Barthou H, Brière C, Caumont C, Petitprez M, Kallerhoff J, Borin C, Souvré A, Alibert G
Laboratoire de Biotechnologie et Amelioration des Plantes, Unite Associée INPT/INRA, ENSAT, 145 Av. de Muret, F-31076, Toulouse, Cedex, France.
Ecole Nationale de Formation Agronomique, BP 87, F-31326, Castanet-Tolosan Cedex, France.
Plant Cell Rep. 1997 Feb;16(5):310-314. doi: 10.1007/BF01088287.
Sunflower protoplasts were cultured in liquid medium under high atmospheric pressure (0.2 to 0.6 MPa) and the plating efficiency, cell wall synthesis and microtubule organization were assessed. In 7-day-old cultures under a pressure of 0.4 MPa and above, the division rate was strongly reduced by more than 60% as compared to the control. Although most of the protoplasts had begun to regenerate a new cell wall they were unable to complete this process. Pressure also had an inhibitory effect on microtubule synthesis. The percentage of protoplasts showing a disassembled cortical network of microtubules was significantly increased up to 60% of the population. These effects were reversible: when protoplasts were transferred to normal pressure most of them rapidly recovered their capacity to divide and afterwards developed normally. Culturing protoplasts under a pressurized atmosphere revealed to be a good model system for studying cortical microtubule dynamics.
将向日葵原生质体在高气压(0.2至0.6兆帕)下于液体培养基中培养,并评估其平板效率、细胞壁合成和微管组织。在0.4兆帕及以上压力下培养7天的培养物中,与对照相比,分裂率大幅降低超过60%。尽管大多数原生质体已开始再生新的细胞壁,但它们无法完成这一过程。压力对微管合成也有抑制作用。显示微管皮质网络解体的原生质体百分比显著增加,高达群体的60%。这些影响是可逆的:当原生质体转移到常压下时,大多数原生质体迅速恢复其分裂能力,随后正常发育。在加压气氛下培养原生质体被证明是研究皮质微管动力学的良好模型系统。