James T W, Jope C
J Cell Biol. 1978 Dec;79(3):623-30. doi: 10.1083/jcb.79.3.623.
The DNA in isolated chloroplasts was visualized by the fluorescent probe 4'6-diamidino-2-phenylindole (DAPI). When excited with light of 360 nm, the DNA-DAPI complex fluoresces brilliantly at 450 nm. Nuclei also fluoresce but their nucleoli do not. RNase and Pronase treatment of chloroplasts did not affect the fluorescence but both pre- and posttreatment of DAPI-stained chloroplasts with DNase specifically destroyed the fluorescence. DNA-DAPI complexes in the chloroplasts show up as bright dots. These are distributed uniformly within the chloroplast except for the outer margins. The fluorescent dots can be seen at different focal levels. The number of DNA dots is roughly proportional to chloroplast area which, in turn, is a function of leaf size. The number of fluorescent dots also gave the impression that large leaves with large chloroplasts contain more chloroplast DNA than nuclear DNA.
用荧光探针4′,6-二脒基-2-苯基吲哚(DAPI)使分离出的叶绿体中的DNA可视化。当用360nm的光激发时,DNA-DAPI复合物在450nm处发出明亮的荧光。细胞核也会发出荧光,但核仁不会。用核糖核酸酶(RNase)和链霉蛋白酶处理叶绿体不会影响荧光,但用脱氧核糖核酸酶(DNase)对DAPI染色的叶绿体进行处理前和处理后都会特异性地破坏荧光。叶绿体中的DNA-DAPI复合物呈现为亮点。这些亮点除了叶绿体的外缘外,在叶绿体内均匀分布。在不同的聚焦水平都能看到这些荧光点。DNA点的数量大致与叶绿体面积成正比,而叶绿体面积又是叶片大小的一个函数。荧光点的数量也让人觉得,叶绿体大的大叶中叶绿体DNA比核DNA更多。