Quinting B, Reyrat J M, Monnaie D, Amicosante G, Pelicic V, Gicquel B, Frère J M, Galleni M
Centre d'Ingénièrie des Proteines, Université de Liège, Institut deChimie, Belgium.
FEBS Lett. 1997 Apr 14;406(3):275-8. doi: 10.1016/s0014-5793(97)00286-x.
Mycobacterium fallax (M. fallax) is naturally sensitive to many beta-lactam antibiotics (MIC < 2 microg/ml) and devoid of beta-lactamase activity. In this paper, we show that the production of the beta-lactamase of Mycobacterium fortuitum by M. fallax significantly increased the MIC values for good substrates of the enzyme, whereas the potency of poor substrates or transient inactivators was not modified. The rates of diffusion of beta-lactams through the mycolic acid layer were low, but for all studied compounds the half-equilibration times were such that they would only marginally affect the MIC values in the absence of beta-lactamase production. These results emphasize the importance of enzymatic degradation as a major factor in the resistance of mycobacteria to penicillins.
伪结核分枝杆菌(M. fallax)对许多β-内酰胺抗生素天然敏感(最低抑菌浓度<2微克/毫升)且无β-内酰胺酶活性。在本文中,我们表明,伪结核分枝杆菌产生的偶然分枝杆菌β-内酰胺酶显著提高了该酶良好底物的最低抑菌浓度值,而不良底物或瞬时灭活剂的效力未改变。β-内酰胺通过分枝菌酸层的扩散速率较低,但对于所有研究的化合物,半平衡时间仅会在不产生β-内酰胺酶的情况下对最低抑菌浓度值产生轻微影响。这些结果强调了酶促降解作为分枝杆菌对青霉素耐药性的主要因素的重要性。