种植结构调整后,农民如何选种

种植结构调整后,即提高了农民的种植热情,也增加了农民的经济收入,但在实际生产中,却发现农民在购种中存在一些问题. 一是片面追求新品种:     

应用喷雾干燥血浆蛋白粉AP920控制猪断奶后多系统衰竭症

目前,猪断奶后多系统衰竭综合症(PMWS)已成为全球养猪业最关注的问题之一。由于PMWS具有传播范围广泛,不同日龄的猪群均存在一定比例的发病率,且患病群猪的死亡率和淘汰率相当高等特点,因而给全球的养猪业造成了严重的危害和经济损失。然而,目前尚未成功研制出能够有效预防和控制PMWS的疫苗。喷雾干燥血浆蛋白(SDP)含有大量活性蛋白,具有抗细菌和抗病毒的功能。很多研究表明,日粮中添加血浆蛋白能够显著提高断奶仔猪的生长性能和免疫机能,但SDP对PMWS的控制效果如何尚未见报道。因此,美国蛋白质公司(APC,INC)在巴西专门研究了喷雾干燥血浆蛋白粉AP920对PMWS的控制作用,结果表明,日粮和饮水中添加AP920可以有效控制PMWS。     

动物血浆蛋白的应用及选择

喷雾干燥动物血浆蛋白粉(Spray-driedanimalplasma/SDAP)在国内仔猪生产中的应用已近10年。血浆产品如何确保其生物安全性,国产血浆产品从生产工艺和质量控制上是否真正能够替代进口产品,如何去评价一个血浆产品业已成为市场和消费者最关心的问题。     

转基因八棱海棠与苹果品种亲和性的微嫁接早期鉴定

用微嫁接法鉴定嫁接亲和性的结果表明,不同培养基和培养方法对嫁接成活率和生根率有较大影响,生根 愈伤同步的方法可以同时获得较高的嫁接成活率和生根率。转番茄铁载体蛋白基因八棱海棠(Malus micromalus)与 苹果(Malus pumila)品种富士,嘎拉以及新红星嫁接成活率分别为93.33％,92.86％,73.34％。嫁接后15 d左右,接穗 新叶开始生长;嫁接后2个月,嫁接苗移栽成活率分别为73.07％,73.91％和55％;移栽后3个月,3种嫁接苗的茎杆 粗度均匀,无大小脚现象。初步结果显示,转基因八棱海棠与富士、嘎拉均具良好的嫁接亲和性,而与新红星的嫁接 亲和性稍差。     

不同化学物质打破葡萄、桃休眠的研究

以保护地栽培的葡萄、桃为试材,对氰氨类、细胞分裂素、赤霉酸和KNO3打破休眠的效果进行了研究。结果表明,1.5%单氰氨、11%石灰氮可明显促使葡萄提前萌芽,提早着色9-10d;50mg/LGA3和100mg/L6-BA对打破休眠基本无效。TDZ与单氰氨混用提高萌芽率的效果最好。在2个葡萄品种上,均没有观察到单氰氨或石灰氮处理对果穗或果实品质性状的不良影响。在华光油桃上,没有观察到化学物质对提早开花或成熟有明显的作用。对葡萄和桃上应用化学物质打破休眠的有关问题进行了讨论。     

某些阳离子在大豆胞囊线虫生防系统中的作用

室内测定了不同浓度的 6种阳离子 :钼、硼、锌、铜、锰和铁对大豆胞囊线虫卵的孵化、大豆种子发芽和根系生长 ,以及对线虫生防菌———厚垣轮枝菌菌丝生长的影响。结果发现 ,在供试所有浓度下 ,铜、锰和铁明显抑制大豆胞囊线虫的卵孵化 ,锌具明显刺激作用 ;在供试浓度水平较低时 ,铜、锰和铁对大豆种子发芽及根系生长有轻微抑制 ,锰的抑制较为明显 ,但均不影响进一步发育 ;在供试浓度较低时 ,铜、锰和铁对厚垣轮枝菌菌丝生长无任何影响。铜可作为线虫生防制剂的添加剂。     

双孢蘑菇子实体多糖的提取及单糖组成

从双孢蘑菇（Agarigus bisporus)子实体中提取多糖，提取率为0．65％，DEAE－Cewllulose-52柱层柱纯化了多糖，聚丙烯酰胺凝胶电泳显示一条带，为蛋白结合多糖，多糖水解液纸层析结果表明，多糖由D－果糖和D－葡萄糖构成。     

芽孢杆菌BC98-Ⅰ抗真菌物质的初步分离及特性

BC98-Ⅰ是一株分离自沤肥浸渍液的蜡状芽孢杆菌，对蔬菜、瓜类、花卉枯萎病具良好的防治效果。它分泌产生的抗真菌物质的粗提物对黄瓜、西瓜、青椒枯萎菌有很强的拮抗作用，当浓度为10mg／mL时，抑菌圈直径分别达到20．33、20．22和22．77mm。该粗提物对高温高压、紫外光和蛋白酶均不敏感。同时，它在中性偏碱(pH8～9)的条件下活性最高；在极性溶剂如水、甲醇、乙醇中溶解度大，抑菌活性高。粗提液经Sephadex G100层析后，得到了两个洗脱峰，活性物质存在于第一峰中。抑菌机制试验表明：它可造成孢子萌发率降低、菌丝生长形态异常、分支加剧并产生大量泡囊。     

Induction of tumor-specific cytotoxic T lymphocytes in vitro by dendritic cells pulsed with different glioma antigens

AIM: The goal of this study was to compare different methods for tumor antigen preparation, to observe the induction of tumor-specific cytotoxic T lymphocytes in rats by dendritic cells (DCs) pulsed with different tumor antigens. METHODS: The precursors of dendritic cells were isolated from bone marrow of rats, stimulated in vitro with recombinent rat granulocyte-macrophage colony-stimulating factor (rrGM-CSF) and interleukin-4 (rrIL-4). Then rat DCs were pulsed with C6 tumor cell antigens prepared with different methods: freeze-thaw, boiling or total protein extracted from ultrasonic crushed tumor cell. Subsequently primed DCs were cocultured with T lymphocytes isolated from spleen to induce CTL. Lymphocyte chemoattractant factor from DCs and cytokine IFN-γ release were determined by ELISA, the cytotoxicity of CTL was assayed by JAM test. RESULTS: DCs pulsed with boiled tumor cell in vitro induced an enhanced ability of T-cell proliferation and cytotoxic T lymphocyte activity.CONCLUSION: Our results demonstrated that DCs primed with boiled tumor cell may represent a method for inducing immune responses against the entire repertoire of tumor antigens of malignancies.     

Changes of MAPKs expression in rat hippocampal neurons after sleep deprivation

AIM: To explore the change and the possible role of MAPKs in rat hippocampus neuron after sleep deprivation. METHODS: The morphology of hippocampus neuron after sleep derivation was observed by TUNEL and HE staining, the activity of ERK was assayed by β-liquid scintillation counting and the expression of JNK was detected by Western blot. RESULTS: In paradoxical sleep deprivation (PSD) group, the number of apoptotic cells in hippocampus was increased. The scores of ERK activity were 1 764.00±941.56. Compared with control groups, the ERK activity was obviously decreased (P<0.05). The JNK expression was 87.5%, which was higher than that in control group. CONCLUSION: These results provide some important evidences that the sleep deprivation could cause changes in MAPKs activity, which may be related to the mechanism of hippocampus neuron apoptosis.