No abstract

No abstract

Summary 1. Procaryotic motility mechanisms are more difficult to investigate than those of the generally larger, hence more easily observable, eucaryotic forms. Furthermore, although the function—namely translational locomotion—is the same, the biomechanisms by which this end is accomplished may be, in fact, quite distinct in the two forms. 2. Observational techniques for studying procaryotic motility are relatively crude and qualitative. Progress toward a greater understanding of motility phenomena will be made correlative with advances derived from devising specific techniques involving approaches adapted from electrical engineering, biophysics and cybernetics. 3. There is a great amount of information at hand concerning the qualitative and quantitative chemical composition of procaryotic flagella, but there is no assurance that preparatory techniques include either the entire organelle on the one hand, or do not introduce subtle errors on the other hand. Similarly, the structural features of flagella as derived from electron‐microscope studies of fixed preparations may be themselves influenced by the techniques employed to reveal them. 4. Chemotactic responses of bacteria have been noted almost since the beginning of bacteriology as a formal scientific endeavour, yet the study of transduction of environmental stimuli, using motile bacteria as experimental subjects, is a relatively recent development. We have proposed that the cytoplasmic membrane may act as a non‐specific receptor‐transmitter of such signals in motile bacteria. If this is found to be the case, perhaps a sensory code may be more amenable to discovery here than with more complex forms of organisms. 5. Knowledge of the physical aspects in procaryotic flagellar movement is extremely fragmentary. There is some information on the movements of living functional flagellar fascicles, but this form of movement of an individual flagellum is purely speculative. We have proposed that the procaryotic flagellum is a rigid or semi‐rigid helix, which does not transmit helical waves of contraction, and that its movements are governed by a specialized area of the cytoplasmic membrane. The flagellum may rotate or wobble within the flagellar basal bulb to produce the motion necessary for propulsion. This view ‘explains’ many of the known properties of procaryotic flagella. 6. The basis of gliding motility remains unknown even after a great deal of experimental work. In our view, the secretion of slime is necessary for adhesion to a solid surface, and movement is believed to be mediated by a mechanism involving contractile waves. 7. Studies on procaryotic motility may yield valuable information on certain areas of general biological interest. Among these are: (a) the transduction of environmental stimuli and the sensory code; (b) the development of reproducible observational techniques for quantitative data on the hydrodynamic and biophysical parameters of cell motion in procaryotic forms; (c) the phenomenon of unicellular ‘behaviour’ and the survival value and evo...

Direct FA staining for S mutans serotypes may be performed on smears made from plaque or strain isolates and on colonies attached to agar plates of black membrane filters. Staining with single conjugates directed to S mutans serotypes (a to e) as well as with polyvalent a-, b-, d-, f-fluorescein label and c-, e-rhodamine label conjugates indicate that serotype c is the most common. This is in agreement with many reports by other investigators. Cross-reactions with many S mutans conjugates occurred with organisms resembling Lancefield groups C and G streptococci.