Wilson Andi, van Dijk Alida, Marx Bianke, du Plessis Deanne, Terblanche Grant, Bornman Simoné, Wilken P Markus, Duong Tuan A, Licht Henrik H De Fine, Wingfield Brenda D
Section for Organismal Biology, Department of Plant and Environmental Sciences, University of Copenhagen, Copenhagen, Denmark.
Forestry & Agricultural Biotechnology Institute, Department of Biochemistry, Genetics and Microbiology, University of Pretoria, Pretoria, South Africa.
Curr Protoc. 2025 Mar;5(3):e70122. doi: 10.1002/cpz1.70122.
The ability to extract protoplasts has contributed significantly to the study of fungi and plants. Protoplasts have historically been used to determine chromosome number via pulsed-field electrophoresis and for the functional characterization of genes via protoplast transformation. More recently, protoplasts have been used to extract the high-molecular-weight DNA required for long-read sequencing projects. The availability of efficient protoplast extraction protocols is thus integral to the study and experimental manipulation of model and non-model fungi. One major hurdle to the development of such protocols has been the discontinuation of enzymes and enzyme cocktails used to digest the fungal cell wall. Here, we provide five protoplast extraction protocols for use in various filamentous ascomycete species spanning the genera Ceratocystis, Fusarium, Metarhizium, Ophiostoma, and Sclerotinia. These protocols all use an inexpensive, readily available enzyme cocktail called Extralyse, a commercially available product commonly used in the wine making industry. Using this enzyme cocktail overcomes reliance on the laboratory-grade enzymes that have frequently been discontinued and are often cost prohibitive at the concentrations required. The protocols described here will allow further research, including genome editing, to be conducted in these fungal genera. Importantly, these protocols also provide a starting point for the development of protoplast extraction techniques in other filamentous fungi. This resource can therefore be used to expand the molecular toolkits available for fungi beyond the species described here, including those with relevance in both medical and biotechnological industries. © 2025 The Author(s). Current Protocols published by Wiley Periodicals LLC. Basic Protocol 1: Protoplast extractions from Ceratocystis eucalypticola and Ceratocystis fimbriata Basic Protocol 2: Protoplast extractions from Fusarium circinatum Basic Protocol 3: Protoplast extractions from Metarhizium acridum, Metarhizium brunneum, and Metarhizium guizhouense Basic Protocol 4: Protoplast extractions from Ophiostoma novo-ulmi Basic Protocol 5: Protoplast extractions from Sclerotinia sclerotiorum.
原生质体提取能力对真菌和植物的研究有显著贡献。历史上,原生质体一直被用于通过脉冲场电泳确定染色体数目,以及通过原生质体转化进行基因功能表征。最近,原生质体已被用于提取长读长测序项目所需的高分子量DNA。因此,高效原生质体提取方案的可用性对于模式真菌和非模式真菌的研究及实验操作至关重要。开发此类方案的一个主要障碍是用于消化真菌细胞壁的酶和酶混合物已停产。在此,我们提供了五种原生质体提取方案,用于多种丝状子囊菌物种,涵盖长喙壳属、镰刀菌属、绿僵菌属、长喙壳属和核盘菌属。这些方案均使用一种名为Extralyse的廉价且容易获得的酶混合物,这是一种在酿酒行业常用的市售产品。使用这种酶混合物克服了对实验室级酶的依赖,这些酶经常停产,并且在所需浓度下成本往往过高。本文所述的方案将允许在这些真菌属中开展进一步研究,包括基因组编辑。重要的是,这些方案也为其他丝状真菌原生质体提取技术的开发提供了起点。因此,该资源可用于扩展可用于真菌的分子工具包,超越本文所述的物种,包括那些在医学和生物技术行业都有相关性的真菌。© 2025作者。由Wiley Periodicals LLC出版的《当前方案》。基本方案1:从桉长喙壳菌和流苏长喙壳菌中提取原生质体 基本方案2:从轮状镰刀菌中提取原生质体 基本方案3:从蝗绿僵菌、布氏绿僵菌和贵州绿僵菌中提取原生质体 基本方案4:从新榆长喙壳菌中提取原生质体 基本方案5:从核盘菌中提取原生质体。