Iandolo J J, Shafer W M
Infect Immun. 1977 May;16(2):610-6. doi: 10.1128/iai.16.2.610-616.1977.
The effect of glucose and the glucose analogues 2-deoxyglucose and alpha-methyl-glucoside on the synthesis and regulation of staphylococcal enterotoxin B was examined. The attenuating effect of glucose on staphylococcal enterotoxin B synthesis was observed. However, when this effect was examined with analogues of glucose, contradictory responses were seen. alpha-Methylglucoside had a slight stimulatory effect on enterotoxin production and other extracellular proteins, whereas 2-deoxyglucose markedly inhibited enterotoxin production. beta-hemolysin and staphylococcal nuclease were also inhibited by 2-deoxy glucose but the synthesis of nuclease could be rescued by the addition of glucose to 2-deoxyglucose-containing cultures. Enterotoxin and beta-hemolysin synthesis were not subject to glucose rescue. The cells used in this study were permeable to cyclic 3',5'-adenosine monophosphate, but the addition of this compound did not reverse glucose repression or 2-deoxyglucose inhibition of enterotoxin B synthesis. We conclude from these data that the regulation of enterotoxin is not under catabolite control as previously reported.
研究了葡萄糖及其类似物2-脱氧葡萄糖和α-甲基葡萄糖苷对葡萄球菌肠毒素B合成及调控的影响。观察到葡萄糖对葡萄球菌肠毒素B合成有减弱作用。然而,当用葡萄糖类似物检测这种作用时,却出现了相互矛盾的反应。α-甲基葡萄糖苷对肠毒素产生及其他细胞外蛋白有轻微的刺激作用,而2-脱氧葡萄糖则显著抑制肠毒素产生。β-溶血素和葡萄球菌核酸酶也受到2-脱氧葡萄糖的抑制,但在含2-脱氧葡萄糖的培养物中添加葡萄糖可挽救核酸酶的合成。肠毒素和β-溶血素的合成不受葡萄糖挽救的影响。本研究中使用的细胞对环磷腺苷酸是可通透的,但添加该化合物并不能逆转葡萄糖对肠毒素B合成的阻遏或2-脱氧葡萄糖对其的抑制作用。根据这些数据我们得出结论,肠毒素的调控并不像先前报道的那样受分解代谢物控制。