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Enterotoxin A production in Staphylococcus aureus: inhibition by glucose
Authors:J L Smith  M M Bencivengo  R L Buchanan  C A Kunsch
Institution:(1) Department of Agriculture, Eastern Regional Research Center, 19118 Philadelphia, PA, USA
Abstract:In this study, we investigated the relationship between carbohydrate metabolism and repression of staphylococcus enterotoxin A (SEA) in Staphylococcus aureus 196E and a pleiotrophic mutant derived from strain 196E. The mutant, designated at strain 196E-MA, lacked a functional phosphoenolpyruvate phosphotransferase system (PTS). The mutant produced acid, under aerobic conditions, from only glucose and glycerol. The parent strain contained an active PTS, and aerobically produced acid from a large number of carbohydrates. Prior growth in glucose led to repression of SEA synthesis in the parent strain; addition to the casamino acids enterotoxin production medium (CAS) led to more severe repression of toxin synthesis. The repression was not related to pH decreases produced by glucose metabolism. When S. aureus 196E was grown in the absence of glucose, there was inhibition of toxin production as glucose level was increased in CAS. The inhibition was related to pH decrease and was unlike the repression observed with glucose-grown strain 196E. The inhibition of SEA synthesis in mutant strain 196E-MA was approximately the same in cells grown with or without glucose and was pH related. Repression of SEA synthesis similar to that seen with glucose-grown S. aureus 196E could not be demonstrated in the mutant. In addition, glucose-grown S. aureus 196E neither synthesized beta-galactosidase nor showed respiratory activity with certain tricarboxylic acid (TCA) cycle compounds. Glucose-grown strain 196E-MA, however, did not show supressed respiration of TCA cycle compounds; beta-galactosidase was not synthesized because the mutant lacked a functional PTS. Cyclic adenosine-3prime, 5prime-monophosphate did not reverse the repression by glucose of SEA or beta-galactosidase synthesis in glucose-grown S. aureus 196E. An active PTS appears to be necessary to demonstrate glucose (catabolite) repression in S. aureus.Abbreviations SEA staphylococcal enterotoxin A - SEB staphylococcal enterotoxin B - SEC staphylococcal enterotoxin C - PTS phosphoenolpyruvate phosphotransferase system - CAS casamino acids salts medium - TCA tricarboxylic acid cycle
Keywords:Phosphoenolpyruvate phosphotransferase system  Catabolite repression  Glucose effect  Cyclic adenosine-3prime" target="_blank">gif" alt="prime" align="BASELINE" BORDER="0">  5prime-monophosphate" target="_blank">gif" alt="prime" align="BASELINE" BORDER="0">-monophosphate  Pleiotrophic mutant  Staphylococcal enterotoxin A  Staphylococcus aureus
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