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11.
给完整的及切除肾上腺的雌性 Wistar 大鼠分別注射地塞米松、去氧皮质酮或地塞米松加去氧皮质酮;冷酚法提取心房总 RNA,用α-~(32P)标记的大鼠心房肽 cDNA 探针与之杂交。完整大鼠接受地塞米松和切除肾上腺后接受地塞米松加去氧皮质酮的大鼠,心房肽基因转录产物增加2倍,其余组无显著变化。结果提示糖皮质激素可促进心房肽基因表达,但此作用依赖于盐皮质激素的同时存在,单纯盐皮质激素不能增强该基因的表达。 相似文献
12.
A determinant of polyomavirus virulence enhances virus growth in cells of renal origin. 总被引:3,自引:2,他引:1 下载免费PDF全文
J B Bolen S E Fisher K Chowdhury T C Shan J E Williams C J Dawe M A Israel 《Journal of virology》1985,53(1):335-339
We have identified a strain of polyomavirus, Py(L), which is unusual in causing acute morbidity and early death after inoculation of newborn mice. We determined that these animals died of kidney failure associated with extensive, virus-mediated destruction of renal tissue. Interestingly, the Py(L) strain infects baby mouse kidney cell cultures more efficiently than do other strains. 相似文献
13.
确定了在pH 5.2到8.7和温度22°到45℃时钼铁蛋白和铁蛋白的稳定性。按logKm和logV分别对pH作图,得到下列参数。于30℃在酸性侧,乙炔络合常数PK_b(C_2H_2)=6.43—6.50,乙炔催化常数pK_b′(C_2H_2)=4.78,在碱性侧乙炔络合常数pK_a(C_2H_2)=7.42—7.55,乙炔催化常数pK_a′(C_2H_2)=7.88—8.29,氮络合常数pK_a(N_2)=7.75—7.9及氮催化常数pK_a′(N_2)=8.08—8.68。既然pK_a与pK_b或pK_a′与pK_b′二者间隔小于3.5个单位,又按V/Km及V′对pH作图,其结果为pKb(C_2H_2)=6.28pK_a(C_2H_2)=7.68和pK_b′(C_2H_2)=5.53和pK_a′(C_2H_2)=8.93。将不同温度下的pK_b或pK_a分别对各自温度的倒数作图,其热力学数据为由pH 5.7到7.3范围内,质子移变基团的解离热⊿H(ioh)=7742卡/克分子,相应的pK_b(C_2H_2)=6.16—6.36;由pH 7.3到8.4范围内⊿H_(ion)=6983卡/克分子,相应的pK_a=8.24—8.44。这些数据指出固氮酶钼铁蛋白络合乙炔的功能基团可能具有咪唑基·巯基和氨基相类似的结构,这种推测正在用化学修饰的方法加以验证。 相似文献
14.
亚急克病人心肌线粒体内膜电子传递链的琥珀酸氧化酶系,琥珀酸脱氢酶和细胞色素氧化酶活性明显低于对照。H~ -ATP酶的活性及其对寡霉素的敏感性都明显下降。ATP能量化后线粒体膜电位的变化也比对照明显降低。膜脂流动性低于对照。亚急克病人心肌线粒体内观察到较多的电子致密无定形物质,经电镜X射线微区等方法分析,认为这些物质不是Ca_3(PO_4)_2,而可能是一种蛋白质凝聚物。此外,心肌线粒体的硒含量远低于对照,而Ca含量明显高于对照。上述结果都反映亚急克病人心肌线粒体明显损伤。根据克山病患者心肌细胞线粒体结构与功能方面呈现的如此广泛与明显的异常,可将克山病称为“心肌线粒体病(Mitochondrial Cardiomyopathy)”。 相似文献
15.
16.
模拟酸雨对七种森林植物生物量的影响 总被引:18,自引:1,他引:17
马尾松(pinus massonina Lamb.)、杉木(Cunninghamia lanceolata(Lamh.) hook)、青冈(Cyclobananopsis glauca Thumb. Oeret)、油茶(Camelia oleifera Abel)、木荷(Schima superba Gardn,et Ghamp. )、黄樟(Cinnamomum porrectum(Roxb)Kosterm)、火力楠(Michelia macclurei)属亚热带森林植物,在我国南方林业生产中占居十分重要的地位。为了探讨酸雨对植物生长和森 相似文献
17.
We have obtained 1H and 13C magic-angle sample-spinning (MAS) nuclear magnetic resonance (NMR) spectra of three glycosyldiacylglycerol-water (1:1, weight ratio) mesophases, at 11.7 T, as a function of temperature, in order to probe lipid headgroup, backbone, and acyl chain dynamics by using natural-abundance NMR probes. The systems investigated were monogalactosyldiacyldiglyceride [MGDG; primarily 1,2-di[(9Z,12Z,15Z)octadec-9,12,15-trienoyl++ +]-3-beta-D-galactopyranosyl- sn-glycerol]; digalactosyldiacyldiglyceride [DGDG; primarily 1,2-di[(9Z,12Z,15Z)octadec-9,12,15-trienoyl++ +]-3- (alpha-D-galactopyranosyl-1-6-beta-D-glactopyranosyl)-sn-glycerol] ; and sulfoquinovosyldiacyldiglyceride [SQDG; primarily 1-[(9Z,12Z,15Z)octadec-9,12,15-trienoyl]-2 -hexadecanoyl-3-(6-deoxyl-6- sulfono-alpha-D-glucopyranosyl)-sn-glycerol]. At approximately 22 degrees C, all three lipid-water systems give well-resoled 13C and 1H MAS NMR spectra, characteristic of fluid, liquid-crystalline mesophases. 13C spin-lattice relaxation times of the headgroup and glycerol backbone carbons of all three materials give, within experimental error, the same NT1 values (approximately 400 ms), implying similar high-frequency motions, independent of headgroup size and charge. Upon cooling, pronounced line broadenings are observed, due to an increase in slow motional behavior. For each lipid, the onset of line broadening is seen with the glycosyl headgroup, glycerol backbone, and the first two or three carbons of the acyl chains. By approximately -20 degrees, all headgroup carbon resonances are broadened beyond detection. Both galactose moieties in DGDG "freeze out" together, implying a rigid-body motion of the disaccharide unit. Upon further cooling, the bulk polymethylene chain resonances in all three systems (in both 13C and 1H MAS) broaden greatly, followed by the olefinic and allylic carbon resonances.(ABSTRACT TRUNCATED AT 250 WORDS) 相似文献
18.
Interferon selectively inhibits the expression of mitochondrial genes: a novel pathway for interferon-mediated responses. 总被引:4,自引:0,他引:4 下载免费PDF全文
As an approach to identifying genes involved in physiological actions of interferons we used differential probes to screen a cDNA library from mouse L-929 cells treated with interferon alpha/beta. We identified two negatively regulated mRNA species which have been examined by analysis of the corresponding mRNAs and by DNA sequencing. Comparison with the GenBank database showed that these cDNA clones corresponded to mitochondrially encoded genes for cytochrome b and subunit I of cytochrome c oxidase. A further cDNA encompassing three mitochondrial genes was used as a probe to show that a third mRNA, NADH dehydrogenase subunit 5, was also down-regulated by interferon while a fourth, NADH dehydrogenase subunit 6, was unaffected. Expression of cytochrome b was also inhibited in mouse NIH 3T3 cells treated with interferon alpha/beta and in human Daudi lymphoblastoid cells treated with interferon alpha. The ability of interferon to reduce mitochondrial mRNA levels could be blocked by cycloheximide suggesting that these effects are mediated by an interferon-responsive nuclear gene which encodes a product capable of regulating mitochondrial gene expression. Analysis of proteins synthesized in the presence of emetine, a specific inhibitor of cytoplasmic translation, showed that the synthesis of several mitochondrial translation products, including cytochrome b, was reduced after treatment with interferon. Our results reveal a novel effect of interferon on cellular physiology which could have important consequences for understanding the effects of interferons as well as suggesting new mechanisms for the regulation of mitochondrial biogenesis and function. 相似文献
19.
兴安落叶松结实规律与长短枝习性的关系 总被引:1,自引:0,他引:1
1987年5月,大兴安岭林区发生的特大森林火灾,实属世界罕见,火灾面积达1.0×10~6ha 多。大量的火烧迹地亟待更新、无论是人工更新还是人工促进天然更新,其中关键的问题之一是种子的来源,在大兴安岭地区,兴 相似文献
20.
用硫酸铵分段盐析、超滤膜分级分离及DEAE-纤维素、Sephadex A-25和Sephadex G-50三种柱层析方法从双胸蚓组织的粗提取液中分离纯化出一种纤溶酶,分子量为29kD,由一条肽链组成。此晦具有强烈的溶解纤维蛋白的作用,对家兎实验性血凝块也具有明显的溶解作用。此酶的最适pH为8.0,在pH7.6~8.4之间活力相差不到2%;酶在PH4.7—11.0范围内稳定;酶作用的最适温度为57℃;此酶热稳定性较好,于25~50℃保温3小时,酶活力基本不变,60℃时,活力保留65%。金属离子Na~(+)、K~(+)、Mg~(2+)等可提高此酶的活力,而Hg~(2+)、Ca~(2+)等金属离子对此酶有不同程度的抑制作用。 相似文献