Gealt M A, Sheir-Neiss G, Morris N R
J Gen Microbiol. 1976 May;94(1):204-10. doi: 10.1099/00221287-94-1-204.
A method has been developed for isolating nuclei from the filamentous fungus Aspergillus nidulans. In this procedure, the mycelia from 14 to 16 h spore-derived cultures of A. nidulans NRI, a stable diploid strain, were frozen with liquid nitrogen and homogenized in a Waring blender. After homogenization, the mycelia were warmed to 4 degrees C and the nuclei were purified from the homogenate by differential centrifugation followed by sedimentation through 2.1 M-sucrose. The final nuclear yield was 15 to 20%, based on DNA estimations. The purified nuclear pellet was free of whole cells. The morphology of the isolated nuclei resembled that of the in situ nuclei; they contained a nucleolus, chromatin, and had a surrounding double membrane. The purified nuclei were characterized by a DNA:RNA:protein ratio of 1:2.8:8.7.
已开发出一种从丝状真菌构巢曲霉中分离细胞核的方法。在此过程中,将稳定二倍体菌株构巢曲霉NRI的14至16小时孢子衍生培养物的菌丝体用液氮冷冻,并在韦林氏搅切器中匀浆。匀浆后,将菌丝体加热至4℃,通过差速离心从匀浆中纯化细胞核,然后通过2.1 M蔗糖沉降。根据DNA估计,最终细胞核产量为15%至20%。纯化的细胞核沉淀不含完整细胞。分离出的细胞核形态与原位细胞核相似;它们含有核仁、染色质,并具有周围的双层膜。纯化的细胞核的DNA:RNA:蛋白质比例为1:2.8:8.7。