Vadeboncoeur C, St Martin S, Brochu D, Hamilton I R
Departement de Biochimie Sciences et Genie, Universite Laval, Ste-Foy, Quebec, Canada.
Infect Immun. 1991 Mar;59(3):900-6. doi: 10.1128/iai.59.3.900-906.1991.
The growth of Streptococcus mutants Ingbritt in continuous culture at low pH or high growth rates repressed the biosynthesis of the components of the phosphoenolpyruvate:sugar phosphotransferase system (PTS). The cellular concentrations of the soluble components HPr, enzyme I (EI), and EIII for mannose (IIIman) and EII activity for glucose, mannose, 2-deoxyglucose (2DG), and fructose were determined in membrane preparations from cells grown at pHs from 8.0 to 5.0 and at dilution (D) or growth rates from 0.1 to 1.0 h-1. The cellular levels of HPr and EI varied less than threefold under all of the growth conditions tested. On the other hand, EII activity in membranes from cells grown at D = 0.1 h-1 was repressed by growth at pHs below 8.0, with cells grown at pH 5.0 completely devoid of EII activity. In addition, cells grown at D = 0.5 and 1.0 h-1 exhibited little PTS activity for glucose, mannose, and 2DG and twofold-lower activity for fructose. These activities were stimulated by the addition of a membrane-free cytoplasmic fraction, and this activating activity was shown to be due to the presence of IIIman. Estimation of the cellular content of IIIman indicated that the synthesis of this factor was repressed by growth above and below pH 7.0 and was particularly sensitive to growth at high rates. These results indicate that with S. mutans Ingbritt, both pH and growth rate regulate the genes for the synthesis of EIIs involved in the phosphorylation of glucose, mannose, 2DG, and fructose and the gene for the formation of IIIman.
在低pH值或高生长速率下进行连续培养时,变异链球菌英布里特菌株(Streptococcus mutants Ingbritt)中磷酸烯醇丙酮酸:糖磷酸转移酶系统(PTS)各组分的生物合成受到抑制。测定了在pH值从8.0至5.0以及稀释率(D)或生长速率从0.1至1.0 h⁻¹条件下生长的细胞的膜制剂中,可溶性组分HPr、酶I(EI)、甘露糖的EIII(IIIman)以及葡萄糖、甘露糖、2-脱氧葡萄糖(2DG)和果糖的EII活性的细胞浓度。在所有测试的生长条件下,HPr和EI的细胞水平变化不到三倍。另一方面,在D = 0.1 h⁻¹条件下生长的细胞,当pH值低于8.0时,其膜中的EII活性受到抑制,在pH 5.0条件下生长的细胞完全没有EII活性。此外,在D = 0.5和1.0 h⁻¹条件下生长的细胞对葡萄糖、甘露糖和2DG几乎没有PTS活性,对果糖的活性则低两倍。添加无膜细胞质组分可刺激这些活性,并且这种激活活性被证明是由于IIIman的存在。对IIIman细胞含量的估计表明,该因子的合成在pH 7.0以上和以下生长时均受到抑制,并且对高速生长特别敏感。这些结果表明,对于变异链球菌英布里特菌株,pH值和生长速率均调节参与葡萄糖、甘露糖、2DG和果糖磷酸化的EII合成基因以及IIIman形成基因。