外源复合酶对移地保护圈养马来熊日粮营养消化率的影响

利用外源复合酶对移地保护圈养的 9只马来熊日粮营养物质及能量消化率进行了测定 ,经单因子方差分析结果表明 ,在圈养马来熊日粮中添加一定量的外源复合酶 ,能提高马来熊对日粮营养物质的消化率 ,其中 ,添加 0 3%饲料量的酶能显著提高日粮粗蛋白的消化率(P <0 0 5) ;添加 0 5%的酶 ,能显著提高日粮粗纤维、粗蛋白质消化率 (P <0 0 5)。此研究结果可应用于马来熊的饲养中 ,提高其饲料报酬     

一氧化氮合酶与寄生虫感染

一氧化氮(NO)在体内由L-精氨酸在一氧化氮合成酶(NOS)的催化下生成。它是一种重要的信使分子,参与血管、气道平滑肌的调节,神经递质的传递,细胞杀伤,肿瘤细胞的溶解及内分泌激素的释放过程,与许多疾病的发生、发展密切相关;既在机体多个系统多种细胞中具有广泛的生理功能,又可能参与多种疾病的发生过程。寄生虫感染时,动物机体内由其诱发产生各种细胞因子。细胞因子激发一氧化氮合酶基因,其转录产生iNOS(induciblenitricoxidesynthase)mRNA,由iNOSmRNA指导一氧化氮合酶(iNOS)生成。iNOS以精氨酸为底物合成NO。本文就NOS的结构、生成和NO对寄生虫的作用以及影响NO抗寄生虫感染的因素作了综述。     

棉花纤维发育后期Mg2+,K+-ATP酶的活性分析

1989～1990年选用陆地棉(G.hirstum L.)北农1号品种和海岛棉(G.barbadenseL.)海7124品种为材料,对棉纤维发育后期的纤维素形成过程进行了研究。结果表明:①随着棉纤维的发育 Mg~(2+),K~+-ATP 酶活性逐渐下降。②Mg~(2+),K~+-ATP 酶活性的最适 pH 值为6.5。Mg~(2+),K~+ATP 酶活性随[Mg~(2+)],[K~+]和[NADH]/[NAD~+]的增大而变大。③Mg~(2+),K~+ATP 酶活性变化与还原性糖含量变化呈显著正相关(r=0.811~*),与纤维素含量变化呈极显著负相关(r=-0.900~(**))。④Mg~(2+),K~+-ATP 酶参与了纤维素的形成过程。     

Protective effect of onychin on the human umbilical vein endothelial cells injured by menadione

AIM: To investigate the protective effect of onychin on the endothelial cells injured by oxidative stress. METHODS: The injured model was established by endothelial cells treated with menadione. The growth inhibitory rate of endothelial cell was determined by MTT assay; NO₂^-／NO₃^- concentration in the medium was determined by nitrate reductase assay; eNOS and caveolin-1 protein levels were determined by Western blot. RESULTS: Onychin significantly decreased the growth inhibitory rate of endothelial cells injured by menadione, increased NO₂^-／NO₃^- concentration in the medium and eNOS activity and up-regulated caveolin-1 expression. CONCLUSION: Onychin possesses a protective effect against endothelial cell injury induced by menadione via caveolin-1/eNOS pathway.     

Importance of Cell Wall Degrading Enzymes Produced by Fusarium graminearum during Infection of Wheat Heads

Cytological studies were carried out to elucidate the importance of cell wall degrading enzymes (CWDE) during infection of wheat spikes by Fusarium graminearum. Scanning electron micrographs revealed that at 6–24 hours after inoculation (hai) of single spikelets with macroconidia of F. graminearum, the fungus germinated by forming several germ tubes and developed a dense hyphal network in the cavity of the spikelet. At 24–36hai, the fungus formed infection hyphae which invaded the ovary and inner surface of the lemma and palea. Transmission electron microscopical studies revealed that the fungus extended inter- and intracellularly in the ovary, lemma and rachis and caused considerable damage and alterations to the host cell walls. In different tissues of healthy and F. graminearum-infected wheat spikes the cell wall components cellulose, xylan and pectin were localized by means of enzyme-gold and immuno-gold labelling techniques. Localization of cellulose, xylan and pectin showed that host cell walls which were in direct contact with the pathogen surface had reduced gold labelling compared to considerable higher labelling densities of walls distant from the pathogen–host interface or in non-colonized tissues. The reduced gold labelling densities in the infected host cell walls indicate that these polysaccharide degrading enzymes might be important pathogenicity factors of F. graminearum during infection of wheat spikes. The results revealed that, infection and colonization of wheat spikes by F. graminearum and reactions of infected host tissue were similar to those reported for F. culmorum.     

‘新红星’苹果果实蔗糖合酶的活性及亚细胞定位

 在‘新红星’苹果果实发育过程中, 伴随果糖、葡萄糖和蔗糖的积累, 蔗糖合酶的分解活性逐渐下降, 而合成活性逐渐升高。苹果果实的蔗糖合酶由分子量为90 kD 的亚基组成, 其免疫信号强度随发育进程而增加。蔗糖合酶主要定位于果肉细胞的细胞质中, 发育中后期该酶的分布密度有一定增加。综合结果认为, 蔗糖合酶调控发育早期蔗糖的降解和发育后期蔗糖的积累。     

Natural tolerance of Cuscuta campestris to herbicides inhibiting amino acid biosynthesis

The response of Cuscuta campestris Yuncker, a non‐specific above‐ground holoparasite, to amino acid biosynthesis inhibitor (AABI) herbicides, was compared with other resistant and sensitive plants in dose–response assays carried out in Petri dishes. Cuscuta campestris was found to be much more resistant to all AABI herbicides tested. The I₅₀ value of C. campestris growth inhibition by glyphosate was eightfold higher than that of transgenic, glyphosate‐resistant cotton (RR‐cotton). The I₅₀ value for C. campestris shoot growth inhibition by sulfometuron was above 500 μM, whereas that of sorghum roots was only 0.004 μM. Cuscuta campestris exposed to glyphosate gradually accumulated shikimate, confirming herbicide penetration into the parasite and interaction with an active form of the target enzyme of the herbicide, 5‐enolpyruvylshikimate‐3‐phosphate synthase. More than half of the C. campestris plants associated with transgenic, glyphosate‐resistant sugarbeet (RR‐sugarbeet) treated with glyphosate or with transgenic, sulfometuron‐resistant tomato (SuR‐tomato) treated with sulfometuron recovered and resumed regular growth 20–30 days after treatment. New healthy stems developed, followed by normal flowering and seed setting. The results of the current study demonstrate the unique capacity of C. campestris to tolerate high rates of AABI. The mechanism of this phenomenon is yet to be elucidated.     

Expression of cyclooxygenase-2 in IL-1β-stimulated mesangial cells is medicated by NF-κB/IκB signal pathway

AIM: To investigate the role of NF-κB/IκB signal pathway in the regulation of cyclooxygenase-2 (COX-2) expression in human mesangial cells (HMC). METHODS: The PGE₂ concentration in supernatants of HMC was measured by radioimmunoassay. COX-2 mRNA and protein expression were determined by RT-PCR and Western blot. Electrophoretic mobility shift assay (EMSA) and Western blot were used to detect the activity of NF-κB and degradation of IκB. RESULTS: IL-1β significantly upregulated COX-2 expression and PGE₂ production in HMC. Significant up-regulation of NF-κB activation, nuclear translocation of p65 subunit, and degradation of IκB α and IκB β were observed in IL-1β-induced HMC. CONCLUSION: Expression of COX-2 in IL-1β-induced HMC is mediated by NF-κB/IκB signal pathway.