大豆花叶病毒种子传毒率测定方法的比较

用苗期症状观察和酶联免疫吸附试验(ELISA)两种方法检查了大豆种子内的大豆花叶病毒(sMV)的传毒率及带毒率,并对两种方法所得的结果进行了比较。带毒大豆种子产生的病苗,其症状主要有花叶、卷叶、叶脉束状、叶脉坏死、凸斑和单叶扭曲等类型。苗期症状观察得到的种子传毒率,与用ELISA法检查去种皮大豆种子的带毒率高度吻合,相关系数r=0.92(n=31),说明此两种方法检查种子传(带)毒率具有相同的生物学和病理学意义。 本文提出了种子“群体病毒浓度”的概念。“群体病毒浓度”=群体内病毒总量/群体内种子总数。38个处理组合和3,591粒种子逐粒用ELISA法检查表明,“群体病毒浓度”与该群体的种子传毒率呈正相关,r=0.93(n=38)。将种子群体作为一个整体用ELISA法检查的结果也证明,“群体病毒浓度”与种子传毒率呈直线相关。因此认为可以用ELISA法对种子群体直接进行测定来估计种子的传毒率。     

一种新病毒——兔出血症病毒的鉴定初报

从我国新发生的一种家兔急性败血性传染病死兔内脏抽提物中,观察到典型的病毒粒子,回归兔可引起典型发病,再从病死兔内脏回收到同样病毒,证明该病系病毒性传染病,暂定名为“兔病毒性出血症”,病原暂定为“兔出血症病毒”。经初步鉴定,认为本病毒可能是一种首次发现的新病毒,属双股RNA病毒。但从病毒大小和核酸节段看,又不同于呼肠病毒科。最终归属正在进一步研究。     

慢性蜜蜂麻痹病病毒核酸与蛋白质组分的研究

从自然感染的意大利麻痹病蜂(APis mellifera)头部,经二次差速离心与蔗糖梯度离心获得纯化的慢性蜜蜂麻痹病病毒(CBPV)。纯化的CBPV制备物感染正常蜜蜂,4天后出现典型的麻痹症状,接着死亡,平均死亡率分别为95％与100％。SDS-聚丙烯酰胺凝胶电泳分析,二次差速离心初步纯化的病毒制备物含有多条蛋白带,而蔗糖密度梯度纯化的病毒制备物仅含有单一的多肽带。5％、7.5％与10％SDS-聚丙烯酰胺凝胶电泳分析,均检测出一种病毒蛋白质,分子量大约为24,200道尔顿,而且不同凝胶浓度检测的蛋白质分子量相近。慢性蜜蜂麻痹病病毒核酸也用SDS-聚丙烯酰胺凝胶电泳分析,结果表明,凝胶中有5条带,对核酸酶敏感,证明该病毒含有5个单股RNA组分。对慢性蜜蜂麻痹病病毒的基因组结构进行了讨论。     

Ca~(++)促进大麦根K~+吸收的过程分析

吸收溶液中CaCl_2促进了大麦根K~+净吸收,Ca~(++)本身对H~+分泌无影响,Cl~-减少了H~+净分泌量。 含有~(86)Rb的大麦根在1m mol/L KCl溶液中发生~(86)Rb外流,在H_2O、1m mol/L NaCl或0.5 m mol/L CaCl_2中没有明显外流。VO_4~(3-)、NaN_3和4℃低温均可以减少根段在1m mol/L KCl溶液中的~(86)Rb外流量。Ca~(++)抑制K~+(~(86)Rb~+)的外流,EDTA加剧外流,Ca~(++)可以逆转EDTA的效应。 Ca~(++)抑制K~+(~(86)Rb)外流和促进K~+净吸收的趋势相吻合。K~+吸收的通量分析结果表明,Ca~(++)抑制K~+通过质膜的外流,促进K~+由细胞质向液泡中转运,而不影响K~+通过质膜的内流速率。     

二氧化硫熏气对小麦叶片中1-氨基环丙烷-1-羧酸、1-(丙二酰氨基)环丙烷-1-羧酸含量的影响及与乙烯产生的关系

在SO_2熏气9h过程中,小麦叶片中乙烯先上升,约6h达高峰,后下降;ACC含量则随熏气时间的延长而上升。停止熏气,乙烯继续下降,ACC含量也明显降低。MACC含量从熏气3h后不断上升,脱离接触后仍继续增加。6-BA预处理对SO_2引起的乙烯和ACC上升有促进作用,但对MACC含量无明显影响。SO_2熏气提高了乙烯形成酶活性。6-BA预处理对SO_2伤害有保护作用。对逆境乙烯的产生与调节作用进行了讨论。     

烟草内生菌根真菌的分离鉴定

本文报道了从烟草(Nicotiana tabacum L.)的根际土壤中分离出内生菌根真菌的孢子,用单孢接种烟苗并在温室内水培条件下培养。选出能在烟草上形成菌根的菌株,经过再次单孢接种确认后,进行种的鉴定。从分离的8个菌株中已鉴定出球囊霉属(Glomus)的3个新记录种:漏斗孢球囊霉[G.mosseae(Nic.& Gerd.)GeM.& Trappe]、根内孢球囊霉(G.intraradics Schenck & Smith)和联结球囊霉(G.constrictum Trappe)。     

Chromosome-mediated transfer of murine alleles for hypoxanthine-guanine phosphoribosyl transferase (HGPRT) and ouabain resistance into human cell lines

Genetic drug-resistance markers were transferred via purified metaphase chromosomes from mouse L cells into the human fibrosarcoma line HT1080 and HeLa S3 cells. Interspecific chromosome-mediated transfer of hypoxanthine-guanine phosphoribosyl transferase (HGPRT; EC 2.4.2.8) from mouse L cells into HGPRT^– HT1080 cells occurred at a frequency of approximately 1×10^–7. The presence of the mouse allele for HGPRT in transferent isolates was confirmed by isoelectric focusing. Transfer of ouabain resistance from mouse L cells to HT1080 and HeLa S3 cells occurred at an average frequency of approximately 4×10^–7. Expression of the mouse trait in transferent isolates was confirmed by their ability to withstand doses of ouabain which would be lethal to spontaneous ouabain-resistant mutants of the human cells but not to mouse L cells. Ouabain-resistant transferents of human cells showed 10⁴- to >10⁵-fold enhanced drug resistance, characteristic of either wild-type or mutant alleles, respectively, from ouabain-resistant donor L cells. Unstable expression of the transferred phenotypes in the absence of selection was seen in some isolates, but expression was lost at slow rates.This work was supported by National Institutes of Health Grant GM30383/21665 to RMB, Core Grants CA14051 to S. E. Luria and CA24538 to E. Mihich, and institutional predoctoral Training Grant GM07287.     

Characterization of some East African Theileria species isolates by isoenzyme analysis, with particular reference to T. parva

Eight different isolates of Theileria parva and one isolate of T. taurotragi, in the form of intra-lymphocytic schizonts and/or purified piroplasms, were subjected to isoenzyme analysis for 24 enzymes by both isoelectric focusing in agarose and electrophoresis in starch gel. Twelve enzymes distinguished between T. parva and T. taurotragi; five enzymes (HK, GPI, PEP1, LDH and SOD) showed variations within T. parva. The metabolism of the host cell was affected by schizont infection, which masked intraspecific variations. Piroplasms were of more potential value for characterization of T. parva.     

食蟹猴疟原虫晚期卵囊、成孢子细胞与子孢子扫描电镜观察

本研究对实验感染食蟹猴疟原虫后9、10和14天的斯氏按蚊阳性蚊胃,进行扫描电镜观察。晚期(分化的)卵囊表面呈现凹凸不平皱褶。成孢子细胞体常呈圆球形或椭圆形,表面光滑,子孢子芽从其表面长出。子孢子体细长,稍弯曲,体表光滑;虫体前部较细,顶端稍平,后部稍粗,末端钝圆。本文对成孢子细胞不同发育阶段的形态予以较详细描述,对子孢子出囊方式做了初步讨论。     

Adenine nucleotide translocase-dependent anion transport in pea chloroplasts

Pea chloroplasts were found to take up actively ATP and ADP and exchange the external nucleotides for internal ones. Using carrier-free [¹⁴C]ATP, the rate of nucleotide transport in chloroplasts prepared from 12–14-day-old plants was calculated to be 330 μmol ATP/g chlorophyll/min, and the transport was not affected by light or temperature between 4 and 22°C. Adenine nucleotide uptake was inhibited only slightly by carboxyatractylate, whereas bongkrekic acid was nearly as effective an inhibitor of the translocator in pea chloroplasts as it was in mammalian mitochondria. There was no counter-transport of adenine nucleotides with substrates carried on the phosphate translocator including inorganic phosphate, 3-phosphoglycerate and dihydroxyacetone phosphate. However, internal or external phosphoenolpyruvate, normally considered to be transported on the phosphate carrier in chloroplasts, was able to exchange readily with adenine nucleotides. Furthermore, inorganic pyrophosphate which is not transported by the phosphate carrier initiated efflux of phosphoenolpyruvate as well as ATP from the chloroplast. These findings illustrate some interesting similarities as well as differences between the various plant phosphate and nucleotide transport systems which may relate to their role in photosynthesis.