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(石蒜科)生物碱分析、抗胆碱酯酶活性及繁殖策略下的生物量生产。

Alkaloids Analysis of (Amaryllidaceae), Anti-Cholinesterase Activity and Biomass Production by Propagation Strategies.

机构信息

Instituto de Biotecnología, Universidad Nacional de San Juan, Av. Libertador General San Martín 1109 (O), C.P. 5400 San Juan, Argentina.

Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Godoy Cruz 2290, C.P. 1425 Ciudad Autónoma de Buenos Aires, Argentina.

出版信息

Molecules. 2021 Jan 2;26(1):192. doi: 10.3390/molecules26010192.

DOI:10.3390/molecules26010192
PMID:33401696
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7795992/
Abstract

Plants in the Amaryllidaceae family synthesize a diversity of bioactive alkaloids. Some of these plant species are not abundant and have a low natural multiplication rate. The aims of this work were the alkaloids analysis of a bulbs extract, the evaluation of its inhibitory activity against cholinesterases, and to test several propagation strategies for biomass production. Eleven compounds were characterized by GC-MS in the alkaloid extract, which showed a relatively high proportion of tazettine. The known alkaloids tazettine, haemanthamine, and the epimer mixture haemanthidine/6-epi-haemanthidine were isolated and identified by spectroscopic methods. Inhibitory cholinesterases activity was not detected. Three forms of propagation were performed: bulb propagation from seed, cut-induced bulb division, and micropropagated bulbs. Finally, different imbibition and post-collection times were evaluated in seed germination assays. The best propagation method was cut-induced bulb division with longitudinal cuts into quarters (T1) while the best conditions for seed germination were 0-day of post-collection and two days of imbibition. The alkaloids analyses of the bulbs showed that they are a source of anti-tumoral alkaloids, especially pretazettine (tazettine) and T1 is a sustainable strategy for its propagation and domestication to produce bioactive alkaloids.

摘要

石蒜科植物合成多种生物活性生物碱。其中一些植物种类不丰富,自然繁殖率低。本工作的目的是分析鳞茎提取物中的生物碱,评估其对胆碱酯酶的抑制活性,并测试几种生物量生产的繁殖策略。通过 GC-MS 在生物碱提取物中鉴定出 11 种化合物,其中 tazettine 的比例相对较高。通过光谱方法分离并鉴定了已知生物碱 tazettine、haemanthamine 和差向异构体混合物 haemanthidine/6-epi-haemanthidine。未检测到抑制胆碱酯酶的活性。进行了三种繁殖形式:种子繁殖鳞茎、切割诱导鳞茎分裂和微繁殖鳞茎。最后,在种子发芽试验中评估了不同的吸胀和收集后时间。切割诱导的鳞茎分裂是最好的繁殖方法,将鳞茎纵向切成四等份(T1),而种子发芽的最佳条件是收集后 0 天和吸胀 2 天。鳞茎的生物碱分析表明,它们是抗肿瘤生物碱的来源,特别是前 tazettine(tazettine),T1 是其繁殖和驯化的可持续策略,可用于生产生物活性生物碱。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4cc/7795992/984ceecef56c/molecules-26-00192-g005a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4cc/7795992/7a1688126a84/molecules-26-00192-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4cc/7795992/f8ddc447ea18/molecules-26-00192-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4cc/7795992/de8bb3870c65/molecules-26-00192-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4cc/7795992/2e05f28313f4/molecules-26-00192-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4cc/7795992/984ceecef56c/molecules-26-00192-g005a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4cc/7795992/7a1688126a84/molecules-26-00192-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4cc/7795992/f8ddc447ea18/molecules-26-00192-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4cc/7795992/de8bb3870c65/molecules-26-00192-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4cc/7795992/2e05f28313f4/molecules-26-00192-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4cc/7795992/984ceecef56c/molecules-26-00192-g005a.jpg

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