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  • tissue culture  (3)
  • Springer  (3)
  • 1995-1999
  • 1985-1989  (3)
  • 1980-1984
  • 1960-1964
Collection
Publisher
  • Springer  (3)
Years
  • 1995-1999
  • 1985-1989  (3)
  • 1980-1984
  • 1960-1964
  • 1990-1994  (1)
Year
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Plant cell, tissue and organ culture 14 (1988), S. 31-40 
    ISSN: 1573-5044
    Keywords: tissue culture ; Malus domestica ; micropropagation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Shoot tips of ‘York’ and ‘Vermont Spur Delicious’ apples (Malus domestica Borkh.) were cultured in vitro to test the influence of K+, Mg++ and gelling agent concentrations on vitrification. These concentrations were 20.05, 14.05 and 8.05 mM K+, 1.5 and 3.0 mM Mg++, 7.0 g/l Difco Bacto agar and 1.0, 1.5 and 2.0 g/l Gelrite. The lowest K+ level produced a higher percentage of vitrified shoots, affected tissue appearance, reduced shoot number and shoot elongation and apparently altered shoot metabolic activity. Gelrite consistently produced vitrified leaves and stems, even though media gelled with 1.5 g/l Gelrite presented the same apparent gel firmness as using 7 g/l Difco Bacto agar, which did not induce vitrification. Less shoot elongation, fewer total shoots, and more usable shoots of ‘York’ were obtained on Bacto-agar, while similar but less noticeable effects were obtained with ‘Vermont Spur Delicious’. The results presented here show that vitrification can be studied in a standardized system in which the only change is substitution of one gelling agent for another.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Plant cell, tissue and organ culture 15 (1988), S. 269-274 
    ISSN: 1573-5044
    Keywords: agar ; Gelrite ; Gossypium hirsutum ; tissue culture
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract A factorial experiment was performed to develop a medium which would support initiation and proliferation of callus in a diverse group of exotic lines of Gossypium hirsutum. Seed hypocotyls of T1, T25 and T133 were cultured on Linsmaier and Skoog (LS) basal medium (1965) with NAA or 2,4-D tested in combination with BA or kinetin. The best medium from this study was then compared to five published media for support of callus initiation and growth of the varieties Acala 1517-75, Coker 500, Dunn 120, Paymaster 303 and TM1. Furthermore, the effects of two gelling agents, Difco-Bacto agar and Kelco Gelrite, were investigated with each of the six media. Significantly more callus was initiated on media solidified with Gelrite than with agar. The best callus production occurred on LS medium supplemented with 30gl-1 glucose, 0.1 mgl-1 BA and 0.1 mgl-1 2,4-D.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Plant cell, tissue and organ culture 16 (1989), S. 75-87 
    ISSN: 1573-5044
    Keywords: Malus domestica ; organogenesis ; tissue culture ; thidiazuron
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Leaves taken from micropropagated shoots of several apple (Malus domestica Borkh.) cultivars were cultured in vitro on Linsmaier & Skoog (LS) medium or the rice anther culture medium of Chu et al. (N6) containing various concentrations of either benzyladenine (BA) or thidiazuron (TDZ) plus naphthaleneacetic acid (NAA). Of the TDZ concentrations tested, 10 μM was most effective and it was equivalent to, or better than, 22 μM BA for both the percentage of leaves regenerating shoots and number of shoots formed per regenerating leaf in almost every experiment. Lower concentrations of NAA (1.1 and 5.4 μM) gave best results with both BA and TDZ. N6 medium gave consistently better results than LS. Lowering total salt concentration or total N concentration of LS to that of N6 did not improve the response nor did changing the NO3:NH4 ratio. The 3–4 leaves on the most distal part of the shoot were most responsive and tended to form the most adventitious shoots. Placing the leaf cultures in the dark for the first 2–3 weeks of the culture period produced the best results. Optimum results were obtained by culturing leaves from the distal part of the shoot in the dark for 2 weeks on N6 medium containing 10 μM TDZ and 1.1 or 5.4 μM NAA, then moving the cultures to 16 h daylight at a photon flux of 60 μmol s-1m-2.
    Type of Medium: Electronic Resource
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