Fukuda A
J Biochem. 1976 Aug;80(2):253-8. doi: 10.1093/oxfordjournals.jbchem.a131271.
At increasing dye concentrations in propidium diiodide-CsCl density gradients, the relative buoyant density shift was largest for open-circular duplex phiX174 DNA (RFII), next largest for single-stranded viral DNA, and least for closed-circular duplex DNA (RFI). These differential relative buoyant density shifts permitted discrete separations of these phiX DNA forms. Further, in propidium diiodide-CsCl density gradients, the distinctive density of single-stranded DNA permitted separations of rolling-circle intermediates with a single-stranded tail that occur during single-stranded phiX DNA synthesis. It is suggested that single-strandedness in a duplex DNA structure influences its buoyand density shift due to differential dye binding to the single-stranded region and is an additional physical basis for relative buoyant separations of DNA molecules in propidium diiodide-CsCl density gradients.
在碘化丙啶 - 氯化铯密度梯度中,随着染料浓度的增加,开环双链φX174 DNA(RFII)的相对浮力密度变化最大,单链病毒DNA次之,闭环双链DNA(RFI)最小。这些不同的相对浮力密度变化使得这些φX DNA形式能够被离散分离。此外,在碘化丙啶 - 氯化铯密度梯度中,单链DNA独特的密度使得在单链φX DNA合成过程中出现的带有单链尾巴的滚环中间体得以分离。有人提出,双链DNA结构中的单链性由于染料与单链区域的差异性结合而影响其浮力密度变化,这是在碘化丙啶 - 氯化铯密度梯度中对DNA分子进行相对浮力分离的另一个物理基础。