| Literature DB >> 34485007 |
Shenglin Hu1,2, Zhefan Wang1, Dongmei Wang1, Jichao Wang1, Jiong Hong1,2.
Abstract
Thermoascus aurantiacus is a thermophilic fungus that belongs to the ascomycetous class and has attracted increasing interest for its ability to produce thermostable cellulolytic enzymes and growth at elevated temperatures. However, studies on this organism have been limited because of the lack of a genetic manipulation system. Here, we developed a polyethylene glycol (PEG)-mediated transformation system for T. aurantiacus based on an orotidine-5'-monophosphate decarboxylase (pyrG)-deficient mutant, with this method achieving a transformation efficiency of 33 ± 3 transformants per microgram of DNA. Intracellular or secretory expression of heterologous proteins, including green fluorescent protein, β-galactosidase and α-amylase, in T. aurantiacus was successful under the inducible endogenous cellobiohydrolase and endoglucanase gene promoter or the constitutive heterologous pyruvate decarboxylase and enolase gene promoter from Trichoderma reesei. To the best of our knowledge, this is the first report on PEG-mediated transformation of T. aurantiacus, which sets the foundation for strain improvement for biotechnological applications and functional genomic studies. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s13205-021-02963-w. © King Abdulaziz City for Science and Technology 2021.Entities:
Keywords: PEG-mediated transformation; Protoplast; Thermoascus aurantiacus; Thermophilic fungus; pyrG
Year: 2021 PMID: 34485007 PMCID: PMC8374019 DOI: 10.1007/s13205-021-02963-w
Source DB: PubMed Journal: 3 Biotech ISSN: 2190-5738 Impact factor: 2.893