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雪滴花离体培养物中加兰他敏的产生

Galanthamine production by Leucojum aestivum cultures in vitro.

作者信息

Stanilova Marina I, Molle Emil D, Yanev Stanislav G

机构信息

Department of Applied Botany, Institute of Botany-Bulgarian Academy of Sciences, 1113 Sofia, Bulgaria.

出版信息

Alkaloids Chem Biol. 2010;68:167-270. doi: 10.1016/s1099-4831(10)06805-7.

Abstract

The results described in these studies proved that the successful in vitro bioproduction of galanthamine from L. aestivum shoot-clumps required mainly the selection of in vitro clones with a genetically determined high ability to produce the desired alkaloids, although the expression of this ability could be additionally influenced by diverse exterior factors, such as some components of the nutrient medium, or the cultivation conditions of the ambience. Tissue differentiation was also of great importance for the biosynthetic capacity of the cultures. The most suitable inocula for in vitro biosynthesis of galanthamine in liquid medium were the directly regenerated shoot-clumps, ensuring high alkaloid concentrations between 1 and 2 mg/g DW for the selected clones. We observed astonishing clone-specific dynamics of the biosynthetic activity of all of the studied in vitro clones. The dynamics were obviously related to the strong biological clock of the species, persisting even in several-year old cultures. These dynamics did not coincide with those usual for the plants growing in situ and under controlled field conditions. In our opinion, the clone specificity of the biosynthetic dynamics could be due to the disturbance of the plant regulation mechanism under the equal conditions of the ambience in the culture room. The sharp decrease of the alkaloid concentrations were transient, followed by an increase, so that cultures were retaining their biosynthetic capacity. The biosynthesis of the main alkaloids, galanthamine and lycorine, was influenced by diverse stimulants such as substances causing stress (JA), feeding with alkaloid precursors (the amino acids phenylalanine and tyrosine, and CH), and physical treatment (acoustic waves). However, the course of the biosynthetic dynamics during the period of the treatments was always the most important factor for the success of secondary metabolism stimulation. As far as scaling-up of the in vitro biosynthesis of valuable compounds, a stable and predictable yield is required, and additional investigations aimed at the annulment of the effect plant biological clock on alkaloid biosynthesis are needed. The elucidation of the relative influences of the diverse factors modulating alkaloid biosynthesis was of great importance. The high galanthamine concentrations of the selected in vitro clones are a promising basis for future studies.

摘要

这些研究中描述的结果证明,从小麦芽丛中成功进行体外生物生产加兰他敏主要需要选择具有遗传决定的高能力来产生所需生物碱的体外克隆,尽管这种能力的表达可能会受到多种外部因素的额外影响,例如营养培养基的某些成分或环境的培养条件。组织分化对培养物的生物合成能力也非常重要。在液体培养基中体外生物合成加兰他敏的最合适接种物是直接再生的芽丛,对于选定的克隆,可确保生物碱浓度在1至2 mg/g干重之间。我们观察到所有研究的体外克隆的生物合成活性具有惊人的克隆特异性动态。这些动态显然与该物种强大的生物钟有关,即使在数年的培养物中也持续存在。这些动态与在原位和受控田间条件下生长的植物通常的动态不一致。我们认为,生物合成动态的克隆特异性可能是由于在培养室环境相同条件下植物调节机制受到干扰。生物碱浓度的急剧下降是短暂的,随后会增加,因此培养物保留了它们的生物合成能力。主要生物碱加兰他敏和石蒜碱的生物合成受到多种刺激物的影响,例如引起胁迫的物质(茉莉酸)、用生物碱前体(氨基酸苯丙氨酸和酪氨酸以及胆碱)喂养以及物理处理(声波)。然而,处理期间生物合成动态的过程始终是次生代谢刺激成功与否的最重要因素。就有价值化合物的体外生物合成放大而言,需要稳定且可预测的产量,并且需要进行额外的研究以消除植物生物钟对生物碱生物合成的影响。阐明调节生物碱生物合成的各种因素的相对影响非常重要。所选体外克隆的高加兰他敏浓度是未来研究的有希望的基础。

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