Montezinos D, Brown R M
Cytobios. 1978;23(90):119-39.
Cell wall biogenesis in the unicellular green alga Oocystis apiculata has been studied. Under normal growth conditions, a cell wall with ordered microfibrils is synthesized. In each layer there are rows of parallel microfibrils. Layers are nearly perpendicular to each other. Terminal linear synthesizing complexes are located in the plasma membrane, and they are capable of bidirectional synthesis of cellulose microfibrils. Granule bands associated with the inner leaflet of the plasma membrane appear to control the orientation of newly synthesized microfibrils. Subcortical microtubules also are present during wall synthesis. Patterns of cell wall synthesis were studied after treatment with EDTA and EGTA as well as divalent cations (MgSO4, CaSO4, Cacl2). 0.1 M EDTA treatment for 15 min results in the disassociation of the terminal complexes from the ends of microfibrils. EDTA-treated cells followed by 15 min treatment with MgSO4 results in reaggregation of the linear complexes into a paired state, remote from the original ends to which they were associated. After 90 min treatment with MgSO4, normal synthesis resumes. EGTA and calcium salts do not affect the linear complexes or microfibril orientation. Treatments with colchicine and vinblastine sulphate do not depolymerize the microtubles, but the wall microfibril orientation is altered. With colchicine or vinblastine, the change in orientation from layer to layer is inhibited. The process is reversible upon removal of the drugs. Lumicolchicine has no effect upon microfibril orientation, but granule bands are disorganized. Treatment with coumarin, a known inhibitor of cellulose synthesis, causes the loss of visualization of subunits of the terminal complexes. The possibility of the existence of a membrane-associated colchicine-sensitive orientation protein for cellulose microfibrils is discussed. Transmembrane modulation of microfibril synthesis and orientation is presented.
对单细胞绿藻尖细卵囊藻的细胞壁生物合成进行了研究。在正常生长条件下,合成了具有有序微纤丝的细胞壁。每层中有平行微纤丝的排。各层几乎相互垂直。末端线性合成复合体位于质膜中,它们能够双向合成纤维素微纤丝。与质膜内小叶相关的颗粒带似乎控制着新合成微纤丝的取向。在壁合成过程中也存在皮层下微管。在用乙二胺四乙酸(EDTA)、乙二醇双四乙酸(EGTA)以及二价阳离子(硫酸镁、硫酸钙、氯化钙)处理后,研究了细胞壁合成模式。用0.1 M EDTA处理15分钟会导致末端复合体从微纤丝末端解离。用EDTA处理过的细胞再用硫酸镁处理15分钟会导致线性复合体重新聚集为配对状态,远离它们原来所关联的末端。用硫酸镁处理90分钟后,恢复正常合成。EGTA和钙盐不影响线性复合体或微纤丝取向。用秋水仙碱和硫酸长春碱处理不会使微管解聚,但壁微纤丝取向会改变。使用秋水仙碱或长春碱时,层与层之间取向的变化受到抑制。去除药物后该过程是可逆的。光秋水仙碱对微纤丝取向没有影响,但颗粒带会紊乱。用香豆素(一种已知的纤维素合成抑制剂)处理会导致末端复合体亚基无法可视化。讨论了存在与膜相关的对纤维素微纤丝有秋水仙碱敏感性的取向蛋白的可能性。提出了微纤丝合成和取向的跨膜调节。