Neu H C, Ashman D F, Price T D
J Bacteriol. 1967 Apr;93(4):1360-8. doi: 10.1128/jb.93.4.1360-1368.1967.
Brief treatment of Escherichia coli with 2 x 10(-4)m ethylenediaminetetraacetic acid (EDTA)-0.12 m tris(hydroxymethyl)aminomethane (Tris), pH 8.0, or 0.12 m Tris alone resulted in the release of the acid-soluble nucleotide pool at 3 or 23 C. Exposure to EDTA-Tris for up to 90 min at 3 C did not result in the release of increasing amounts of 260-mmu-absorbing material. At 23 and 37 C, EDTA-Tris resulted in a steady increase in acid-soluble 260-mmu-absorbing material. Previous growth environment did not alter the release. There appeared to be degradation of 23S ribonucleic acid (RNA) after 10 min of exposure at 23 C. In addition, there was degradation of nucleotides to nucleosides and bases. This occured either within the cells with altered permeability or in the periplasmic space. This occurred in the presence of EDTA and Tris but was not seen with EDTA-phosphate. The mechanism of this degradation is unclear, since it occurs in ribonuclease I-deficient strains. Exposure to Tris buffer for long periods of time at 23 C resulted in release of the nucleotide pool and in degradation of RNA and nucleotides. These studies point out that the EDTA-Tris effect on E. coli must be divided into two parts, an early (4 to 5 min) change in permeability and a later phase of actual RNA breakdown and nucleotide degradation. Studies utilizing EDTA and Tris as agents altering permeability must thus be viewed with caution. Although the cells are viable, they have lost their acid-soluble nucleotide pool and have undergone degradation of some ribosomal RNA.
用2×10⁻⁴m乙二胺四乙酸(EDTA)-0.12m三(羟甲基)氨基甲烷(Tris),pH 8.0或单独用0.12m Tris对大肠杆菌进行短暂处理,会导致在3℃或23℃下酸溶性核苷酸库的释放。在3℃下暴露于EDTA-Tris长达90分钟,不会导致260纳米吸收物质的释放量增加。在23℃和37℃下,EDTA-Tris导致酸溶性260纳米吸收物质稳步增加。先前的生长环境不会改变这种释放。在23℃暴露10分钟后,似乎有23S核糖核酸(RNA)降解。此外,核苷酸降解为核苷和碱基。这发生在通透性改变的细胞内或周质空间中。这在EDTA和Tris存在的情况下发生,但在EDTA-磷酸盐存在时未观察到。这种降解的机制尚不清楚,因为它发生在核糖核酸酶I缺陷菌株中。在23℃下长时间暴露于Tris缓冲液会导致核苷酸库的释放以及RNA和核苷酸的降解。这些研究指出,EDTA-Tris对大肠杆菌的影响必须分为两部分,早期(4至5分钟)的通透性变化和后期实际的RNA分解和核苷酸降解阶段。因此,使用EDTA和Tris作为改变通透性的试剂的研究必须谨慎看待。虽然细胞是有活力的,但它们已经失去了酸溶性核苷酸库并且经历了一些核糖体RNA的降解。