Girardeau J P, Dubourguier H C, Gouet P
J Gen Microbiol. 1982 Mar;128(3):463-70. doi: 10.1099/00221287-128-3-463.
The effect of various culture media on K99 antigen production by enterotoxigenic Escherichia coli strains of bovine origin was investigated by slide agglutination tests, enzyme-linked immunosorbent assays and in vitro attachment to intestinal villi. A-Alanine at concentrations higher than 0.7 g 1(-1) was responsible for the inhibition of K99 synthesis observed on media rich in amino acids. The increased inhibitory activity of L-alanine in glucose-rich media after autoclaving suggested the formation of inhibitory products via Maillard's reaction. Of various L-alanine derivatives tested, only those that hydrolysed to L-alanine were inhibitory. L-Alanine analogues were without effect and the addition of 10 mM-cyclic AMP did not overcome the repression of K99 biosynthesis by L-alanine. Enzymes involved in cell wall synthesis such as L-alanine racemase or D-alanyl-D-alanine synthetase were evidently were evidently unaffected by L-alanine.
通过玻片凝集试验、酶联免疫吸附测定以及体外对肠绒毛的黏附,研究了各种培养基对源自牛的产肠毒素大肠杆菌菌株产生K99抗原的影响。浓度高于0.7 g l(-1)的α-丙氨酸导致在富含氨基酸的培养基上观察到的K99合成受到抑制。高压灭菌后,富含葡萄糖的培养基中L-丙氨酸的抑制活性增加,这表明通过美拉德反应形成了抑制产物。在测试的各种L-丙氨酸衍生物中,只有那些水解为L-丙氨酸的衍生物具有抑制作用。L-丙氨酸类似物没有作用,添加10 mM-环磷酸腺苷也不能克服L-丙氨酸对K99生物合成的抑制。参与细胞壁合成的酶,如L-丙氨酸消旋酶或D-丙氨酰-D-丙氨酸合成酶,显然不受L-丙氨酸的影响。