230 resultados para SP NOV.


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研究了不同Pb2+浓度(0.1、1、10、50、100、200、400 mg/L)处理对绿球藻(Chlorococcum sp.)生长、形态结构及生理特性的影响。与对照BG11培养的绿球藻比较,Pb2+浓度≤50 mg/L条件下培养的绿球藻细胞壁无明显增厚,色素变化不大;而暴露到Pb2+浓度>50 mg/L条件下培养,绿球藻细胞壁明显增厚,蛋白核消失。低浓度Pb2+(0.1~10 mg/L)对绿球藻生长基本没有影响;浓度在50 mg/L时,绿球藻仍能维持一定的生长速率;但当Pb2+浓度≥100 mg/L时

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二苯并呋喃(DF)是研究二英类化合物生物降解的模式化合物之一。本文报道了一种降解菌Janibacter sp.对活性污泥降解二苯并呋喃的强化作用,以及对其降解基因的分析结果。向反应器中添加5%的降解菌,与活性污泥共同作用,可在48h内将约56mg/L剂量的DF几乎完全降解,提高降解率28%以上。利用PCR方法,克隆和测序分析证明有DF降解基因丛的存在,并且发现以丰富培养基在高温下培养可去除该基因丛;丢失该基因丛的突变株同时失去利用DF作为唯一碳源进行生长的能力,显示其很可能位于一个大质粒上。

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CO2浓度提高时,微拟球藻吸收醋酸钠的速率增加2倍。混养生长的藻细胞最大光合作用速率、光合作用效率、无机碳半饱和常数和无机碳饱和的光合作用速率均显著低于光自养条件下生长的。

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以单细胞蓝藻聚球藻Synechococcussp.PCC7942为材料,利用甲基磺酸乙酯(EMS)进行化学诱变获得了一个高CO2 需求突变株。它能在 4%CO2 下生长而不能在空气中生长。对突变株的初检表明:其回复突变率约为 10 -7。该突变株从高CO2 条件下转到空气中后,细胞在 2~ 3d内逐渐趋于死亡;其光合作用对外源无机碳的依赖性高于野生型细胞,碳酸酐酶活性也低于野生型细胞。在超微结构水平,突变株细胞内出现了不同类型的异常羧体:有的为棒状;有的为不规则状;有的为 空羧体",而且,类囊体周围糖原颗

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将蓝藻培养于含 0 .0 5 mol/ L Na Cl的液体培养基 ,3d后细胞结构改变 ,出现无色透明区 .将此材料经溶菌酶处理形成原生质球 ,然后降低渗透压 ,原生质球破裂 ,液泡释放 .此液泡为极为标准的园球状 ,完全透明 ,泡体内无可辩物质 .电镜检查表明为一个单一膜所包围 ,泡内没有内囊体等细胞内物质 ,该膜亦显示典型三明治状单位膜结构 .

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在丝状蓝藻Anabaena sp.PCC7120细胞粗提液的碳酸酐酶(CA)分析中,发现了两种形式的CA活性.高CO_2下生长的细胞,在35μmol/L EZ(Ethoxyzolamide,碳酸酐酶的抑制剂)存在的情况下,CA总活性的85%左右被抑制,其半抑制浓度I_(50)为7.4μmol/L;随着EZ浓度的继续增加,CA活性在EZ浓度达到约150μmol/L处出现了第二个抑制峰,在250μmol/L处抑制程度达到最大,使CA总活性的15%被抑制,其半抑制浓度I_(50)为190μmol/L。在空气条件

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比较了红球藻HB748株在MCM,BBM及BG-11.3种培养基中的生长.结果表明:HB748在这3种培养基中前4d的平均生长速率分别为0.97d-1,0.77d-1和0.63d-1,存在显著差异;然而,在BBM和BG-11中添加MCM中所含等量VB12后,748株在3种培养基中的生长速率趋于一致,表明VB12,是HB748维持较好的前期生长的必需成分;在VB12的需求满足后.3种培养基无机组分的差异对HB748前期生长影响甚微.

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研究分析了混合鱼腥藻粉的营养成分,结果表明混合鱼腥藻粉蛋白质含量为40.5%;氨基酸组成符合联合国粮农卫生组织(FAO/WHO)规定的标准;并含有较丰富的糖类、脂肪酸、无机元素和色素。证实了鱼腥藻可以作为蛋白饲料资源开发和利用。

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用光合膜片增溶和SDS-聚丙烯酰胺凝胶电泳方法,从固氮蓝藻Anabaena sp.7120分离到7条色素带。迁移率较慢的五条叶绿素蛋白复合体带,具有相同的吸收光谱和室温荧光光谱特性。它们的红区最大吸收峰在676nm;蓝区最大吸收峰在438nm。它们的室温荧光发射最高峰在672—673nm;在710,732和740nm都有小峰。这些是CPⅠ叶绿素所特有的。我们认为这5条带都是属于光系统Ⅰ的叶绿素蛋白复合体。另一条迁移率稍快的叶绿素蛋白复合体带为CPⅡ。它的红区最大吸收峰在672nm;蓝区最大吸收峰在436n

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本文报道了血腥藻(Anabaena spp.)的一种异常生长现象和从鱼腥藻中分离得到的柄杆菌1017—41株的生物学特性。此菌株除具有柄杆菌特有的形态和发育周期外,还出现分叉状和长的分节状菌体,与已有记载的柄杆菌明显不同,故定为柄杆菌属(Caulobacter)的一个新种,命名为多态柄杆菌(Caulobacter polymorphus nov.sp.)。

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Pseudomonas sp.CTP-01的对硫磷水解酶具有底物诱导合成性质。停滞生长期的细胞接触底物半小时即产生相应酶的合成,而指数生长期的细胞接触底物48小时后才发生酶的合成。甲基对硫磷及对硝基酚也具有诱导作用,可见合成对硫磷水解酶的诱导特异基团可能与对硝基酚及其苯环上的取代基有密切关系。

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本文首次报导了武汉市郊区三带喙库蚊(Culex tritaeniorhynchus)孑孓体内寄生等索线虫(Isomermis sp.)的生活史。等索线虫在6月至9月份对宿主的寄生率的幅度为5%~48%。等索线虫一年内可发生多代,当气温在26°~33℃时,完成一代生活史的周期为22~28天;并成功地进行了室内人工感染;此外就等索线虫对宿主的感染强度,寄生部位;雌雄性比等问题也进行了初步的研究。

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Khawia saurogobii n. sp. is described from the intestine of the cyprinid fishes Saurogobio dabryi and Saurogobio dumerili in China. The new species belongs to the Lytocestidae and is placed in Khawia because of its afossate scolex, vitelline follicles in the cortical parenchyma, uterus not looping anterior to the cirrus sac, gonopores separate but close together in distinct genital atrium, external seminal vesicle absent, and postovarian follicles present. The new species differs from other congeneric species by the shape of the body markedly tapering posteriorly from the end of the anterior third, the shape of the scolex that is very short and markedly wider than the neck, spatulate without incisions, but shallow superficial grooves, vitelline follicles and testes starting immediately posterior to the scolex, and an ovary with long, posterior arms bent medially, thus giving the shape of an inverted A.

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In Synechocystis sp. PCC 6803, gene sll1384 encodes a protein with a DnaJ domain at its N-terminal portion and a TPR domain at the C-terminal portion. An sll1384 mutant shows no difference from the wild type in adaptation to different temperatures, but almost completely loses its capability of phototactic movement. After complementation with sll1384, the mutant regains the phototaxis. As shown with electron microscopy, on the cell surface, mutant cells have pili that appear to be the same as that of the wild type. Also, the transformation efficiency remains unchanged in the mutant. It is postulated that Sll1384 regulates phototaxis of Synechocystis through protein-protein interaction. It is the first DnaJ-like protein gene identified in a cyanobacterium for a role in phototaxis.

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Iron deficiency can induce cyanobacteria to synthesize siderophore receptor proteins on the outer membrane to enhance the uptake of iron. In this study, an outer membrane of high purity was prepared from Anabaena sp. PCC 7120 based on aqueous polymer two-phase partitioning and discontinuous sucrose density ultra-centrifugation, and the induction of outer membrane proteins by iron deficiency was investigated using 2-D gel electrophoresis. At least. five outer membrane proteins were newly synthesized or significantly up-regulated in cells transferred to iron-deficient conditions, which were all identified to be siderophore receptor proteins according to MALDI-TOF-MS analyses. Bacterial luciferase reporter genes luxAB were employed to monitor the transcription of the encoding genes. The genes were induced by iron deficiency at the transcriptional level in different responsive modes. Luciferase activity expressed from an iron-regulated promoter may be used as a bioreporter for utilizable iron in natural water samples. (C) 2009 National Natural Science Foundation of China and Chinese Academy of Sciences. Published by Elsevier Limited and Science in China Press. All rights reserved.