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Resistance and mechanism of Acinetobacter baumannii to carbapenem antibiotics(such as meropenem and imipenem)
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作者 Huo Lirui 《Science International Innovative Medicine》 2025年第1期86-92,共7页
The mortality rate ofAcinetobacter baumannii is as high as 47%,This is inseparable From its strong resistance to carbapenems,polymyxins,aminoglycosides,quinolone antibiotics.This article will analyze the resistance of... The mortality rate ofAcinetobacter baumannii is as high as 47%,This is inseparable From its strong resistance to carbapenems,polymyxins,aminoglycosides,quinolone antibiotics.This article will analyze the resistance of Acinetobacter baumannii to carbapenem antibiotics(meropenem and imipenem)and explore why Acinetobacter baumannii is so resistant.The data I used comes from the NCBI database,which includes six resistant groups(R)to meropenem and imipenem,and five sensitive groups(S).The level of the resistant group is complete genome,three sensitive groups are contig,and two are complete genome.Subsequently,I used Prokka in Galaxy to convert the Fasta.file into various forms such as Faa,gbk,ffn.After performing Fisher's test on all GFF files,I obtained the result chart,which includes the search for relevant domains and protein descriptions on Interpro using the chart.ProteinPlus also performed drug pocket prediction and constructed protein models using Swissmodel,as well as different multi sequence comparisons.Finally,I analyzed the functions of the proteins corresponding to the genes specific to the resistance group and the reasons for the development of drug resistance,making future research on the drug resistance of Acinetobacter baumannii easier.And further research can be conducted on the drug pocket in the protein ofAcinetobacter baumannii that has developed resistance,and drugs can be administered. 展开更多
关键词 acinetobacter baumannii A.baumanii baumanii CARBAPENEMS carbapenem carbopenems GENOME protein model
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Genetic variabilities of Acinetobacter baumannii in a hospital setting using ISSR markers
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作者 Poonamrani Mishra Mahesh Chandra Sahu Debasish Sahoo 《Asian Pacific Journal of Tropical Medicine》 2025年第7期334-336,I0001,共4页
Acinetobacter(A.)baumannii is a Gram-negative,non-fermenting opportunistic pathogen increasingly implicated in nosocomial infections,particularly in intensive care units(ICUs).Its ability to acquire multidrug resistan... Acinetobacter(A.)baumannii is a Gram-negative,non-fermenting opportunistic pathogen increasingly implicated in nosocomial infections,particularly in intensive care units(ICUs).Its ability to acquire multidrug resistance(MDR),including to carbapenems,poses a major public health threat.Infections caused by A.baumannii-ranging from pneumonia to bloodstream and wound infections-are difficult to treat and associated with high mortality,especially in critically ill patients[1]. 展开更多
关键词 nosocomial infections genetic variabilities nosocomial infectionsparticularly acinetobacter baumannii opportunistic pathogen multidrug resistance mdr including ISSR markers intensive care units
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Antibiotic resistance pattern and biofilm formation among clinical Acinetobacter baumannii isolates:A cross-sectional study
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作者 Vahab Hassan Kaviar Zahra Farshadzadeh +8 位作者 Azar Dokht Khosravi Mohammad Hossein Haddadi Somayeh Karamolahi Marzieh Hashemian Nazanin Omidi Moloudsadat Motahar Nourkhoda Sadeghifard Saeed Khoshnood Fatemeh Shahi 《Journal of Acute Disease》 2025年第3期1-12,共12页
Objective:To investigate the pattern of antibiotic resistance and biofilm production capabilities of clinical Acinetobacter baumannii(A.baumannii)isolates in this study.Methods:A.baumannii isolates were collected from... Objective:To investigate the pattern of antibiotic resistance and biofilm production capabilities of clinical Acinetobacter baumannii(A.baumannii)isolates in this study.Methods:A.baumannii isolates were collected from Tehran Imam Khomeini Hospital in this cross-sectional study,and the minimum inhibitory concentrations for 16 antibiotics were determined using Vitek2®systems.All isolates were analyzed for biofilm production,then presence of biofilm-associated genes,and class Ⅰ and Ⅱ integron genes.Results:60 non-replicate A.baumannii isolates were included in this study.The resistance rates reached 100%for aztreonam,cefepime,ceftazidime,ciprofloxacin,piperacillin-tazobactam,piperacillin,ticarcillin,and trimethoprim-sulfamethoxazole.A.baumannii isolates were most sensitive to colistin and rifampicin being the most effective treatments.Multi-drug resistant and extensively drug-resistant isolates accounted for 83.3%and 16.7%,respectively.Of the isolates,91.6%formed biofilms,categorized as 10%strong,31.6%moderate,and 50%weak.No correlation was found between antibiotic resistance and biofilm formation.The genes csuE,abaI,and ompA were prevalent,but their distribution was similar across biofilm categories.A relationship between Int1 and biofilm production was noted.Conclusions:The high rates of antibiotic resistance and biofilm formation,alongside the presence of integrons including class Ⅰ and Ⅱ,underscore the necessity for ongoing monitoring of A.baumannii.Notably,classⅠintegron presence was significantly linked to biofilm formation.Further research is needed to explore the connection between antibiotic resistance and biofilm production in A.baumannii. 展开更多
关键词 acinetobacter baumannii Antibiotic resistance BIOFILM Biofilm-associated genes INTEGRON
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The Acinetobacter baumannii group:a systemic review 被引量:7
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作者 Hua-zhong Zhang Jin-song Zhang Li Qiao 《World Journal of Emergency Medicine》 CAS 2013年第3期169-174,共6页
BACKGROUND:The Acinetobacter baumannii group,including Acinetobacter baumannii,Acinetobacter genomospecies 3 and 13 TU,is phenotypically indistinguishable and uniformly identified as Acinetobacter baumannii by laborat... BACKGROUND:The Acinetobacter baumannii group,including Acinetobacter baumannii,Acinetobacter genomospecies 3 and 13 TU,is phenotypically indistinguishable and uniformly identified as Acinetobacter baumannii by laboratories of clinical microbiology.This review aimed to demonstrate the differences among them.METHODS:Literatures associated with the Acinetobacter baumannii group were identified and selected from PubMed databases and relevant journals.RESULTS:Acinetobacter genospecies 3 and 13 TU possess a certain proportion in clinical isolates.There were considerable differences in epidemiologic features,clinical manifestations,antimicrobial resistances and therapeutic options among the Acinetobacter baumannii group.Compared with Acinetobacter genomospecies 3 and 13 TU,Acinetobacter baumannii with a higher resistance to antimicrobial agents are easier to be treated inappropriately,and present a worse outcome in patients.CONCLUSION:The Acinetobacter baumannii group comprises three distinct clinical entities,and their clinical value are not equal. 展开更多
关键词 acinetobacter baumannii acinetobacter genomospecies 3 acinetobacter genomospecies 13TU DIFFERENCE
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好氧异养硝化菌Acinetobacter sp. YY-5的分离鉴定及脱氮机理 被引量:30
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作者 金敏 王景峰 +6 位作者 孔庆鑫 赵祖国 王新为 谌志强 陈照立 邱志刚 李君文 《应用与环境生物学报》 CAS CSCD 北大核心 2009年第5期692-697,共6页
通过异养硝化培养基获得一株高效脱氮细菌,并通过形态学特征、生理生化反应及16S rDNA同源性比较对筛得菌株进行了鉴定;分别以NO3--N和NO2--N为唯一氮源,通过对脱氮过程中各种含氮代谢物的定量及对脱氮相关基因氨单加氧酶基因(amoA)、... 通过异养硝化培养基获得一株高效脱氮细菌,并通过形态学特征、生理生化反应及16S rDNA同源性比较对筛得菌株进行了鉴定;分别以NO3--N和NO2--N为唯一氮源,通过对脱氮过程中各种含氮代谢物的定量及对脱氮相关基因氨单加氧酶基因(amoA)、羟胺氧化酶基因(hao)、周质硝酸盐还原酶亚基基因(napA)的扩增及测序比较,对该菌株的生理途径及脱氮机理进行了研究.结果表明,高效脱氮细菌YY-5不能发生好氧反硝化,但能在3d内将氨氮由95.23mg/L降解至1.29mg/L,降解率达到98.6%,同时未发现亚硝酸盐氮、硝酸盐氮积累;对该菌主要代谢气体产物进行检测,发现CO2和N2明显增多,无N2O生成;经鉴定,初步判定该菌为不动杆菌属,命名为Acinetobacter sp. YY-5;从该菌基因组中均能扩增出amoA、hao、napA等基因,其中napA与hao基因与已报道的napA与hao基因进行Blast比较,发现具有较大差别. 展开更多
关键词 好氧异养硝化菌 acinetobacter sp. YY-5 机理 脱氮
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一株高效烷烃降解菌Acinetobacter sp. LAM1007的分离鉴定及降解特性 被引量:10
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作者 朱杰 阮志勇 +5 位作者 董卫卫 郭翔 孔德龙 张琪 赵述淼 张伟 《微生物学通报》 CAS CSCD 北大核心 2017年第7期1535-1546,共12页
【目的】挖掘高效烷烃降解菌,为后续石油烃污染修复工程提供优良菌种资源。【方法】以正十六烷为唯一碳源,将大庆石油污染土样中分离筛选到的高效烷烃降解菌经形态观察、生理生化试验、细胞化学组分及16SrRNA基因序列分析等方法进行初... 【目的】挖掘高效烷烃降解菌,为后续石油烃污染修复工程提供优良菌种资源。【方法】以正十六烷为唯一碳源,将大庆石油污染土样中分离筛选到的高效烷烃降解菌经形态观察、生理生化试验、细胞化学组分及16SrRNA基因序列分析等方法进行初步鉴定与系统分类;同时通过单因素试验研究环境因素(温度、pH、接种量和转速)以及不同初始浓度的正十六烷(0.1%、0.3%、0.5%、1.0%、1.5%、2.0%,体积比)对菌株降解效率的影响。【结果】筛选到一株高效烷烃降解菌LAM1007,经初步鉴定该菌株为不动杆菌属(Acinetobacter)。该菌株在添加正十六烷的无机盐培养基中的最适降解条件为:30°C,pH 7.0,接种量1%(体积比),转速180 r/min,在该条件下浓度为0.3%(体积比)的正十六烷60 h内降解率高达90%。【结论】菌株LAM1007是一株在石油烃污染修复方面极具应用潜力的高效烷烃降解菌。 展开更多
关键词 正十六烷 acinetobacter sp. 柴油 液体石蜡
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阿特拉津降解菌Acinetobacter sp.DNS32对无机氮源的响应 被引量:7
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作者 王志刚 张颖 +1 位作者 郭火生 伊欢 《微生物学通报》 CAS CSCD 北大核心 2014年第8期1541-1546,共6页
【目的】研究Acinetobacter sp.DNS32的生长、阿特拉津降解能力和降解基因转录水平的表达对无机氮素的响应关系,为菌株的工程应用提供指导与理论基础。【方法】以Acinetobactersp.DNS32为对象,采用摇瓶法研究菌株在阿特拉津培养基中菌... 【目的】研究Acinetobacter sp.DNS32的生长、阿特拉津降解能力和降解基因转录水平的表达对无机氮素的响应关系,为菌株的工程应用提供指导与理论基础。【方法】以Acinetobactersp.DNS32为对象,采用摇瓶法研究菌株在阿特拉津培养基中菌株生长情况及降解能力对外加硝态氮与铵态氮的响应关系,利用荧光定量PCR技术检测DNS32降解基因表达量对外加无机氮源的响应关系。【结果】外加无机氮源可以促进DNS32菌株的生长,提高阿特拉津降解能力,无机氮源对DNS32菌株的trzN、atzB和atzC 3种降解基因表达均有促进作用,加入无机氮源的试验处理中DNS32菌株trzN基因的表达量最高可达对照的11.252±2.408倍,推断DNS32菌株的这3种降解基因所编码的酶是稳定表达的组成酶。【结论】DNS32降解阿特拉津不受"氮饥饿"诱导机制调控,且无机氮源的存在对菌株的生长与降解有促进作用,因此菌株在土壤修复实践中具有广阔的应用前景。 展开更多
关键词 阿特拉津 acinetobacter SP DNS32 无机氮源 降解能力 基因表达
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Acinetobacter sp. XA05和Sphingomonas sp. FG03苯酚生物降解特性研究 被引量:3
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作者 刘永军 刘金光 +1 位作者 李华 王晓昌 《西安建筑科技大学学报(自然科学版)》 CSCD 北大核心 2010年第3期420-426,共7页
从活性污泥和苯酚污染的土壤中分离出来两个菌株,分别编号为XA05和FG03.通过16S rRNA基因序列分析表明,XA05属于Acinetobacter sp.,而FG03属于Sphingomonas sp..将XA05和FG03在以不同浓度的苯酚作为唯一碳源的基础培养液中培养,结果显示... 从活性污泥和苯酚污染的土壤中分离出来两个菌株,分别编号为XA05和FG03.通过16S rRNA基因序列分析表明,XA05属于Acinetobacter sp.,而FG03属于Sphingomonas sp..将XA05和FG03在以不同浓度的苯酚作为唯一碳源的基础培养液中培养,结果显示,在初始苯酚浓度分别为800 mg/L和1000 mg/L时,作用45 h和60 h后,XA05和FG03对苯酚的去除率分别是99.5%、78.3%和97.6%、68.1%.两个菌株按1:1的体积比混合后,当苯酚的初始浓度分别为800 mg/L和1000 mg/L时,作用35 h和60 h后,苯酚去除率分别为99.8%,97.2%.XA05和FG03的苯酚降解动力学研究表明,在Haldane’s模型中,XA05和FG03都有较高的KS和KSI值. 展开更多
关键词 苯酚 acinetobacter sp. XA05 SPHINGOMONAS sp. FG03 生物降解 动力学
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固定化Acinetobacter sp. XA05和Sphingomonas sp. FG03降解苯酚 被引量:3
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作者 李华 刘永军 刘金光 《化工环保》 CAS CSCD 北大核心 2010年第1期12-15,共4页
从活性污泥和受苯酚污染的土壤中分离出的菌株XA05和FG03均具有很强的苯酚生物降解能力。16srDNA序列分析表明,XA05和FG03菌株分别属于不动杆菌属(Acinetobacter sp.)和鞘氨醇单胞菌属(Sphin-gomonas sp.)。实验结果表明,在苯酚初始质... 从活性污泥和受苯酚污染的土壤中分离出的菌株XA05和FG03均具有很强的苯酚生物降解能力。16srDNA序列分析表明,XA05和FG03菌株分别属于不动杆菌属(Acinetobacter sp.)和鞘氨醇单胞菌属(Sphin-gomonas sp.)。实验结果表明,在苯酚初始质量浓度为800.0mg/L、培养时间为35h的条件下,自由悬浮细胞和固定化细胞的苯酚降解率均高于95.0%。 展开更多
关键词 苯酚 生物降解 固定化细胞 acinetobacter sp.XA05 SPHINGOMONAS sp.FG03
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异养硝化菌Acinetobacter harbinensis HITLi 7T冷休克蛋白基因生物信息学分析与不同温度下的表达 被引量:2
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作者 马银鹏 李伟光 +2 位作者 孟利强 姜威 张淑梅 《基因组学与应用生物学》 CAS CSCD 北大核心 2020年第9期4003-4009,共7页
Acinetobacter harbinensis HITLi 7T是一株低温氨氮去除能力较强的异养硝化细菌,在其基因组信息中发现一个冷休克蛋白基因SE27RS01265,基因全长624 bp,编码207个氨基酸。系统发育分析发现,该蛋白与Acinetobacter属菌株的冷休克蛋白同... Acinetobacter harbinensis HITLi 7T是一株低温氨氮去除能力较强的异养硝化细菌,在其基因组信息中发现一个冷休克蛋白基因SE27RS01265,基因全长624 bp,编码207个氨基酸。系统发育分析发现,该蛋白与Acinetobacter属菌株的冷休克蛋白同源性为64.73%~82.13%,与菌株A.kookii(GenBank No:WP092820441)同源性最高。预测该蛋白分子量为23.68 kD,没有信号肽,是非分泌型的不稳定碱性疏水蛋白;二级结构主要由Alpha螺旋、延伸链、Beta转角和无规则卷曲等四部分组成。荧光定量PCR研究发现,该基因在低温条件下高表达,在12.5℃相对表达量最高。本研究为解析冷休克蛋白在菌株HITLi 7T低温生长与氨氮去除中的作用提供理论基础。 展开更多
关键词 acinetobacter harbinensis HITLi 7T 冷休克蛋白基因 生物信息学分析 荧光定量PCR
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Acinetobacter lwoffii ChI-06合成几丁质酶抑制剂的发酵动力学研究 被引量:2
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作者 金伟军 姚祥春 张礼星 《科技通报》 2008年第5期631-635,共5页
对Acinetobacter lwoffii ChI-06合成几丁质酶抑制剂的发酵过程和发酵动力学进行了研究。应用Logistic方程和Luedeking-Piret方程,得到了描述菌体生长、抑制剂合成及基质消耗的动力学模型。模型反映了该菌体合成抑制剂过程的动力学特征... 对Acinetobacter lwoffii ChI-06合成几丁质酶抑制剂的发酵过程和发酵动力学进行了研究。应用Logistic方程和Luedeking-Piret方程,得到了描述菌体生长、抑制剂合成及基质消耗的动力学模型。模型反映了该菌体合成抑制剂过程的动力学特征,模型值与实验数据拟合良好。 展开更多
关键词 acinetobacter lwoffii ChI-06 几丁质酶抑制剂 发酵动力学
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不动杆菌Acinetobacter sp.NG3固定化处理抗生素制药废水的研究 被引量:1
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作者 王俊峰 王萍萍 刘志健 《安徽农业科学》 CAS 2014年第35期12633-12634,12728,共3页
[目的]研究PVA复合栽体包埋固定化微生物颗粒处理抗生素废水的工艺条件.[方法]采用包埋固定化技术处理抗生素废水中的COD,考察了不同因素对COD去除效果的影响.[结果]其最佳处理条件:曝气时间为25h,处理温度为25~35℃,pH为6~8.在该条... [目的]研究PVA复合栽体包埋固定化微生物颗粒处理抗生素废水的工艺条件.[方法]采用包埋固定化技术处理抗生素废水中的COD,考察了不同因素对COD去除效果的影响.[结果]其最佳处理条件:曝气时间为25h,处理温度为25~35℃,pH为6~8.在该条件下,其对抗生素废水的COD去除率达85%以上.[结论]包埋固定化增强了菌体抵抗环境的能力,使包埋固定化菌处理抗生素废水的最适温度、pH和进水COD范围变宽. 展开更多
关键词 固定化 抗生素废水 acinetobacter sp.NG3
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响应面法优化菌种Acinetobacter gerneri CLX-6降解苯胺印染废水 被引量:2
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作者 蔡莉 王敏 《染整技术》 CAS 2019年第2期28-32,共5页
筛选菌种Acinetobacter gerneri CLX-6降解苯胺印染废水,考察培养温度、培养pH、装液量对苯胺降解率的影响,确定单因素培养条件:培养温度30℃、培养pH=7.0、装液量150 mL,苯胺的降解率高达92.19%。然后利用数学软件SAS系统,通过中心响... 筛选菌种Acinetobacter gerneri CLX-6降解苯胺印染废水,考察培养温度、培养pH、装液量对苯胺降解率的影响,确定单因素培养条件:培养温度30℃、培养pH=7.0、装液量150 mL,苯胺的降解率高达92.19%。然后利用数学软件SAS系统,通过中心响应面分析法中的旋转中心组合设计法优化了苯胺降解条件,最佳培养条件为培养温度33℃、培养pH=6.0,装液量为180 mL,苯胺降解率可达96.7%。菌种CLX-6对印染废水的应用研究表明,将其用于处理苯胺印染废水前景可观。 展开更多
关键词 acinetobacter gerneri CLX-6 响应面分析法 苯胺降解率
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Cellular Fatty Acids as Chemical Markers for Differentiation of Acinetobacter baumannii and Acinetobacter calcoaceticus 被引量:1
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作者 YANG Chao GUO Zhao Biao +4 位作者 DU Zong Min YANG Hui Ying BI Yu Jing WANG Gui Qin TAN Ya Fang 《Biomedical and Environmental Sciences》 SCIE CAS CSCD 2012年第6期711-717,共7页
Objective Gas chromatography (GC) was used to investigate the cellular fatty acid (CFA) composition of 141 Acinetobacter boumannii and 32 A. calcoaceticus isolates from different locations in China and to find che... Objective Gas chromatography (GC) was used to investigate the cellular fatty acid (CFA) composition of 141 Acinetobacter boumannii and 32 A. calcoaceticus isolates from different locations in China and to find chemical markers to differentiate these two closely related bacteria. Methods Whole cell fatty acid methyl esters (FAMEs) were obtained by saponification, methylation, and extraction for GC analysis, followed by a standardized Microbial Identification System (MIS) analysis. Results All A. baumannii and A. calcoaceticus strains contained some major fatty acids, namely, 18:1 co9c, 16:0, Sum In Feature 3, 12:0, 17:1co8c, 3-OH-12:0, 17:0, Sum In Feature 2, 2-OH-12:0, and 18:0 compounds. Although most of the total CFAs are similar between A. baumannii and A. calcoaceticus strains, the ratios of two pairs of CFAs, i.e., Sum In Feature 3/18:1 co9c versus 16:0/18:1 co9c and Sum In Feature 3/18:1 co9c versus unknown 12.484/18:1 co9c fatty acids, could differentiate these two closely related bacteria. A. baumannii could be easily classified into two subgroups by plotting some ratios such as Sum In Feature 3/16:0 versus 17:0 and Sum In Feature 3/2-OH-12:0 versus17:0 fatty acids. Conclusion The ratios of some CFAs could be used as chemical markers to distinguish A. baumannii from A. colcoaceticus. 展开更多
关键词 acinetobacter baumannii acinetobacter calcoaceticus DIFFERENTIATION Fatty acids Gaschromatography.
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Antibacterial resistance patterns of Acinetobacter baumannii complex:The results of Isfahan Antimicrobial Resistance Surveillance-1 Program 被引量:1
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作者 Sayed Nassereddin Mostafavi Soodabeh Rostami +6 位作者 Zary Nokhodian Behrooz Ataei Azam Cheraghi Parisa Ataabadi Naser Almasi Zohreh Norouzi Roya Kelishadi 《Asian Pacific Journal of Tropical Medicine》 SCIE CAS 2021年第7期316-322,共7页
Objective: To determine the antibiotic resistance patterns of the Acinetobacter(A.) baumannii complex isolates that cause the confirmed infection. Methods: The present descriptive study was performed from March 2016 t... Objective: To determine the antibiotic resistance patterns of the Acinetobacter(A.) baumannii complex isolates that cause the confirmed infection. Methods: The present descriptive study was performed from March 2016 to March 2018 in three referral hospitals in Isfahan, Iran. All A. baumannii complex strains isolated from different clinical samples were identified by conventional phenotypic methods and antibiotic susceptibility pattern was detected. After the clinical investigation, contaminated samples were excluded and the source(hospital/community) and site of the infection were determined. Data on antibiotic susceptibility testing were extracted from WHONET software and analysis was done with SPSS.Results: From 254 patients who had confirmed A. baumannii complex infection, 158(62.20%) cases were male, 27(10.63%) were less than 20 years old, 172(67.72%) had healthcare-associated infections and 96(37.79%) were admitted in intensive care units. The most frequent infection was bloodstream infections(111, 43.70%). Our results showed that most of the isolates were resistant to most of the antibiotics(more than 75.00%) and a lower rate of non-susceptibility was observed against minocycline(20, 44.44%) and colistin(0%). The rate of multidrug-resistant isolates was 88.97%. There was no significant difference between resistance of A. baumannii complex isolates according to age. However, the resistance to amikacin and minocycline and the rate of multidrug resistance(MDR) were significantly different between males and females. In patients with healthcare associated infection(HAI), MDR isolates were significantly different regarding admission in ICU ward. Resistance to levofloxacin and ciprofloxacin were lower in isolates from patients with bloodstream infections in comparison to other diagnoses.Conclusions: In our study, a high level of antibiotic resistance was detected in both community-acquired and healthcare-associated A. baumannii complex infections. Appropriate antibiotic prescription in a clinical setting is an essential need for the control and prevention of A. baumannii resistant infections. 展开更多
关键词 acinetobacter baumannii acinetobacter infections Anti-bacterial agents Drug resistance Iran
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离子环境对Acinetobacter sp. ADP1的salR基因活性的影响 被引量:1
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作者 李超 周琳 +2 位作者 张永军 宋福平 张杰 《生物技术通报》 CAS CSCD 北大核心 2009年第9期57-63,共7页
革兰氏阴性菌Acinetobacter sp. ADP1可以利用水杨酸作为惟一的碳源和能源生长,与这一代谢过程相关的基因为sal基因。利用sal基因启动子与细菌荧光素酶基因(lux)编码区融合而构建的工程菌Acinetobacter ADPWH_lux,通过定量测定活细胞发... 革兰氏阴性菌Acinetobacter sp. ADP1可以利用水杨酸作为惟一的碳源和能源生长,与这一代谢过程相关的基因为sal基因。利用sal基因启动子与细菌荧光素酶基因(lux)编码区融合而构建的工程菌Acinetobacter ADPWH_lux,通过定量测定活细胞发光度可以检测出salR基因在不同离子环境中的活性。本试验测定了不同浓度梯度的10种金属离子对处于指数期和稳定期的细菌的salR基因活性的影响。发光度检测表明重金属离子均会抑制指数期和稳定期的细菌的发光能力。RT-PCR试验也证明,凡能够抑制细菌发光能力的离子,均会抑制细菌的salA基因的转录。 展开更多
关键词 acinetobacter sp. ADP1 salR基因 LysR型转录调节子 离子耐受性 生物发光
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Acinetobacter johnsonii G2细胞的固定化及其非水相介质中催化合成葛根素糖苷 被引量:1
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作者 许婷婷 项梦 +1 位作者 潘扬 吴薛明 《现代化工》 CAS CSCD 北大核心 2018年第4期131-134,共4页
利用海藻酸钠包埋法固定化Acinetobacter johnsonii G2细胞,在非水相介质中生物催化葛根素合成葛根素糖苷,考察了细胞的固定化条件、转化条件以及固定化细胞的操作稳定性。结果表明,最佳固定化条件为:海藻酸钠质量分数为2%,氯化钙质量... 利用海藻酸钠包埋法固定化Acinetobacter johnsonii G2细胞,在非水相介质中生物催化葛根素合成葛根素糖苷,考察了细胞的固定化条件、转化条件以及固定化细胞的操作稳定性。结果表明,最佳固定化条件为:海藻酸钠质量分数为2%,氯化钙质量分数为2%,细胞包埋量的体积分数为50%;最佳转化条件为:温度为40℃,p H为6.47,二甲基亚砜体积分数为20%。在最佳条件下,葛根素在催化体系中质量浓度提高至31.92 g/L,产率达93%,且固定化细胞的重复使用稳定性好。与游离细胞相比,固定化细胞对p H、温度及有机溶剂表现出更强的稳定性,且在非水相介质中催化效率更高。 展开更多
关键词 acinetobacter johnsonii 非水相介质 固定化 葛根素 生物合成
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芳烃诱导Acinetobacter sp.CZ合成靛蓝及染布应用研究 被引量:1
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作者 陈卓 郭鑫宇 +3 位作者 吴炜泽 戴春晓 荆佳维 曲媛媛 《环境科学学报》 CAS CSCD 北大核心 2023年第10期37-46,共10页
靛蓝是一种古老的天然染料,被广泛应用于食品、染色以及医药等行业.利用微生物转化废水中的含氮杂环污染物吲哚合成靛蓝对于污染物的绿色资源化具有重要意义.本研究从焦化废水处理厂二沉池中分离得到靛蓝合成菌CZ,经形态学观察和16S rRN... 靛蓝是一种古老的天然染料,被广泛应用于食品、染色以及医药等行业.利用微生物转化废水中的含氮杂环污染物吲哚合成靛蓝对于污染物的绿色资源化具有重要意义.本研究从焦化废水处理厂二沉池中分离得到靛蓝合成菌CZ,经形态学观察和16S rRNA基因测序鉴定为不动杆菌属(Acinetobacter sp.).采用液相色谱/飞行时间-质谱联用仪(LC/TOF-MS)测定菌株代谢的中间产物,发现靛红、靛红酸及邻氨基苯甲酸是菌株CZ降解吲哚的中间产物,降解过程中有副产物靛蓝生成.同时,条件优化结果表明菌株CZ在受到苯酚及联苯刺激作用下合成靛蓝产量得到显著提升.进一步利用响应曲面法考察菌株CZ合成靛蓝的最佳条件为:吲哚浓度292.88 mg·L^(-1)和苯酚浓度135.89 mg·L^(-1)、吲哚浓度286.83 mg·L^(-1)和联苯518.96 mg·L^(-1).靛蓝产量分别达到34.86 mg·L^(-1)以及29.51 mg·L^(-1),相较于初始条件分别提升12.58倍及10.65倍.将合成的生物靛蓝应用于染布,证明了其具备染色能力,K/S值在3.22~3.45之间.本研究可为探索吲哚污水的资源化合成靛蓝及其应用提供有力的理论支持. 展开更多
关键词 acinetobacter sp. 吲哚降解 靛蓝合成 芳烃诱导 响应曲面法
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Antimicrobial resistance in Acinetobacter baumannii : From bench to bedside 被引量:58
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作者 Ming-Feng Lin Chung-Yu Lan 《World Journal of Clinical Cases》 SCIE 2014年第12期787-814,共28页
Acinetobacter baumannii(A. baumannii) is undoubtedly one of the most successful pathogens in the modern healthcare system. With invasive procedures, antibiotic use and immunocompromised hosts increasing in recent year... Acinetobacter baumannii(A. baumannii) is undoubtedly one of the most successful pathogens in the modern healthcare system. With invasive procedures, antibiotic use and immunocompromised hosts increasing in recent years, A. baumannii has become endemic in hospitals due to its versatile genetic machinery, which allows it to quickly evolve resistance factors, and to its remarkable ability to tolerate harsh environments. Infections and outbreaks caused by multidrugresistant A. baumannii(MDRAB) are prevalent and have been reported worldwide over the past twenty or more years. To address this problem effectively, knowledge of species identification, typing methods, clinical manifestations, risk factors, and virulence factors is essential. The global epidemiology of MDRAB is monitored by persistent surveillance programs. Because few effective antibiotics are available, clinicians often face serious challenges when treating patients with MDRAB. Therefore, a deep understanding of the resistance mechanisms used by MDRAB can shed light on two possible strategies to combat the dissemination of antimicrobial resistance: stringent infection control and antibiotic treatments, of which colistin-based combination therapy is the mainstream strategy. However, due to the current unsatisfying therapeutic outcomes, there is a great need to develop and evaluate the efficacy of new antibiotics and to understand the role of other potential alternatives, such as antimicrobial peptides, in the treatment of MDRAB infections. 展开更多
关键词 acinetobacter BAUMANNII Antibiotic resistance EPIDEMIOLOGY GENOMICS Infection control
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Biodegradation of phenol by free and immobilized Acinetobacter sp.strain PD12 被引量:24
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作者 WANG Ying TIAN Ye +3 位作者 HAN Bin ZHAO Hua-bing BI Jian-nan CAI Bao-li 《Journal of Environmental Sciences》 SCIE EI CAS CSCD 2007年第2期222-225,共4页
A new phenol-degrading bacterium with high biodegradation activity and high tolerance of phenol, strain PD 12, was isolated from the activated sludge of Tianjin Jizhuangzi Wastewater Treatment Facility in China. This ... A new phenol-degrading bacterium with high biodegradation activity and high tolerance of phenol, strain PD 12, was isolated from the activated sludge of Tianjin Jizhuangzi Wastewater Treatment Facility in China. This strain was capable of removing 500 mg phenol/L in liquid minimal medium by 99.6% within 9 h and metabolizing phenol at concentrations up to 1100 mg/L. DNA sequencing and homologous analysis of 16S rRNA gene identified PD12 to be an Acinetobacter sp. Polyvinyl alcohol (PVA) was used as a gel matrix to immobilize Acinetobacter sp. strain PDI2 by repeated freezing and thawing. The factors affecting phenol degradation of immobilized cells were investigated, and the results showed that the immobilized cells could tolerate a high phenol level and protected the bacteria against changes in temperature and pH. Storage stability and reusability tests revealed that the phenol degradation functions of immobilized cells were stable after reuse for 50 times or storing at 4℃ for 50 d. These results indicate that immobilized Acinetobacter sp. strain PD 12 possesses a good application potential in the treatment of phenol-containing wastewater. 展开更多
关键词 PHENOL BIODEGRADATION acinetobacter sp. PD 12 immobilized bacterium
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