共查询到17条相似文献,搜索用时 62 毫秒
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【背景】金纳米颗粒(AuNPs)凭借其稳定性、抗氧化性能和生物相容性在许多领域有广泛应用。目前关于微生物合成金纳米颗粒的研究较少。【目的】对微生物合成金纳米颗粒的可能性以及影响因素进行探究,有利于揭示具体的合成机制,发现AuNPs的特性以及合成位置与菌丝和影响因素的关系。【方法】以绿色木霉菌(Trichoderma viride)菌株(GIM3.141)为菌种资源,通过目视检测法、紫外可见分光光度计、X射线衍射和透射电镜等手段分析合成AuNPs的特征。探讨细胞内生物合成金纳米颗粒(AuNPs)的可能性,研究生物量、初始金离子浓度、溶液pH等因素对细胞内合成AuNPs的影响。【结果】X射线衍射分析表明AuNPs以金纳米晶体形态存在。透射电镜分析表明AuNPs主要位于细胞壁膜间隙,一小部分附着在细胞壁上。紫外可见分光光度计分析表明,金纳米颗粒粒径随着生物量添加量和溶液pH的升高而变小,随着初始金离子浓度的升高而变大。【结论】非致病性真菌绿色木霉菌可以在细胞内合成AuNPs,其中包括伪球形、三角形、四边形和六边形等多种形状,粒径范围从几纳米到三百纳米,为大规模、低成本、无污染地生物合成纳米颗粒工艺提供了菌种资源。 相似文献
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【目的】考察菌株Trichosporon montevideense WIN合成纳米金的催化特性及应用。【方法】利用活性WIN菌作用不同浓度HAu Cl_4(1、2和4 mmol/L)合成纳米金的特性,分别利用活性WIN菌和灭活WIN菌合成纳米金,分析合成纳米金的形貌、粒径及其催化特性。【结果】HAu Cl_4浓度为1 mmol/L时,菌株WIN合成了纳米金,HAu Cl_4浓度为2 mmol/L和4 mmol/L时,菌株WIN合成了纳米金及较大尺寸的金颗粒。通过紫外-可见光谱扫描、透射电子显微镜分析,发现活性和灭活WIN菌均能还原Au~(3+)合成纳米金,合成的纳米金均以球形为主,还有少量三角形、四边形及六边形。活性WIN菌合成的纳米金粒径范围为3 nm-252 nm,平均粒径为45.2 nm,而灭活WIN菌合成的纳米金为1 nm-271 nm,平均粒径为38.3 nm。活性和灭活WIN菌合成的纳米金对还原4-硝基苯酚的催化速率分别为2.76×10~(-3)s~(-1)和4.84×10~(-3)s~(-1)。【结论】菌株Trichosporon montevideense WIN的活性及灭活细胞均可以合成纳米金,且合成的纳米金具有良好的催化特性,在催化去除环境中难降解污染物中具有一定的应用前景。 相似文献
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基于发展纳米材料"绿色合成技术"重要性,生物合成纳米材料已成为纳米合成技术研究热点。微生物具有廉价、易培养、繁殖快等优点被应用于多种纳米材料的生物合成研究,成为生物合成纳米材料的重要生物类群。本文综述了细菌、放线菌、酵母菌以及真菌等微生物应用于纳米生物合成技术的发展;着重评述了纳米材料微生物合成生物方法、纳米材料微生物合成相关机制、纳米材料形貌和尺寸微生物调控合成方法以及应用研究进展;并对纳米材料微生物合成技术未来发展趋势进行了展望。 相似文献
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利用晶种生长法制备金纳米棒,在其表面依次用聚丙烯酸(PAA)和聚乙烯亚胺(PEI)修饰,降低了CTAB的细胞毒性,同时也增强了金纳米棒在盐和细胞培养液中的稳定性。又利用静电吸附作用,成功的将DNA连接到了金纳米棒的表面,制备了DNA传感器,可用于生物研究。 相似文献
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纳米金新型基因芯片检测系统的研制及其在临床病原微生物快速检测中的应用 总被引:2,自引:0,他引:2
本研究在纳米放大基因芯片检测专利技术的基础上 ,研制纳米金新型基因芯片检测系统 ,从而充分利用纳米金与银反应可将信号放大 10 6倍的优势以取代目前通用的荧光、同位素、酶标等信号报告材料 ,实现芯片技术与纳米技术的有机结合 ,使之具有设备简单 ,技术稳定易于掌握 ,灵敏度高 ,应用范围广等特点。并在此基础上构建针对临床常见致病菌的实用型纳米金基因芯片 ,从而为临床致病性病原微生物的快速、简便、准确诊断探索一条新的途径。试验的主要方法及结果如下 :(1)扩增实验表明 :引物巯基修饰后必须经过TCEP预还原处理 ,才能获得较好的P… 相似文献
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金的微生物浸出和回收 总被引:1,自引:1,他引:1
金是最稳定的元素之一。它常和银,铜以及其他微量元素结合。在化合物中,常见一价和三价金。金的三价化合物较稳定。在碱性条件下,一价金离子可与含有氧和硫的配位基形成可溶于水的复合物,该复合物在岩石圈的表面层易流动。在一定的条件下,金的溶解、迁移和沉淀是由微生物的作用产生的。金在自然界的复杂循环过程中,微生物起着重要的作用。由于微生物和金有密切的关系,在黄金工业中,人们有可能多方面的利用微生物。例如:加拿大温哥华基因探针有限公司研制了探测金矿的微生物探测器[1];加拿大、南非和美国巳用微生物预处理难浸含砷命矿,提高了金的浸出率[2]。本文仅就国外用微生物从矿石中直接浸出和从溶液中回收金的研究现状作一简要介绍。 相似文献
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In this study, the rapid biosynthesis of gold nanoparticles (AuNPs) by Aspergillus flavus culture supernatant was achieved by reducing 1 mM of chloroauric acid (HAuCl4) within 2 min at pH 7 and 30 °C. The biosynthesized nanoparticles exhibited maximum absorbance at 545 nm in UVvis spectroscopy. Transmission electron microscopy exhibited that AuNPs tend to take nearly spherical shapes with an average size of 12 nm. Fourier transform infrared analysis indicated that carboxyl, amine, and hydroxyl groups may participate in the biosynthesis and stabilization of AuNPs. Its zeta potential was found to be -33.01 mV. Energy dispersive X-rays showed a strong and typical beak of gold nanocrystallites with 80.84 % of analyzed sample. X-Ray diffraction spectrum displayed Bragg reflections identical to the gold nanocrystals. The results confirmed that biosynthesized AuNPs are a potent anticancer agent against A549, HepG2 and MCF7 cell lines with IC50 value 53.5, 60.7 and 100 μg/mL, respectively. Crystal violet assay confirmed the cytopathic effects of AuNPs on HepG2 and A549 cell lines. Annexin-V FITC assay and cell cycle confirmed the apoptotic effect and cell cycle arrest in G2/M phase, respectively for A549 cell line. Moreover, the results showed a degradation efficiency of AuNPs to 4-nitrophenol within 16 min. 相似文献
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Gold nanoparticles (Au-NPs) have been widely used in biomedical fields such as imaging, diagnosis, and treatment because of their special characteristics. Au-NPs can be synthesized using several methods, including the biological method, also called green or eco-friendly synthesis. Recent studies have reported the anticancer activity of biosynthesized Au-NPs, especially in lung cancer. This review focused on the advances in the antilung cancer activity of biosynthesized Au-NPs and its potential mechanisms. 相似文献
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放线菌中铁载体生物合成机制研究进展 总被引:2,自引:1,他引:2
铁载体是由微生物产生,对铁元素具有高亲和性的小分子化合物。这类天然产物所展现的结构多样性引起人们对其生物合成机制的极大兴趣。目前已有研究报道的铁载体生物合成途径主要有2种,一是直接由非核糖体肽合成酶(Nonribosomal peptide synthetases,NRPSs)家族的多酶复合体负责合成,另一种是以不依赖于NRPS(NRPS-independent,NIS)的方式,由一类特殊合成酶家族参与合成。在过去的十多年中,铁载体生物合成成为天然产物生物合成研究领域的热点之一,其中几种依赖于NRPS途径合成的铁载体生物合成机制已得到充分阐明,而对NIS方式合成的铁载体研究也获得了诸多进展。作为放线菌的一类重要次级代谢产物,通过遗传学、化学等手段对放线菌所产生铁载体生物合成途径的遗传学和生物化学研究,能够为发展新的抗菌药物提供契机,同时也能加深我们对这一类生物活性物质形成机制的认识。综述近期该研究方向的进展。 相似文献
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Min Lin Ying Zhao ShuQi Wang Ming Liu ZhenFeng Duan YongMei Chen Fei Li Feng Xu TianJian Lu 《Biotechnology advances》2012
Lanthanide (Ln)-doped upconversion nanoparticles (UCNPs) with appropriate surface modification can be used for a wide range of biomedical applications such as bio-detection, cancer therapy, bio-labeling, fluorescence imaging, magnetic resonance imaging and drug delivery. The upconversion phenomenon exhibited by Ln-doped UCNPs renders them tremendous advantages in biological applications over other types of fluorescent materials (e.g., organic dyes, fluorescent proteins, gold nanoparticles, quantum dots, and luminescent transition metal complexes) for: (i) enhanced tissue penetration depths achieved by near-infrared (NIR) excitation; (ii) improved stability against photobleaching, photoblinking and photochemical degradation; (iii) non-photodamaging to DNA/RNA due to lower excitation light energy; (iv) lower cytotoxicity; and (v) higher detection sensitivity. Ln-doped UCNPs are therefore attracting increasing attentions in recent years. In this review, we present recent advances in the synthesis of Ln-doped UCNPs and their surface modification, as well as their emerging applications in biomedicine. The future prospects of Ln-doped UCNPs for biomedical applications are also discussed. 相似文献
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Robert Granet René Faure Gautier Mark-Arthur Ndong Ntoutoume Jean Pierre Mbakidi David Yann Leger Bertrand Liagre Vincent Sol 《Bioorganic & medicinal chemistry letters》2019,29(9):1065-1068
A new gold nanoparticle-based construct has been designed to hydrophobic drugs delivery into cancer cells. Cyclodextrin scaffolds adsorbed on polyethyleneimine-coated gold nanoparticles (AuNP@PEI@CD) have been used to encapsulate hydrophobic tetrapyrrolic compounds consisting of gold complexes of 5,10,15,20-tetraphenyl porphyrin (AuTPPCl) and 5-(4-acetoxyphenyl)-10,15,20-triphenyl porphyrin (AuTPPOAcCl). These two nanoparticles have been tested for their cytotoxic activities against the two colorectal cancer cell lines HT-29 and HCT-116 and have shown significant increases in toxicity when compared to the corresponding non-vectorized tetrapyrrolic macrocycles. 相似文献
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The goal of this work was to synthesize gold nanoparticles (AuNPs) using electrode-respiring Geobacter sulfurreducens biofilms. We found that AuNPs are generated in the extracellular matrix of Geobacter biofilms and have an average particle size of 20 nm. The formation of AuNPs was verified using TEM, FTIR and EDX. We also found that the extracellular substances extracted from electrode-respiring G. sulfurreducens biofilms reduce Au3+ to AuNPs. From FTIR spectra, it appears that reduced sugars were involved in the bioreduction and synthesis of AuNPs and that amine groups acted as the major biomolecules involved in binding. 相似文献
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The nonlinear optical properties of protein-modified gold nanoparticles has been studied by the hyper-Rayleigh scattering (HRS) technique. HRS signals from the nanoparticles coated with goat-anti-human IgG have been obtained when pumped with a laser pulse with a wavelength of 1064 nm. The HRS signals of gold nanoparticles with IgG were larger than those of bare gold nanoparticles. This can be explained by a noncentrosymmetric effect. It was also found that the HRS signals from the IgG-coated gold nanoparticles could be greatly increased when the antigen was added due to gold nanoparticle aggregation. Our experiment found that the HRS method could produce a measurable signal with 10 microg/ml antigen added, while the colorimetric method using UV spectrum detection required 100 microg/ml of added antigen. The results show that the HRS measurement of immunogold nanoparticles could become a potential immunoassay in determining small levels of antigen in aqueous samples. 相似文献