Extracting Protoplasts from Filamentous Fungi Using Extralyse, An Enzyme Used in the Wine Industry

Andi Wilson, Alida van Dijk, Bianke Marx, Deanne du Plessis, Grant Terblanche, Simoné Bornman, P. Markus Wilken, Tuan A. Duong, Henrik H. De Fine Licht, Brenda D. Wingfield
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Abstract

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

Abstract Image

利用酿酒工业中常用的酵素从丝状真菌中提取原生质体
提取原生质体的能力极大地促进了对真菌和植物的研究。原生质体历来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确定基因的功能特征。最近,原生质体又被用于提取长读程测序项目所需的高分子量 DNA。因此,高效的原生质体提取方案对于研究和实验操作模式真菌和非模式真菌不可或缺。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的停产。在此,我们提供了五种原生质体提取方案,可用于各种丝状子囊菌属,包括子囊菌属、镰刀菌属、担子菌属、子囊菌属和硬菌属。这些方案都使用了一种名为 Extralyse 的廉价易得的鸡尾酒酶,这是一种商用产品,常用于酿酒业。使用这种鸡尾酒酶克服了对实验室级酶的依赖,因为实验室级酶经常停产,而且在所需浓度下成本往往过高。本文所述的方案将有助于对这些真菌属开展进一步的研究,包括基因组编辑。重要的是,这些方案还为开发其他丝状真菌的原生质体提取技术提供了一个起点。因此,该资源可用于扩大真菌分子工具包的范围,使其超出本文所述的真菌种类,包括与医疗和生物技术行业相关的真菌。© 2025 作者。当前协议》由 Wiley Periodicals LLC 出版。基本方案 1:从桉角孢子菌(Ceratocystis eucalypticola)和杉角孢子菌(Ceratocystis fimbriata)中提取原生质体基本方案 2:从环状镰刀菌(Fusarium circinatum)中提取原生质体基本方案 3:基本程序 4:从 Ophiostoma novo-ulmi 中提取原生质体基本程序 5:从 Sclerotinia sclerotiorum 中提取原生质体
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