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Mineralization by nanobacteria

机译:纳米菌的矿化

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Nanobacteria are the smallest cell-walled bacteria, only recently discovered in human and cow blood and in commercial cell culture serum. In this study, we identified with energy-dispersive x-ray microanalysis and chemical analysis that all growth phases of nanobacteria produce biogenic apatite on their cell envelope. Fourier transform IR spectroscopy revealed the mineral as carbonate apatite. Previous models for stone formation have lead to a hypothesis that an elevated pH due to urease and/or alkaline phosphatase activity are important lithogenic factors. Our results indicate that carbonate apatite can be formed without these factors at pH 7.4 at physiological phosphate and calcium concentrations. Due to their specific macromolecules, nanobacteria can produce apatite very efficiency in media mimicking tissue fluids and glomerular filtrate and rapidly mineralizing most of available calcium and phosphate. This can be also monitored by $+85$/Sr incorporation and provides a unique model for in vitro studies on calcification. Recently, bacteria have been implicated in the formation of carbonate (hydroxy)fluorapatite in marine sediments. Apatite grains are found so commonly in sedimentary rocks that apatite is omitted in naming the stone. To prove that apatite and other minerals are formed by bacteria would implicate that the bacteria could be observed and their actions followed in stones. We have started to approach this in two ways. Firstly, by the use of sensitive methods for detecting specific bacterial components, like antigens, muramic acid and nucleic acids, that allow for detecting the presence of bacteria and, secondly, by follow-up of volatile bacterial metabolites observed by continuous monitoring with ion mobility spectrometry, IMCELL, working like an artificial, educatable smelling nose. The latter method might allow for remote real time detection of bacterial metabolism, a signature of life, in rocks via fractures of drillholes with or without injected substrate solutions. Nanobacteria may provide a model for primordial life-forms, such as replicating clay crystallites in a sandstone, where minerals and metal atoms associated to membranes, may play catalytic and structural roles reducing the number of enzymes and structural proteins needed for life. Such simple metabolic pathways may support the 10,000-fold slower growth rate of nanobacteria, as compared to the usual bacteria. They may also explain the endurability of this life-form in extreme environmental conditions. Altogether such properties do suggest that nanobacteria may have evolved from environmental sources, such a shot springs, to take advantage of the steady-state calcium and phosphate supply of the mammalian blood. Based upon our findings of nanobacteria, a novel theory for the early development of life, based on apatite-mediated chemistry on membranes selecting itself for its own catalytical machinery, is presented.
机译:纳米杆菌是最小的细胞围绕细菌,最近在人和牛血液和商业细胞培养血清中发现。在这项研究中,我们用能量分散X射线微基分析和化学分析,即纳米菌的所有生长阶段都会在其细胞包膜上产生生物磷灰石。傅里叶变换IR光谱显示矿物磷酸盐磷灰石。以前的石材模型已经导致假设,即由于释放脲和/或碱性磷酸酶活性导致的pH升高是重要的型型型型岩性因子。我们的结果表明,在生理磷酸盐和钙浓度下,可以在pH7.4处没有这些因素形成碳酸盐磷灰石。由于它们的特异性大分子,纳米杆菌可以在模拟组织液和肾小球滤液中产生磷灰石非常效率,并且迅速矿化大多数可用钙和磷酸盐。这也可以通过$ + 85 $ / SR合并监控,并为钙化的体外研究提供独特的模型。最近,细菌涉及在海洋沉积物中形成碳酸盐(羟基)氟磷灰石。磷灰石谷物被发现如此通常在沉积岩石中,在铭记石头时省略了磷灰石。为了证明磷灰石和其他矿物质由细菌形成会暗示可以观察到细菌,并且它们的行为遵循石头。我们已经开始以两种方式接近这一点。首先,通过使用敏感方法来检测特异性细菌组分,如抗原,蛋白酸和核酸,其允许检测细菌的存在,其次通过通过连续监测离子迁移率观察到的挥发性细菌代谢物的随访光谱法,Imcell,像人工,教育的嗅觉一样工作。后一种方法可能允许远程实时检测细菌新陈代谢,植物签名,通过钻孔骨骼的骨折,具有或不注入底物溶液。纳米杆菌可以提供原始寿命的模型,例如复制砂岩中的粘土微晶,其中与膜相关的矿物质和金属原子,可能发挥催化和结构作用,从而减少寿命所需的酶数和结构蛋白。与通常的细菌相比,这种简单的代谢途径可以支持纳米菌的10,000倍的生长速率。他们还可以在极端环境条件下解释这种生命形式的耐用性。此类特性确实表明纳米杆菌可能已经从环境源,这种射击弹簧中发展,以利用哺乳动物血液的稳态钙和磷酸盐供应。基于我们的纳米菌的发现,提出了一种基于磷灰石介导的生命的早期发展的新理论,基于磷灰石介导的化学在膜上选择自身的催化机械。

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