亚硝化单胞菌的分离鉴定及其降解特性的研究

对含有亚硝化菌的活性污泥进行富集和分离得到6株亚硝化菌,对其中降解效果最好的一株YS6菌株进行鉴定和降解特性研究。结果表明:该菌为亚硝化单胞菌(Nitrosomonas sp.),最适碳源CaCO_3和NaHCO_3,最适温度30℃,最适pH值8,250mL锥形瓶最佳装瓶量50 mL,接种量12×10~9个。     

光倒刺鲃、白鲢协同投放抑制丝状藻(水绵)藻华围隔研究

为探究高效与安全抑制丝状藻藻华的方法,利用光倒刺鲃(Spinibarbus hollandi)、白鲢(Hypophthalmichthys molitrix)的食性特点,研究了不同密度(低密度(L)40 g·m-3、高密度(H)80 g·m-3)与不同投放比例(光倒刺鲃∶白鲢=3∶1、1∶1、1∶3)协同作用下,对围隔内水体丝状藻水绵(Spirogyra sp.)的抑制效果,以及对水生植物和水质的影响.结果表明,光倒刺鲃可以显著摄食丝状藻水绵,且在低密度、高比例(3∶1)时,即对丝状藻的生长具有明显抑制作用.高密度(80 g·m-3)投放光倒刺鲃、白鲢,无论比例如何,都会引起水体水质下降,引起轻微富营养化,并导致浮游藻类生物量上升,不适用于本试验水体.在本试验条件下,高密度(80 g·m-3)投放条件下,白鲢可以抑制浮游生物总量,H(1∶3)、H(1∶1)组中,呈现藻类小型化的趋势;而在低密度(40 g·m-3)投放条件下,未发现浮游藻类有小型化趋势.本试验L(3∶1)组,即光倒刺鲃30 g·m-3、白鲢10 g·m-3,可以有效控制试验水体丝状藻水绵滋生,且能够兼顾改善水质.     

Pseudomonas sp. QJX-1的锰氧化特性研究

从锰矿土壤样品中分离、纯化出1株高效锰氧化细菌(QJX-1),经16S rDNA序列鉴定为Pseudomonas sp.QJX-1.研究表明,Pseudomonas sp.QJX-1含有锰氧化的必需成分多铜氧化酶基因CumA,当初始Mn2+为5.05 mg·L-1,菌密度D600为0.020时,该菌可在48 h内将Mn2+转化,且转化率高达99.4%.在寡营养条件下该菌锰氧化速率较富营养条件下有显著提高;添加石英砂滤料促使生物膜的快速形成,进而促进Mn2+的生物转化.根据研究结果推测地下水处理过程中生物锰氧化速率较快.     

Evaluation of Bacillus sp. MZS10 for decolorizing Azure B dye and its decolorization mechanism

To evaluate decolorization and detoxification of Azure B dye by a newly isolated Bacillus sp. MZS10 strain, the cultivation medium and decolorization mechanism of the isolate were investigated. The decolorization was discovered to be dependent on cell density of the isolate and reached 93.55%(0.04 g/L) after 14 hr of cultivation in a 5 L stirred-tank fermenter at 2.0 g/L yeast extract and 6.0 g/L soluble starch and a small amount of mineral salts. The decolorization metabolites were identified with ultra performance liquid chromatography-tandem mass spectroscopy(UPLC-MS). A mechanism for decolorization of Azure B was proposed as follows: the C=N in Azure B was initially reduced to –NH by nicotinamide adenine dinucleotide phosphate(NADPH)-dependent quinone dehydrogenase, and then the –NH further combined with –OH derived from glucose to form a stable and colorless compound through a dehydration reaction. The phytotoxicity was evaluated for both Azure B and its related derivatives produced by Bacillus sp. MZS10 decolorization, indicating that the decolorization metabolites were less toxic than original dye. The decolorization efficiency and mechanism shown by Bacillus sp. MZS10 provided insight on its potential application for the bioremediation of the dye Azure B.     

Biodegradation of benzo[a]pyrene in soil by Mucor sp. SF06 and Bacillus sp. SB02 co-immobilized on vermiculite

Two indigenous microorganisms, Bacillus sp. SB02 and Mucor sp. SF06, capable of degrading polycyclic aromatic hydrocarbons （PAHs） were co-immobilized on vermiculite by physical adsorption and used to degrade benzo[a] pyrene （BaP）. The characteristics of BaP degradation by both free and co-immobilized microorganism were then investigated and compared. The removal rate using the immobilized bacterial-fungal mixed consortium was higher than that of the freely mobile mixed consortium. 95.3% of BaP was degraded using the co-immobilized system within 42 d, which was remarkably higher than the removal rate of that by the free strains. The optimal amount of inoculated co-immobilized system for BaP degradation was 2%. The immobilized bacterial-fungal mixed consortium also showed better water stability than the free strains. Kinetics of BaP biodegradation by co-immobilized SF06 and SB02 were also studied. The results demonstrated that BaP degradation could be well described by a zero-order reaction rate equation when the initial BaP concentration was in the range of 10--200 mg/kg. The scanning electronic microscope （SEM） analysis showed that the co-immobilized microstructure was suitable for the growth of SF06 and SB02. The mass transmission process of co-immobilized system in soil is discussed. The results demonstrate the potential for employing the bacterial-fungal mixed consortium, co-immobilized on vermiculite, for in situ bioremediation of BaP.     

滏阳河河流水体中重金属污染特征及其对青海弧菌和斜生栅藻的毒性效应

为调查滏阳河水系的重金属污染状况,研究河流重金属污染对水生生物的毒性,根据河流结构、水文条件、排污口分布并考虑空间分布的均匀性,选取66个采样位点,采集河水及对应的表层沉积物样品,分析了样品中的重金属含量。用斜生栅藻和青海弧菌Q67作为模式生物,根据滏阳河水重金属污染较严重的邯郸近郊2号采样点采集水样的重金属含量配制系列重金属浓度的模拟河水进行重金属污染河水的生态毒性测试。结果表明,在全部66个采样点中,29个采样点河水重金属含量超过国家地表水III类水体重金属含量标准,主要污染元素是Hg、Pb、Cr、Zn。几乎所有采样点河水Mn和Fe含量都大大高于国家集中式生活饮用水地表水源地补充项目规定的标准限值。根据2号采样点河水样品中的重金属含量配成的模拟河水对青海弧菌Q67的EC₅₀值为6.65%,为毒性极强的污染物。模拟河水样品对斜生栅藻的抑制作用较小,在实验的最高浓度下(1000倍河水重金属含量)暴露4 d尚未引起半数藻细胞死亡。随河水重金属浓度上升,斜生栅藻超氧化物歧化酶(SOD)活性总体上呈现先升高后降低的趋势,丙二醛(MDA)含量变化则与此相反,反映河水重金属污染可引起藻细胞的氧化损伤。叶绿素a和b含量则随暴露浓度的提高逐渐降低。在重金属浓度达到2号采样点河水的10%时,斜生栅藻叶绿素a含量已有显著降低,MDA含量显著升高,海河流域重金属污染对生态系统的影响应予以重视。河水发光菌Q67的生长抑制率、斜生栅藻的叶绿素a和MDA含量可以作为评估河流重金属污染生态危害的指标。     

微生物絮凝剂产生菌的筛选及其絮凝特性

采用常规的微生物学方法,从垃圾渗滤液中筛选到一株高效微生物絮凝剂产生菌LB1,根据其形态学和生理生化特征初步鉴定该菌株属于假单胞菌属,命名为Pseudonomas sp. LB1。LB1所产微生物絮凝剂的絮凝特性的研究结果表明,LB1的最佳产絮凝时间为96 h,所产絮凝活性物质主要是其生长过程中的胞外分泌物和细胞生长后期的次级代谢产物,菌体细胞本身具有一定的助凝作用。LB1所产絮凝剂最佳加样量为3％（体积分数V/V）;对pH的适应范围较宽,在4～10之间具有较高的絮凝活性,均大于75％;温度为25℃时絮凝率为86.3％,在25～60℃之间,絮凝率基本保持稳定;LB1所产絮凝剂对几种废水具有较好的絮凝效果。     

氯氰菊酯降解菌CY22-7的分离鉴定及降解特性研究

从采集的多种土壤样品中.获得了19株在3种筛选平板上均生长良好的候选氯氰菊酯降解菌.通过生理生化特性鉴定和16S rDNA序列的测定及比对.将其中的氯氰菊酯降解菌CY22-7鉴定为中华根瘤菌属(Sinorhizobium sp.).同时,对氯氰菊酯降解菌CY22-7的降解特性研究结果表明:(1)氯氰菊酯降解菌CY22-7以5%(体积分数)的接种鼍接种到氯氰菊酯起始质量浓度为100 mg/L的氯氰菊酯乙醇培养基后,于200 r/min、30℃摇床中培养.经过6 d的培养,氯氰菊酯降解菌CY22-7降解了约60%的氯氰菊酯.(2)加人外源营养物质有利于促进氯氰菊酯的降解.其中,葡萄糖和酵母提取物的促进作用最为明显.(3)氯氰菊酯降解菌CY22-7降解氯氰菊酯的最适温度为30℃,最佳pH为6.0.     

应用细胞合成计量关系模型分析鱼腥藻7120的混合营养生长

根据文献中鱼腥藻细胞大分子的含量和组成情况,计算了细胞合成所需要的小分子单体和前体代谢物的量,得到代谢意义上的细胞生物合成计量关系,此计量关系模型,对鱼腥藻7120细胞在气升式光生物反应器中光自养和混合营养生长的对数生长阶段进行了代谢通量分析。结果表明,葡萄糖的利用影响细胞初级碳代谢的流动状况,混合营养生长过程比光自养生长过程磷酸戊糖途径氧化性分支的反应程度明显加强,随着培养的进行,葡萄糖被细胞用作碳源的比例可能减小,而用作能源的比例可能增大。     

Degradation of poly(3-hydroxybutyrate), PHB,by bacteria and purification of a novel PHB depolymerase fromComamonas sp.

Bacteria capable of growing on poly(3-hydroxybutyrate), PHB, as the sole source of carbon and energy were isolated from various soils, lake water, activated sludge, and air. Although all bacteria utilized a wide variety of monomeric substrates for growth, most of the strains were restricted to degrade PHB and copolymers of 3-hydroxybutyrate and 3-hydroxyvalerate, P(3HB-co-3HV). Five strains were also able to decompose a homopolymer of 3-hydroxyvalerate, PHV. Poly(3-hydroxyoctanoate), PHO, was not degraded by any of the isolates. One strain, which was identified asComamonas sp., was selected, and the extracellular depolymerase of this strain was purified from the medium by ammonium sulfate precipitation and by chromatography on DEAE-Sephacel and Butyl-Sepharose 4B. The purified PHB depolymerase was not a glycoprotein. The relative molecular masses of the native enzyme and of the subunits were 45,000 or 44,000, respectively. The purified enzyme hydrolyzed PHB, P(3HB-co-3HV), and—at a very low rate—also PHV. Polyhydroxyalkanoates, PHA, with six or more carbon atoms per monomer or characteristic substrates for lipases were not hydrolyzed. In contrast to the PHB depolymerases ofPseudomonas lemoignei andAlcaligenes faecalis T₁, which are sensitive toward phenylmethylsulfonyl fluoride (PMSF) and which hydrolyze PHB mainly to the dimeric and trimeric esters of 3-hydroxybutyrate, the depolymerase ofComamonas sp. was insensitive toward PMSF and hydrolyzed PHB to monomeric 3-hydroxybutyrate indicating a different mechanism of PHB hydrolysis. Furthermore, the pH optimum of the reaction catalyzed by the depolymerase ofComamonas sp. was in the alkaline range at 9.4.