Esterases of 62 Serratia marcescens, S. liquefaciens, S. plymuthica and S. marinorubra strains were analysed by horizontal slab electrophoresis in polyacrylamide-agarose gel. Five principal bands hydrolysed P-naphthyl acetate but differed in their range of activity towards other substrates and in their sensitivity to di-isofluoropropyl phosphate. Additional bands were detected in some strains of S. marcescens and S. marinorubra. The comparative distribution of bands showed that the four Serratia species were characterized by distinct electrophoretic patterns of their esterases. Serratia marcescens, S. Ziquefaciens and S. plymuthica appeared to be more closely related to one another than to S. marinorubra. In the case of S.plymuthica and S. marinorubra, congruence was found between biovars and esterase patterns. The numerous electrophoretypes observed within Serratia species might provide useful epidemiological markers.
I N T R O D U C T I O NPrevious investigations have revealed that esterases of several taxa in the family Enterobacteriaceae (Goullet, 1973(Goullet, , 1975(Goullet, , 1977Goullet & Richard, 1977) give distinct and reproducible species-specific zymogram banding patterns when assayed after electrophoresis in polyacrylamide-agarose gel. In the present study, the esterases produced by the four Serratia species recognized by Grimont et al. (1977a, b) were examined.
METHODSThe names and sources of the test strains are given in Table 1. Growth conditions, preparation of extracts, inhibition by di-isofluoropropyl phosphate (DFP), protein estimation, acrylamide-agarose gel electrophoresis, esterase staining and estimation of electrophoretic mobility (MF value) have all been described previously (Goullet, 1977).
RESULTSThe esterase profiles resolved from multiple runs of the same and different soluble extracts from each strain were reproducible. Electrophoretic relationships were established between the strains by numerous replicate assays comparing esterase bands in adjacent positions on the same gel. Esterase bands were found in all of the test strains.Five principle esterase bands varying in sharpness and colour intensity, designated as E,, E,, ES, E, and E, in order of decreasing electrophoretic mobility, were defined ( Fig. 1 a),The El band hydrolysed a-naphthyl acetate and to a lesser degree a-naphthyl butyrate, indoxyl acetate and P-naphthyl acetate; the Ez band hydrolysed a-and P-naphthyl acetates;