Yasuda Y, Tochikubo K
Microbiol Immunol. 1984;28(11):1203-10. doi: 10.1111/j.1348-0421.1984.tb00778.x.
Glucose interfered with the inhibitory action of hydrophobic compounds, such as n-octanol, diphenylamine and 2-tert-butylphenol, during L-alanine-initiated germination of Bacillus subtilis spores. The action of glucose on the action of the hydrophobic compounds was not competitive, and the binding affinity of glucose was not essentially affected by the hydrophobic compounds, indicating the presence of separate binding sites for glucose and the hydrophobic compounds. The binding affinity of D-alanine, a competitive inhibitor of L-alanine, was not affected by the hydrophobic compounds, indicating separate binding sites for D-alanine and the hydrophobic compounds. A possible arrangement of the binding sites for glucose and for the hydrophobic compounds in relation to those for L- and D-alanine on the spores is discussed.
在枯草芽孢杆菌孢子由L-丙氨酸引发的萌发过程中,葡萄糖会干扰疏水性化合物(如正辛醇、二苯胺和2-叔丁基苯酚)的抑制作用。葡萄糖对疏水性化合物作用的影响并非竞争性的,且葡萄糖的结合亲和力基本上不受疏水性化合物的影响,这表明葡萄糖和疏水性化合物存在各自独立的结合位点。L-丙氨酸的竞争性抑制剂D-丙氨酸的结合亲和力也不受疏水性化合物的影响,这表明D-丙氨酸和疏水性化合物也存在各自独立的结合位点。本文讨论了孢子上葡萄糖、疏水性化合物与L-丙氨酸和D-丙氨酸结合位点的可能排列方式。