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无激素培养基将支持某些甜菜(Beta vulgaris L.)群体的完整植株叶片外植体产生愈伤组织,并随后再生芽。

Hormone-free medium will support callus production and subsequent shoot regeneration from whole plant leaf explants in some sugarbeet (Beta vulgaris L.) populations.

机构信息

Graduate Research Assistant, Department of Crop and Soil Sciences, Michigan State University, 48824, East Lansing, MI, USA.

出版信息

Plant Cell Rep. 1989 Apr;8(4):222-5. doi: 10.1007/BF00778538.

DOI:10.1007/BF00778538
PMID:24233142
Abstract

Sugarbeet plants representing 14 of 16 germplasm sources (4 to 5 plants per source) produced callus from leaf disks on a hormone-free Murashige and Skoog based medium. Overall, 49.2% of explants from partially expanded leaves of whole plants initiated callus (53 of 74 plants tested), in an average time of 96.7 days. The time to callus was considerably longer than the 4-6 weeks observed when 1 mg/L N(6)-benzyladenine has been used in the medium. Shoots were regenerated on the hormone-free medium without subculture from callus of eight individual genotypes, representing 3 of the 14 populations that produced callus. Shoots produced by 'Gartons White Knight' and 'L53' appeared to be of somatic embryo origin. Rhizogenic calli were also produced by the same three populations that regenerated shoots. Significant differences among populations were found for frequency of root formation from leaf disks and time to callus. Variation among plants within a population was significant for four of the five traits examined. The results indicate the ease of hormone autonomization in sugarbeet, and should be of value in designing regeneration media for a wider range of beet germplasm.

摘要

甜菜植株代表 16 个种质资源中的 14 个(每个资源 4-5 株),在无激素 Murashige 和 Skoog 基础培养基上从叶片圆盘产生愈伤组织。总体而言,74 株试验植株中有 49.2%(53 株)来自部分展开的整株叶片的外植体启动了愈伤组织,平均时间为 96.7 天。与在培养基中使用 1 mg/L N(6)-苄基腺嘌呤时观察到的 4-6 周相比,愈伤组织的时间要长得多。来自产生愈伤组织的 8 个个体基因型的愈伤组织在无激素培养基上无需继代培养即可再生出芽。来自 'Gartons White Knight' 和 'L53' 的芽似乎来自体细胞胚胎的起源。同样的三个种群也产生了生根的愈伤组织。在叶片圆盘生根频率和愈伤组织形成时间方面,种群之间存在显著差异。在五个检查的性状中,有四个在种群内的植物之间存在显著差异。结果表明,甜菜中激素自主化很容易,这对于设计更广泛的甜菜种质资源的再生培养基应该是有价值的。

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本文引用的文献

1
Suspension culture of sugarbeet (beta vulgaris L.). induction and habituation of dedifferentiated and self-regenerating cell lines.甜菜(Beta vulgaris L.)悬浮培养。去分化和自我再生细胞系的诱导和驯化。
Plant Cell Rep. 1985 Apr;4(2):66-9. doi: 10.1007/BF00269208.
2
An improved medium for adventitious shoot formation and callus induction in Beta vulgaris L. in vitro.提高离体甘蓝型油菜不定芽形成和愈伤组织诱导的培养基。
Plant Cell Rep. 1988 Jan;7(1):30-4. doi: 10.1007/BF00272972.
3
An approximate distribution of estimates of variance components.
甜菜(Beta vulgaris L.)下胚轴离体培养再生植株和再生体的流式细胞术核 DNA 分析。
Plant Cell Rep. 1992 Jul;11(7):329-33. doi: 10.1007/BF00233359.
4
In planta 2,3,5 truodobenzoic acid treatment promotes high frequency and routine in vitro regeneration of sugarbeet (Beta vulgaris L.) plants.在植物体内,2,3,5 三羟基苯甲酸处理促进了甜菜(Beta vulgaris L.)植物的高频常规离体再生。
Plant Cell Rep. 1996 Dec;16(3-4):142-6. doi: 10.1007/BF01890855.
方差分量估计值的近似分布。
Biometrics. 1946 Dec;2(6):110-4.