During the past few years the authors have been interested in studying the effects of high centrifugal force upon the structure of various types of cells in both plants and animals (Beams and King, 1940). In the course of these investigations a large flagellated bacterium, Spirillum volutans, appeared among our cultures of protozoa. Because of its large size it was thought that this organism might prove to be valuable bacteriological material for cytological study, since a review of the literature on this subject disclosed it to be in a considerable state of uncertainty. In addition, to our knowledge, ultracentrifugal force has not been applied to bacteria with the view of studying its effects upon the cytology of these organisms. MATERIALS AND METHODS Spirillum volutanrs appeared in a boiled wheat culture of mixed infusoria. The bacteria grew and multiplied rapidly when subcultured at intervals of about two weeks. Both normal and ultracentrifuged organisms were fixed in 100 per cent alcohol, Schaudinn's, Bouin's, Champy's and Regaud's solutions. They were stained in Heidenhain's hematoxylin, Delafield's hematoxylin, Regaud's hematoxylin, aceto-carmine, by Feulgen's method, in silver nitrate, in osmic acid and in nigrosin. In addition they were vitally stained by Janus green B, neutral red, methylene-blue and brilliant-cresyl-blue. They were also observed in the living unstained condition, in dark field and under polarized light; the microincineration technique was likewise carried out. The bacteria were centrifuged at 400,000 times gravity for 10 to 20 minutes in the air-driven ultracentrifuge developed by J. W. Beams at the University of Virginia, to whom we are indebted for having constructed the apparatus for us. DESCRIPTION Spirillum volutans is a large, quite rigid, corkscrew-shaped bacterium which is equipped with a group of flagella at each end (fig. 1). It moves in a rather tight spiral, the movement appearing to be quite without jerkiness. There are numerous granules and vacuole-like inclusions in the protoplasm which appear highly refractive or dark, depending upon the focus at which they are observed (fig. 4). Vital staining with nigrosin reveals these structures much more clearly than under ordinary unstained conditions (fig. 6). Due to their rigid covering, these organisms do not break up nor are they greatly distorted by ultracentrifuging but all the granules and vacuoles are con-Aided by a grant from the Rockefeller Foundation for work in Cellular Biology.