不适宜生长条件对混菌降解苯胺的影响

分别从台州和衢州某化工厂的好氧池中分离筛选得到2株苯胺降解菌TZ1和JH1,经16S rDNA测序鉴定为Comamonas sp.TZ1和Pseudomonas sp.JH1,均具有较强的苯胺降解能力,培养24 h后,可使初始浓度为800 mg/L的苯胺去除率达到96.4%~98.4%。在此基础上,按体积比1∶1将2株菌液进行混合构建了混合菌体系,进而对比考察了苯胺初始浓度、pH、盐度和重金属等环境因子对单一菌和混合菌生长量及降解苯胺效果的影响,重点探讨混合菌对不适宜生长环境的适应性及其对苯胺的降解特性。通过单一菌和混合菌对比实验发现,在适宜苯胺初始浓度、pH和盐度条件下,混合菌的生长量略高于单一菌;在不适宜生长的高浓度苯胺、pH和盐度条件下,混合菌也表现出了更强的适应性和苯胺矿化能力。Zn2+和Cr6+耐受实验则表明,对于Cr6+,混合菌表现出了更强的耐受能力,而对于Zn2+并没有表现出更强的耐受能力。     

Shewanellasp．XB缺氧反硝化降解苯酚

苯酚的生物降解一直受到关注。以苯酚为惟一电子供体,研究了Shewanellasp．XB对苯酚的缺氧降解特性。研究结果表明,在反硝化条件下,当C／N为13．3时,苯酚可以完全降解,NO2--N积累量很少。另外,当加入氧化还原介体,如核黄素3μmol／L、AQDS0．01mmol／L、AQS0．05mmol／L和LQ0．01mmol／L时,苯酚降解速率分别为不加介体时的1．45、1．77、1．67和1．63倍。当以氯化铵代替硝酸盐时,苯酚也能进行厌氧发酵降解。另外,菌株XB反硝化降解苯酚可能是厌氧和好氧降解的混合过程。     

Shewanella sp.XB缺氧反硝化降解苯酚

苯酚的生物降解一直受到关注。以苯酚为惟一电子供体,研究了Shewanella sp.XB对苯酚的缺氧降解特性。研究结果表明,在反硝化条件下,当C/N为13.3时,苯酚可以完全降解,NO-2-N积累量很少。另外,当加入氧化还原介体,如核黄素3μmol/L、AQDS 0.01 mmol/L、AQS 0.05 mmol/L和LQ 0.01 mmol/L时,苯酚降解速率分别为不加介体时的1.45、1.77、1.67和1.63倍。当以氯化铵代替硝酸盐时,苯酚也能进行厌氧发酵降解。另外,菌株XB反硝化降解苯酚可能是厌氧和好氧降解的混合过程。     

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。     

Fenton (H2O2/Fe) reaction involved in Penicillium sp. culture for DDT [1,1,1-trichloro-2,2-bis(p-chlorophenyl)ethane)] degradation

The purpose of this work was to demonstrate that a Fenton (H₂O₂/Fe) reaction was involved in DDT [1,1,1-trichloro-2,2-bis(p-chlorophenyl)ethane)] degradation in a culture of Penicillium sp. spiked with FeSO₄. A commercial DDT mixture (10% DDE [1,1-dichloro-2,2-bis(p-chlorophenyl)ethylene], 30% o,p-DDT and 60% of p,p′ -DDT) of 10 mg L^{? 1} was used. Hydrogen peroxide (H₂O₂), tartaric acid and oxalic acid were identified at 18 h in culture media, with and without added DDT; this correlated positively with lowering of pH from 5.8 to 2.7. Lower concentrations of oxalic acid and H₂O₂ (7.9 and 52.6 mg L^{? 1}, respectively) occurred in media with DDT at 30 h, in comparison to that one without DDT mixture (27.9 and 65.3 mg L^{? 1}, respectively), at this time there was maximum degradation (87.7, 91.7 and 94.2%) for DDE, o,p-DDT and p,p′-DDT, respectively. We propose that the degradation of the DDT mixture by Penicillium sp. was through a Fenton reaction (H₂O₂/Fe) under acidic conditions produced in situ during the fungal culture amended with FeSO₄.     

氮源对克雷伯氏菌NⅢ2分泌絮凝剂特性的影响

实验研究了蔗糖为碳源,硝酸钠、脲、蛋白胨、硫酸铵和氯化铵等氮源对NⅢ2发酵产絮凝剂的影响。结果表明,发酵液起始pH值为7.50,以硝酸钠为氮源,发酵液pH会上升,升至7.60～8.34时,NⅢ2菌株开始大量分泌微生物絮凝剂,发酵72 h,产量可达7.5 g/L,该产量是目前报道的克雷伯氏菌产絮凝剂的最高值。脲为氮源,pH则下降,降至5.04～6.49时,大量分泌絮凝剂,发酵72 h产量达5.2 g/L。蛋白胨、氯化铵和硫酸铵等为氮源时,pH下降十分明显,pH小于3.71时有絮凝剂分泌,发酵72 h产量约2.0 g/L或更小。以硝酸钠和脲为氮源时,发酵液中有黄色物质分泌,该黄色物质出现或黄色逐渐加深,是NⅢ2菌高产絮凝剂的标志。除硫酸铵外,其他氮源发酵所产絮凝剂为O-糖蛋白。当以硝酸钠、脲、蛋白胨、硫酸铵和氯化铵为氮源时,絮凝剂中蛋白的含量分别为9.55%、33.28%、19.39%、13.81%和15.51%,且蛋白含量越高,絮凝剂活性越大。     

Effects of a gradually increased load of fish waste silage in co-digestion with cow manure on methane production

This study examined the effects of an increased load of nitrogen-rich organic material on anaerobic digestion and methane production. Co-digestion of fish waste silage (FWS) and cow manure (CM) was studied in two parallel laboratory-scale (8 L effective volume) semi-continuous stirred tank reactors (designated R1 and R2). A reactor fed with CM only (R0) was used as control. The reactors were operated in the mesophilic range (37 °C) with a hydraulic retention time of 30 days, and the entire experiment lasted for 450 days. The rate of organic loading was raised by increasing the content of FWS in the feed stock. During the experiment, the amount (volume%) of FWS was increased stepwise in the following order: 3% – 6% – 13% – 16%, and 19%. Measurements of methane production, and analysis of volatile fatty acids, ammonium and pH in the effluents were carried out. The highest methane production from co-digestion of FWS and CM was 0.400 L CH4 gVS^?1, obtained during the period with loading of 16% FWS in R2. Compared to anaerobic digestion of CM only, the methane production was increased by 100% at most, when FWS was added to the feed stock. The biogas processes failed in R1 and R2 during the periods, with loadings of 16% and 19% FWS, respectively. In both reactors, the biogas processes failed due to overloading and accumulation of ammonia and volatile fatty acids.     

沙雷氏菌发酵蓝藻生产蛋白酶

以富含蛋白质的蓝藻作有机氮源进行微生物发酵生产蛋白酶,为蓝藻的资源化利用提供一条新途径。采用单因素实验,研究了影响沙雷氏菌发酵蓝藻生产蛋白酶的培养基主要成分。结果发现,在实验范围内,沙雷氏菌发酵蓝藻生产蛋白酶的最佳碳源是蔗糖,最佳速效氮源是尿素,最佳金属离子(盐)是ZnSO4,最佳产酶促进剂是吐温80。在单因素实验中,发酵上清液的蛋白酶活最高可达到941 U/mL,而且发酵周期短,发酵培养18 h即可达到最高酶(活)值。     

Effects of dissolved inorganic carbon and nutrient levels on carbon fixation and properties of Thermosynechococcus sp. in a continuous system

The concept of CO₂ chemo-absorption by sodium hydroxide in a wet scrubber followed by microalgae cultivation was used as a means to reduce the major greenhouse gas. A thermophilic and alkaline tolerable cyanobacterium named Thermosynechococcus CL-1 (TCL-1) was cultivated in continuous system, with a carbonate-bicarbonate buffer as carbon source. The effects of dissolved inorganic carbon (DIC_in) and nutrient levels in influent on cell mass productivity, DIC removal efficiency, and alkaline solution regeneration by TCL-1 were investigated. The results show the highest cell mass productivity reaches 1.7 g L⁻¹ d⁻¹ under the highest DIC and nutrients level. Conversely, the best regeneration of alkaline solution proceeds from pH 9.5 to 11.3 under the lowest level. In addition, the highest ΔDIC (DIC consumption) and DIC removal efficiency are 42 mM and 43% at 113.2 and 57 mM DIC_in, respectively.     

Characterization of the first step involved in enzymatic pathway for microcystin-RR biodegraded by Sphingopyxis sp. USTB-05

Enzymes encoded by genes biodegrading microcystins (MCs) can help reveal the function of genes and biodegradation pathway of MCs. Here the first and important gene (USTB-05-A, 1,008 bp) involved in biodegradation of microcystin-RR (MC-RR) was cloned from Sphingopyxis sp. USTB-05 and firstly expressed in Escherichia coli BL21 (DE3) with an expression vector of pGEX4T-1 successfully. The nucleotide sequences of cloned USTB-05-A possessed 92.5% homology to that of mlA reported in Sphingomonas sp. strain ACM-3962. The deduced amino acid sequences containing the cleavage sites of 26th (alanine) and 27th (leucine) showed 83% identical to that of MlrA. The cell-free extract (CE) of recombinant E. coli BL21 (DE3) containing USTB-05-A had high activity for biodegrading MC-RR. Initial MC-RR of 40 mg L⁻¹ was completely biodegraded under total protein of 350 mg L⁻¹ within 0.25 h. A product derived from MC-RR appeared distinctly with the decrease of MC-RR peak on the profile of HPLC. The product (m/z 1056.5) had molecular weight of 18 higher than that of MC-RR (m/z 1038.7). The findings provided the positive evidences that biodegradation of MC-RR began with the breakage of cyclic MC-RR and then it was converted to linear MC-RR as the first product catalyzed by first enzyme of Sphingopyxis sp. USTB-05.