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In vitro kavapyrone production and genomic stability of in vitro kava cultures.

机译:体外卡瓦酮的体外生产和体外卡瓦培养物的基因组稳定性。

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摘要

A possibility of establishing a reliable tissue culture system for a medicinal plant, kava (Piper methysticum) was investigated by minimizing the incidence of necrosis and contamination. In addition, in vitro phytochemical production and genomic stability of in vitro kava cultures were explored with the established tissue culture system.; Utilization of foliar explants as well as medium supplementation with plant preservative mixture resulted in the reduction of contamination incidence that was not attained with high osmoticum medium, alternative sterilants or post sterilization with AgNO3. A medium treatment of N 6-benzyladenine (0.5 mg L−1) and (2,4-dichlorophenoxy)acetic acid (0.5 mg L−1) resulted in the highest callus generation and the low necrosis incidence. Optimization of shoot primordia and microshoots formation was achieved with a medium containing N6-benzyladenine at 1.0 mg L−1.; A gradual increase in kavapyrone content was observed with in vitro cultures over a period of time although the total amount was very low (0.446–1.208 g/100 g DW). In in vitro plantlets, the total kavapyrone content was the highest in leaves (0.942 g/100 g DW), while the content was the lowest in roots (0.117 g/100 g DW). A significant increase in the total kavapyrone content (2.080 g/100 g DW) was observed one month after in vitro plantlets were acclimatized. This suggests a positive effect of plant development, ontogeny and growth environment on kavapyrone production.; In addition to ontogenic effects on kavapyrone production, a particular pattern of kavapyrone accumulation was observed in different organs of the greenhouse grown plant, in vitro plantlet and acclimatized plants, confirming an earlier report on tissue specificity of kavapyrone accumulation.; Of the four signaling compounds used, salicylic acid and γ-aminobutyric acid elicited time- and concentration-dependent overproduction of kavapyrones. Treatments of callus cultures with sodium acetate resulted in a significant increase in kavapyrone production (∼400%) although responses did not appear to be time- or concentration-dependent.; Inter simple sequence repeat (ISSR) markers were used for detection of polymorphism among in vitro kava cultures. An absence of normally observed bands was observed among organogenic callus cultures, while a small degree of ISSR polymorphism was detected among regenerated plantlets.
机译:通过使坏死和污染的发生率最小化,研究了建立一种可靠的药用植物卡瓦(卡瓦)组织培养系统的可能性。此外,利用已建立的组织培养系统,探讨了体外植物化学生产和体外卡瓦培养物的基因组稳定性。叶面外植体的使用以及添加有植物防腐剂的培养基可减少高渗透压培养基,替代消毒剂或用AgNO 3 消毒后无法实现的污染发生率。 N 6 -苄腺嘌呤(0.5 mg L -1 )和(2,4-二氯苯氧基)乙酸(0.5 mg L -1 )导致愈伤组织生成量最高,坏死发生率低。用浓度为1.0 mg L -1 N 6 -苄基腺嘌呤的培养基优化了芽原基和微枝的形成。尽管一段时间总量(0.446-1.208 g / 100 g DW)非常低,但在体外培养物中观察到卡瓦吡隆含量逐渐增加。在体外植物中,卡瓦吡隆的总含量在叶片中最高(0.942 g / 100 g DW),而在根中最低(0.117 g / 100 g DW)。在体外小苗适应后1个月,观察到卡伐吡酮的总含量显着增加(2.080 g / 100 g DW)。这表明植物发育,个体发育和生长环境对卡瓦吡隆的生产具有积极作用。除了对卡瓦吡隆的生产产生影响外,还在温室植物,体外苗和驯化植物的不同器官中观察到了卡瓦吡隆积累的特定模式,这证实了卡瓦吡隆积累的组织特异性的早期报道。 。;在使用的四种信号传导化合物中,水杨酸和γ-氨基丁酸引起卡瓦吡酮的时间和浓度依赖性过量生产。用乙酸钠处理愈伤组织培养物导致卡瓦吡隆产量显着增加(〜400%),尽管反应似乎不依赖于时间或浓度。使用简单序列重复(ISSR)标记检测体外卡瓦培养物中的多态性。在器官发生的愈伤组织培养物中没有观察到正常观察到的条带,而在再生的小植株中发现了少量的ISSR多态性。

著录项

  • 作者

    Kobayashi, Hideka.;

  • 作者单位

    University of Illinois at Urbana-Champaign.;

  • 授予单位 University of Illinois at Urbana-Champaign.;
  • 学科 Biology Plant Physiology.; Agriculture Plant Culture.
  • 学位 Ph.D.
  • 年度 2003
  • 页码 122 p.
  • 总页数 122
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 植物学;作物生物学原理、栽培技术与方法;
  • 关键词

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