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芽孢杆菌属JH7中胞外多糖对碳酸钙沉淀的调控作用

Modulation of calcium carbonate precipitation by exopolysaccharide in Bacillus sp. JH7.

作者信息

Kim Hyun Jung, Shin Bora, Lee Yun Suk, Park Woojun

机构信息

Laboratory of Molecular Environmental Microbiology, Department of Environmental Science and Ecological Engineering, Korea University, Seoul, 02841, Republic of Korea.

出版信息

Appl Microbiol Biotechnol. 2017 Aug;101(16):6551-6561. doi: 10.1007/s00253-017-8372-8. Epub 2017 Jun 22.

Abstract

Extracellular polymeric substance (EPS) is proposed to facilitate calcium ion supersaturation through its nucleation effect during the microbially induced calcium carbonate precipitation (MICP) process. However, the supersaturation effect of Ca via EPS in MICP has not been clearly demonstrated. Enhanced exopolysaccharide production of the alkali- and halotolerant MICP-capable bacteria, Bacillus sp. JH7, was achieved through glycerol addition. This was demonstrated by measuring cellular precipitation and Congo red binding. Interestingly, field emission scanning electron microscopy and energy-dispersive X-ray spectrometry analysis demonstrated that there was no MICP under glycerol-amended conditions. Although glycerol promoted exopolysaccharide capture of Ca ions, Ca embedded onto EPS did not participate in MICP formation. The pH was reduced in glycerol-added media, which led us to analyze high acetate production under our test conditions. Purified glycerol-induced exopolysaccharide showed a higher capacity of Ca capture than the control. Quantitative RT-PCR analysis showed that three genes involved in exopolysaccharide production were highly upregulated by glycerol. The amounts of three detected monosaccharides (arabinose, glucose, and mannose) were altered by glycerol. Cell hydrophobicity measurements indicated that glycerol could confer more hydrophilic characteristics to cells, which might enhance Ca binding onto EPS. Unexpectedly, our data demonstrated, for the first time, that glycerol could promote exopolysaccharide and acetate production under our test condition, which could inhibit MICP by reducing the availability of free Ca.

摘要

胞外聚合物(EPS)被认为在微生物诱导碳酸钙沉淀(MICP)过程中通过其成核作用促进钙离子过饱和。然而,在MICP过程中EPS对钙离子的过饱和效应尚未得到明确证实。通过添加甘油提高了具有耐碱和耐盐特性的能进行MICP的芽孢杆菌属JH7菌株的胞外多糖产量。这通过测量细胞沉淀和刚果红结合得以证明。有趣的是,场发射扫描电子显微镜和能量色散X射线光谱分析表明,在添加甘油的条件下没有发生MICP。尽管甘油促进了EPS对钙离子的捕获,但嵌入EPS的钙离子并未参与MICP的形成。添加甘油的培养基中pH值降低,这使我们分析了在我们的测试条件下高乙酸盐的产生情况。纯化的甘油诱导的胞外多糖显示出比对照更高的钙离子捕获能力。定量逆转录聚合酶链反应分析表明,参与胞外多糖产生的三个基因被甘油高度上调。检测到的三种单糖(阿拉伯糖、葡萄糖和甘露糖)的含量因甘油而改变。细胞疏水性测量表明,甘油可以赋予细胞更多的亲水性特征,这可能增强钙离子与EPS的结合。出乎意料的是,我们的数据首次表明,在我们的测试条件下甘油可以促进胞外多糖和乙酸盐的产生,这可能通过降低游离钙离子的可用性来抑制MICP。

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