不同MLSS对低温低碳氮比污水处理效果的影响

利用SBR反应器驯化低温、低碳氮比活性污泥,经过30 d的驯化,活性污泥颜色由原来的深黑色、散状转变为浅色、絮状,考察不同MLSS对污水的处理效果并探讨基质降解动力学。结果表明:在进水COD和NH4+-N浓度一定的前提下,MLSS在3~4 g/L时,出水水质最好,COD的去除率达到97.1%,总氮的去除率达到63.1%。铵态氮降解过程符合Monod一级动力学方程Se/S0=e-KXt;拟合曲线的相关指数R为(-0.9548~-0.9856)。     

产广谱细菌素米酒乳杆菌C2发酵培养基的研究

为了提高米酒乳杆菌C2发酵产细菌素的水平,对发酵培养基的组成进行研究。采用琼脂扩散法,以金黄色葡萄球菌为指示菌,对发酵的基础培养基、碳源、氮源、无机盐和氨基酸对细菌素产生的影响进行研究,并确定最佳的培养基组成。实验结果表明：米酒乳杆菌C 2发酵产细菌素的最佳基础培养基为SL培养基,培养基中的碳源、氮源、无机盐及补加氨基酸对细菌素产生的影响显著。当培养基的组成为：葡萄糖20 g·L^-1,酵母浸粉25 g·L^-1,MgSO4.7H2O 0.38 g·L^-1,L-半胱氨酸1 g·L^-1,柠檬酸三铵2g·L^-1,乙酸钠2.5 g·L^-1,吐温80 1 ml.L-1时细菌素的产量最大,抑菌圈直径可达28.97 mm。     

新垦淡灰钙土微生物生物量碳、氮、磷及玉米产量的研究

通过设置在宁夏红寺堡灌区开垦4 a的淡灰钙土上的定位试验,研究了不同施肥对新垦淡灰钙土微生物生物量碳、氮、磷及玉米产量的影响。结果表明:各施肥处理可以明显提高土壤微生物生物量碳、氮、磷含量,不同处理相比,化肥配合羊粪效果最好,单施羊粪次之,单施化肥最低;与对照相比各施肥处理对玉米的增产效果极显著,各处理作用效果的排序为:氮磷 羊粪>氮磷锌钾>氮磷锌>氮磷>氮>羊粪>不施肥,氮磷 羊粪处理与单施氮肥和单施羊粪之间差异达极显著水平。化肥与有机肥羊粪配合施用既能显著增加土壤微生物生物量碳、氮、磷含量又能使玉米产量显著提高,因此是新垦淡灰钙土施肥的最佳选择。土壤微生物量碳与有机碳呈极显著正相关,与全氮呈显著正相关,表明其与土壤肥力关系密切,可作为评价新垦地土壤质量变化的生物学指标。     

一种用C18柱纯化低浓度微量寡核苷酸的新方法

通过比较4种不同的回收方法和C18硅胶4种不同的用量对回收的影响,提出了回收低浓度微量寡核苷酸的最佳方案:分别用1 mL乙腈、2 mL灭菌双蒸水和1 mL 10 mmol/L乙酸铵平衡装填10 mg硅胶的C18 Sep-Pak反相层析柱;再将寡核苷酸溶液通过C18柱;然后用1 mL 25 mmol/L碳酸氢铵洗脱C18柱,并以3000 r/m in离心2 m in;最后用1 mL 30%乙腈洗脱C18柱,将收集的溶液离心冻干后即得到纯化的寡核苷酸。该方法的回收率可达53.7%±3.0%。     

在草鱼免疫反应中莨菪佐剂性的初步观察

在草鱼免疫反应中莨菪佐剂性的初步观察赵建培（福州市郊区水产技术推广站，福州３５００１１）史维舟，陈昌福（华中农业大学水产学院，武昌４３００７０）已有研究报道指出，英若具有增强鱼类免疫力的作用［１］。但是，关于度著究竟是如何作用于鱼类的免疫系统，即为什...     

Effect of ischemia or hypoxia on vascular endothelial growth factor production in rat myocardium and its significance

AIM:To determine the relationship between ischemia, hypoxia and the production of vascular endothelial growth factor in rat myocardium and its basic mechanism. METHODS:(1) 28 Wistar rats were randomly divided into 4 groups: group A, normal control;group B, 1 day's acute myocardial infarction;group C, 3 day's acute myocardial infarction;group D, 7 day's acute myocardial infarction. (2) Rat cardiac myocytes cultured were primarily divided into some groups, hypoxia incubated 24 hours; PMA groups, hypoxia incubated 24 hours with PKC activator (PMA), A 0 ng/mL; B 10 ng/mL; C 100 ng/mL; D 1 000 ng/mL; Chelerythrine groups, hypoxia incubated 24 hours with PKC inhibitor (chelerythrine), A 0 nmol/L; B 10 nmol/L. (3) By computer scanned and quantitated, vascular endothelial growth factor (VEGF) protein was detected with immunohistochemical technique. RESULTS:The longer time of ischemia and hypoxia was, the higher the VEGF production.The relat ionship was found between the time of ischemia or hypoxia and the production of VEGF.The product ion of VEGF protein was further promoted by PMA with different concentrat ion, decreased by chelerythrine.CONCLUSION: Ischemia or hypoxia strongly stimulated the production of VEGF in myocardium, which played an important role in autoprotecting of ischemic or hypoxic myocardium. Hypoxia-induced PKC activation is one kind of basic mechanisms in this course.     

中华鲟ASDIGIRR与ASTRAF6基因的克隆与表达

中华鲟是处在硬骨鱼类与软骨鱼类之间的中国古老的珍稀鱼类之一,但在人工繁殖和养殖过程中,容易受到不同疾病的危害,因此,需要深入研究其免疫调控,为其疾病预防提供理论依据。单个免疫球蛋白白细胞介素-1受体相关分子(SIGIRR)和肿瘤坏死因子受体相关因子6(TRAF6)是toll样受体(TLR)信号通路的2个重要的信号转导元件。本研究鉴定了中华鲟的SIGIRR和TRAF6的同源物,分别命名为ASDIGIRR (Acipenser sinensis DIGIRR)和ASTRAF6 (A. sinensis TRAF6),并研究它们在正常组织中的表达和Poly(I:C)诱导后的表达模式。结果显示,ASDIGIRR和ASTRAF6在健康鲟的10个组织中均有表达,且分别在肠道和头肾组织中表达量最高;用Poly (I:C)孵育中华鲟脾脏细胞后,ASDIGIRR在3 h时的表达量显著下调,在6 h时恢复至正常水平,后在24 h显著上调达到最高值,随后开始下调,至48 h时仍显著高于对照组,而ASTRAF6在6 h达到最高表达量,维持到24 h后再下调,48 h时下降至最低水平。研究表明,ASDIGIRR和ASTRAF6在中华鲟抵御病原入侵的免疫防御过程中起着重要作用。     

A Case of Wound Botulism in a Foal Affected by Gastric Ulcers in Italy

The case of a 50-day-old Thoroughbred foal affected by sudden muscular weakness and failure to swallow associated with recumbency is described. The clinical picture suggested a diagnosis of botulism. At necropsy, nonglandular gastric mucosa presented deep ulcerations. No other macroscopic nor microscopic lesions were detected. Clostridium botulinum type B was isolated from the lesions of gastric mucosa, whereas the cecal and colonic content, assayed for both spores and toxins, were negative. Moreover, analyses of all potential environmental sources of toxins near the feeding areas were negative. It was concluded that the colonization of gastric ulcers may have contributed to this unusual case of botulism. To the best of our knowledge, this is the first case of botulism in horses reported in Italy, which is also the first case anywhere of wound botulism caused by infection of gastric mucosa lesions.     

The absorption, tissue distribution and excretion of enteraly administered alpha-ketoglutarate in rats

The absorption, tissue distribution and excretion of enteral alpha-ketoglutarate (AKG) was studied in four experiments. Six male Sprague Dawley rats were used to investigate the excretion of AKG in urine and faeces. Thirty rats, randomly assigned to five groups, were used to investigate the distribution of AKG in body tissues. They were gavaged with AKG enriched with 3 muCi/kg BW of (14)C uniformly marked AKG. Fourteen male Sprague Dawley rats were used to study the absorption of AKG (duodenum vs. ileum). Intestinal recovery of NaAKG vs. CaAKG was investigated in 36 rats. There was no significant excretion of non-metabolized AKG in the urine and faeces. There was no significant difference in the systemic levels of AKG when comparing the proximal to distal small intestine infusion. Up to 50%, 30% and 20% of gastrically delivered AKG was recovered in the stomach, 0.5, 1 and 2 h after gavage; the jejunal recovery achieved a maximum of 3%, 30 min after gavage, and was not detectable 2 h later. There was a relatively high distribution of (14)C-AKG in the tissues (e.g. liver, brain, bones, skin, muscles), 3 h after gavage, up to 70% of the administered dose. In conclusion, the high rate of retention of the carbon from AKG allows the postulation that there is a non-energetic mode of metabolism of intragastrically administered AKG. After conversion to final metabolites, AKG penetrates into all tissues and organs of rats, including the bone tissue. Intestinal absorption of AKG does not depend on the type of AKG salt administered.     

O型口蹄疫病毒P1-2A3C基因在家蚕杆状病毒表达系统中的表达

口蹄疫是一种严重危害畜牧业生产的烈性传染病。为了促进O型口蹄疫病毒(FMDV)基因工程活载体疫苗的研制,选取O型FMDV编码序列中的衣壳蛋白前体P1-2A基因和蛋白酶3C基因,插入家蚕杆状病毒转移载体pVL1393中,构建重组载体pVL-P1-2A3C,并与线性化病毒Bm-BacPAK6 DNA共转染家蚕BmN细胞,获得重组病毒Bm-P1-2A3C。将重组病毒感染家蚕5龄幼虫,以双抗体夹心ELISA法和间接血凝方法检测血淋巴中的表达产物:目的蛋白在感染病毒后120 h的蚕血淋巴中表达量最高,抗原表达呈阳性的最大稀释倍数为1∶128。结果显示O型FMDV的P1-2A3C基因已在家蚕体内获得表达。