was developed for Gerbera (Gerbera jamesonii Bolus) var. orange using flower bud explants. The young (7 days) explants were found to be suitable culture and highest (100%) callus induction obtained MS medium supplemented with 5.0 mg/l BAP 1.0 NAA. maximum shoot regeneration (95%) the number of shoots (10) observed 6.0 0.3 multiplication frequency (60) only ...

In vitro propagation of Dendrobium macrostachyum, a threatened and endemic species was achieved through nodal explants. The nodal explants were cultured on Murashige and Skoog (MS) basal medium and MS medium supplemented with N6-benzyladenine (BA-2.22, 4.44 and 8.88 microM), Kinetin (KN-2.32, 4.65, and 9.29 microM) and Coconut water (CW, 5, 10 and 15%) individually or in combination with 2.69 m...

Above-ground plant architecture is dictated to a large extent by the fates and growth rates of aerial meristems. Shoot apical meristem gives rise fundamental form generating new leaves. However, axillary meristems located in leaf axils have great influence on affect harvest index, yield potential cultural practices. Improving breeding facilitates denser plantations, better resource use efficien...

It has been suggested that one of the major functions of the apical ectodermal ridge (AER) of the embryonic chick limb-bud is to maintain mesenchymal cells directly subjacent to it (i.e. cells extending 0.4-- 0.5 mm from the AER) in a labile, undifferentiated condition. We have attempted to directly test this hypothesis by subjecting the undiffertiated subridge mesoderm of stage-25 embryonic ch...

In Arabidopsis (Arabidopsis thaliana), the carotenoid cleavage dioxygenases MORE AXILLARY GROWTH3 (MAX3) and MAX4 act together with MAX1 to produce a strigolactone signaling molecule required for the inhibition of axillary bud outgrowth. We show that both MAX3 and MAX4 transcripts are positively auxin regulated in a manner similar to the orthologous genes from pea (Pisum sativum) and rice (Oryz...

The embryo is shown at the stage when axons are starting to grow from the trigeminal ganglion (TG) to the maxillary (Mx) and mandibuSelected Reading lar (Md) processes. The collagen gel coculture paradigm is shown in which directed axonal growth is observed from the trigeminal Buchman, V.L., and Davies, A.M. (1993). Development 118, 989– ganglion to explants of its targets but not to explants o...

The capacity to form flower buds in thin-layer explants was studied in flowering plants of several species, cultivars, and lines of Nicotiana differing in their response to photoperiod. This capacity was found in all biotypes examined and could extend into sepals and corolla. It varied greatly, depending on genotype, source tissue and its developmental stage, and composition of the culture medi...

MS (Murashige and Skoog) media supplemented with benzylaminopurine (BAP) showed that the number of bud formation in shoot cultures of Musa acuminata cv.Berangan during the initiation stage increased proportionately with the concentrations used (11, 22 and 33 μM). However, the highest concentration of BAP (33 μM) simultaneously increased the formation of abnormal shoots. After the first apical b...

Axillary shoot formation is a key determinant of plant architecture. Formation of the axillary shoot is regulated by initiation of the axillary meristem or outgrowth of the axillary bud. Here, we show that rice (Oryza sativa) TILLERS ABSENT1 (TAB1; also known as Os WUS), an ortholog of Arabidopsis thaliana WUS, is required to initiate axillary meristem development. We found that formation of th...