Department of Biochemistry, University of Otago, P.O. Box 56, Dunedin, New Zealand.
Planta. 1988 Dec;176(4):441-50. doi: 10.1007/BF00397650.
The cell walls of Chlamydomonas gametes are multilayered structures supported on frameworks of polypeptides extending from the plasma membrane. The wall-polypeptide catalogue reported by Monk et al. (1983, Planta 158, 517-533) and extended by U.W. Goodenough et al. (1986, J. Cell Biol. 103, 405-417) was re-evaluated by comparative analysis of mechanically isolated cell walls purified from several strains. The extracellular locus of wall polypeptides was verified by in vivo iodogen-catalysed iodination and by autolysin-mediated elimination of the bulk of these polypeptides from the cell surface. Three (w15, w16, w17) and possibly four (w14) polypeptides were located to the most exterior aspect of the wall because of their susceptibility to Enzymobeadcatalysed iodination and their retention by a cell-wall-less mutant. The composition of shed walls stabilised with ethylenediaminetetraacetic acid during natural mating and kinetic analysis of the dissolution of walls purified from a bald-2 mutant demonstrated the rapid and specific destruction of polypeptide w3. Differential solubilisation of wall polypeptides occurred after loss of w3. Wall dissolution, characterised by the generation of fishbone structures from the W2 layer, gave as many as four additional polypeptides. Charged detergents and sodium perchlorate extracted a comparable range of polypeptides at room temperature from mechanically isolated walls, i.e. components of the W4-W6 layers, hot sodium dodecyl sulphate solubilised framework polypeptides, while reducing agent was required to solubilise the W2 layer. A model of wall structure is presented.
衣藻配子的细胞壁是多层结构,由从质膜延伸出来的多肽框架支撑。Monk 等人(1983 年,《植物学》158, 517-533)报告的细胞壁多肽目录,并由 U.W. Goodenough 等人(1986 年,《细胞生物学》103, 405-417)扩展,通过比较分析从几种菌株中分离的机械分离细胞壁进行了重新评估。细胞壁多肽的细胞外位置通过体内碘代催化剂催化的碘标记和自溶酶介导的这些多肽从细胞表面的大部分消除来验证。由于它们易受酶珠催化的碘化作用和细胞无壁突变体对其的保留,因此三种(w15、w16、w17)和可能四种(w14)多肽被定位到壁的最外表面。在自然交配过程中稳定的脱落细胞壁的组成,以及从 bald-2 突变体中纯化的细胞壁溶解的动力学分析表明,多肽 w3 迅速而特异性地被破坏。在 w3 丢失后,发生了细胞壁多肽的差异溶解。壁溶解,其特征是从 W2 层产生鱼骨结构,产生了多达四种额外的多肽。带电荷的去污剂和高氯酸钠在室温下从机械分离的壁中提取了类似范围的多肽,即 W4-W6 层的成分,热十二烷基硫酸钠溶解了框架多肽,而还原剂则需要溶解 W2 层。提出了一种壁结构模型。