De Voe I W, Thompson J, Costerton J W, MacLeod R A
J Bacteriol. 1970 Mar;101(3):1014-26. doi: 10.1128/jb.101.3.1014-1026.1970.
The outer layers of the cell envelope of a pseudomonad of marine origin were removed by washing the cells in 0.5 m NaCl followed by suspension in 0.5 m sucrose. The term mureinoplast has been suggested for the rod-shaped forms which resulted from this treatment. As previously established, these forms lacked the outer cell wall layers but still retained a rigid peptidoglycan structure. Mureinoplasts remained stable if suspended in a balanced salt solution containing 0.3 m NaCl, 0.05 m MgSO(4), and 0.01 m KCl but, unlike whole cells, lost ultraviolet (UV)-absorbing material if suspended in 0.5 m NaCl or 0.05 m MgCl(2). Sucrose added to the balanced salt solution also enhanced the loss of UV-absorbing material. Addition of lysozyme to suspensions of mureinoplasts in the balanced salt solution produced spherical forms which, by electron microscopy and the analysis of residual cell wall material, appeared to be true protoplasts. Only undamaged mureinoplasts, as judged by their capacity to fully retain alpha-aminoisobutyric acid, were capable of being converted to protoplasts. Protoplasts and undamaged mureinoplasts retained 100% transport capacity when compared to an equal number of whole cells. The Na(+) requirement for transport of alpha-aminoisobutyric acid and the sparing action of Li(+) on this Na(+) requirement were the same for both protoplasts and whole cells. These observations indicate that, in this gram-negative bacterium, the cell wall does not participate in the transport process though it does stabilize the cytoplasmic membrane against changes in porosity produced by unbalanced salt solutions. The results also indicate that the requirements for Na(+) for transport and for the retention of intracellular solutes are manifested at the level of the cytoplasmic membrane.
通过在0.5m NaCl中洗涤细胞,然后悬浮于0.5m蔗糖中,去除海洋来源假单胞菌细胞包膜的外层。对于经此处理产生的杆状形态,有人建议使用“胞壁质体”这一术语。如先前确定的那样,这些形态缺乏外细胞壁层,但仍保留刚性的肽聚糖结构。如果将胞壁质体悬浮于含有0.3m NaCl、0.05m MgSO₄和0.01m KCl的平衡盐溶液中,它们会保持稳定,但与完整细胞不同的是,如果悬浮于0.5m NaCl或0.05m MgCl₂中,它们会失去紫外线(UV)吸收物质。添加到平衡盐溶液中的蔗糖也会增强UV吸收物质的损失。向平衡盐溶液中的胞壁质体悬浮液中添加溶菌酶会产生球形形态,通过电子显微镜和对残留细胞壁物质的分析,这些球形形态似乎是真正的原生质体。只有通过其完全保留α-氨基异丁酸的能力判断为未受损的胞壁质体才能转化为原生质体。与相同数量的完整细胞相比,原生质体和未受损的胞壁质体保留了100%的转运能力。对于原生质体和完整细胞而言,α-氨基异丁酸转运的Na⁺需求以及Li⁺对该Na⁺需求的节约作用是相同的。这些观察结果表明,在这种革兰氏阴性细菌中,细胞壁虽能稳定细胞质膜以防止不平衡盐溶液引起的孔隙率变化,但不参与转运过程。结果还表明,转运和保留细胞内溶质对Na⁺的需求在细胞质膜水平体现。