Barug D, Bastiaanse H B, van Rossum J M, Kerkenaar A
Antimicrob Agents Chemother. 1986 Aug;30(2):238-44. doi: 10.1128/AAC.30.2.238.
Lombazole had no effect on respiration at any tested concentration and had little effect on the K+ permeability of Staphylococcus epidermidis. Of the major metabolic processes investigated in this bacterium, only de novo synthesis of the cell envelope was inhibited by lombazole well in advance of an effect on growth. The time course of inhibition indicated that lombazole exerted its primary effect via inhibition of lipid synthesis; other induced changes, such as reduced synthesis of lipoteichoic acid and cell wall components, were considered to be secondary effects. Although the precise site of action in S. epidermidis has to be established, the absence of alterations in lipid patterns after treatment with lombazole suggests the toxicant may affect an essential step in lipid biosynthesis. In Candida albicans, lombazole inhibited the sterol C-14 demethylation step in the ergosterol biosynthesis pathway.
在任何测试浓度下,隆巴唑对呼吸均无影响,对表皮葡萄球菌的钾离子通透性影响很小。在该细菌中研究的主要代谢过程中,只有细胞膜的从头合成在对生长产生影响之前就被隆巴唑很好地抑制了。抑制的时间进程表明,隆巴唑通过抑制脂质合成发挥其主要作用;其他诱导变化,如脂磷壁酸和细胞壁成分合成减少,被认为是次要作用。虽然隆巴唑在表皮葡萄球菌中的精确作用位点有待确定,但用隆巴唑处理后脂质模式没有改变,这表明该毒物可能影响脂质生物合成中的一个关键步骤。在白色念珠菌中,隆巴唑抑制了麦角固醇生物合成途径中的固醇C-14去甲基化步骤。