Garcia E, Lopez P, Ureña M T, Espinosa M
J Bacteriol. 1978 Sep;135(3):731-40. doi: 10.1128/jb.135.3.731-740.1978.
The addition of ethylenediaminetetraacetate to competent cultures of Bacillus subtilis irreversibly inhibited the transformability as well as the cellular binding of DNA. Our results show that the inhibition of DNA binding by ethylenediaminetetraacetate in whole cells, protoplasts, and membrane vesicles is mainly due to a permanent alteration of the DNA receptors. Transformation absolutely requires free magnesium ions, whereas DNA binding is a magnesium-independent step. In contrast to ethylenediaminetetraacetate, the absence of Mg2+ does not irreversibly affect the capacity of the competent cells to be transformed DNA-binding receptors located at the cell surface remain associated with the plasma membrane after protoplasting and after isolation of membrane vesicles. A Mg2+-dependent endonucleolytic activity associated with the membrane appears to be responsible for the lower levels of binding by protoplasts in the presence of this ion.
向枯草芽孢杆菌感受态培养物中添加乙二胺四乙酸会不可逆地抑制其转化能力以及DNA的细胞结合。我们的结果表明,在全细胞、原生质体和膜泡中,乙二胺四乙酸对DNA结合的抑制主要是由于DNA受体的永久性改变。转化绝对需要游离镁离子,而DNA结合是一个不依赖镁离子的步骤。与乙二胺四乙酸不同,镁离子的缺失不会不可逆地影响感受态细胞被转化的能力,位于细胞表面的DNA结合受体在原生质体形成后以及膜泡分离后仍与质膜相关联。与膜相关的一种依赖镁离子的核酸内切酶活性似乎是在该离子存在下原生质体结合水平较低的原因。