应用生物素标记的NDV－cDNA探针检测感染尿囊液中NDV－RNA的初步研究

本文应用聚合酶链反应（ＰＣＲ）技术从构建的新城疫病毒（ＮＤＶ）ｃＤＮＡ文库中扩增含编码Ｆ糖蛋白前体──Ｆｏ酶切位点序列的３５９ｂｐ的Ｆ蛋白基因ｃＤＮＡ片段。将此３５９ｂｐｃＤＮＡ片段经光敏生物素标记后,即成ＮＤＶ－ｃＤＮＡ探针。该探针能特异性地从感染的尿囊液中检测出ＮＤＶ强毒株和疫苗毒株的基因组ＲＮＡ,而不与ＩＢＤｖ－ｄｓＲＮＡ、ＡＩＢｖ－ｓｓＲＮＡ、ＥＤＳ７６－ｄｓＤＮＡ、ＭＤＶ－ｄｓＤＮＡ,ＦＰＶ－ｄｓＲＮＡ及ＡＩＬＶ－ｄｓＤＮＡ发生交叉杂交反应。试验结果表明：尽管该探钎含有编码Ｆｏ蛋白酶切位点序列的碱基顺序,但它还是不能把ＮＤＶ的强、弱毒株区分开。这说明ＮＤＶ强、弱毒株比区域内的碱基存在着相当大的同源性。不过,此探针对ＮＤＶ来说具有特异性,这就为ＮＤＶ的诊断技术开创了基因水平检测的新途径。     

Unsaturated vitamin b(12) binding capacity in human and ruminant blood serum - a comparison of techniques including a new technique by high performance liquid chromatography

A new technique by High Performance Liquid Chromatography (HPLC-gel permeation) shows promise as a tool to separate and quantitate the Unsaturated Vitamin B(12) Binding Capacity (UBSC) of the individual Vitamin B(12) binders in blood serum. This method, although not as rapid as protein-coated charcoal or cellulose separation techniques, is more applicable for use with large numbers of samples than gel filtration. The use of a radioactivity detector to monitor the eluant from the column permitted automation of the method. Comparable results for UBBC and for the UBBC of individual binders were obtained when samples were analyzed by gel filtration and HPLC. The HPLC method proved suitably precise and the recovery of added cyanocobalamin was acceptable. It is proposed that HPLC be the method of choice for measurement of the USBC of binders of Vitamin B(12) in blood serum.     

家蚕第2隐性赤蚁的遗传学研究——Ⅱ.ch-2基因的连锁分析

Ch-2基因是继ch之后新发现的一种隐性赤蚁ch-2基因与pM(2)、Ze(3)、L(4)、Pe(5)、E~(EL)(6)、q(7)、st(8)、I(9)、w-2(10)、ms(12)、cf(13)、U(14)、Se(15)、cts(16)、B_m(17)、nb(19)、rb(21)、or(22)、sp(23)、Nd(25)、及Y_m等各标志基因都是独立遗传.Ch-2与mln杂交F_2代分离+ch-2+min:ch-2+min:ch-2mln:ch-2mln=523:284:231:0≈2:1:1:0;ch-2与elp杂交F_2代分离+ch-2+elf:ch-2+elp:+ch-2elp:ch-2elp=219:97:68:0≈2:1:1:0,充分说明ch-2与mln、elp是连锁遗传的,即ch-2基因位于第18连锁群.     

柞树害虫栎粉舟蛾的初步研究

栎粉舟蛾Femtoma ocypete(Bremer)是柞树的重要害虫之一。此虫在辽宁一年发生一代,以蛹在土中越冬。翌年7月中旬开始羽化,持续到8月中旬。羽化后即可交配产卵。7月下旬到8月下旬均有幼虫孵出。幼虫经6个龄期,于9月中、下旬入土化蛹。防治方法:8月中旬往柞树上喷洒0.025％浓度的“杀虫灵”农药,能杀死各龄幼虫,防治效果为90％左右,七天后养蚕无害。     

苎麻自交一代分离和变异的研究

1983～1985年以“黄壳早”、“芦竹青”、“古巴苎麻”和“武冈红皮种”为材料进行自交,并观测了自交一代的分离和变异情况,研究结果表明:a.根据自交一代的形态分类,可将“芦竹青”繁殖后代分为40个类型,“芦竹青”自交一代的麻骨颜色分离为四种,其分离比例为9.3:4.2:3:0.7,基本符合孟德尔遗传规律;b.个体间产量性状差异很大,株高变冥为0.23～1.68m,茎粗变异为0.48～1.14 cm,有效株变异为1～23株;c.40个类型的纤维细度的变异呈正态分布,变异为1168～1905公支,最细的类型和最粗的类型相差747支上述结果表明:苎麻自交后代的形态性状、产量性状和纤维细度均产生显著的分离和差异。     

陆地棉核雄性不育材料在山东不同地区的育性转变及应用研究

对在山东的济南、平度、莱西、烟台种植的几种陆地棉（Ｇｏｓｓｙｐｉｕｍ　ｈｉｒｓｕｔｕｍＬ．）核雄性不育材料的育性表现进行了研究,结果表明：洞Ａ不育系的衍生材料ＭＢ、ＭＡ在不同气候条件下有育性的变化。在济南高度不育,可作为不育系。在其他几个地区表现不同程度的可育。其中ＭＢ在平度有相当好的育性,能正常结铃。而双隐性核不育材料５９Ａ、６２Ａ未能观察到育性变化。本文就核不育材料在棉花杂交制种中的应用前景及需深入研究的问题作了探讨。     

光敏核不育水稻选育与利用的几个问题讨论

对现有光敏核不育材料进行了分类,分为４种遗传类型;其中,温光弱感到光敏核不育系是最为理 想的遗传工具,并就其选育途径和选择“粳不籼恢”繁殖制种技术体系进行了论证．     

包心菜无菌苗子叶及叶片原生质体高频分裂和高频植株再生

以包心菜子叶和叶片原生质体为材料。经不同液体培养基(Bp1,Bp2,B1)浅层培养,再生细胞高频分裂并形成愈伤组织。愈伤组织经扩增后转移到分化培养基上诱导植株分化,从这两种原生质体中获得了再生植株。在原生质体培养过程中,原生质体及细胞团的褐化程度与培养基中的有机成分的多少有关。原生质体的分化频率与培养基中植物激素种类关系甚大。在植株分化时,谷氨酰胺和腺嘌呤对植株分化有很大促进作用。另外,原生质体的来源及原生质体培养基对原生质体植株分化能力均有不同的影响。     

Identification of feline blood B and T lymphocytes by cell electrophoresis.

The electrokinetic properties of feline blood lymphocytes isolated by centrifugation over Ficoll-Isopaque gradient were investigated. A biphasic electrophoretic mobility (EPM) distribution was regularly observed with a low-mobility (LM) population (mean EPM: 0.82) accounting for 32% of blood lymphocytes and a high-mobility (HM) population (mean EPM: 1.09) representing 68% of blood lymphocytes. Following fractionation on nylon-wool columns, lymphocytes with B-cell properties (64% sIg⁺; 9% guinea pig erythrocytes (GPE)-rosette⁺, PHA and Con A unresponsive) were enriched in the adherent fraction and belonged mainly (78%) to the LM population. In contrast, lymphocytes with T properties (5% sIg⁺, 42% GPE-rosette⁺, PHA and Con A responsive) were recovered in the effluent fraction and comprised 84% of HM elements.Thus, in cat blood, LM lymphocytes are likely to represent in majority B cells and HM lymphocytes T cells. This indicates that cell electrophoresis provides an interesting mean for differentiating B and T cells in the cat.