Mera M U, Beveridge T J
Department of Microbiology, College of Biological Science, University of Guelph, Ontario, Canada.
J Bacteriol. 1993 Apr;175(7):1936-45. doi: 10.1128/jb.175.7.1936-1945.1993.
To investigate the chemical mechanism of silicate binding to the surface of Bacillus subtilis, we chemically modified cell wall carboxylates to reverse their charge by the addition of an ethylenediamine ligand. For up to 9 weeks, mixtures of Si, Al-Fe-Si, and Al-Fe-Si plus toxic heavy metals were reacted with these cells for comparison with control cells and abiotic solutions. In general, more Si and less metal were bound to the chemically modified surfaces, thereby showing the importance of an electropositive charge in cell walls for fine-grain silicate mineral development. The predominant reaction for this development was the initial silicate-to-amine complexation in the peptidoglycan of ethylenediamine-modified and control cell walls, although metal ion bridging between electronegative sites and silicate had an additive effect. The binding of silicate to these bacterial surfaces can thus be described as outer sphere complex formation because it occurs through electrostatic interaction.
为了研究硅酸盐与枯草芽孢杆菌表面结合的化学机制,我们通过添加乙二胺配体对细胞壁羧酸盐进行化学修饰,以逆转其电荷。在长达9周的时间里,将硅、铝铁硅以及铝铁硅加有毒重金属的混合物与这些细胞反应,用于与对照细胞和非生物溶液进行比较。总体而言,更多的硅和更少的金属与化学修饰表面结合,从而表明细胞壁中的正电荷对细粒硅酸盐矿物形成的重要性。这种形成过程的主要反应是乙二胺修饰的和对照细胞壁的肽聚糖中最初的硅酸盐与胺的络合作用,尽管负电位点与硅酸盐之间的金属离子桥接具有累加效应。因此,硅酸盐与这些细菌表面的结合可以描述为外层球络合物的形成,因为它是通过静电相互作用发生的。