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离体繁殖美丽芦荟(Aloe elegans Tod.)的方法是使用侧芽扦插。

In vitro micropropagation of Aloe elegans Tod. using offshoot cuttings.

机构信息

Department of Biology, College of Natural and Computational Sciences, Mekelle University, PO Box 231, Mekelle, Ethiopia.

Department of Biological and Chemical Engineering, Mekelle Institute of Technology, Mekelle University, PO Box 1632, Mekelle, Ethiopia.

出版信息

BMC Res Notes. 2023 Sep 12;16(1):215. doi: 10.1186/s13104-023-06490-0.

Abstract

OBJECTIVE

Aloe elegans Tod. is an ecologically, environmentally, medicinally, and commercially useful aloe species in Ethiopia and Eritrea. Unfortunately, it is highly threatened due to industrial and urban expansion and traditional mining and agricultural activities. As a consequence, it is included in the IUCN List of Threatened Species since 2013. The plant is getting thinly populated in many parts of the Tigrai floristic region since it is being exploited for traditional and commercial purposes. Therefore, this study was aimed to develop a reproducible, large-scale micropropagation protocol using offshoot cuttings in Murashige and Skoog (MS) media enriched with plant growth regulators (PGRs).

RESULTS

Sterilized explants cultured in full-strength MS media enriched with 0.25 mg/L benzyl amino purine (BAP) and 0.10 mg/L naphthaleneacetic acid (NAA) resulted in 100% healthy and live (i.e., initiated) explants after four weeks of initiation study. Unsupplemented initiation media (control) yielded only 14.3% initiated explants. The initiated explants were tested for their shooting response to produce microshoots by incubating in different concentrations and combinations of BAP and NAA for four weeks. Fewer days to shooting (13.0 ± 1.0 days), higher mean shoot number (5.0 ± 1.0), and higher mean shoot length (9.20 ± 2.35 cm) were observed with 1.0/0.50, 1.0/0.25, and 1.0 /0.50 mg/L BAP/NAA combinations, respectively. The rooting responses of the microshoots toward producing plantlets were also tested by incubating them in half-strength MS media enriched with different concentrations of NAA and indole-3-butyric acid (IBA) for four weeks. Fewer mean days to rooting (12.0 ± 1.0 days), higher mean root number (8.0 ± 4.0), and higher mean root length (7.53 ± 3.03 cm) were observed in MS media enriched with 0.75, 0.75, and 1.25 mg/L IBA, respectively. The responses of A. elegans plantlets to primary (in greenhouse) and secondary (in nursery shade and direct sunlight) acclimatization in coco peat, composted soil, and manured soil media were high - with survival percentages of 87.5-97.8% in three to four weeks.

摘要

目的

在埃塞俄比亚和厄立特里亚,翠绿芦荟(Aloe elegans Tod.)是一种具有生态、环境、药用和商业价值的芦荟物种。不幸的是,由于工业和城市扩张以及传统采矿和农业活动,它受到了高度威胁。因此,自 2013 年以来,它已被列入 IUCN 濒危物种名录。由于其被用于传统和商业用途,在提格雷植物区系的许多地区,该植物的种群数量正在减少。因此,本研究旨在利用 MS 培养基中的侧芽切段建立可重复、大规模的微繁殖体系,该 MS 培养基中添加了植物生长调节剂(PGRs)。

结果

在含有 0.25 mg/L 苄氨基嘌呤(BAP)和 0.10 mg/L 萘乙酸(NAA)的完全 MS 培养基中培养的消毒外植体,在起始研究四周后,100%的外植体健康且存活(即起始)。未添加起始培养基(对照)的外植体仅产生 14.3%的起始外植体。将起始外植体在不同浓度和 BAP 和 NAA 组合下孵育四周,以测试其产生微芽的出芽反应。用 1.0/0.50、1.0/0.25 和 1.0/0.50 mg/L BAP/NAA 组合,观察到更短的出芽天数(13.0±1.0 天)、更高的平均芽数(5.0±1.0)和更高的平均芽长(9.20±2.35 cm)。将微芽在含有不同浓度 NAA 和吲哚丁酸(IBA)的半强度 MS 培养基中孵育四周,以测试其生根反应。在含有 0.75、0.75 和 1.25 mg/L IBA 的 MS 培养基中,观察到更短的生根天数(12.0±1.0 天)、更高的生根数(8.0±4.0)和更高的生根长度(7.53±3.03 cm)。在椰糠、堆肥和施肥土壤介质中,翠绿芦荟幼苗在温室(一级)和苗圃遮荫和直射阳光(二级)驯化中的反应较高,在三到四周内存活率为 87.5-97.8%。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a363/10498563/ab41a053807d/13104_2023_6490_Fig2_HTML.jpg

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