设施菜田不同施氮处理对硝酸盐迁移和积累的影响

在设施菜地条件下,研究了氮肥减施及配施抑制剂处理在黄瓜生长期对土壤NO3--N迁移累积的影响。结果表明,氮肥减施处理可显著降低土壤表层和整个土体的NO3--N含量。常规施氮量时0~40 cm土层的NO3--N含量均高于其它处理,减氮30%后0~40 cm土层未出现NO3--N显著积累现象;氮肥配施抑制剂处理不同程度降低了土壤NO3--N含量,且抑制硝态氮向下层土壤淋失,其中抑制剂组合的效果最好。氮肥配施抑制剂,可以有效控制NO3--N在土壤和植物体内的过量累积,减少硝态氮淋溶损失。     

荞麦中2种重要的功能性蛋白cDNA片段克隆与序列分析

以乌克兰甜荞为材料提取总RNA,反转录后采用cDNA末端快速克隆技术(RACE)克隆蛋白酶抑制剂和硫氰酸生成酶基因的3′端序列,并采用生物信息学技术进行序列分析。结果表明:获得的蛋白酶抑制剂和硫氰酸生成酶的3′端基因序列片段长度分别为307 bp和372 bp,生物信息学分析结果表明所获得的蛋白酶抑制剂基因片段与GenBank上已发表的苦荞蛋白酶抑制剂同源性为67%,获得的硫氰酸生成酶基因片段与Gen-Bank上已发表的拟南芥硫氰酸生成酶的同源性为65%。     

许氏平鮋消化道中部分消化酶的研究

对许氏平 (Sebastesschlegeli)消化道内的 5种与消化吸收有关的酶进行分布和活性测定。结果表明 ,(1)肠道各段均具很高碱性磷酸酶活性 ,最适 pH为 9.7。食道和胃几乎没有碱性磷酸酶活性。 (2 )消化道各部位均含酸性磷酸酶 ,肠道活性最高 ,自幽门盲囊起依次递降。食道和胃酸性磷酸酶活性明显低于肠 ,胃和肠酸性磷酸酶的最适 pH均为 5 .3。 (3)肠道中羧酸酯酶活性明显高于胃 ,且 2者羧酸酯酶最适 pH差别较大 ,分别为 8.4和 6 .8。(4)胃蛋白酶活性明显高于肠道 ,胃蛋白酶最适pH为 2 .6 ,肠蛋白酶最适 pH为 9.4。 (5 )胃淀粉酶活性明显低于肠道 ,胃淀粉酶最适 pH为 4 .6 ,肠道淀粉酶最适pH为 7.0。这表明许氏平对蛋白质的初步消化在胃中进行 ,在肠中进一步消化和吸收 ,而对糖类和脂类的消化和吸收主要在肠道进行     

Purification and characterization of two anionic trypsins from the hepatopancreas of carp

SUMMARY: Two trypsins, designated as trypsin A and trypsin B, have been purified from the hepatopancreas of carp. The purification procedures consisted of ammonium sulfate fractionation, and chromatographies on DEAE-Sephacel, Ultrogel AcA54 and Q-Sepharose. Trypsin A was purified to homogeneity with the molecular mass of approximately 28 kDa, while trypsin B gave two close bands of 28.5 kDa and 28 kDa on sodium dodecylsulfate polyacrylamide gel electrophoresis both under reducing and non-reducing conditions. On native-PAGE, both trypsin A and trypsin B showed a single band. Trypsin A and trypsin B revealed optimum temperature of 40°C and 45°C, respectively, and shared the same optimum pH 9.0 using Boc-Phe-Ser-Arg-MCA as substrate. Both enzymes were effectively inhibited by trypsin inhibitors and their susceptibilities were similar. The NH₂-terminal amino acid sequences of trypsin A and trypsin B were determined to 37th and 40th amino acid residue, respectively. Their sequences were very homologous, but not identical to that of a trypsin-type serine proteinase from carp muscle and these of other trypsins. Immunoblotting test using the antibody raised against trypsin A cross-reacted with trypsin B positively.     

Effect of human tissue factor pathway inhibitor gene transfection in vein grafts on thrombus formation and early patency rate

AIM: To reduce thrombus formation after coronary artery bypass graft,we investigated the antithrombotic effect of human tissue factor pathway inhibitor (TFPI) gene delivery on vein grafts. METHODS: The eukaryotic expressed plasmid vector pCMV-(Kozak)TFPI was constructed. Through pressurizing infusion,vein endotheliocytes were transfected with cationic liposome containing the plasmid vector pCMV-(Kozak)TFPI. After operation, vein grafts were harvested at third day for immunohistochemical, RT-PCR and Western blotting analysis of exogenous gene expression and for observation of thrombus formation by pathological method and scanning electron microscopy. At 30th days, the patency rate was recorded by vessel Doppler ultrasonography. RESULTS: Human TFPI mRNA and protein were detected in TFPI gene transferred vein grafts. Thrombosis was found in 8 animals of empty plasmid control group and in 7 animals of empty control group, but in only 1 of the TFPI group (P<0.05). Thirty days after operation, 5 vein grafts were occluded in both empty plasmid control group and empty control group, but none of vein grafts were occluded in TFPI group (P<0.05). The endothelial surfaces of the vein grafts in both control groups were covered with aggregated erythrocytes and platelets, but not in TFPI group. CONCLUSION: Human tissue factor pathway inhibitor gene transfection reduces thrombus formation and improves early patency rate in vein grafts.     

不同类型添加材料在新型肥料生产中的应用

就目前新型肥料研制过程中所选用的添加材料或包膜材料进行了归类划分,并对高表面活性矿物、高分子聚合物、抑制剂等材料的化学性质、与肥料养分离子相互作用机理等进行了分析和阐述。分析了不同材料对肥料的溶出速率或释放速率的影响,从提高营养元素有效性和生态环境建设方面讨论了这些材料的应用前景。     

Efficacy of various concentrations of synthetic hormones on the induced breeding of Channa marulius (Sole)

A study was conducted to determine the artificial breeding response, embryonic and larval development of giant snakehead, Channa marulius, with the application of various dosages of stimulatory hormones: Suprefact® (LHRH) agonist and Ovaprim® (GnRH + dopamine inhibitor). First and second hormonal dosages of Suprefact® (diluted) and Ovaprim® (0.3, 0.4, and 0.5 ml for male and 0.8, 0.9, and 1.0 ml for females per kilogram body weight) were used. There were three treatments T₁, T₂, and T₃ and each treatment had three replicates. Male fish were treated with T₁ (0.3), T₂ (0.4), T₃ (0.5) ml kg⁻¹ of body weight while female fish with T₁ (0.8), T₂ (0.9), T₃ (1.0) ml kg⁻¹ of body weight. The results showed that fish stimulated with T₃ (1.0) obtained better fecundity rate (2951.7) followed by T₂ (0.4) (2678.3), while the lowest fecundity (466.7) was recorded in T₁. The numerically higher values of gonado-somatic index (males and females) and fertilization rate appeared in T₂. The highest survival rate (97.1%) was found in T₃ followed by T₂ (97.0%), while the lowest (32.2%) in T₁. In conclusion, the application of Suprefact® and Ovaprim® at 0.4 and 0.5 ml kg⁻¹ body weight for male and 0.9 and 1.0 ml kg⁻¹ for female fish successfully stimulated snakehead fish induced breeding.     

A review of cyanobacterial odorous and bioactive metabolites: Impacts and management alternatives in aquaculture

Increased demand has pushed extensive aquaculture towards intensively operated production systems, commonly resulting in eutrophic conditions and cyanobacterial blooms. This review summarizes those cyanobacterial secondary metabolites that can cause undesirable tastes and odors (odorous metabolites) or are biochemically active (bioactive metabolites) in marine and freshwater, extensive and intensive aquaculture systems. For the scope of this paper, biochemically active metabolites include (1) toxins that can cause mortality in aquaculture organisms or have the potential to harm consumers via accumulation in the product (hepatotoxins, cytotoxins, neurotoxins, dermatoxins, and brine shrimp/molluskal toxins), (2) metabolites that may degrade the nutritional status of aquaculture species (inhibitors of proteases and grazer deterrents) or (3) metabolites that have the potential to negatively affect the general health of aquaculture species or aquaculture laborers (dermatoxins, irritant toxins, hepatotoxins, cytotoxins). Suggestions are made as to future management practices in intensive and extensive aquaculture and the potential exposure pathways to aquaculture species and human consumers are identified.