Werner Antonia, Otte Kolja L, Stahlhut Gertrud, Pöggeler Stefanie
Department of Genetics of Eukaryotic Microorganisms, Institute of Microbiology and Genetics, Georg-August-University of Göttingen, Grisebachstr. 8, 37077, Göttingen, Germany.
AMB Express. 2020 Dec 21;10(1):222. doi: 10.1186/s13568-020-01160-x.
The engineered monomeric version of the lancelet Branchiostoma lanceolatum fluorescent protein, mNeonGreen (mNG), has several positive characteristics, such as a very bright fluorescence, high photostability and fast maturation. These features make it a good candidate for the utilization as fluorescent tool for cell biology and biochemical applications in filamentous fungi. We report the generation of plasmids for the expression of the heterologous mNG gene under the control of an inducible and a constitutive promoter in the filamentous ascomycete Sordaria macrospora and display a stable expression of mNG in the cytoplasm. To demonstrate its usefulness for labeling of organelles, the peroxisomal targeting sequence serine-lysine-leucine (SKL) was fused to mNG. Expression of this tagged version led to protein import of mNG into peroxisomes and their bright fluorescence in life cell imaging.
文昌鱼(Branchiostoma lanceolatum)荧光蛋白mNeonGreen(mNG)的工程单体形式具有几个积极特性,如非常明亮的荧光、高光稳定性和快速成熟。这些特性使其成为丝状真菌细胞生物学和生化应用中用作荧光工具的良好候选者。我们报告了在丝状子囊菌大孢粪壳菌(Sordaria macrospora)中,用于在诱导型和组成型启动子控制下表达异源mNG基因的质粒的构建,并展示了mNG在细胞质中的稳定表达。为了证明其对细胞器标记的有用性,将过氧化物酶体靶向序列丝氨酸-赖氨酸-亮氨酸(SKL)与mNG融合。这种标记形式的表达导致mNG蛋白导入过氧化物酶体,并在活细胞成像中发出明亮荧光。