REVIEW REVIEW use of a technique that had recently been reported by Godson and Sinsheimer 6 that utilized a detergent mixture of Brij 58 (a neutral detergent) and deoxycholate for lysis of phageinfected E. coli. During a relatively low-speed centrifugation step, the vast majority of chromosomal DNA pelleted leaving the supernatant greatly enriched in plasmid DNA. Sucrose gradient analyses of these "cleared lysates" revealed a ColE1-protein complex sedimenting slightly faster (24S) than the 23S protein-free supercoiled DNA. Surprisingly, when the 24S complex was exposed to conditions expected to affect protein structure such as proteases, strong ionic detergents or heat, the 24S complex converted to a 17S relaxed (open circular) configuration. The relaxation event involved the introduction of a strand-specific nick in the supercoiled plasmid; we therefore called the 24S entity a "relaxation complex". 7,8 The percentage of plasmid DNA that was present in the complexed state varied from less than 30%, when glucose was in the growth medium, to more than 80% when glucose was absent.