Department of Microbiology, University of Toronto, 100 College Street, #214, M5G 1L5, Toronto, Ontario, Canada.
Plant Cell Rep. 1990 Jul;9(3):117-20. doi: 10.1007/BF00232084.
Nicotiana tabacum var. Carlson protoplast culture conditions were modified to contain a cell wall inhibitor, 2,6-dichlorobenzonitrile, in order to delay cell wall regeneration and to allow efficient nuclear and cytoplasmic microinjections. Under modified conditions, the protoplast preparations appeared healthier as compared to the control protoplasts and showed no resistance at all during microinjection. Furthermore, the duration of protoplast microinjection was extended for up to 3-4 days. In order to set up nuclear microinjections, the nuclei of these protoplasts were stained either before or after immobilization without any adverse effect on their mitotic activity. Successful cytoplasmic microinjections were demonstrated by injecting Alfalfa mosaic virus (AMV) RNA, which resulted in viral infection of 14% of the injected protoplasts.
为了延迟细胞壁再生并允许有效的核和细胞质显微注射,对烟草细胞原生质体培养条件进行了修改,使其包含细胞壁抑制剂 2,6-二氯苯腈。在改良条件下,与对照原生质体相比,原生质体制备物看起来更健康,并且在显微注射过程中完全没有抗性。此外,原生质体显微注射的持续时间延长至 3-4 天。为了进行核显微注射,在固定之前或之后对这些原生质体的核进行染色,而不会对其有丝分裂活性产生任何不利影响。通过注射紫花苜蓿花叶病毒 (AMV) RNA 成功地进行了细胞质显微注射,结果导致 14%的注射原生质体被病毒感染。