RT Journal Article SR Electronic(1) A1 Gombas, David E. A1 Labbe, Ronald G.YR 1981 T1 Extraction of Spore-lytic Enzyme from Clostridium perfringens Spores JF Microbiology, VO 126 IS 1 SP 37 OP 44 DO https://doi.org/10.1099/00221287-126-1-37 PB Microbiology Society, SN 1465-2080, AB Various chemical reagents known to extract spore coat protein were used to extract spore-lytic enzyme (SLE) from intact and germinated spores of Clostridium perfringens. Of the reagents tested, 7·2m-urea plus 10% (v/v) mercaptoethanol, pH2·85, solubilized the most SLE activity per mg spores. The quantity of SLE extracted was dependent on the initial pH of the reagent, with a maximum between pH 2·7 and 3·0. Germinated spores yielded more SLE than non-germinated spores upon urea/mercaptoethanol extraction. SLE release during spore germination probably utilizes a trigger mechanism not satisfied by germination alone. Significant amounts of SLE were released during germination when spores were suspended in potassium chloride or a complex germinant mixture containing brain-heart infusion, yeast extract and chloramphenicol, but not during germination with sodium nitrite, which non-enzymically lysed the cortical peptidoglycan. Greater solubilization of SLE activity was obtained by urea/mercaptoethanol extraction of spores germinated with nitrite than of spores germinated with either potassium chloride or the complex germinant., UL https://www.microbiologyresearch.org/content/journal/micro/10.1099/00221287-126-1-37