Insights on the synthesis of iron-oxide nanoparticles and the detection of iron-reducing genes from soil microbes

Oluwafemi Bamidele Daramola , Reama Chinedu George , Nkem Torimiro , Afusat Ajoke Olajide
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Abstract

This study explores the potential of some soil bacteria in the synthesis of iron oxide nanoparticles (IONPs), highlighting their advantages in terms of iron uptake and tolerance capacity. Soil samples collected from a metal fabricating workshop were successively screened in nutrient broth containing 1% iron salts (Fe2O3, FeCl3, and FeSO4) following a standard microbiological sampling technique. The recovered bacterial isolates (persister cells) were identified using polymerase chain reaction (PCR) and 16S rRNA sequencing. Ten bacterial isolates identified as Sporosarcina luteola, Bacillus badius (2), Bacillus subtilis (2), Bacillus tropicus, Bacillus cereus, Klebsiella pneumoniae, Klebsiella quasipneumoniae and Klebsiella africana were recovered. The method reports that six of the bacterial isolates extracellularly synthesize IONPs and the result from the energy dispersion x-ray (EDX) spectral analysis indicated varying weight percentages of bio-reduced iron by Bacillus subtilis-A12 (48.59%), Klebsiella quasipneumoniae (39.99%), Bacillus subtilis-B1 (39.97%), Bacillus cereus (38.62%), Bacillus badius (33.79%) and Klebsiella africana (32.61%). The IONPs exhibited absorbance peaks in the range of 250–350 nm, with a mean area size estimated between 31–72 nm using ImageJ software. Additionally, the presence of iron reductase (fhu) and cysteine desulfurase (suf) genes were detected in the recovered Bacillus and Klebsiella species through PCR analysis. This study has provided valuable insights into the physiology and genomic functions essential for microbial synthesis of IONPs and their relevance to nano-bioremediation.

氧化铁纳米粒子的合成及土壤微生物铁还原基因检测的启示
本研究探讨了一些土壤细菌在合成氧化铁纳米粒子(IONPs)方面的潜力,突出了它们在铁吸收和耐受能力方面的优势。按照标准的微生物采样技术,在含有 1%铁盐(Fe2O3、FeCl3 和 FeSO4)的营养肉汤中对从金属加工车间采集的土壤样本进行了连续筛选。利用聚合酶链式反应(PCR)和 16S rRNA 测序对回收的细菌分离物(宿主细胞)进行鉴定。回收的 10 个细菌分离物被鉴定为 Sporosarcina luteola、Bacillus badius (2)、Bacillus subtilis (2)、Bacillus tropicus、Bacillus cereus、Klebsiella pneumoniae、Klebsiella quasipneumoniae 和 Klebsiella africana。能量色散 X 射线(EDX)光谱分析结果表明,枯草芽孢杆菌-A12(48.59%)、准肺炎克雷伯氏菌(39.99%)、枯草芽孢杆菌-B1(39.97%)、蜡样芽孢杆菌(38.62%)、坏死芽孢杆菌(33.79%)和非洲克雷伯氏菌(32.61%)。IONPs 在 250-350 纳米范围内显示出吸光度峰值,使用 ImageJ 软件估算的平均面积大小在 31-72 纳米之间。此外,通过聚合酶链式反应(PCR)分析,在回收的芽孢杆菌和克雷伯氏菌中检测到了铁还原酶(fhu)和半胱氨酸脱硫酶(suf)基因。这项研究为了解微生物合成 IONPs 所必需的生理学和基因组功能及其与纳米生物修复的相关性提供了宝贵的见解。
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