Setlow B, Cowan A E, Setlow P
Department of Biochemistry, University of Connecticut Health Center, Farmington, CT 06032, USA.
J Appl Microbiol. 2003;95(3):637-48. doi: 10.1046/j.1365-2672.2003.02015.x.
To determine the properties of Bacillus subtilis spores germinated with the alkylamine dodecylamine, and the mechanism of dodecylamine-induced spore germination.
Spores of B. subtilis prepared in liquid medium were germinated efficiently by dodecylamine, while spores prepared on solid medium germinated more poorly with this agent. Dodecylamine germination of spores was accompanied by release of almost all spore dipicolinic acid (DPA), degradation of the spore's peptidoglycan cortex, release of the spore's pool of free adenine nucleotides and the killing of the spores. The dodecylamine-germinated spores did not initiate metabolism, did not degrade their pool of small, acid-soluble spore proteins efficiently and had a significantly lower level of core water than did spores germinated by nutrients. As measured by DPA release, dodecylamine readily induced germination of B. subtilis spores that: (a) were decoated, (b) lacked all the receptors for nutrient germinants, (c) lacked both the lytic enzymes either of which is essential for cortex degradation, or (d) had a cortex that could not be attacked by the spore's cortex-lytic enzymes. The DNA in dodecylamine-germinated wild-type spores was readily stained, while the DNA in dodecylamine-germinated spores of strains that were incapable of spore cortex degradation was not. These latter germinated spores also did not release their pool of free adenine nucleotides.
These results indicate that: (a) the spore preparation method is very important in determining the rate of spore germination with dodecylamine, (b) wild-type spores germinated by dodecylamine progress only part way through the germination process, (c) dodecylamine may trigger spore germination by a novel mechanism involving the activation of neither the spore's nutrient germinant receptors nor the cortex-lytic enzymes, and (d) dodecylamine may trigger spore germination by directly or indirectly activating release of DPA from the spore core, through the opening of channels for DPA in the spore's inner membrane.
These results provide new insight into the mechanism of spore germination with the cationic surfactant dodecylamine, and also into the mechanism of spore germination in general. New knowledge of mechanisms to stimulate spore germination may have applied utility, as germinated spores are much more sensitive to processing treatments than are dormant spores.
确定用烷基胺十二烷基胺萌发的枯草芽孢杆菌孢子的特性,以及十二烷基胺诱导孢子萌发的机制。
在液体培养基中制备的枯草芽孢杆菌孢子能被十二烷基胺高效萌发,而在固体培养基上制备的孢子用该试剂萌发效果较差。十二烷基胺诱导的孢子萌发伴随着几乎所有孢子吡啶二羧酸(DPA)的释放、孢子肽聚糖皮层的降解、孢子中游离腺嘌呤核苷酸池的释放以及孢子的死亡。十二烷基胺萌发的孢子不启动代谢,不能有效降解其小的、酸溶性孢子蛋白池,且其核心水含量显著低于营养物萌发的孢子。通过DPA释放测量发现,十二烷基胺能轻易诱导以下几种枯草芽孢杆菌孢子的萌发:(a)脱壳的;(b)缺乏所有营养萌发剂受体的;(c)缺乏对皮层降解至关重要的任何一种裂解酶的;或(d)具有不能被孢子皮层裂解酶攻击的皮层的。十二烷基胺萌发的野生型孢子中的DNA很容易被染色,而不能进行孢子皮层降解的菌株的十二烷基胺萌发孢子中的DNA则不能被染色。这些后一种萌发的孢子也不释放其游离腺嘌呤核苷酸池。
这些结果表明:(a)孢子制备方法在确定十二烷基胺诱导孢子萌发的速率方面非常重要;(b)十二烷基胺萌发的野生型孢子仅在萌发过程中进行到部分阶段;(c)十二烷基胺可能通过一种新机制触发孢子萌发,该机制既不涉及孢子营养萌发剂受体的激活,也不涉及皮层裂解酶的激活;(d)十二烷基胺可能通过直接或间接激活孢子核心中DPA的释放来触发孢子萌发,通过打开孢子内膜中DPA的通道。
这些结果为阳离子表面活性剂十二烷基胺诱导孢子萌发的机制以及一般孢子萌发的机制提供了新的见解。刺激孢子萌发机制的新知识可能具有实际应用价值,因为萌发的孢子比休眠孢子对加工处理更敏感。