山杏幼苗水分生理生态特性及凋萎湿度的研究

对山杏幼苗进行 3种施水量的水分培养和干旱处理。结果表明 :随施水量的减少 ,叶片的净光合速率、蒸腾速率、气孔导度和水分利用效率等指标都随之下降 ,叶片温度提高。 40 9.2和 1 89.2 mm施水量对山杏幼苗各项指标的影响呈显著差异 ,而 40 9.2和 32 1 .2 mm之间与 32 1 .2和 1 89.2 mm之间均无差异。随土壤干旱的加剧 ,山杏幼苗叶片的蒸腾速率和水势与土壤含水量呈规律性变化 ;当干旱持续 39天时 ,1 .44%的土壤含水量可视为山杏幼苗的凋萎湿度     

Characteristics in the secretion of liver TNF-α induced by infusion of LPS into veins in goats

AIM: To study the role of liver in immune regulation in experimental endotoxemia. METHODS: 17 castrated male goats were subjected to simultaneously installing catheters in jugular, hepatic and portal veins by surgery. Four days later, lipopolysaccharide (LPS) was infused in term of three groups as followings: In group ①, LPS of 20 EU (endotoxin unit, EU)·kg^-1 was infused into portal vein; In group ②, LPS of 20 EU·kg^-1 was infused into jugular vein and LPS of 1 500 EU·kg^-1 infused into jugular vein in group ③. Before and after infusion, blood samples were collected from the three veins through the catheters for 8 h.The plasma levels of TNF-α were measured by RIA. RESULTS: In group ①, the plasma TNF-α levels of hepatic and portal vein rose to peak value at 5 h, but that of the jugular vein did not changed. In group ②, the plasma TNF-α levels in hepatic vein rose to peak value at 3 h. The TNF-α levels of jugular vein rose to peak value at 1 h and the one in portal vein enhanced continuously between 0-8 h. In group ③, the plasma TNF-α levels in jugular, hepatic and portal vein rose to significant peaks at 1 h simultaneously. CONCLUSION: During experimental endotoxemia,liver showed different dynamic characteristics in TNF-α secretion according to the pathway and doses of LPS delivery.     

Effects of β-ME and RA on expression of GFAP in mesenchymal cells derived from mouse fetal liver

AIM: To investigate the effects of β-mercaptoethanol (β-ME) and all-trans rentinal acid (RA) on glial fibrillary acidic protein (GFAP) expression in mesenchymal cells derived from mouse fetal liver in vitro. METHODS: Cells suspension from 14.5-days-old mouse fetal liver were cultured in DMEM/HEPES/F12 supplemented with 20％ FCS and mesenchymal cells were acquired after discarding nonadherent cells. The 5th passage cells were induced by β-ME and RA. The characteristics of treated cells were assayed by immunocytochemistry staining at 5 hours and 5 days after induction. β-actin as an internal control, GFAP gene expression of mesenchyal cells was detected with semi-quantitative RT-PCR. RESULTS: After being inducted by β-ME and RA, 80％ approximately of the cells exhibited typical neural morphology and about 85％ expressed GFAP phenotype. Semi-quantitative RT-PCR showed that mRNA expression of GFAP increased in treated cells versus untreated cells (P<0.01). CONCLUSION: GFAP expression in mesenchymal cells derived from mouse fetal liver in vitro increases after being treated with β-ME and RA.     

Meiotic competence of mouse oocytes reconstructed by replacing the germinal vesicle with a male pronucleus and somatic nucleus

The present study examines the contribution of the nucleus to meiotic competence in mouse oocytes that were reconstructed using nuclear transfer. Three types of reconstructed oocytes were produced: MP‐GV, by transplanting the male pronucleus (MP) into germinal vesicle (GV) stage oocytes; 3T3‐GV, by transplanting the nucleus of a National Institute of Health (NIH) 3T3 cell into a GV stage oocyte; and 3T3‐MII, by transplanting the nucleus of an NIH 3T3 cell into a metaphase II (MII) stage oocyte. The fusion rates differed, but not significantly, in the MP‐GV, 3T3‐GV, and 3T3‐MII groups (77, 63, 56%, respectively). Then, meiotic competence was compared in MP‐GV, 3T3‐GV and non‐manipulated GV stage oocytes as a control. Nuclear envelope breakdown occurred in all the reconstructed oocytes, as well as the control ones. The percentage of first polar body extrusion differed between the MP‐GV (100%), 3T3‐GV (72%), and control (67%) groups. DNA staining with Hoechst 33342 revealed that in the MP‐GV‐group oocytes that had reached MII stage, the chromosomes were condensed and aligned in a regular array similar to the normal metaphase plate. By contrast, in 3T3‐GV group oocytes, the condensed chromosomes were irregularly scattered in the cytoplasm. These results suggest that the donor nucleus affects meiotic competence in reconstructed oocytes.     

猪胸膜肺炎放线杆菌外膜蛋白(OMP)5′末端保守区基因的克隆、表达及其免疫活性研究

以猪胸膜肺炎放线杆菌血清7型25-4株基因组DNA为模板,PCR方法扩增外膜蛋白(OMP)5′末端保守区基因片段(OMPc),酶切及核苷酸序列分析鉴定后,与原核表达载体质粒pGEX-6P-1进行连接,构建成重组表达载体pGEX-OM-Pc,转入大肠杆菌BL21中,以IPTG进行诱导,SDS-PAGE电泳分析发现,转化了重组质粒的菌株所表达的融合蛋白相对分子量为34 kD,与实际预测相符,命名为GST-OMPc.GST亲和层析柱进行纯化,ELISA方法对纯化蛋白进行检测.结果表明:纯化蛋白GST-OMPc能够与兔抗猪胸膜肺炎放线杆菌血清7型的阳性血清反应.OMPc蛋白的成功表达为其功能的研究打下基础.     

鸡抗球虫药的体外筛选综述

抗鸡球虫药的筛选分为体内筛选和体外筛选。体外筛选具有简易、迅速、准确和经济的优点。本文在前人大量工作的基础上，总结了体外筛选的全过程，并分述了细胞培养筛选法和鸡胚培养筛选法。     

草地土壤肥力及其营养管理的必要性

介绍了草地土壤肥力的来源,土壤基本养分对草地生产的作用,草地植物与动物对养分的需求量及缺乏症状,说明了加强草地营养管理以及维持草地生态系统营养平衡的重要性,指出增强对土壤肥力和营养管理是提高草地生产能力、保证草地生态系统平衡、保障草地可持续利用的关键技术措施.     

过氧化氢提高燕麦幼苗耐碱性的活性氧代谢和渗透调节

为探明过氧化氢(H₂O₂)提高燕麦耐碱性的作用,以‘定莜6号’幼苗为材料,采用珍珠岩栽培方法,在幼苗三叶一心期根部浇灌75 mmol·L^-1 NaHCO₃或添加二甲基硫脲(DMTU,H₂O₂淬灭剂)或抗坏血酸(ASA,H₂O₂清除剂)模拟碱胁迫,通过叶面喷施0.01 mmol·L^-1 H₂O₂来观测H₂O₂对碱胁迫下幼苗生长、活性氧代谢和渗透溶质积累的影响。结果表明:喷施H₂O₂ 能够缓解NaHCO₃胁迫对燕麦幼苗生长的抑制,降低幼苗叶片O2·-、H₂O₂和丙二醛含量,提高超氧化物歧化酶、抗坏血酸过氧化物酶等抗氧化酶活性和非酶抗氧化剂抗坏血酸、谷胱甘肽含量;使过氧化氢酶、过氧化物酶活性及渗透溶质可溶性糖、游离氨基酸和脯氨酸含量显著降低,有机酸和叶绿素含量明显提高,而可溶性蛋白质含量则变化不大;添加DMTU和ASA后有效逆转了喷施H₂O₂对NaHCO₃胁迫燕麦生长受抑和生理响应的调节。采用主成分和隶属函数分析显示,喷施H₂O₂显著提高了NaHCO₃胁迫下燕麦幼苗的综合评价值,添加DMTU和ASA完全或部分逆转了H₂O₂的作用。因此,外源H₂O₂是通过调控活性氧代谢和渗透调节来缓解碱胁迫导致的氧化伤害和生长抑制,从而增强燕麦幼苗的耐碱性。     

铅胁迫对金丝草生长及生理生化的影响

采用土培方法,探究不同梯度铅胁迫(0、1000、2000和3000 mg·kg^-1)对金丝草生长形态、体内抗氧化系统和渗透调节物质的影响。结果表明:低浓度(1000 mg·kg^-1)处理会诱导金丝草叶片过氧化物酶(POD)活性、可溶性蛋白(SP)含量和根系抗超氧阴离子自由基活力(ASAFR)、可溶性糖(SS)及脯氨酸(Pro)含量增加,使得金丝草植株总抗氧化能力(T-AOC)处于较高水平,促进了金丝草株高、叶长和生物量的增加。随胁迫浓度增加,高浓度(2000~3000 mg·kg^-1)处理下,金丝草叶片和根系丙二醛(MDA)含量迅速增加,株高、叶长、叶面积和生物量下降,生长受到抑制。但金丝草通过增强叶片和根系POD、过氧化氢酶(CAT)活性来抵御过氧化作用,提高可溶性蛋白和可溶性糖含量维持细胞正常运作,增加根系生物量占比来加强根系发育,一定程度适应了高浓度铅胁迫。综上表明,金丝草主要通过叶片和根系不同抗氧化酶差异化响应、提高渗透调节物质含量,提升金丝草植株总抗氧化能力等途径来提高Pb耐性,对Pb污染矿区植物修复有较大潜力。     

小黑麦与黑麦花序结构和籽粒特性比较

植物的花序结构及其形态特征是影响种子生产性能的重要因素。对于禾本科植物而言,其花序大小、小穗数、小花数及小花的外稃、内稃和芒的性状特征直接影响种子形成和产量。本研究通过测定小黑麦品系C2、C35和黑麦品系C13、C33的花序结构特征,得到以下结果:小黑麦花序[(14.30±0.52) cm×(1.24±0.09) cm]明显大于黑麦[(13.20±0.35) cm×(0.82±0.02) cm],小黑麦花序长而粗,黑麦花序短而细;小黑麦花序的小穗数[(21.35±1.47)个]少于黑麦[(30.20±0.79)个];小黑麦每个小穗的小花数较多,为3~4朵,黑麦的小花数趋于稳定,每个小穗有2朵小花。从花序中部小穗的小花结构看,小黑麦下位护颖长[(1.27±0.11) cm]和宽[(0.26±0.03) cm]、上位护颖长[(1.30±0.09) cm]和宽[(0.23±0.04) cm]均显著大于黑麦下位护颖长[(1.04±0.05) cm]和宽[(0.08±0.01) cm]、上位护颖长[(0.94±0.10) cm]和宽[(0.06±0.01) cm];小黑麦中部小穗第1小花的外稃宽[(0.32±0.03) cm]、外稃高[(0.24±0.03) cm]和芒长[(8.35±0.51) cm]、第2小花的外稃宽[(0.35±0.04) cm]、外稃高[(0.25±0.05) cm]和芒长[(8.37±1.19) cm]极显著大于黑麦相应值[(0.26±0.01),(0.15±0.01),(5.50±0.19),(0.25±0.01),(0.17±0.01)和(5.18±0.23) cm];第1和第2小花的外稃长[(1.35±0.06),(1.37±0.06) cm]和内稃长[(0.84±0.04),(1.41±0.06) cm]均小于黑麦的外稃长[(1.49±0.05),(1.47±0.05) cm]和内稃长[(1.45±0.05),(1.47±0.04) cm]。小黑麦的穗粒数[(52.50±1.80)粒]显著低于黑麦[(58.50±2.50)粒] (P<0.05),但其穗粒重[(2.08±0.04) g]、粒重[(0.04±0.00) g]和籽粒宽[(3.04±0.32) mm]均极显著高于黑麦 (P<0.01),每个花序的籽粒不仅体积大,而且质量较重,其籽粒的生产性能高于黑麦。小黑麦籽粒呈椭圆形或长卵圆形,浅黄色,表皮皱缩,饱满度差;黑麦籽粒呈窄纺锤形,青灰色,表皮光滑,籽粒饱满。小黑麦和黑麦花序结构与籽粒性状的Pearson相关分析表明,小黑麦花序宽和花序基部小穗数与籽粒长显著正相关(P<0.05),花序长与籽粒宽极显著正相关(P<0.01),花序中部小穗的下、上位护颖宽分别与穗粒重和穗粒数极显著正相关(P<0.01);黑麦花序中部小穗第2小花的内稃长与籽粒长显著正相关(P<0.05),外稃高与穗粒数极显著负相关(P<0.01)。研究小黑麦和黑麦的花序结构和籽粒特征,对正确区分二者和了解其籽粒的生产性能具有重要意义,同时有利于小黑麦的示范推广。