甲胺磷农药降解菌HS-A32的分离鉴定及降解特性

从长期受有机磷农药污染的土壤中分离到一株降解菌HS-A32,能以甲胺磷作为唯一的碳源和氮源生长.HS-A32菌降解甲胺磷的最适温度为30℃,最适pH值为7.0,甲胺磷的最适降解浓度为1 000 mg/L,降解率达82%.聚酰胺薄层色谱(TLC)可检测到降解产物中有NH4 生成.HS-A32菌能以多种碳、氮源生长,外加可利用的碳源和氮源能促进甲胺磷的降解.通过16S rDNA扩增、测序,运用BLAST检索分析,构建系统进化树.结合生理生化鉴定,初步确定HS-A32为不动杆菌属(Acinetobacter).HS-A32菌还能降解甲基对硫磷等多种有机磷农药.图6表1参14     

Interspecific transmission of Paederus endosymbionts: relationship to the genetic divergence among the bacteria associated with pederin biosynthesis

Summary. Endosymbiotic bacteria implicated in pederin production of Paederus (+)-females (Coleoptera: Staphylinidae) can be transmitted horizontally within and less frequently among the three species analyzed (P. melanurus, P. riparius, P. sabaeus). The 16S rDNA isolated from (+)-females reveals closely related bacterial sequences in the three species as well as in Paederus fuscipes and Paederidus ruficollis. This confirms the association of the undescribed endosymbiont and pederin biosynthesis in 5 of the 13 species that have been shown to contain the substance. In spite of the high sequence identities (> 99.5%), which suggest one species of endosymbiont, some of the heterospecific hosts were incompatible. This indicates adaptation and specific preferences of the endosymbiont for their natural host. Received 5 December 2001; accepted 11 March 2002.     

极端嗜热厌氧纤维素菌的分离鉴定、系统发育分析及其酶学性质的研究

从云南高温温泉、油井等热源地区采集的大量样品中,获得了一株特殊的极端嗜热厌氧纤维素分解菌B2.分离菌株直杆,革兰氏阴性(G-),未观察到孢子,细胞单个或成对出现.菌体大小为0.4μm×(2-4)μm,严格厌氧,生长温度范围50-70℃,最适生长温度65℃.pH范围4-8,最适pH 7.0.在纤维素粉琼脂上菌落直径2-4 mm,乳白色.分离菌株能利用纤维二糖、葡萄糖、蔗糖、松子糖、淀粉、覃糖等作为碳源,分离菌株还可利用纤维素滤纸、纤维素粉、微晶纤维素、纤维素粉MN300和甘蔗渣、水稻秸杆.发酵纤维素产生乙醇、乙酸.在菌株B2的纤维素酶系中,C1酶、Cx酶和β-葡萄糖苷酶的最适温度分别为80℃、80℃和70℃,其比值为1:9:10,同时发现Cx酶具有较高的热稳定性.部分长度的16S rDNA序列分析表明,分离菌株B2与Thermoanaerobacter ethanalicus具有99.8％相似性.分离菌株B2为Thermoanaerobacter属.图5表3参21     

菲降解菌的筛选鉴定及其降解酶基因的研究

经过富集从活性污泥中筛选出两株菲降解菌WSCII和WSCIII,经16SrDNA鉴定,它们分别属于鞘氨醇单胞菌属(Sphingomonassp. )和假单胞菌属(Pseudomonassp. ),在28℃下4d内对菲( 0. 6g/L)的降解率分别达到了70. 9%和78. 1%;在LB、萘和菲为碳源的培养条件下,测得菌体的双加氧酶比活力不同.在菲的诱导下,两株菌的双加氧酶比活力最高,而以LB和萘为碳源时酶的比活力较低,其中WSCII在萘中不能生长;这表明该酶在两菌中皆为底物诱导表达.以其它菌的萘双加氧酶基因大亚基片段做模板制备异源探针,与两菌总DNA进行斑点杂交;结果表明,这两株菌可能含有不同的菲双加氧酶基因.利用简并引物进行PCR扩增菲双加氧酶,结果仅能从WSCIII的总DNA中扩增得到目的片段,序列分析证明,该基因与已报道的(P. putidaNCIB9816 -4, AF491307 )双加氧酶同源性最高为98%. 图5参10     

底泥中红霉素耐受菌群的多样性分析

为了正确评估抗生素残留的环境风险,了解长期受低浓度红霉素污染条件下,水体底泥中红霉素耐受菌群结构的变化特点,采用传统的微生物培养法和分子生物学方法对长期受低浓度红霉素污染的水体底泥中红霉素耐受菌群结构的多样性进行了分析.结果表明:采用传统的培养方法,从底泥中可分离筛选出3株对红霉素有耐受能力的菌株,根据其形态学特征及16S rDNA序列分析,初步鉴定为赖氨酸芽孢杆菌(Lysinibacillussp.)、土壤芽孢杆菌(Solibacillus silvestris)以及蜡样芽孢杆菌(Bacillus cereus),其中敏感菌蜡样芽孢杆菌经低浓度红霉素诱导对红霉素表现出一定的耐药性.进一步构建底泥耐药菌群16S rDNA克隆文库发现,底泥中红霉素耐受菌群可分为三大类群,其中未获培养的细菌(Uncultured bacterium)在整个文库中比例最大,占65.06%,其次为芽孢杆菌纲(Bacilli)和梭菌纲(Clostridia),分别占文库比例33.73%和1.20%.文库中可培养的耐药菌优势类群为芽孢杆菌纲,与传统培养方法得到的结果相一致.上述研究表明,在长期受低浓度红霉素污染的环境中,红霉素耐药菌的存在具有一定的广泛性和潜在性,将可能威胁人类健康和生态系统,应当重视其生态风险评价与管理.     

两株菲降解菌株的特性及其系统发育分析

从石油污染土壤中分离到两株可以菲为唯一碳源的细菌菌株,经形态和生理生化特性分析,脂肪酸含量分析和16S rDNA序列同源性鉴定, 两菌均属鞘氨醇单胞菌属(Sphingomonas),菌株ZX4为少动鞘氨醇单胞菌(Sphingomonas paucimobilis),而菌株EVA17与该属内已知菌的序列同源性在93%~98%之间,推测可能为一新种.两菌株在不同碳源培养基上的生长曲线表明菲对细菌生长有明显的延滞作用.菌株EVA17全细胞蛋白质电泳图谱揭示该细菌在菲诱导下可出现诱导性蛋白,推测可能为一些解毒酶或降解酶.菲降解细菌在以结晶态菲为碳源时生长速率明显低于以粉末态菲为碳源时的生长速率,表明细菌与菲间的接触面积是限制其利用菲的一个重要因素.分离菌株谷胱甘肽S-转移酶(GST酶)具有可与1-氯-2,4-二硝基苯(CDNB)结合的活性.添加表面活性剂吐温-80可促进细菌对菲的利用.     

Microbial community structures in an integrated two-phase anaerobic bioreactor fed by fruit vegetable wastes and wheat straw

The microbial community structures in an integrated two-phase anaerobic reactor（ITPAR）were investigated by 16 S r DNA clone library technology. The 75 L reactor was designed with a 25 L rotating acidogenic unit at the top and a 50 L conventional upflow methanogenic unit at the bottom, with a recirculation connected to the two units. The reactor had been operated for 21 stages to co-digest fruit/vegetable wastes and wheat straw, which showed a very good biogas production and decomposition of cellulosic materials. The results showed that many kinds of cellulose and glycan decomposition bacteria related with Bacteroidales,Clostridiales and Syntrophobacterales were dominated in the reactor, with more bacteria community diversities in the acidogenic unit. The methanogens were mostly related with Methanosaeta, Methanosarcina, Methanoculleus, Methanospirillum and Methanobacterium; the predominating genus Methanosaeta, accounting for 40.5%, 54.2%, 73.6% and 78.7% in four samples from top to bottom, indicated a major methanogenesis pathway by acetoclastic methanogenesis in the methanogenic unit. The beta diversity indexes illustrated a more similar distribution of bacterial communities than that of methanogens between acidogenic unit and methanogenic unit. The differentiation of methanogenic community composition in two phases, as well as pH values and volatile fatty acid（VFA） concentrations confirmed the phase separation of the ITPAR. Overall, the results of this study demonstrated that the special designing of ITPAR maintained a sufficient number of methanogens, more diverse communities and stronger syntrophic associations among microorganisms, which made two phase anaerobic digestion of cellulosic materials more efficient.     

不同溶解氧条件下A/O系统的除碳脱氮效果和细菌群落结构变化

应用一个在不同的溶解氧(3、2、1和0.5 mg·L-1)浓度下长期运行的缺氧/好氧(A/O)小试系统考察了溶解氧浓度的变化对系统的除碳和脱氮效果以及细菌群落结构的影响.结果表明,A/O系统的除碳和脱氮效果不随溶解氧(DO)的降低而降低,在低溶解氧(0.5 mg·L-1)条件下,系统仍具有很好的除碳和脱氮效果,即化学需氧量(COD)、氨氮(NH+4-N)和总氮(TN)的去除率分别为89.7%、98.3%和88.0%.通过PCR-DGGE方法,对系统中的细菌群落结构随DO浓度的变化规律进行了分析,结果表明,微生物群落结构随DO浓度的变化有所不同,高DO和低DO环境中的细菌群落结构差异较大,但是与高DO条件下系统内的细菌群落相比,在低DO条件下系统内细菌群落仍具有较高的生物多样性.在低DO条件下,系统内的优势细菌主要被鉴定为Proteobacteria.     

CANON在SBAF中的快速启动及其微生物特征

启动周期长是单级全程自养脱氮工艺(CANON)的主要制约因素之一.本文研究了基于淹没式生物滤池(SBAF)的CANON工艺的快速启动方法.首先,以城镇污水处理厂二沉池中普通活性污泥为种泥,在(30±2)℃、不添加有机碳源,控制DO(阶段Ⅰ:0.3~0.5 mg·L~(-1),阶段Ⅱ~Ⅳ:0.1~0.2 mg·L~(-1))的实验条件下,经过48 d对污泥微生物的驯化,成功启动了CANON工艺,氨氮(NH+4-N)和总氮(TN)最大去除率分别达到99.9%和86.5%.其次,采用16S r DNA宏基因组高通量测序技术研究了体系内微生物种群结构特性.测序结果显示体系内两个优势微生物菌门是Proteobacteria(变形菌门)和Planctomycetes(浮霉菌门),平均分别占比26.6%和17.8%,主要脱氮微生物是β-Proteobacteria中的Nitrosomonas和Brocadiae中的Candidatus brocadia.通过以上实验分析得出:采用SBAF启动CANON技术,具有可实现体系快速启动、生物高效脱氮、过程稳定运行等特性.     

2株好氧反硝化菌的筛选及其强化贫营养生物膜脱氮效果

经富集培养、BTB培养基初筛与反硝化能力测定,从城市污水处理厂活性污泥中筛选得到2株好氧反硝化细菌.通过16S rDNA同源性分析对2株菌进行鉴定;并将这2菌株接种到贫营养生物膜体系中以探究它们对系统总氮的去除能力的强化.结果表明,这2株菌分别属于Pseudomonas aeruginosa和Pseudomonas putida,2株好氧反硝化菌单独存在时,对模拟废水的TN去除率分别达78%和82%;2株细菌强化后的生物膜系统对TN去除率达68%和64%,较非强化对照系统分别提高47%和43%,且NH4+-N去除率均接近100%.说明这2株好氧反硝化细菌具有较强的反硝化能力,并能够有效强化生物膜在贫营养条件下的反硝化能力,并且不会抑制生物膜硝化能力,可实现生物膜系统同步硝化反硝化.