Department of Developmental Biology, Research School of Biological Sciences, Australian National University, 2601, Canberra, A.C.T., Australia.
Planta. 1979 Jan;146(1):41-8. doi: 10.1007/BF00381253.
Protoplasts of the filamentous green alga Mougeotia sp. are spherical when isolated and revert to their normal cylindrical cell shape during regeneration of a cell wall. Sections of protoplasts show that cortical microtubules are present at all times but examination of osmotically ruptured protoplasts by negative staining shows that the microtubules are initially free and become progressively cross-bridged to the plasma membrane during the first 3 h of protoplast culture. Cell-wall microfibrils areoobserved within 60 min when protoplasts are returned to growth medium; deposition of microfibrils that is predominantly transverse to the future axis of elongation is detectable after about 6 h of culture. When regenerating protoplasts are treated with either colchicine or isopropyl-N-phenyl carbamate, drugs which interfere with microtubule polymerization, they remain spherical and develop cell walls in which the microfibrils are randomly oriented.
丝状绿藻 Mougeotia sp. 的原生质体在分离时呈球形,在细胞壁再生过程中恢复为正常的圆柱细胞形状。原生质体的切片显示,皮质微管始终存在,但通过负染色观察渗透压破裂的原生质体表明,微管最初是游离的,并在原生质体培养的最初 3 小时内逐渐与质膜交联。当原生质体返回生长培养基时,在 60 分钟内观察到细胞壁微纤维;在培养约 6 小时后,可以检测到主要横向于伸长未来轴的微纤维沉积。当用秋水仙素或异丙基-N-苯基氨基甲酸酯处理再生原生质体时,这些药物会干扰微管聚合,使它们保持球形并形成微纤维随机定向的细胞壁。