棉枯萎抗性定向培育对棉籽球蛋白与棉紫素的影响

研究了同源的抗枯萎病品种西农87岱16抗和感枯萎病品种原岱16棉花种子的生化成分及其性质差异.结果表明,抗病性不同的两类品种的种子球蛋白的种类,不同分子量球蛋白的合成比率及次生代谢物棉紫素的含量都有较大变化.本项研究结果支持定向培育法是一种科学的棉花抗病育种方法.     

茶树病程相关蛋白基因CsPR5的克隆及表达分析

为探究茶树中病程相关蛋白5(pathogenesis-related protein 5,PR5)在茶树中的功能,采用cDNA末端快速扩增(rapid amplification of cDNA end,RACE)技术克隆了PR5基因的全长;通过荧光定量PCR方法检测了CsPR5在龙井43茶树不同组织部位、植物激素(茉莉酸、乙烯利和水杨酸)处理、茶炭疽病菌Colletotrichum camelliae侵染和小贯小绿叶蝉Empoasca onukii为害后的表达特征。结果表明,CsPR5基因开放阅读框为843 bp,编码281个氨基酸。CsPR5基因在茶树根、茎、嫩叶、花和种子5个组织中的相对表达量分别为0.187、3.093、0.928、0.045和0.012,且五者之间差异显著,主要在茎和叶中表达,其分别为根中相对表达量的16.54倍与4.96倍。水杨酸处理6 h及乙烯利处理6、12 h后,茶树CsPR5基因的相对表达量分别为1.622、2.344和1.845,分别比对照显著上调2.20倍、3.18倍和2.35倍;但是外施茉莉酸对茶树CsPR5基因的相对表达量无影响。茶炭疽病菌侵染显著诱导了茶树CsPR5基因的相对表达量,处理后的相对表达量为1.977,是对照的1.90倍;小贯小绿叶蝉取食显著抑制了其为害部位CsPR5的相对表达量,为7.273,仅为对照的38.80%,但该诱导不具系统性。     

日粮中添加不同有机酸对肉鸡生产性能的影响

选择体重相近、健康的1日龄罗曼肉用雏120只,在基础日粮中分别添加0.2%柠檬酸、乳酸和延胡索酸,观察有机酸对肉鸡生产性能的影响。结果表明:在22～42日龄,添加柠檬酸组和延胡索酸组采食量均比对照组显著增加(P<0.05);在1～21日龄及全期,添加柠檬酸组日增重比对照组显著增加(P<0.05),在22～42日龄添加柠檬酸组日增重比对照组和添加乳酸组有显著增加(P<0.05);3种有机酸对料肉比指标影响有下降趋势,但均未达到显著水平(P>0.05)。     

黄嘌呤氧化酶传感器的研制及其对鱼鲜度的检测

将黄嘌呤氧化酶以共价连接法固定于二醋酸纤维素薄膜上，制成的酶膜与极谱式氧电极共同组成对次黄嘌呤进行定量测定的黄嘌呤氧化酶传感器。该传感器测定范围为１０～１２０ｍｇ／Ｌ，响应时间１０ｓ，不同浓度次黄嘌呤标准溶液对传感器１０ｓ响应值的相关系数为γ＝－０．９９６６，次黄嘌呤标准溶液重复测定６０次（１０ｓ响应值）的变异系数为ＣＶ＝０．３０３％。应用该传感器与分光光度法对鱼体次黄嘌呤含量进行了测定比较，二者具有良好的相关性。     

Immunomodulatory effect of γ‐irradiated Astragalus polysaccharides on immunosuppressed broilers

In this study, we irradiated Astragalus polysaccharides (APS) using 25 kGy ⁶⁰Co γ ray to obtain γ‐irradiated Astragalus polysaccharides (IAPS) and then investigated the effects of IAPS on growth performance and immune function of cyclophosphamide (CPM)‐treated broilers. The physicochemical properties of APS and IAPS (molecular weight, water solubility, viscosity, morphological and structural properties) were evaluated. Then, 384 one‐day‐old Arbor Acres broiler chicks with similar initial weight were randomly assigned into 6 groups: the non‐treated group (control), and CPM‐treated groups were fed either a basal diet or the diets containing 900 mg/kg APS, or 900, 600, 300 mg/kg IAPS, respectively. On days 16, 18, and 20, all broilers except for the control group were intramuscularly injected with 0.5 ml CPM (40 mg/kg·BW). Broilers in the control group were intramuscularly injected with 0.5 ml sterilized saline (0.75%, wt/vol). This trial lasted for 21 days. The physicochemical treatment showed that γ irradiation could decrease the molecular weight and viscosity, and increase the water solubility of APS (p < 0.05), whereas the structural properties of APS was not affected. In the animal trial, 900 mg/kg APS or 900, 600 mg/kg IAPS relieved the decreased growth performance, thymus index, T lymphocytes proliferation, serum IgG concentration, NOS activity and the increased blood heterophil:lymphocyte ratio in CPM‐treated broilers (p < 0.05). CPM‐induced decreases in B lymphocytes proliferation and serum IgM concentration were only increased by IAPS at 900 mg/kg (p < 0.05). Overall, both APS and IAPS alleviated CPM‐induced immunosuppression. Especially, IAPS possessed better immunomodulatory effect than APS, indicating that γ irradiation could be used as an effective method to enhance the immunomodulatory activity of APS.     

表达马立克氏病病毒CVI988／Rispens株糖蛋白B基因的重组鸡痘病毒疫苗的免疫保护研究

用鸡痘病毒载体表达马立克氏病病毒（MDV）糖蛋白B（gB）基因构建成重组鸡痘病毒（rFPV）。以MDV　GA或Md5和RBIB混合攻毒，在不同品种的鸡中评价rFPV－gB／R单价苗和与火鸡疱疹病毒（HVT）组成的二价苗的免疫保护效力。试验结果表明，MDV疫苗和FPV母源抗体阴性的SPF鸡和母源抗体阳性的商品鸡中，rFDV－gB／R均能提供免疫保护作用，且其中一种商品蛋鸡中rFPV－gB／R与HVT液氮苗或HVT冻干苗结合使用，均有显著的免疫协同保护作用。免疫学研究指出，rFPV－gB／R与常规疫苗一样，可显著地降低疫苗免疫攻毒鸡的病毒血症和羽囊排毒。     

小麦水分和装满度对磷化氢吸附率的影响

在小麦含水量分别为9.3%、12.6%和14.4%,装满度分别为100%、70%、50%、30%和0%,气体浓度为100mL/m3和400mL/m3的条件下,测定小麦对磷化氢的吸附率,结果表明小麦对磷化氢的吸附率随着粮食水分增加,磷化氢浓度和装满度增大有不同程度增加.在药量较大的施药初期和装满度大时,检测到的磷化氢浓度高于设定浓度,磷化氢浓度、小麦水分和装满度较低时,小麦对磷化氢的吸附较容易达到平衡.     

梨不同砧穗组合光合特性

 用CIRAS-1 便携式光合作用测定系统研究了豆梨(Pyrus betulaefolia Bunge) 、杜梨(P.calleryana Dcen.) 幼树以及豆梨、杜梨与砂梨(P. pyrifolia Nakai) 品种丰水、新高4 种砧穗组合幼树叶片的光合作用。结果表明, 砧木显著影响栽培品种的光合作用, 杜梨比豆梨以及以杜梨为砧木的丰水、新高幼树比以豆梨为砧木的两品种幼树叶片净光合速率(Pn) 、表观量子产量(Φi) 、羧化效率(CE) 、水分利用效率(WUE) 高。新高的Pn、Φi 、CE 和WUE 值较丰水高, 且在两种砧木上均表现出同样的结果。     

猪圆环病毒2型GD株ORF2基因的序列分析

根据GenBank中猪圆环病毒2型（PCV2）0RF2基因序列，设计一对引物，应用PCR从本室鉴定分离的PCV2 GD株的细胞培养物中扩增出ORF2基因（702bp）。将此基因片段克隆入pMD18-T载体，筛选获得重组质粒pMD—ORF2并对其测序，结果表明所克隆的ORF2基因与其他PCV2的0RF2基因核苷酸序列同源性在92．1％～99．9％之间，推导的氨基酸序列同源性在90．2％～99．5％之间。     

Crop milk protein is synthesised following activation of the IRS1/Akt/TOR signalling pathway in the domestic pigeon (Columba livia)

1. The experiment was conducted to study whether insulin receptor substance 1 (IRS1) / Protein kinase B (Akt)/target of the rapamycin (TOR) signalling pathway activation stimulates crop milk protein synthesis in the domestic pigeon (Columba livia).

2. Crop milk was collected from ten 1-d-old squabs and analysed for nutrient content. During the non-breeding period and the first day of lactation, blood samples were collected from 5 pairs of breeding pigeons and the levels of prolactin and insulin were determined.

3. Crop samples were collected from 5 pairs of breeders at d 14 and 16 of the incubation period and d 1, 3 and 7 of the lactation period. Crop samples were evaluated for changes in crop weight and thickness and changes in the expression patterns of IRS1/Akt/TOR signalling pathway–related proteins.

4. The results demonstrated that prolactin induces a gradual increase in the relative weight and thickness of the crop, with crops reaching a maximum size at the third day of lactation.

5. Pigeon crop milk contains 64.1% crude protein and 29.7% crude fat based on dry weight.

6. Serum prolactin and insulin levels in the lactation period were significantly higher than those in the non-breeding period. Compared with non-breeding pigeons, the expression of the phosphorylated IRS1 phosphorylated Akt, phosphorylated TOR, phosphorylated ribosomal protein S6 kinase, phosphorylated S6, phosphorylated eukaryotic initiation factor 4E binding protein 1 and eukaryotic initiation factor 4E were significantly up-regulated in the crop of pigeons in the lactation period.

7. In conclusion, prolactin might induce changes in crop tissue and form the physiological structure for crop milk synthesis. Furthermore, the synthesis of crop milk protein is regulated by activation of the IRS1/Akt/TOR signalling pathway.