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1.
研究放电等离子体灭活大肠杆菌的效果。采用远程氧等离子体反应器,分别考察探究放电功率、处理时间、氧气流量、远程距离及有机污染物对灭菌效果的影响,并观察灭菌前后大肠杆菌的显微结构。结果表明在100W,60s,40cm3/min条件下,远程氧等离子体的杀菌效果值在距放电区0、20、40cm处分别为3.42、3.38和3.32。有机物浓度升高,灭菌效果急剧下降。结论为氧等离子体在距放电区040cm内均能有效灭活大肠杆菌,但有机污染物影响较大。氧等离子体场中高能粒子的刻蚀作用是导致细菌死亡的主要原因。  相似文献   
2.
高选择性基因工程菌E.coli SE5000生物富集水体中的镍离子   总被引:4,自引:0,他引:4  
利用基因工程菌E.coli SE5000对水体中的镍离子进行富集研究.菌体细胞对Ni^2 的富集速率很快,富集过程满足Langmuir等温线模型.经基因改造的基因工程菌不仅最大镍富集容量与原始宿主菌相比增加了4倍多,而且对pH值的变化呈现出更强的适应性.对离子强度及其它共存重金属离子的影响的实验结果表明:Na^ ,Ca^2 ,Cd^2 ,Pb^2 的影响较小,但Mg^2 ,Hg^2 ,Cr^3 和Cu^2 所引起的负面效应较大.金属螯合剂EDTA的存在对基因工程菌的富集行为影响很大.  相似文献   
3.
四环素对大肠杆菌抗生素抗性基因进化的影响   总被引:1,自引:0,他引:1  
为了解环境中低浓度抗生素对抗生素抗性发展的影响,以大肠杆菌(Escherichia coli,E.coli)为基础材料,通过亚抑菌浓度四环素处理,得到由敏感到抗性的菌株,研究了四环素对大肠杆菌产生抗生素抗性基因(antibiotic resistance genes,ARGs)的影响,采用同位素标记相对和绝对定量技术(isobaric tags for relative and absolute quantification,iTRAQ),分析四环素处理前后,大肠杆菌总蛋白差异表达情况.结果表明,大肠杆菌经1/2MIC浓度的四环素诱导,20 d后可由敏感转至耐药,表明环境中的低浓度四环素的刺激对大肠杆菌耐药性的形成影响较大.并且,检测到四环素抗性基因tetA、tetE和tetZ,β-内酰胺类抗性基因blaTEM和blaFOX,多重耐药性基因acrA、marA和marR.蛋白结果表明大肠杆菌在四环素胁迫下以特定的节能存活模式,通过诱导细胞防御和修复系统来应对环境压力,并表现出对离子传输的严格调节,来抵抗四环素毒性的影响.研究结果为进一步解析环境中抗生素胁迫的抗性机制提供了参考.  相似文献   
4.
载铜蒙脱石对大肠杆菌K88吸附性能的研究   总被引:1,自引:0,他引:1  
以蒙脱石(MMT)和硫酸铜为主要原料,制备了载铜蒙脱石(MMT-Cu),并对MMT-Cu吸附大肠杆菌K88的能力进行比较研究.结果表明:MMT和MMT-Cu对大肠杆菌K88均有较强的吸附作用,但载铜后蒙脱石吸附大肠杆菌的能力明显增强.细菌与吸附材料作用90min后可达到吸附平衡.介质pH值、离子强度和吸附温度对MMT和MMT-Cu吸附细菌的能力均有不同程度的影响.  相似文献   
5.
IntroductionIncreasing public interests have been concerned onsafety foods and the environmental aspects recently,especially on the so-called organic foods , which are madefromcrops grown with organic fertilizers or compost but notchemical fertilizers .Pu…  相似文献   
6.
载银活性碳纤维对大肠杆菌吸附作用的研究   总被引:10,自引:0,他引:10  
以大肠杆菌(Escherichiacoli)为对象,通过细菌吸附实验研究了载银活性碳纤维(ACF(Ag))对大肠杆菌的吸附特性.借助扫描电子显微镜(SEM)进行细菌分布形态的观察和细菌数量的计算.结果表明,大肠杆菌易分布于ACF(Ag)表面的沟槽处;ACF(Ag)吸附的细菌数量随银含量、比表面积的增加而增大.此外,细菌吸附量还与ACF(Ag)表面银颗粒的大小有关.对吸附细菌的动力学亦进行了研究.  相似文献   
7.
The aim of the research was to develop new products and processes from a manufacturing waste from an Italian metallurgic company. The company produced thin silver metallic films and the production scraps were silver flakes. The possibility to use the silver flakes in water disinfection processes was studied. The antimicrobial activity of the flakes was investigated in batch using Escherichia coli as Gram-negative microorganism model. The flakes did not show any antimicrobial activity, so they were activated with two different processes: thermal activation in reducing atmosphere and chemical activation, obtaining, respectively, reduced flakes (RF) and chemical flakes (CF). The flakes, activated with either treatment, showed antimicrobial activity against E. coli. The kill rate was dependent on the type of activated flakes. The chemical flakes were more efficient than reduced flakes. The kill rate determined for 1 g of CF, 1.0 ± 0.2 min−1, was greater than the kill rate determined for 1 g of RF, 0.069 ± 0.004 min−1. This was confirmed also by the minimum inhibitory concentration values. It was demonstrated that the antimicrobial capability was dependent on flakes amount and on the type of aqueous medium. Furthermore, the flakes maintained their properties also when used a second time. Finally, the antimicrobial activities of flakes were tested in an effluent of a wastewater treatment plant where a variety of heterotrophic bacteria were present.  相似文献   
8.
The ongoing development of microbial source tracking has made it possible to identify contamination sources with varying accuracy, depending on the method used. The purpose of this study was to test the efficiency of the antibiotic resistance analysis (ARA) method under low resistance by tracking the fecal sources at Turkey Creek, Oklahoma exhibiting this condition. The resistance patterns of 772 water-isolates, tested with nine antibiotics, were analyzed by discriminant analysis (DA) utilizing a five-source library containing 2250 isolates. The library passed various representativeness tests; however, two of the pulled-sample tests suggested insufficient sampling. The resubstitution test of the library individual sources showed significant isolate misclassification with an average rate of correct classification (ARCC) of 58%. These misclassifications were explained by low antibiotic resistance (Wilcoxon test P < 0.0001). Seasonal DA of stream E. coli isolates for the pooled sources human/livestock/deer indicated that in fall, the human source dominated (P < 0.0001) at a rate of 56%, and that human and livestock respective contributions in winter (35 and 39%), spring (43 and 40%), and summer (37 and 35%) were similar. Deer scored lower (17–28%) than human and livestock at every season. The DA was revised using results from a misclassification analysis to provide a perspective of the effect caused by low antibiotic resistance and a more realistic determination of the fecal source rates at Turkey Creek. The revision increased livestock rates by 13–14% (0.04 ≤ P ≤ 0.06), and decreased human and deer by 6–7%. Negative misclassification into livestock was significant (0.04 ≤ P ≤ 0.06). Low antibiotic resistance showed the greatest effect in this category.  相似文献   
9.
Fed-batch cultures of recombinantEscherichia coli strains were carried out for the production of poly(3-hydroxybutyric acid) (PHB) in a chemically defined medium. TheE. coli strains used were XL1-Blue, harboring pSYL105, a stable high-copy number plasmid containing theAlcaligenes eutrophus polyhydroxyalkanoate (PHA) genes, and XL1-Blue, harboring pSYL107, which is pSYL105 containing theE. coli ftsZ gene to suppress filamentation. With XL1-Blue(pSYL105) the final cell mass and PHB concentration obtained in 62 h were 102 and 22.5 g/L, respectively. Fed-batch culture of XL1-Blue(pSYL107) under identical conditions resulted in a final cell mass and PHB concentration of 127.5 and 48.2 g/L, respectively. The PHB contents obtained with XL1-Blue(pSYL105) and XL1-Blue(pSYL107) were 22.1 and 37.8%, respectively. Therefore, PHB was more efficiently produced in a defined medium by employing filamentation-suppressed recombinantE. coli.  相似文献   
10.
SOS/umu测试法被广泛应用于化合物和复杂混合物遗传毒性的评价,由于该技术所用菌种为致病菌且操作步骤繁琐等原因,制约了技术的推广应用。研究建立了基于重组大肠杆菌SOS效应的水质遗传毒性检测方法(专利号:ZL201110022476.1),应用该方法评价了某市4座污水厂出水的直接遗传毒性效应,同时以污水处理一厂为例考察了直接遗传毒性效应的季节变化规律以及不同的工艺对水中直接遗传毒性物质的去除情况。结果显示:各污水厂出水均表现出一定的直接遗传毒性,对应的4-NQO毒性当量浓度范围为0.018~0.514 mg·L-1;一年四季中夏季进出水直接遗传毒性效应最高,现有工艺中生化处理工艺段对直接遗传毒性去除效果最佳,去除率为33.33%。该方法操作便利、检测敏感性较高、操作危险性较低,可用于水中直接遗传毒性效应的测试。  相似文献   
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