Rapid production and field testing of homozygous transgenic tobacco lines with virus resistance conferred by expression of satellite RNA and coat protein of cucumber mosaic virus

A procedure for the fast production of homozygotic transgenic plants was developed. Leaf discs of haploid tobacco plants from anther cultures were transformed with a chimaeric vector containing coat protein (CP) and satellite RNA (Sat-RNA) genes from cucumber mosaic virus (CMV). One-hundred-and-twelve Kanamycin-resistant transformed haploid plants were subjected to selection based on the expression of both CP and Sat-RNA. Eighty-nine transgenic plants expressing both genes were selected and tested for their resistance to CMV by inoculation with high concentration of CMV (200 g ml^–1). Only five plants showed no symptoms of viral infection 30 days after inoculation. These plants were then diploidized by colchicine treatment. Three homozygous diploid lines with high levels of resistance to CMV were obtained after only one generation. The three transgenic lines were further tested under field conditions. The results showed that the progenies of these transgenic lines were homozygous and were highly resistant to CMV under natural field infection and manual inoculation conditions.     

菌紫质光生物分子器件及其超快过程

菌紫质是嗜盐菌紫膜中的一种光能转换蛋白.它具有光致色变和光驱动质子泵功能,其原初光异构化过程极其迅速,可在430fs内完成.由于菌紫质具有一系列独特的光电和光学特性,如对光强的微分响应,高的空间分辨率,高的光灵敏度,高循环次数等,使得它在光电探测,仿视觉系统,人工神经网络,非线性光学及光学信息记录和处理方面有很多重要应用.利用超短脉冲激光技术,高时间分辨光谱学技术及高速取样探测技术,对菌紫质的光循环,原初光异构化,激发态动力学,质子泵机制等方面的研究已取得了许多有意义的结果.     

Haemodynamic and renin responses to prostacyclin infusion in Na depleted and Na restricted sheep

The haemodynamic and renin responses to prostacyclin (PGI2) infusion were examined in sheep during sodium depletion and dietary sodium restriction. The haemodynamic effects of PGI2 infusion in sodium depleted and sodium restricted sheep were similar to those obtained in the sodium replete animal. The renin proportionate response to PGI2 was not altered by sodium restriction but blunted by sodium depletion, compatible with the hypothesis that endogenous PGI2 is high in Na depletion.     

Effect of prenatally and postnatally induced hypoxia on blood volume of newborn lambs

The effect of both prenatally and postnatally induced acute hypoxia on the blood volume was studied in 16 newborn lambs. Hypoxia was induced by 8% O₂ inhalation for 10–20 minutes prenatally in 7 term pregnant ewes immediately before caesarean section delivery of the lambs (Group 1), and postnatally in nine 2–4 day old lambs born spontaneously (Group 11). The umbilical cords of Group 1 lambs were clamped early (E.C.) within 10 seconds after birth. Group 11 lambs had their cords severed within one minute of birth by the ewes. Blood volume (BV) was measured by the double label, radioiodinated human serum albumin-125 (RIHSA-125) plasma tag and radiochromium-51 (Cr⁵¹) red cell tag dilution technique. The red cell volume (RCV), which reflects the size of placental transfusion best, is significantly higher in Group 1 (42.1 ± 1.6 ml/kg) than in normal E.C. lambs (29.8 ± 2.0 ml/kg). The RCV in Group 1 was smaller than that in late clamped (L.C.) lambs, in whom an almost complete placental transfusion (RCV = 50.4 ± 2.3 ml/kg) had occurred; and close to those of spontaneously born lambs (S.B.) who received a partial placental transfusion (RCV = 36.7 ± 2.1 ml/kg). This finding in Group 1 suggests that with prenatal hypoxia, a partial placental transfusion had occurred in utero. In Group 11 lambs in whom hypoxia was postnatally induced, the BV, RCV, and plasma volume (109.7 ± 5.2, 44.1 ± 1.7 and 65.1 ± 4.2 ml/kg) were slightly, but not significantly, increased from control values of 101.6 ± 4.9, 40.8 ± 1.7 and 60.8 ± 4.3 mg/kg), respectively. It is suggested that postnatally induced hypoxia does not significantly increase the blood volume of newborn lambs due to the absence of placental reservoir of blood. Prenatally induced hypoxia appeared to bring about a higher blood volume than expected in E.C. lambs due to a transfer of placental blood to the fetus in utero. Blood volume redistribution in the feto-placental unit in utero is an unique adaptational response to prenatal hypoxia.     

猕猴桃品种‘金桃’采收指标与果实软熟品质相关性研究

分别对河南省27个果园的中华猕猴桃（Actinidia chinensis Planch.）品种‘金桃’果实的5项采收生理指标及果实软熟时的8项品质性状进行测定,采用主成分分析法对果实软熟时的品质指标进行综合评分,并对果实的采收生理指标、果实软熟品质指标及综合分值间进行相关性分析。结果显示,采收时的生理指标（干物质、色度角、硬度和可溶性固形物）均与果实软熟品质综合分值间呈极显著相关,其中干物质相关系数最高,为0.437。干物质与体现果实软熟品质的关键指标（可溶性固形物、总糖和糖酸比）均呈极显著性相关。研究结果表明‘金桃’果实采收时,干物质含量是果实软熟时品质的重要评价指标,而可溶性固形物和色度角是评判采收期的辅助指标。     

交联琼脂糖珠固定化蛋白酶在纯化牛肺Kunitz抑制剂中的应用

本文介绍了珠状交联琼脂糖及以此作为载体,经氯代环氧丙烷活化后与蛋白酶(胰蛋白酶或糜蛋白酶)结合,制成固定化蛋白酶亲和吸附剂,进而用以亲和层析牛肺提取液中的Kunitz抑制剂的方法。纯化出的抑制剂在SDS-聚丙烯酰胺凝胶电泳上呈现单一条带,与参照物Trasytol(商品Kunitz抑制剂)具有相对应的电泳迁移率,其分子量也相符。纯化产品每毫克蛋白的抑制活力相当于16 000胰蛋白酶BAEE单位。纯化效果为90倍,收率约85％。     

在古尔班通古特沙漠中柽柳（Tamarix spp.）群落的侵移与更新研究

 柽柳(Tamarix spp.)在荒漠的非河岸区自然侵移现象已被发现。生长季偶发大雨引起暂时性积水,在土层结构和种源的适当配合下,有可能引起柽柳的自然发生过程。这种机遇较少出现。故实生苗群数量较少,年龄结构亦非连续性。但植丛寿命长,在漫长生活周期中,这种机遇终将出现,如无人为因素干扰,这类植丛将能持续地补充幼体而实现更新。     

Acetylation of O-specific lipopolysaccharides from Shigella flexneri 3a and 2a occurs in Escherichia coli K-12 carrying cloned S. flexneri 3a and 2a rfb genes.

Most of the Shigella flexneri O-specific serotypes result from O-acetyl and/or glucosyl groups added to a common O-repeating unit of the lipopolysaccharide (LPS) molecule. The genes involved in acetylation and/or glucosylation of S. flexneri LPS are physically located on lysogenic bacteriophages, whereas the rfb cluster contains the biosynthesis genes for the common O-repeating unit (D.A.R. Simmons and E. Romanowska, J. Med. Microbiol. 23:289-302, 1987). Using a cosmid cloning strategy, we have cloned the rfb regions from S. flexneri 3a and 2a. Escherichia coli K-12 containing plasmids pYS1-5 (derived from S. flexneri 3a) and pEY5 (derived from S. flexneri 2a) expressed O-specific LPS which reacted immunologically with S. flexneri polyvalent O antiserum. However, O-specific LPS expressed in E. coli K-12 also reacted with group 6 antiserum, indicating the presence of O-acetyl groups attached to one of the rhamnose components of the O-repeating unit. This was confirmed by measuring the amounts of acetate released from purified LPS samples and also by the chemical removal of O-acetyl groups, which abolished group 6 reactivity. The O-acetylation phenotype was absent in an E. coli strain with an sbcB-his-rfb chromosomal deletion and could be restored upon conjugation of F' 129, which carries sequences corresponding to a portion of the deleted region. Our data demonstrate that E. coli K-12 strains possess a novel locus which directs the O acetylation of LPS and is located in the sbcB-rfb region of the chromosomal map.     

Crystallization and preliminary X-ray structure analysis of pigeon egg-white lysozyme.

Calcium binding lysozyme from pigeon egg-white was crystallized by the hanging drop vapor diffusion technique using ammonium sulphate as a precipitant. The crystals belong to the orthorhombic system, space group P2(1)2(1)2(1), and have unit cell dimensions of a = 34.2 A, b = 34.8 A, and c = 99.4 A. One asymmetric unit contains one molecule of the pigeon lysozyme. The crystals diffract X-rays at least to 2.0 A resolution and are suitable for high resolution structure analysis. The diffraction data up to 3.0 A resolution were collected with a diffraction image processor, DIP100, using a Fuji imaging plate as an area detector. The structure was solved by the molecular replacement technique and refined to an R factor of 0.216. Least-squares fitting of the main-chains of pigeon egg-white lysozyme with those of chicken egg-white lysozyme and baboon alpha-lactalbumin showed that the main-chain folding of pigeon lysozyme is more similar to that of chicken lysozyme than that of alpha-lactalbumin. The largest differences between the pigeon and chicken lysozymes are in the surface loop regions.     

A soluble mitochondrial protein increases the voltage dependence of the mitochondrial channel,VDAC

A soluble protein isolated from mitochondria has been found to modulate the voltage-dependent properties of the mitochondrial outer membrane channel, VDAC. This protein, called the VDAC modulator, was first found inNeurospora crassa and then discovered in species from other eukaryotic kingdoms. The modulator-containing fraction (at a crude protein concentration of 20 µg/ml) increases the voltage dependence of VDAC channels over 2–3-fold. At higher protein concentrations (50–100 µg/ml), some channels seem to remain in a closed state or be blocked while others display the higher voltage dependence and are able to close at low membrane potentials. By increasing the steepness of the voltage-dependent properties of VDAC channels, this modulator may serve as an amplifierin vivo to increase the sensitivity of the channels in response to changes in the cell's microenvironment, and consequently, regulate the metabolic flux across the outer mitochondrial membrane by controlling the gating of VDAC channels.