Paul M, Setlow B, Setlow P
Department of Molecular, Microbial and Structural Biology, University of Connecticut Health Center, Farmington, CT 06030-3305, USA.
J Appl Microbiol. 2007 Apr;102(4):954-62. doi: 10.1111/j.1365-2672.2006.03162.x.
To determine the effectiveness of tert-butyl hydroperoxide (tBHP) plus the cationic surfactant cetyltrimethyl ammonium bromide (CTAB) and a tetra-amido macrocyclic ligand (TAML) activator in killing spores of Bacillus subtilis and the mechanisms of spore resistance to and killing by this reagent.
Killing of spores of B. subtilis by tBHP was greatly stimulated by the optimum ratio of concentrations of a TAML activator (1.7 micromol l(-1)) to tBHP (4.4%, vol/vol) plus a low level (270 mg l(-1)) of CTAB. Rates of killing of spores lacking most DNA protective alpha/beta-type small, acid-soluble spore proteins (alpha(-)beta(-) spores) or the major DNA repair protein, RecA, by tBHP plus CTAB and a TAML activator were essentially identical to that of wild-type spore killing. Survivors of wild-type and alpha(-)beta(-) spores treated with tBHP plus CTAB and a TAML activator also exhibited no increase in mutations. Spores lacking much coat protein either because of mutation or chemical decoating were much more sensitive to this reagent than were wild-type spores, but were more resistant than growing cells. Wild-type spores killed with this reagent retained their large pool of dipicolinic acid (DPA), and the survivors of spores treated with this reagent were sensitized to wet heat. The tBHP plus CTAB and TAML activator-killed spores germinated with nutrients, albeit more slowly than untreated spores, but germinated faster than untreated spores with dodecylamine. The killed spores were also germinated by application of 150 and 500 megaPascals of pressure for 15 min and by lysozyme treatment in hypertonic medium, but these spores lysed shortly after their germination.
The combination of tBHP plus CTAB and a TAML activator is effective in killing B. subtilis spores. The spore coat is a major factor in spore resistance to this reagent system, which does not kill spores by DNA damage or by inactivating some component needed for spore germination. Rather, this reagent system appears to kill spores by damaging the spore's inner membrane in some fashion.
This work demonstrates that tBHP plus CTAB and a TAML activator is an effective and mild decontaminant for spores of Bacillus species. Evidence has also been obtained on the mechanisms of spore resistance to and killing by this reagent system.
确定叔丁基过氧化氢(tBHP)与阳离子表面活性剂十六烷基三甲基溴化铵(CTAB)以及四酰胺大环配体(TAML)活化剂组合在杀灭枯草芽孢杆菌孢子方面的有效性,以及孢子对该试剂的抗性和被其杀灭的机制。
TAML活化剂(1.7 μmol l⁻¹)与tBHP(4.4%,体积/体积)的最佳浓度比,再加上低水平(270 mg l⁻¹)的CTAB,极大地促进了tBHP对枯草芽孢杆菌孢子的杀灭作用。缺乏大多数具有DNA保护作用的α/β型小的酸性可溶性孢子蛋白(α⁻β⁻孢子)或主要DNA修复蛋白RecA的孢子,被tBHP加CTAB和TAML活化剂杀灭的速率与野生型孢子杀灭速率基本相同。用tBHP加CTAB和TAML活化剂处理的野生型和α⁻β⁻孢子的存活者,其突变率也没有增加。由于突变或化学脱壳而缺乏大量外壳蛋白的孢子,对该试剂比野生型孢子更敏感,但比生长中的细胞更具抗性。用该试剂杀灭的野生型孢子保留了大量的吡啶二羧酸(DPA),用该试剂处理的孢子的存活者对湿热敏感。tBHP加CTAB和TAML活化剂杀灭的孢子在有营养物质的情况下能够萌发,尽管比未处理的孢子慢,但比用十二胺处理的未处理孢子萌发得快。通过施加150和500兆帕的压力15分钟以及在高渗培养基中用溶菌酶处理,也能使被杀死的孢子萌发,但这些孢子在萌发后不久就会裂解。
tBHP加CTAB和TAML活化剂的组合在杀灭枯草芽孢杆菌孢子方面是有效的。孢子外壳是孢子对该试剂系统产生抗性的主要因素,该试剂系统不是通过DNA损伤或使孢子萌发所需的某些成分失活来杀灭孢子。相反,该试剂系统似乎是以某种方式通过损伤孢子的内膜来杀灭孢子。
这项工作表明,tBHP加CTAB和TAML活化剂是一种对芽孢杆菌属孢子有效且温和的去污剂。还获得了关于孢子对该试剂系统的抗性和被其杀灭的机制的证据。