A mushroom-shaped budding bacterium, isolated from fresh pond water, is unlike any previously described aquatic budding bacteria (Whittenbury & McLee, I 967 ; Hirsch & Rheinheimer, 1968 ; Staley, 1968). Its morphological 'life-cycle' and other properties are described.
METHODS
Media.The organism was grown routinely in glucose-salts medium (pH 6.9) of the following composition: (NH4)2S04, 0.1 % (w/v); NaCI, 0.05 % (w/v); MgS04, 7H20, 0.05 % (w/v); NaH2P04, 12H20, 0.07 % (w/v); NaH,PO,, 2H20, 0.03 % ( Substrate utilization. Ability to use a variety of combined carbon and energy sources, aerobically and anaerobically, was tested using a soft agar salts medium (glucose-salts medium without glucose) containing 0.004 % bromothymol blue distributed in 3 in. test tubes. Substrates (0.5 %, w/v, final concentration) were filter-sterilized before adding to melted, autoclaved medium. Tubed medium was melted, cooled to 3 5 ' ' inoculated with a drop of 24 h. culture, swirled to distribute inoculum and allowed to set.Slide culture. Molten agar medium, generally glucose-salts agar, was poured on sterile glass slides and a sterile cover-slip was dropped immediately onto the surface of the medium to cast a flat surface. After the medium solidified, the coverslip was removed and the agar surface allowed to dry partially before being inoculated from a 24 h. culture. A trough was cut in the agar and a cover-slip placed over the inoculated surface with the trough (air supply) lying centrally under the coverslip. The edges of the coverslip, cleared of excess agar, were sealed with a paraffin wax-petroleum jelly mixture, to prevent drying out. Growth was obseryed under phase contrast over 24 h. at 3 0 ' . Electron microscopy was as described by Davies & Whittenbury (1970).
RESULTS A N D DISCUSSIONPhysiological properties. The organism was a capsulated Gram-negative, non-spore forming, non-photosynthetic, strictly aerobic heterotroph. Nitrate was not reduced, catalase and oxidase activities were detected; a-, b-and c-type cytochromes were identified in suspensions of the organism scanned in a Unicam SP800 ultraviolet spectrophotometer. Organic growth factors were not required. Glucose, D-and L-arabinose, galactose, fructose, mannitol, glycerol, sodium gluconate, formate, acetate, propionate, lactate, fumarate, succinate, citrate or glutarate were utilized as combined carbon and energy sources. Acid was produced from sugars and sugar alcohols. Mannose, lactose, maltose, sucrose, dulcitol,