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首页> 外文期刊>Ciência Florestal >Influence of culture medium, explant length and genotype on micropropagation of Pinus taeda L.
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Influence of culture medium, explant length and genotype on micropropagation of Pinus taeda L.

机译:培养基,外植体长度和基因型对松微繁的影响。

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摘要

This work aimed to establish a micropropagation protocol for Pinus taeda L. Apical shoots from 5-day seedlings, of different genotypes (F27, B05 and PC), were cultured on WV5 medium supplemented with 44 µM 6-benzylaminopurine (BAP) and 0.05 µM α-naphtaleneacetic acid (NAA), for 14 days, followed by subcultures on growth regulator-free medium. Explants were sectioned into apical shoots and nodal segments for multiplication. Different lengths of explants, BAP concentrations and cultivation periods were tested. Rooting was induced on WV5/2, WV3/2, GDm/2 and agar-water culture media supplemented with 2.68 µM NAA and 0.44 µM BAP for nine days, followed by a 4-week subculture on growth regulator-free medium. It was verified that genotype influenced shoot formation and rooting. The length of 1.0 cm is recommended for nodal segment explants to obtain a high number of axillary shoots. For apical shoots, 0.5 cm explant and WV5 medium formulation allowed the best results for elongation. The best period of subculture was eight weeks, both for nodal segments and for apical shoots. The higher percentage of nodal segments with shoots (99.2%) and the higher average number of shoots per explant (4.0) were obtained with F27 genotype in medium culture containing 2.5 µM BAP. For apical shoots, the best result for elongation was observed for the shorter explants (0.5 cm) on WV5 culture medium (218.3%). The maintenance of in vitro clonal micro garden of vigorous shoots was obtained for two years of 8-week subcultures on WV5 culture medium. The best rooting rate (55.6%) was obtained when shoots were inoculated in agar-water medium with 2.68 μM NAA and 0.44 μM BAP for nine days. Plantlets were successfully acclimatized (85% of survival), so a micropropagation protocol was established.
机译:这项工作旨在建立针叶松的微繁协议。将5天不同基因型(F27,B05和PC)幼苗的顶端芽在补充有44 µM 6-苄基氨基嘌呤(BAP)和0.05 µM的WV5培养基上进行培养。 α-萘乙酸(NAA),持续14天,然后在无生长调节剂的培养基上进行亚培养。将外植体切成顶端芽和节节以繁殖。测试了不同长度的外植体,BAP浓度和培养时间。在补充有2.68 µM NAA和0.44 µM BAP的WV5 / 2,WV3 / 2,GDm / 2和琼脂水培养基上诱导生根9天,然后在无生长调节剂的培养基上进行4周传代培养。证实基因型影响芽的形成和生根。对于结节外植体,建议使用1.0 cm的长度,以获得大量的腋生芽。对于顶芽,0.5 cm外植体和WV5培养基配方可实现最佳的伸长效果。无论是节段还是顶端芽,亚培养的最佳时期均为八周。在含有2.5 µM BAP的培养基中,使用F27基因型获得的带有芽的节节百分数更高(99.2%),每个外植体的平均芽数更高(4.0)。对于顶芽,在WV5培养基(218.3%)上观察到较短的外植体(0.5 cm)的最佳伸长效果。在WV5培养基上进行了为期8周的2年传代培养,获得了有活力的芽的体外克隆微花园。当将芽苗接种在琼脂水培养基中并接种2.68μMNAA和0.44μMBAP九天时,可获得最佳生根率(55.6%)。幼苗已成功地适应环境(存活的85%),因此建立了微繁殖方案。

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