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直接叶剥皮法用于槟榔原生质体:一种简单高效的槟榔原生质体分离和转化系统。

Direct leaf-peeling method for areca protoplasts: a simple and efficient system for protoplast isolation and transformation in areca palm (Areca catechu).

机构信息

Sanya Nanfan Research Institute, Key Laboratory of Green Prevention and Control of Tropical Plant Diseases and Pests (Ministry of Education), School of Plant Protection, Hainan University, Haikou, Hainan, 570228, China.

Key Laboratory of Biology and Genetic Resources of Tropical Crops, Ministry of Agriculture and Rural Affairs & Institute of Tropical Bioscience and Biotechnology, Chinese Academy of Tropical Agricultural Sciences, Haikou, Hainan, 571101, China.

出版信息

BMC Plant Biol. 2023 Jan 26;23(1):56. doi: 10.1186/s12870-023-04048-7.

Abstract

BACKGROUND

Areca palm (Areca catechu) is a woody perennial plant of both economical and medicinal importance grown in tropical and subtropical climates. Yet, the molecular biology study of areca palm is extremely impeded by its unavailability of a transformation method. An efficient protoplast isolation and transformation system could be highly desirable to overcome this barrier.

RESULTS

Here, we described a simple and efficient method for protoplast isolation and transformation from the perennial plant areca palm. A high yield of protoplasts (2.5 × 10 protoplasts per gram of fresh leaf tissues) was obtained from the fresh light green leaflet from the newly-emerged leaf digested overnight in the enzyme solution [2% (w/v) cellulase R10, 0.5% (w/v) macerozyme R10, 0.7 M mannitol, 10 mM CaCl, 20 mM KCl, 20 mM MES and 0.1% (w/v) BSA, pH 5.7] by the direct leaf-peeling method. The isolated areca protoplasts maintain viability of 86.6% and have been successfully transformed with a green fluorescent protein (GFP)-tagged plasmid (pGreen0029-GFP, 6.0 kb) via the polyethylene glycol (PEG)-mediated transformation. Moreover, the mannitol concentration (optimal: 0.7 M) was determined as a key factor affecting areca protoplast isolation. We also demonstrated that the optimal density of areca protoplast for efficient transformation was at 1.0-1.5 × 10 cells/ml. With the optimization of transformation parameters, we have achieved a relatively high transformation efficiency of nearly 50%.

CONCLUSION

We have established the first efficient protocol for the high-yield isolation and transformation of areca palm protoplasts. This method shall be applied in various biological studies of areca palm, such as gene function analysis, genome editing, protein trafficking and localization and protein-protein interaction. In addition, the protoplast system offers a great genetic transformation approach for the woody perennial plant-areca palm. Moreover, the established platform may be applied in protoplast isolation and transformation for other important species in the palm family, including oil palm and coconut.

摘要

背景

槟榔(Areca catechu)是一种经济和药用价值都很高的木本植物,生长在热带和亚热带气候中。然而,由于缺乏转化方法,槟榔的分子生物学研究受到了极大的阻碍。一个高效的原生质体分离和转化系统将是克服这一障碍的理想选择。

结果

本文描述了一种从多年生植物槟榔中分离和转化原生质体的简单而有效的方法。通过直接叶片剥离法,从新鲜浅绿色的幼叶中获得了高产量的原生质体(每克新鲜叶片组织 2.5×10 个原生质体),这些原生质体在酶解液[2%(w/v)纤维素酶 R10、0.5%(w/v)离析酶 R10、0.7 M 甘露醇、10 mM CaCl2、20 mM KCl、20 mM MES 和 0.1%(w/v)BSA,pH 5.7]中过夜消化。分离的槟榔原生质体保持 86.6%的活力,并通过聚乙二醇(PEG)介导的转化成功转化了绿色荧光蛋白(GFP)标记的质粒(pGreen0029-GFP,6.0 kb)。此外,甘露醇浓度(最佳:0.7 M)被确定为影响槟榔原生质体分离的关键因素。我们还证明,有效转化的槟榔原生质体最佳密度为 1.0-1.5×10 个细胞/ml。通过转化参数的优化,我们实现了近 50%的相对较高的转化效率。

结论

我们建立了槟榔原生质体高效分离和转化的第一个有效方案。该方法将应用于槟榔的各种生物学研究,如基因功能分析、基因组编辑、蛋白质运输和定位以及蛋白质-蛋白质相互作用。此外,原生质体系统为木本多年生植物-槟榔提供了一种很好的遗传转化方法。此外,该平台可应用于棕榈科其他重要物种(包括油棕和椰子)的原生质体分离和转化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/056a/9878809/fafb8b191c99/12870_2023_4048_Fig1_HTML.jpg

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