Mattila T, Honkanen-Buzalski T, Pösö H
Biochem J. 1984 Nov 1;223(3):823-30. doi: 10.1042/bj2230823.
The effect of dicyclohexylamine on seven freshly isolated bacterial strains of mastitis pathogens was studied. Streptococcus uberis was the most sensitive strain investigated, since 5 mM-dicyclohexylamine totally arrested its growth and 1.25 mM of the drug caused 60% growth inhibition. The Staphylococcus aureus, Escherichia coli and Pseudomonas aeruginosa strains were also sensitive to the drug, but less so than Strep. uberis, since 5 mM drug caused only partial inhibition of growth. Micrococcus sp. and Klebsiella sp. grew in the presence of 10.0 mM-dicyclohexylamine, and, finally the growth of Streptococcus agalactiae was not at all affected by dicyclohexylamine. These different sensitivities towards dicyclohexylamine in vivo were paralleled by different sensitivities of the bacteria's spermidine synthase to the drug in vitro, and also by the ability of the drug to lower spermidine concentration in bacterial cells. Spermidine synthase from sensitive bacteria was inhibited by more than 90% by 50 microM-dicyclohexylamine in vitro, and the concentration of spermidine was decreased in E. coli and Ps. aeruginosa by 70% and in Strep. uberis by 95%, whereas in Strep. agalactiae 5 mM-dicyclohexylamine did not affect the concentration of spermidine at all. Dicyclohexylamine treatment led to the accumulation of putrescine in Strep. uberis. Spermidine synthesis catalysed by the extracts of Micrococcus sp. required 500 microM-dicyclohexylamine for 90% inhibition, and Strep. agalactiae contained a spermidine synthase that was still active at 1000 microM-dicyclohexylamine, The observed inhibition of growth was totally reversed by adding 50 microM-spermidine (final concentration) to the medium. Putrescine reversed the inhibition only when bacteria had a spermidine synthase activity insensitive to dicyclohexylamine. Spermine did not overcome the inhibition of growth caused by dicyclohexylamine, probably because it was not taken up by the bacterial cells used in this study. The inhibition of the growth by dicyclohexylamine (even in the case of Strep. uberis) was reversible in the sense that addition of 50 microM-spermidine 18 h after dicyclohexylamine still restored the growth rate of untreated controls.
研究了二环己胺对七种新鲜分离的乳腺炎病原菌菌株的影响。乳房链球菌是所研究的最敏感菌株,因为5 mM二环己胺完全抑制其生长,1.25 mM该药物导致60%的生长抑制。金黄色葡萄球菌、大肠杆菌和铜绿假单胞菌菌株对该药物也敏感,但不如乳房链球菌敏感,因为5 mM药物仅导致部分生长抑制。微球菌属和克雷伯菌属在10.0 mM二环己胺存在下生长,最后无乳链球菌的生长完全不受二环己胺影响。这些细菌在体内对二环己胺的不同敏感性与它们的亚精胺合酶在体外对该药物的不同敏感性以及该药物降低细菌细胞中亚精胺浓度的能力相对应。敏感细菌的亚精胺合酶在体外被50 microM二环己胺抑制超过90%,大肠杆菌和铜绿假单胞菌中的亚精胺浓度分别降低70%和95%,而在无乳链球菌中降低95%,而在无乳链球菌中5 mM二环己胺根本不影响亚精胺浓度。二环己胺处理导致乳房链球菌中腐胺积累。微球菌属提取物催化的亚精胺合成需要500 microM二环己胺才能达到90%的抑制率,无乳链球菌含有一种亚精胺合酶,在1000 microM二环己胺时仍有活性。向培养基中添加50 microM亚精胺(终浓度)可完全逆转观察到的生长抑制。只有当细菌具有对二环己胺不敏感的亚精胺合酶活性时,腐胺才能逆转抑制作用。精胺不能克服二环己胺引起的生长抑制,可能是因为它未被本研究中使用的细菌细胞摄取。二环己胺对生长的抑制(即使在乳房链球菌的情况下)在某种意义上是可逆的,即在二环己胺处理18小时后添加50 microM亚精胺仍能恢复未处理对照的生长速率。