S U M M A R YThe symbionts called 'lambda' present in the cytoplasm of killer stocks 239 (syngen 4) and 299 (syngen 8) of Paramecium aurelia have been investigated. Observations with the electron microscope of ultrathin sections and of negatively stained material revealed that these symbionts have peritrichous flagellation. The ultrastructures of symbionts from both stocks were identical and were those of flagellated bacteria. (1950, 1959, 1965). These stocks are referred to as rapid lysis killers, since sensitive paramecia are lysed within 20 min. after being exposed to them. Paramecia of syngen 3 are especially sensitive to the action of all lambda-bearing killers. Lambda particles are much larger than most of the other symbionts which have been described for P. aurelia. Van Wagtendonk, Clark & Godoy (1963) reported that it was possible to grow lambda particles in cell-free cultures in an axenic medium. There has been little electron microscopy of lambda reported. Sonneborn (1965) published one micrograph of this symbiont. The present paper reports investigations on lambda of P. aurelia stocks 239 and 299 by use of phase-contrast and electron microscopy.
M E T H O D SBoth stocks of Paramecium were grown in lettuce medium previously inoculated with Aerobacter aerogenes (Sonneborn, 1950). Lambda particles outside the host cytoplasm were observed with a bright phase-contrast microscope (American Optical Co.) in animals freshly crushed between a slide and coverslip. To observe the symbionts in situ two methods were used. In the first, whole paramecia were observed with a dark phase-contrast microscope (Carl Zeiss), using paramecia treated with lactoorcein according to the method of Beale & Jurand (1966). In the second, I p Araldite sections were mounted on slides, stained with toluidine blue and observed with ordinary bright-field microscopy.The ultrastructure of lambda symbionts was investigated by examination of ultrathin sections and of negatively stained isolated symbionts with the A.E.I. 6 electron microscope. For ultrathin sectioning mass cultures of each stock were fixed in one of two ways. In the first method the paramecia were concentrated by centrifugation,