一株芽孢杆菌产生物絮凝剂去除赤潮微藻的研究

以赤潮微藻米氏凯伦藻(Karenia mikimotoi)和塔玛亚历山大藻(Alexandrium tamarense)为受试对象,对一株芽孢杆菌WZ01所产的生物絮凝剂去除赤潮微藻的性能进行了研究。结果表明:芽孢杆菌WZ01所产生物絮凝剂对人工培养的米氏凯伦藻和塔玛亚历山大藻藻液均有去除能力,适宜的絮凝剂质量浓度为40.0~60.0 mg/L,絮凝时间为90~120 min,pH=7.5~8.5,在20~40℃范围内生物絮凝剂对2种微藻的絮凝率无显著区别;Ca~(2+)和Mg~(2+)浓度对生物絮凝剂去除2种微藻有一定影响,适宜浓度为4.0~6.0 mmol/L;适宜条件下生物絮凝剂对人工培养的米氏凯伦藻和塔玛亚历山大藻藻液的絮凝率均超过80.0%。研究表明,芽孢杆菌WZ01所产的生物絮凝剂在去除赤潮微藻方面有应用潜力。     

Repeated batch and continuous degradation of chlorpyrifos by Pseudomonas putida

The present study was undertaken with the objective of studying repeated batch and continuous degradation of chlorpyrifos (O,O-diethyl O-3,5,6-trichloropyridin-2-yl phosphorothioate) using Ca-alginate immobilized cells of Pseudomonas putida isolated from an agricultural soil, and to study the genes and enzymes involved in degradation. The study was carried out to reduce the toxicity of chlorpyrifos by degrading it to less toxic metabolites. Long-term stability of pesticide degradation was studied during repeated batch degradation of chlorpyrifos, which was carried out over a period of 50 days. Immobilized cells were able to show 65% degradation of chlorpyrifos at the end of the 50th cycle with a cell leakage of 112 × 10³ cfu mL^?1. During continuous treatment, 100% degradation was observed at 100 mL h^?1 flow rate with 2% chlorpyrifos, and with 10% concentration of chlorpyrifos 98% and 80% degradation was recorded at 20 mL h^?1 and 100 mL h^?1 flow rate respectively. The products of degradation detected by liquid chromatography–mass spectrometry analysis were 3,5,6-trichloro-2-pyridinol and chlorpyrifos oxon. Plasmid curing experiments with ethidium bromide indicated that genes responsible for the degradation of chlorpyrifos are present on the chromosome and not on the plasmid. The results of Polymerase chain reaction indicate that a ~890-bp product expected for mpd gene was present in Ps. putida. Enzymatic degradation studies indicated that the enzymes involved in the degradation of chlorpyrifos are membrane-bound. The study indicates that immobilized cells of Ps. putida have the potential to be used in bioremediation of water contaminated with chlorpyrifos.     

Isolation and characterisation of a carbofuran degrading Burkholderia sp. PCL3 from carbofuran-phytoremediated rhizosphere soil

A bacterial strain capable of degrading carbofuran as the sole carbon source was isolated from carbofuran-phytoremediated rhizosphere soil of rice. A 16S rRNA study identified the strain as Burkholderia sp. (isolate PCL3). Free cells of isolate PCL3 possessed inhibitory-type degradation kinetics with a q _max of 0.087 day^?1 and S _m of 248.76 mg·L^?1. Immobilised PCL3 on corncob and sugarcane bagasse possessed Monod-type degradation kinetics with a q _max of 0.124 and 0.098 day^?1, respectively. The optimal pH and temperature with the highest degradation rate coefficient of carbofuran were pH 7.5 and 35 °C, respectively.     

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.     

Biodegradation of indole by a newly isolated Cupriavidus sp. SHE

Indole, a typical nitrogen heterocyclic aromatic pollutant, is extensively spread in industrial wastewater. Microbial degradation has been proven to be a feasible approach to remove indole, whereas the microbial resources are fairly limited. A bacterial strain designated as SHE was isolated and found to be an efficient indole degrader. It was identified as Cupriavidus sp. according to 16S rRNA gene analysis. Strain SHE could utilize indole as the sole carbon source and almost completely degrade 100 mg/L of indole within 24 hr. It still harbored relatively high indole degradation capacity within pH 4–9 and temperature 25°C–35°C. Experiments also showed that some heavy metals such as Mn^2 +, Pb^2 + and Co^2 + did not pose severe inhibition on indole degradation. Based on high performance liquid chromatography–mass spectrum analysis, isatin was identified as a minor intermediate during the process of indole biodegradation. A major yellow product with m/z 265.0605 (C₁₅H₈N₂O₃) was generated and accumulated, suggesting a novel indole conversion pathway existed. Genome analysis of strain SHE indicated that there existed a rich set of oxidoreductases, which might be the key reason for the efficient degradation of indole. The robust degradation ability of strain SHE makes it a promising candidate for the treatment of indole containing wastewater.     

烟嘧磺隆降解菌SY-6的固定化、降解特性及其工程化应用

以海藻酸钠为载体,对烟嘧磺隆降解菌SY-6进行细胞固定化,通过单因素实验明确了菌株包埋SY-6的最优条件,并对其降解特性进行研究。结果表明,当海藻酸钠含量为4%,Ca Cl2含量为3%,固化时间为4 h,制得的固定化小球具有较强的机械强度和较好的传质性能及其对烟嘧磺隆的降解率较高。固定化细胞降解烟嘧磺隆的最佳条件为p H为7.0、温度为30℃、包菌量为5%。在不同p H或温度下,与游离细胞相比,固定化细胞有较宽泛的耐受性。将包埋的SY-6投加到序批式反应器(简称SBR)中处理烟嘧磺隆废水,结果表明,菌株SY-6在合适的使用周期内稳定性较高且对烟嘧磺隆废水降解效果较好,为烟嘧磺隆固定化细菌的工程化应用奠定了基础。     

n(NO3--N)/n(NO2--N)对混培养菌与纯培养菌同步脱氮除硫的影响

在温度30℃、pH为7、硫氮比为5/3、厌氧条件下,对比研究了不同n(NO-3-N)/n(NO-2-N)对荧光假单胞菌和铜绿假单胞菌混培养菌同步脱氮除硫影响.随着n(NO-3-N)/n(NO-2-N)减小,荧光假单胞菌、铜绿假单胞菌对NOx-N去除率逐渐增高,而S2-去除率却依次减少,混培养菌对NOx-N去除效率先增加后趋于平稳.n(NO-3-N)/n(NO-2-N)对混培养菌去除S2-几乎没有影响.荧光假单胞菌能迅速将NO-3-N转化为NO-2-N,但NO-2-N转为N2却相对缓慢,培养液中出现NO-2-N累积;而铜绿假单胞菌将NO-2-N还原N2的能力明显比荧光假单胞菌强,培养液未反应的NOx-N以NO-3-N为主,未出现NO-2-N累积.混培养菌对NOx-N转化的情况介于荧光假单胞菌与铜绿假单胞菌之间.荧光假单胞菌同时获得较高NOx-N、S2-去除的n(NO-3-N)/n(NO-2-N)为5/5,铜绿假单胞菌为10/0,混培养菌为5.0/5.0.混培养菌对NOx-N、S2-的同步去除效果优于单菌株荧光假单胞菌和铜绿假单胞菌.     

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.