乙草胺降解菌B-2的分离鉴定及其降解特性的分析

作为一种被广泛使用的氯代酰胺类除草剂,乙草胺进入环境中很难被降解。本研究从长期施用乙草胺的稻田土壤中分离筛选到一株以乙草胺为唯一碳源的菌株B-2,经形态、生理生化特性及16S r RNA基因序列同源性分析,最终鉴定为Klebsiella variicola。通过研究培养温度、初始p H值、菌体接种量、装液量、Na Cl浓度和乙草胺浓度对该菌株生长和降解的影响,确定了最佳生长条件。结果表明,菌株B-2以5%接种量接入浓度为100 mg/L乙草胺、p H 7.0的无机盐培养基(含0.1%Na Cl)中,30℃条件下培养5 d,对乙草胺的降解率可达90.31%。     

苯酚降解菌F6的筛选鉴定及降解特性

本研究利用逐级驯化的方法,从广西某工厂的废水中分离得到一株能利用苯酚作为唯一碳源生长的高效苯酚降解菌F6。采用16S r DNA序列分析的方法,将菌株F6鉴定为芽孢杆菌(Bacillus sp.)。F6菌株在8 h内几乎完全降解100 mg/L的苯酚,降解率达99.9%,该菌株的菌体生长与苯酚降解呈同步趋势,主要在对数生长期降解苯酚。F6最高耐受苯酚浓度为1 800 mg/L,在温度25~40℃,p H值6.0~9.0,盐度0~40 g/L范围内,F6菌株均能保持对苯酚良好的降解能力。菌株F6的降解底物具有广谱性,除了能够利用苯酚作为唯一碳源,还可以利用邻苯二酚、间苯二酚、对苯二酚、连苯三酚、甲苯、氯苯等酚类化合物为其生长代谢提供碳源和能源。综上所述,菌株F6在应用于处理成分复杂、含酚浓度较高的废水中将具有很大的潜力。     

一株毒死蜱降解新菌株Sphingopyxis terrae R17的分离鉴定及降解特性

从农药厂排污沟污泥中分离到一株能降解毒死蜱的新菌株,命名为R17,经生理生化和16S rDNA序列同源性分析,鉴定为Sphingopyxis terrae.R17可以利用毒死蜱作为唯一碳源生长,该菌株的最适生长温度为35℃、最适pH为7～8,在此条件下培养28 h后,菌落浓度达9.18×108cfu/mL.研究了该菌在...     

一株苯酚降解菌的筛选、鉴定及其降解特性

本研究采用逐量分批驯化的方法,从造纸废水中分离得到一株能够以苯酚为唯一碳源生长的苯酚降解菌株F5-1.经形态观察、生理生化特性鉴定及16S rDNA序列分析,将该菌株鉴定为克雷伯菌(Klebsie-lla sp.).该菌株能够在7 h时完全降解初始浓度为100 mg/L的苯酚,降解苯酚主要发生在生长对数期;在pH 5.0～9.0,NaCl浓度0～80 g/L,温度20～40℃范围内,菌株F5-1均可有效降解初始浓度为100～1 200 mg/L的苯酚;能够耐受的最大苯酚浓度为1 500 mg/L.本研究结果表明,F5-1菌株对处理环境条件复杂的含酚废水具有潜在的应用前景.     

聚乙烯醇高效降解菌的筛选及降解特性研究

以聚乙烯醇为唯一碳源从环境中筛选获得了高效降解聚乙烯醇的微生物菌株XT11, 初步鉴定为假单胞菌属(Pseudomonas sp.)。对菌株Pseudomonas XT11的生长过程及PVA降解过程进行了研究, 发现该菌株在54 h内可将1 g/L的聚乙烯醇(PVA)降解。同时研究了温度、pH值及酵母膏浓度对该菌株降解PVA的影响, 结果表明其最适温度、pH值和酵母膏浓度分别为30℃、7.0和0.5 g/L。研究了PVA浓度对PVA降解率的影响, 发现随着PVA浓度的增大, PVA的降解率降低。     

聚乙烯醇高效降解菌的筛选及降解特性研究

以聚乙烯醇为唯一碳源从环境中筛选获得了高效降解聚乙烯醇的微生物菌株XT11,初步鉴定为假单胞菌属(Pseudomonas sp.).对菌株Pseudomonas XT11的生长过程及PVA降解过程进行了研究,发现该菌株在54 h内可将1 g/L的聚乙烯醇(PVA)降解.同时研究了温度、pH值及酵母膏浓度对该菌株降解PVA的影响,结果表明其最适温度、pH值和酵母膏浓度分别为30℃、7.0和0.5 g/L.研究了PVA浓度对PVA降解率的影响,发现随着PVA浓度的增大,PVA的降解率降低.     

粪臭素高效降解菌YKSW-6的分离、鉴定及降解特性

【背景】粪臭素是畜牧堆肥中有机污染物的主要成分,造成养殖场及周边环境恶化,粪臭素污染问题亟待解决,利用微生物降解粪臭素是一种环保节能的有效方法。【目的】分离鉴定粪臭素高效降解菌株,研究其降解特性,为粪臭素降解提供高效的菌种资源,为该菌株应用于臭味污染环境的净化提供基础。【方法】以粪臭素为唯一碳源的无机盐培养基作为培养基质,从猪粪堆肥样品中分离筛选粪臭素高效降解菌株,通过形态特征和16S rRNA基因序列分析进行分离菌株的初步鉴定,分析其生长规律及粪臭素降解特性,并利用气相色谱质谱联用(GC-MS)对菌株代谢粪臭素的产物进行分析。【结果】从样品中分离获得一株能以粪臭素为唯一碳源的细菌YKSW-6菌株,形态学和16S rRNA基因序列分析初步鉴定该菌株为戈登氏红球菌(Rhodococcus gordoniae)。接种量为10%时,该菌培养14 h对100 mg/L的粪臭素降解率达到100%。其能够利用D-山梨醇、溴-丁二酸等18种碳源,对亚碲酸钾、溴酸钾等13种化学敏感物具有抗性。菌株YKSW-6在5%接种量、温度30-42℃和pH值为6.0-9.0时对100 mg/L的粪臭素降解效率均能达到100%,菌株生长和降解粪臭素的最佳条件为：pH 7.2,温度37℃,转速180 r/min。GC-MS结果表明,粪臭素在菌株的作用下C2先被氧化,转变为3-甲基羟基吲哚,随后进一步被氧化为N-(2-乙酰基苯基)甲酰胺。同时中间产物还有苯乙醛和苯乙酸。【结论】红球菌YKSW-6为目前已报道的降解粪臭素能力较强的菌株,丰富了粪臭素降解菌种的资源库,为实际环境微生物修复应用提供了理论参考。     

苯酚降解菌的分离及培养特性研究

对南充市郊炼油厂活性污泥进行富集,驯化筛选得到2株能以苯酚作为唯一碳源和能源生长的菌株,编号为S1,S2,两菌株可耐10,000mg/L左右的苯酚浓度,实验得出其最佳生长条件为pH7-8,温度25℃-30℃,在适宜条件下,对苯酚有较好的降解能力,而且苯对两菌株的生长表现为抑制作用。     

一株耐低温石油烃降解菌的分离鉴定及其降解特性

目的:从污染环境中分离耐低温石油降解菌,并对其降解特性进行研究。方法:采用摇瓶富集培养和平板划线分离的方法,得到一株能以原油为碳源、能源生长的细菌菌株,采用分子生物学方法对该降解菌进行初步鉴定。结果:从天津大港油田污染土壤和水体中分离到一株耐低温石油降解菌DSY171,该菌株能够在10℃条件下,以石油为惟一碳源生长。经过对其形态特征、生理生化及16S rDNA序列分析,初步鉴定该菌株归属红球菌属。菌株DSY171在低温条件下(10～15℃)12 d的石油降解率显著优于常温条件(20～30℃),原油降解率为60%左右;菌株DSY171的pH适应范围较广,初始pH值为6～9时均能代谢生长,但在偏碱性环境下(pH7～9)的代谢生长好于偏酸性环境(pH6～7)。除了降解石油外,菌株DSY171对柴油、食用油等不同碳源也均能够降解代谢,具有一定的碳源利用广谱性。结论:耐低温石油降解菌DSY171的分离及其降解特性的研究,为生物学方法解决低温环境石油污染问题提供了高效菌种,在环境微生物学理论研究和实践应用中具有一定的意义和价值。     

高效芘降解菌N12的分离鉴定与降解特性

以芘为目标降解物,利用选择性富集培养方法,从沈抚灌区污染土壤中分离到一株高效芘降解菌N12,经生理生化试验和16S rDNA测序分析,该菌被鉴定为分枝杆菌属（Mycobacterium sp.）.菌株N12能以菲、苊、芴和芘为唯一碳源和能源生长,不能以蒽、萘和苯并芘为唯一碳源和能源生长.在菲和芘共同存在的情况下菌株N12可降解苯并芘,9 d内对苯并芘降解率可达79.0%.摇瓶降解试验表明,菌株N12可在7 d内将100 mg·L^-1的芘降解94.4%,14 d内将其完全降解;可将600 mg·L^-1的芘在7 d内降解56.1%,14 d内降解95.5%.添加葡萄糖可促进N12对芘的降解.菌株N12是一株优良的多环芳烃降解菌,可作为多环芳烃污染土壤生物修复的菌种资源.     

复合酶产生菌的筛选及其在烟叶醇化中的应用

从进口烟叶表面分离筛选出5株产复合酶的菌株,其中菌株HY-2能产多种复合酶,且活性相对较高,通过生理生化及16SrDNA序列分析,鉴定该菌株为解淀粉芽孢杆菌（Bacillus amyloliquefaciens）。利用该菌株配制成的生物制剂（编号MR—HY）,分别采用回潮控温控湿及直接添加的方式在烟叶醇化中进行应用。结果表明,采用回潮控温控湿方式,生物制剂能在短时间内快速作用烟叶中组分,可使得烟叶糖氮比、糖碱比更趋于协调,品质得到一定的提升;采用直接添加方式也能有效的加速烟叶醇化过程,同时烟叶的香气量增加,香气质感变好,杂气及刺激降低。可见,通过添加该菌株配制的生物制剂能有效的改善烟叶醇化过程,有较好的应用空间。     

一株产油微藻的筛选及分子鉴定

利用通气培养系统, 对10株经过初步生长筛选的微藻进行培养, 以总脂单位体积产率为主要指标, 筛选具有产油潜力的优良藻种。结果表明, 10株微藻的生物质干重、总脂含量分别为0.81.6 g/L、14.8%39.7%, 总脂单位体积产率大于30 mg/(Ld)的有6株, 其中藻株HY-6总脂单位体积产率达到最高的50.8 mg/(Ld), 是一株具有潜力的产油微藻。运用形态学特征和18S rDNA及ITS系统学分析相结合的方法对藻种HY-6进行分类鉴定。依据形态学特征, HY-6为球状单细胞, 具有1个明显的蛋白核, 杯状色素体周生, 从而初步判断该藻株可能属于小球藻属(Chlorella)或拟小球藻属(Parachlorella); 18S rDNA及ITS系统学分析表明HY-6与小球藻属分为两个不同的进化支, 但与凯氏拟小球藻(Parachlorella kessleri)的亲缘关系较近, 且具有较高的自展支持率, 因此将其鉴定为凯氏拟小球藻(P. kessleri)。研究结果将为产油微藻资源的收集、筛选及后续研究提供基础。       

The influence of six pharmaceuticals on freshwater sediment microbial growth incubated at different temperatures and UV exposures

Pharmaceutical compounds have been detected in freshwater for several decades. Once they enter the aquatic ecosystem, they may be transformed abiotically (i.e., photolysis) or biotically (i.e., microbial activity). To assess the influence of pharmaceuticals on microbial growth, basal salt media amended with seven pharmaceutical treatments (acetaminophen, caffeine, carbamazepine, cotinine, ibuprofen, sulfamethoxazole, and a no pharmaceutical control) were inoculated with stream sediment. The seven pharmaceutical treatments were then placed in five different culture environments that included both temperature treatments of 4, 25, 37°C and light treatments of continuous UV-A or UV-B exposure. Microbial growth in the basal salt media was quantified as absorbance (OD(550)) at 7, 14, 21, 31, and 48d following inoculation. Microbial growth was significantly influenced by pharmaceutical treatments (P?相似文献   

Evidence for permanent enhancement of residual ADH induced by antidiuretic agents (chlorpropamide, carbamazepine, clofibrate) in patients with pituitary diabetes insipidus.

Excretion of free water was studied in 7 patients with pituitary diabetes insipidus before treatment and after withdrawal of antidiuretic drugs (chlorpropamide, carbamazepine, clofibrate) used on a long-term basis. A statistically significant decrease in free water clearance was found after 2-4 weeks of withdrawal of antidiuretic agents. This was considered as a clinical evidence for the permanently enhanced release of residual ADH induced by chlorpropamide, carbamazepine and clofibrate in patients with partial defect in ADH secretion.     

Simultaneous activated carbon adsorption within a membrane bioreactor for an enhanced micropollutant removal

Significant adsorption of sulfamethoxazole and carbamazepine to powdered activated carbon (PAC) was confirmed by a series of adsorption tests. In contrast, adsorption of these micropollutants to the sludge was negligible. The removal of these compounds in membrane bioreactor (MBR) was dependent on their hydrophobicity and loading as well as the PAC dosage. Sulfamethoxazole exhibited better removal rate during operation under no or low (0.1 g/L) PAC dosage. When the PAC concentration in MBR was raised to 1.0 g/L, a sustainable and significantly improved performance in the removal of both compounds was observed - the removal efficiencies of sulfamethoxazole and carbamazepine increased to 82 ± 11% and 92 ± 15% from the levels of 64 ± 7%, and negligible removal, respectively. The higher removal efficiency of carbamazepine at high (1.0 g/L) PAC dosage could be attributed to the fact that carbamazepine is relatively more hydrophobic than sulfmethoxazole, which subsequently resulted in its higher adsorption affinity toward PAC.     

Divergence of binding, signaling, and biological responses to recombinant human hybrid IFN.

Three human IFN-alpha hybrids, HY-1 [IFN-alpha21a(1-75)/alpha2c(76-165)], HY-2 [IFN-alpha21a(1-95)/alpha2c(96-165)], and HY-3 [IFN-alpha2c(1-95)/alpha21a(96-166)], were constructed, cloned, and expressed. The hybrids had comparable specific antiviral activities on Madin-Darby bovine kidney (MDBK) cells but exhibited very different antiproliferative and binding properties on human Daudi and WISH cells and primary human lymphocytes. Our data suggest that a portion of the N-terminal region of the molecule is important for interaction with components involved in binding of IFN-alpha2b while the C-terminal portion of IFN is critical for antiproliferative activity. A domain affecting the antiproliferative activity was found within the C-terminal region from amino acid residues 75-166. The signal transduction properties of HY-2 and HY-3 were evaluated by EMSA and RNase protection assays. Both HY-2 and HY-3 induced activation of STAT1 and 2. However, HY-2 exhibited essentially no antiproliferative effects at concentrations that activated STAT1 and 2. Additionally, at concentrations where no antiproliferative activity was seen, HY-2 induced a variety of IFN-responsive genes to the same degree as HY-3. RNase protection assays also indicate that, at concentrations where no antiproliferative activity was seen for HY-2, this construct retained the ability to induce a variety of IFN-inducible genes. These data suggest that the antiproliferative response may not be solely directed by the activation of the STAT1 and STAT2 pathway in the cells tested.     

微生物转化连翘苷制备连翘脂素的研究

本文旨在开发一种微生物转化工艺,将连翘苷转化为活性更高的连翘脂素.结果从土壤中分离筛选到一株桔青霉(Penicillium citrinum)LB菌株,转化连翘苷为连翘脂素的专一性较高.经培养基主要组成和转化条件优化,得出较佳的产酶培养组成为:蔗糖7 g/L,(NH4)2 SO45 g/L,NaCl 5 g/L,KH2 PO45 g/L,MgSO41 g/L,MnSO40.5 g/L,pH 6.0.LB菌株经产酶培养后,过滤收集菌体悬浮于2倍发酵液体积的磷酸盐缓冲液中,加入2 g/L的底物连翘苷,于30℃、200 r/min转化20 h,连翘脂素的转化得率可达94.1%.利用微生物将连翘苷转化为连翘脂素,具有方法简单、转化得率高、产物容易纯化和副产物少等优点,有潜在的工业化应用价值.     

磷酸三(1-氯-2-丙基)酯降解菌筛选及其降解特性

【背景】磷酸三(1-氯-2-丙基)酯[tris-(1-chloro-2-propyl)phosphate,TCIPP]作为全球广泛关注的新兴有机污染物,具有环境赋存含量高、不易生物降解等特点,亟须开发TCIPP的高效去除技术。【目的】获得具有较高TCIPP降解效率并可用于TCIPP污染修复的新菌株。【方法】利用梯度提高无机盐培养基中TCIPP浓度的方法,从TCIPP污染土壤中筛选出1株能够降解液体中高浓度TCIPP (100 mg/L)的菌株,根据16S rRNA基因序列分析对其进行鉴定,并首次对其降解液体中TCIPP的特性进行研究。【结果】所筛选的TCIPP降解菌株DT-6为苍白杆菌(Ochrobactrum sp.),它能够利用TCIPP作为唯一碳源和能源;当TCIPP初始浓度为50 mg/L、培养时间为7 d时DT-6的生物量最大,对TCIPP的降解率也达到最高,为34.6%;蔗糖的加入能够显著促进DT-6的生长,但却抑制了其对TCIPP的降解。【结论】本研究报道了一株TCIPP高效降解菌Ochrobactrum sp. DT-6,能够为环境中TCIPP污染的生物修复提供新的种质...     

Effects of selected pharmaceuticals on riverine biofilm communities

Although pharmaceutical and therapeutic products are widely found in the natural environment, there is limited understanding of their ecological effects. Here we used rotating annular bioreactors to assess the impact of 10 microg.L(-1) of the selected pharmaceuticals ibuprofen, carbamazepine, furosemide, and caffeine on riverine biofilms. After 8 weeks of development, community structure was assessed using in situ microscopic analyses, fluor-conjugated lectin binding, standard plate counts, fluorescent in situ hybridization, carbon utilization spectra, and stable carbon isotope analyses. The biofilm communities varied markedly in architecture although only caffeine treated biofilms were significantly thicker. Cyanobacteria were suppressed by all 4 compounds, whereas the nitrogen containing caffeine, furosemide, and carbamazepine increased algal biomass. Ibuprofen and carbamazepine reduced bacterial biomass, while caffeine and furosemide increased it. Exopolymer content and composition of the biofilms was also influenced. Significant positive and negative effects were observed in carbon utilization spectra. In situ hybridization analyses indicated all treatments significantly decreased the gamma-proteobacterial populations and increased beta-proteobacteria. Ibuprofen in particular increased the alpha-proteobacteria, beta-proteobacteria, cytophaga-flavobacteria, and SRB385 probe positive populations. Caffeine and carbamazepine additions resulted in significant increases in the high GC354c and low GC69a probe positive cells. Live-dead analyses of the biofilms indicated that all treatments influenced the ratio of live-to-dead cells with controls having a ratio of 2.4, carbamazepine and ibuprofen being 3.2 and 3.5, respectively, and furosemide and caffeine being 1.9 and 1.7, respectively. Stable isotope analyses of the biofilms indicated delta 13C values shifted to more negative values relative to control biofilms. This shift may be consistent with proportional loss of cyanobacteria and relative increase in algal biomass rather than incorporation of pharmaceutical carbon into microbial biofilm. Thus, at 10 microg.L(-1) levels pharmaceuticals exhibit both nutrient-like and toxic effects on riverine microbial communities.     

Substrate specificity for the 12beta-hydroxylation of bufadienolides by Alternaria alternata

Hydroxylation is an important route to synthesize more hydrophilic compounds of pharmaceutical significance. Microbial hydroxylation offers advantages over chemical means for its high specificity. In this study, a fungal strain Alternaria alternata AS 3.4578 was found to be able to catalyze the specific 12beta-hydroxylation of a variety of cytotoxic bufadienolides. Cinobufagin and resibufogenin could be completely metabolized by A. alternata to generate their 12beta-hydroxylated products in high yields (>90%) within 8 h of incubation. A. alternata could also convert 3-epi-desacetylcinobufagin into 3-epi-12beta-hydroxyl desacetylcinobufagin as the major product (70% yield). C-3 dehydrogenated products were detected in these reactions in fair yields, while their accumulation was relatively slow. The 12beta-hydroxylation of bufadienolides could be significantly inhibited by the substitution of 1beta-, 5-, or 16alpha-hydroxyl groups, and the 14beta,15beta-epoxy ring appeared to be a necessary structural requirement for the specificity. For the biotransformation of bufalin, a 14beta-OH bufadienolide, this reaction was not specific, and accompanied by 7beta-hydroxylation as a parallel and competing metabolic route. The biotransformation products were identified by comparison with authentic samples or tentatively characterized by high-performance liquid chromatography-diode array detection-atmospheric pressure chemical ionization-mass spectrometry analyses.