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巴氏芽孢八叠球菌是迄今为止所知的利用尿素降解进行生物矿化的最为高效的微生物系统之一,基于其碳酸钙生物矿化形成的"超强能力",巴氏芽孢八叠球菌已经被成功地应用于沙石、土壤等生物固化中,成为一种全新的、具有极大潜力的生物建筑辅助技术,被称为"生物水泥"。由于巴氏芽孢八叠球菌分离自土壤,没有病原性并具有极好的环境友好性。近年来,其应用领域被拓展到环境治理乃至健康医疗领域,成为全新的研究热点。然而,与应用研究相比,人们对巴氏芽孢八叠球菌生物矿化背后的分子机理还知之甚少。因此,这里针对迄今为止国内外对于巴氏芽孢八叠球菌生物矿化相关的分子机理的研究进行分析介绍,在此基础上综述了包括建工、环境、及医疗健康领域在内的巴氏芽孢八叠球菌的应用,希望能够促进对于该球菌矿化的研究。  相似文献   
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Heavy metals (HMs) pollution is a serious problem, worldwide. The present study focuses on HMs removal (HMs mobility restricted within soil) by microbial induced mineral precipitation (MIMP) using indigenous isolates. Indigenous isolates were identified as Bacillus subtilis C(225)(MK334652), Oceanobacillus indicireducens 5(225)(MK334653), and Bacillus pumilus 7(225)(MK334654) by 16S-rRNA from HMs polluted industrial-soil (soil-225) that is used for bioremediation. The studied soil contained high level (mg/kg) of Cr(307.41?±?1.02), Cu(576.35?±?1.02), and Zn(708.81?±?1.50) as per Taiwan permissible limit (TPL) and/or Canadian Soil Quality Guidelines (CSQG). Minimum inhibitory concentration (MIC) of Bacillus species were higher compare to Oceanobacillus. Bioavailable-fraction (F1) of HMs (Cr/Cu/Zn) in untreated 225-soil was noticed to be higher compared to F2–F5 fraction. Bacillus subtilis C(225) are more efficient for HMs-mineralization, compared to other isolates where Cr/Cu/Zn immobilized within soil, transforming from bioavailable-fraction (F1) (high-mobility) (60–90% reduction) to residual-fraction F5 (low-mobility) (50–80% increment). Organic-bound-fraction (F4) (medium-mobility) of Cr increased (42.66?±?2.1%), compared to Cu/Zn, by Bacillus subtilis C(225). Urease (40.8%) and dehydrogenase (8.3%) activity increased in bio-remediated soil, compared to control. MIMP of HMs by ingenious bacteria reflects the transformation-pathway from F1 to F5 of HMs to fix strongly within soils with inadequate mobility. Thus, MIMP by indigenous microbe can be applicable for HMs stabilization/removal in contaminated soil for ecofriendly environmental cleanup.  相似文献   
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目的:为了研究碳酸酐酶1(carbonic anhydrase I,CA1)在生物矿化和骨形成过程中的作用。方法:选择HeLa细胞为研究对象,用地塞米松(dexamethasone,DEX)、β-磷酸甘油(β-glycerophosphate,β-GP)和维他命C(ascorbic acid,AA)诱导其钙化,茜素红染色法观察矿化结节的形成,荧光定量PCR检测细胞骨化标志蛋白Runx2/cbfa1的表达。CA1表达水平的变化采用Western blot和荧光定量PCR的方法检测。同时用碳酸酐酶抑制剂乙酰唑胺处理HeLa细胞,观察CA1表达被抑制后对HeLa细胞钙化的影响。结果:HeLa细胞在诱导后形成大量矿化结节,Runx2/cbfa1转录水平明显升高,显示DEX、β-GP和AA可诱导HeLa细胞钙化和骨化,HeLa细胞钙化后CA1表达明显增高。HeLa细胞经乙酰唑胺处理后,CA1的表达量减少,矿化结节形成明显减少,说明抑制CA1表达可以抑制HeLa细胞矿化和骨化过程。结论:CA1在生物矿化和新骨形成过程中起着重要作用。  相似文献   
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