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巴比妥抑制细菌孢子萌发的机制及影响因素

Mechanism and factors influencing the veronal inhibition of bacterial spore germination.

作者信息

Sierra G, Bowman A

出版信息

Appl Microbiol. 1969 Mar;17(3):372-8. doi: 10.1128/am.17.3.372-378.1969.

Abstract

The inhibitory effect of sodium 5,5-diethyl barbiturate (Veronal) on the L-alanine-induced initiation of germination of Bacillus subtilis spores was examined. Veronal reversibly inhibited the initiation of germination by a noncompetitive mechanism. The inhibition was time-independent and it took place whether L-alanine was or was not allowed to permeate the spore before the addition of the inhibitor. The concentration of the inhibitor and the pH of the initiation system were important factors determining the effectiveness of Veronal as an inhibitor. The magnitude of the inhibition increased linearly with decreasing pH at constant concentration and with increasing concentration at constant pH. These results suggest that the inhibition involves a permeability phenomenon related to the access of drug to the active sites in the spore and that the entry of Veronal into the spores is regulated by the concentration of undissociated molecule. At the physiologically important pH of 7.4, initiation with alanine in phosphate buffer at high spore densities (about 10(9) spores per ml) was 50% inhibited by 4 mM Veronal, and 8mM Veronal inhibited initiation completely. L-Alanine initiation in tris(hydroxymethyl)amino-methane-hydrochloride buffer was completely inhibited by 5 mM Veronal. The inhibition could be partially reversed by the combined addition of D-fructose, D-glucose, and K(+). Possible reasons for the failure of otherwise inhibitory concentrations of Veronal to inhibit completely the L-alanine-induced initiation when a combination of fructose, glucose, and K(+) was present and a suggested relationship to two functional roles of L-alanine in the initiation of germination are discussed.

摘要

研究了5,5 - 二乙基巴比妥酸钠(佛罗那)对L - 丙氨酸诱导的枯草芽孢杆菌孢子萌发起始的抑制作用。佛罗那通过非竞争性机制可逆地抑制萌发起始。这种抑制与时间无关,并且无论在添加抑制剂之前L - 丙氨酸是否被允许渗透到孢子中,抑制作用都会发生。抑制剂的浓度和起始系统的pH值是决定佛罗那作为抑制剂有效性的重要因素。在恒定浓度下,抑制程度随pH值降低呈线性增加,在恒定pH值下随浓度增加而增加。这些结果表明,抑制作用涉及与药物进入孢子活性位点相关的通透性现象,并且佛罗那进入孢子受未解离分子浓度的调节。在生理重要pH值7.4时,在高孢子密度(约每毫升10⁹个孢子)的磷酸盐缓冲液中用丙氨酸起始萌发,4 mM佛罗那可抑制50%,8 mM佛罗那可完全抑制起始。在三(羟甲基)氨基甲烷 - 盐酸盐缓冲液中用L - 丙氨酸起始萌发,5 mM佛罗那可完全抑制。联合添加D - 果糖、D - 葡萄糖和K⁺可部分逆转这种抑制作用。讨论了在存在果糖、葡萄糖和K⁺组合时,否则具有抑制作用浓度的佛罗那未能完全抑制L - 丙氨酸诱导起始的可能原因,以及与L - 丙氨酸在萌发起始中的两种功能作用的建议关系。

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