ABSTRACT
To visualize the fine structure of compacted DNA of Synechococcus elongatus PCC 7942, which appears at a specific time in the regular light/dark cycle prior to cell division, ChromEM with some modifications was applied. After staining DNA with DRAQ5, the cells were fixed and irradiated by red laser in the presence of 3,3'-diaminobenzidine and subsequently fixed with OsO4. A system with He-Ne laser (633 nm) was set up for efficient irradiation of the bacterial cells in aqueous solution. The compacted DNA was visualized by transmission electron microscopy, in ultrathin sections as electron dense staining by osmium black.
Subject(s)
DNA, Bacterial/ultrastructure , Synechococcus/ultrastructure , 3,3'-Diaminobenzidine/chemistry , Anthraquinones/chemistry , DNA, Bacterial/chemistry , Fluorescent Dyes/chemistry , Lasers , Microscopy, Electron, Transmission , Osmium/chemistry , Staining and Labeling/methods , Synechococcus/geneticsABSTRACT
A fiber-optic mirror magneto-optical trap (mirror-MOT) that uses a pair of circularly polarized light-emitting optical fibers as an optical access is demonstrated. The fiber is fabricated so that a length of birefringence fiber, designed to be a quarter wave retarder at both wavelengths of 780 and 852 nm, is attached directly onto a polarization-maintaining normal fiber. The polarization states of light emitted from the fibers are sufficiently circular for the operation of a mirror-MOT with 87Rb atoms. The mirror-MOT is able to capture approximately the same number of atoms obtainable with a conventional mirror-MOT. The technique makes it possible to fabricate a compact MOT apparatus by introducing the optical fibers directly into an ultrahigh-vacuum chamber.
