A/California/7/2009与A/California/4/2009病毒感染力比较

目的甲型H1N1流感病毒A/California/7/2009与A/California/4/2009病毒序列比较同源性在99%以上,本实验旨在比较两株病毒感染BALB/c小鼠研究感染力强弱。方法分别将A/California/7/2009（CA7）与A/California/4/2009（CA4）两株病毒分别连续10倍稀释后,对4~6周龄雌性BALB/c小鼠经乙醚麻醉后进行滴鼻攻毒,每个稀释度接种10只实验小鼠,测定CA7 MLD50为101.24/0.05 mL,检测小鼠感染、致病的多项指标,观察期为14 d。结果相同TCID50的CA7和CA4病毒感染小鼠,CA4感染小鼠后14 d内死亡率为20%,而CA7感染小鼠后8 d内死亡率为100%。CA7 106TCID50感染的小鼠病理表现为重度弥漫性间质性肺炎,CA4 106TCID50感染的小鼠病理表现为中度-重度间质性肺炎。结论在相同条件下,CA7感染力明显强于CA4。     

Preparation of copoly (γ-benzyl-l-glutamyl-N5-β-d-glucopyranosyl-l-glutamine) and its interaction with fibroblast cells

Copoly(α-amino acid)s consisting of γ-benzyl-l-glutamate and $\text{N}{}^5\text{-β-}\text{d}\text{-glucopyranosyl-}\text{l}\text{-glutamine}$ were prepared by the reaction of copoly(l-glutamate) containing succinimide ester, which served as active site for the coupling reaction with β-d-glucopyranosylamine. The α-helical conformation of these copolymers became unstable in DMF as the content of glutamine derivative increased. A dry film made from this copolymer could take a full α-helical conformation even at such a high content as 80% of the glutamine derivative, but in a wet film this ordered structure was partially disrupted by hydration. The hydraulic permeability of this copoly(α-amino acid) was clearly dependent on the molar content of glucopyranosyl groups. The attachment of fibroblast cells to these hydrated copolymer films was effectively depressed in the presence of a serum-free medium. The cells attached to the substrate were spherical in shape.     

Metabolism of Δ4-cis-PGF1α in the monkey

This isomer of PGF_2α is relatively resistant to metabolic degradation in the Cynomolgus monkey. Thus, 16–20 per cent of the amount injected was excreted unchanged in the urine. Five metabolites with 20, 18, 16 and 14 carbon atoms in the skeleton were identified. The data are similar to those earlier seen in the rat and further support the idea that this analogue of PGF_2α could have a long half-life time in the mammalian body and thus a long duration of its pharmacological actions.     

Conformational studies on poly(N-δ-trimethyl-l-ornithine)

$\text{Poly}\text{(N-δ-}\text{trimethyl-}\text{l}\text{-ornithine}$), (Me₃Orn)_n, is usually not able to attain the α-helical conformation in aqueous solution independent of its pH value; however, it becomes α-helical at low concentrations of sodium perchlorate over a wide pH range according to the circular dichorism (c.d.) spectra. Cl^?, SO₄^2? and H₂PO₄^? do not induce α-helix formation. One can conclude that a distinct topology of the anions bound by the side chains is responsible for the α-helix-inducing effect of some water-structure-breaking anions such as perchlorate. This means that the anions are inserted between the ?N⁺ of the side groups shielding the positive charges repelling one another. The insertion of the anions requires that the water molecules surrounding the ions can be stripped off, which is easily possible if they are water-structure-breaking ones. At higher perchlorate concentrations, the c.d. spectrum changes. It is characterized by a negative shoulder near 208 nm and a pronounced minimum at ≈ 226 nm. With increasing temperature, the c.d. spectrum of the α-helix occurs. Finally the α-helix undergoes a conformational change to the random coil. The apparent transition enthalpy ΔH_vH is remarkably lower than that of the homologue (Me₃Lys)_n, obviously due to a lower cooperativity of the transition. In contrast to poly(l-ornithine), (Orn)_n, the c.d. spectrum of (Me₃Orn)_n remains almost unchanged after adding anionic surfactants such as sodium octyl sulphate (SOS) or sodium dodecyl sulphate (SDS). In organic solvents like methanol or isopropanol, in contrast to (Orn)_a and (Lys)_n, no α-helix formation occurs. However, in mixtures of these alcohols or dioxane with water, α-helix formation is induced by perchlorate, as in pure water. The thermal stability of the α-helix in these systems is increased.     

Dissimilatory nitrate uptake in Paracoccus denitrificans via a Δ\̃gmH+-dependent system and a nitrate-nitrite antiport system

Respiration-driven proton translocation has been studied with the oxidant pulse method for cells of denitrifying Paracoccus denitrificans oxidizing H₂ during reduction of O₂, NO^?₃, NO^?₂ or N₂O. A simplified scheme of anaerobic electron transport and associated proton translocation is shown that is consistent with the measured $\text{H}{}^{\mathrm{+}}\text{oxidant ratios}$. Furthermore, the kinetics and energetics of NO^?₃ uptake in whole cells of P. denitrificans were studied. For this purpose, we measured H₂ consumption or N₂O production after addition of NO^?₃ to a cell suspension, which indirectly gave information about uptake (and reduction) of NO^?₃. It was found that a lag phase in H₂ consumption or N₂O production appeared whenever the membrane potential was dissipated by addition of thiocyanate, carbonyl cyanide m-chlorophenylhydrazone or triphenyl-methylphosphonium bromide. However, these lag phases were not observed when NO^?₂ was present at the moment of introduction of NO^?₃. On the basis of these findings we conclude that there are two uptake systems for NO^?₃. One system is dependent on the proton-motive force and is probably used for initiation of NO^?₃ uptake. The other is an $\text{NO}{}^{\mathrm{?}}{}_3\text{NO}{}^{\mathrm{?}}{}_2$ antiport and its function is to take over NO^?₃ uptake from the first system.     

Comparison of red cell and kidney (Na+ + K+)-ATPase at 0°C

Human red cell and guinea pig kidney $\text{(}\text{Na}{}^{\mathrm{+}}\text{+}\text{K}{}^{\mathrm{+}}\text{)-}\text{ATPase}$ were phosphorylated at 0°C. Using concentrations of ATP ranging from 10^?6 to 10^?8 M, ATP-dependent regulation of reactivity is observed with red cell but not kidney $\text{(}\text{Na}{}^{\mathrm{+}}\text{+}\text{K}{}^{\mathrm{+}}\text{)-}\text{ATPase}$ at 0°C. In particular, with the red cell enzyme only, the following are observed: (i) the ratio of enzyme-bound ATP (E·ATP, measured by the pulse-chase method of Post, R.L., Kume, S., Tobin, T., Orcutt, B. and Sen, A.K. (1969) J. Gen. Physiol. 54, 306s-326s) to steady-state level of total phosphoenzyme (EP) decreases with decrease in ATP concentration and (ii) the apparent turnover of phosphoenzyme (ratio of Na⁺-stimulated ATP hydrolysis to level of total EP at steady state) also varies as a function of ATP concentration. In addition, when EP is formed at very low ATP (0.02 μM), and then EDTA is added, rapid disappearance of a fraction of EP occurs, presumably due to ATP resynthesis, only with the red cell enzyme. These differences in behaviour of the red cell and kidney enzymes are explained on the basis of the observed predominance of K⁺-insensitive EP in red cell, but K⁺-sensitive EP in kidney $\text{(}\text{Na}{}^{\mathrm{+}}\text{+}\text{K}{}^{\mathrm{+}}\text{)-}\text{ATPase}$ at 0°C.     

Determination of H+e− ratios in chloroplasts with flashing light

Using a rapid pH electrode, measurements were made of the flash-induced proton transport in isolated spinach chloroplasts. To calibrate the system, we assumed that in the presence of ferricyanide and in steady-state flashing light, each flash liberates from water one proton per reaction chain. We concluded that with both ferricyanide and methylviologen as acceptors two protons per electron are translocated by the electron transport chain connecting Photosystem II and I. With methyl viologen but not with ferricyanide as an acceptor, two additional protons per electron are taken up due to Photosystem I activity. One of these latter protons is translocated to the inside of the thylakoid while the other is taken up in H₂O₂ formation. Assuming that the proton released during water splitting remains inside the thylakoid, we compute $\text{H}{}^{\mathrm{+}}\text{e}{}^{\mathrm{?}}$ ratios of 3 and 4 for ferricyanide and methyl viologen, respectively.In continuous light of low intensity, we obtained the same $\text{H}{}^{\mathrm{+}}\text{e}{}^{\mathrm{?}}$ ratios. However, with higher intensities where electron transport becomes rate limited by the internal pH, the $\text{H}{}^{\mathrm{+}}\text{e}{}^{\mathrm{?}}$ ratio approached 2 as a limit for both acceptors.A working model is presented which includes two sites of proton translocation, one between the photoacts, the other connected to Photosystem I, each of which translocates two protons per electron. Each site presents a ≈ 30 ms diffusion barrier to proton passage which can be lowered by uncouplers to 6–10 ms.     

Characterization of a β-actinin-like protein in purified non-muscle cell membranes. Its activity on (Na+ + K+)-ATPase

Treatment by EDTA of purified plasma membranes from MF₂S cells (a variant of the murine plasmacytoma MOPC 173) solubilized proteins and increased by a 1000-fold the sensitivity of $\text{(}\text{Na}{}^{\mathrm{+}}\text{+}\text{K}{}^{\mathrm{+}}\text{)-}\text{ATPase}$ to ouabain. When added back with Ca²⁺ to treated plasma membranes, these EDTA-solubilized proteins restored the initial sensitivity of the enzyme to its inhibitor. We report the purification of a protein of $\text{M}{}_{\mathrm{<mtext>r</mtext>}}$ 32 000, isolated from the EDTA-treated membrane supernatant. This protein was purified by a one-step procedure involving a preparative polyacrylamide gel electrophoresis without detergent. In the presence of Ca²⁺ it was able to restore the original sensitivity to ouabain of $\text{(}\text{Na}{}^{\mathrm{+}}\text{+}\text{K}{}^{\mathrm{+}}\text{)-}\text{ATPase}$ from EDTA-treated membrane. This protein was shown to be similar to the β-actinin described by Maruyama by the following criteria: (1) molecular weight and amino acid composition; (2) cross-reactivity with their respective antisera; (3) in the presence of Ca²⁺ the same quantitative biological activity on ouabain sensitivity of the $\text{(}\text{Na}{}^{\mathrm{+}}\text{+}\text{K}{}^{\mathrm{+}}\text{)-}\text{ATPase}$. A possible interaction between β-actinin, calmodulin and membrane-bound $\text{(}\text{Na}{}^{\mathrm{+}}\text{+}\text{K}{}^{\mathrm{+}}\text{)-}\text{ATPase}$ is discussed.     

不同氮效率水稻全生育期内对增硝营养的响应及其生理机制

通过添加硝化抑制剂（二氰胺,DCD）来控制硝化作用的水培试验方法,研究了氮高效水稻品种南光和氮低效水稻品种ELIO的籽粒产量对增硝营养（NH4＋∶NO3-比例为100∶0和75∶25）的响应,同时从产量构成、不同生育时期水稻生长、氮素吸收和同化4个方面研究了造成其产量差异的生理机制。结果表明：增NO3-营养可以显著促进氮高效水稻品种南光的生长,从而使其籽粒产量水平提高21%,而对氮低效水稻品种ELIO的籽粒产量没有显著影响。进一步分析表明：在增NO3-营养条件下,南光的穗粒数增加了25%,结实率增加了16%,而氮低效水稻品种ELIO的结实率和穗粒数在两种营养条件下没有显著变化;增NO3-营养可以促进南光对氮素的吸收,使其在苗期、分蘖盛期、齐穗期和成熟期对氮素的吸收量平均增加了36%,进而促进了其生长,干物质积累量在四个生育时期平均增加了30%;南光叶片硝酸还原酶和根系谷氨酰胺合成酶的活力在增硝营养条件下分别增加了100%和95%,说明增硝营养促进了南光对NH4＋和NO3-的同化利用。与氮低效水稻品种（ELIO）相比,氮高效水稻品种（南光）对增硝营养表现出较强的生理响应。     

盐渍区农田氮肥施用量对土壤硝态氮动态变化的影响

土壤硝态氮动态变化和残留与农田硝态氮淋溶以及地下水硝态氮污染密切相关。为了促进海河低平原盐渍区农田氮肥合理利用以及农业可持续发展,试验在盐化潮土条件下,通过设计不同施氮量（0,70,140,210kg N hm^-2）处理,重点研究了该区农田氮肥施用量对土壤硝态氮动态、残留以及土壤氮损失的影响。结果表明：（1）0～100cm土壤剖面硝态氮总量随施氮量显著增加,施用氮肥没有改变剖面硝态氮总量随玉米生育进程波状变化趋势,但明显增强了其变化幅度;（2）施氮改变了硝态氮土壤剖面空间分布状态,表现出施氮后上部土层（0～40cm）硝态氮比例显著增加而后迅速降低的趋势;（3）硝态氮残留与氮素损失随施氮量增加而增加,且N210和N140处理下氮素损失量显著高于N70和N0。     

不同品种菠菜叶肉及叶柄中硝态氮累积与硝酸还原酶活性的关系

盆栽试验条件下,菠菜体内的硝态氮含量及硝酸还原酶（NR）活性因品种和部位而异。硝态氮含量以短缩茎中最高,叶和叶柄中次之,根中最低,且根,冠比越大的品种,其整体植株中的硝态氮含量越低;根尤其是侧根NR活性较高;叶肉和叶柄中硝态氮含量均与根中以内、外源硝酸盐为底物的NR活性呈一定的负相关。     

不同氮浓度和形态比例对水曲柳幼苗叶绿素合成、光合作用以及生物量分配的影响 (英文)

 水曲柳（Fraxinus mandshurica）是我国东北林区重要的工业用材树种,在东北林区广泛种植,因而其培育近来日益得到高度重视。在水曲柳的种植区域内,尽管林地内凋落物丰富,但该地区气温低,冬季长,氮素矿化速度低,氮素供给显得不足。本研究采用沙培的方式,在为幼苗提供完     

水氮配合对绿洲沙地农田玉米产量、土壤硝态氮和氮平衡的影响

在黑河中游边缘绿洲沙地农田研究了不同的水氮配合对玉米产量、土壤硝态氮在剖面中的累积和氮平衡的影响.结果表明,施氮处理较不施氮处理产量增加48.22%～108.6%,施氮量超过225 kg hm-2,玉米产量不再显著增加.受土壤结构影响土壤硝态氮在土壤中呈"W"型分布,即土壤硝态氮含量在0～20 cm、140～160 cm和260～300 cm土层均出现峰值,并随施氮量增加,峰值增高.在常规高灌溉量处理硝态氮含量峰值最高值出现在260～300 cm土层,节水25%灌溉处理硝态氮含量峰值最高值出现在土壤表层0～20 cm土层.在常规高灌溉量处理0～300 cm土层中200～300土层硝态氮累积量所占比例最高,介于27.56%～51.86%之间;节水25%灌溉处理在0～300 cm土层中100～200土层硝态氮累积量所占比例最高,介于32.94%～38.07%之间;表明低灌溉处理下土壤硝态氮在土壤浅层累积较多,而高灌溉处理使更多的硝态氮淋溶至土壤深层.与2006年相比,2007年不施氮处理0～200 cm土层土壤硝态氮含量和积累量均明显减少;而施氮处理变化很小,在低灌溉处理甚至表现出硝态氮含量和积累量增加,表明施氮是土壤硝态氮累积的主要来源,而灌溉则使硝态氮向土壤深层淋溶.0～200 cm 土层土壤硝态氮累积量平均介于27.66～116.68 kg hm-2、氮素表观损失量平均介于77.35～260.96 kg hm-2,和施氮量均呈线性相关,即随施氮量增加,土壤硝态氮累积量和氮素表观损失量均增加,相关系数R2介于0.79～0.99之间,相关均显著.随施氮量增加,玉米总吸氮量和氮收获指数增加,氮的农学利用率降低,而灌溉的影响较小.施氮量超过225 kg hm-2时,地上部植株氮肥吸收利用率和籽粒氮肥吸收利用率开始有降低趋势.所以,在沙地农田,节水10%～25%的灌溉水平和225 kg hm-2的施氮水平可以在避免水肥过量投入的基础上减少土壤有机氮淋溶对地下水造成的污染威胁.     

外源脯氨酸对盐胁迫下甜瓜幼苗硝酸还原的影响

采用营养液水培方法,以＂雪美＂品种甜瓜（Cucumis melo L.）为材料,研究了外源脯氨酸（Proline）对盐胁迫下甜瓜幼苗叶片和根系硝酸还原的影响。结果表明：（1）盐胁迫提高了甜瓜幼苗叶片和根系内铵态氮（NH4＋-N）和可溶性蛋白含量;降低了硝态氮（NO-3-N）含量和硝酸还原酶（nitrate reductase,NR）活性。（2）外源施用脯氨酸明显地提高了盐胁迫下甜瓜幼苗叶片和根系内NO-3-N和可溶性蛋白含量;降低了盐胁迫下甜瓜幼苗叶片和根系内NH＋4-N含量;增强了盐胁迫下甜瓜幼苗体内NR活性。研究结果表明,外源脯氨酸可以通过调节甜瓜幼苗体内硝酸还原酶活性和氮化合物含量来缓解盐胁迫对甜瓜幼苗植株的伤害。     

好氧反硝化微生物多样性及其反硝化功能初步研究

为研究污水厂/养殖池中好氧反硝化微生物的多样性及菌株反硝化能力,本研究采集了位于福建省厦门市和漳州市的污水处理厂、排污口、污水池、对虾养殖池的污水和污泥样品进行好氧反硝化微生物的富集、分离、鉴定和功能筛选。分别以NaNO3、NaNO2作为唯一氮源共分离纯化获得128株单菌。其中以NaNO3为唯一氮源分离得到63株,以NaNO2为唯一氮源分离得到65株。16SrRNA基因序列分析表明,128株单菌分属于γ-变形菌纲(Gammaproteobacteria,58.6%)、芽胞杆菌纲(Bacilli,6.4%)、放线菌纲(Actinobacteria,11.7%)、α-变形菌纲(Alphaproteobacteria,8.6%)、纤维菌纲(Cytophagia,2.3%)、鞘脂杆菌纲(Sphingobacteria,0.8%)和黄杆菌纲(Flavobacteria,1.6%)7个纲中的38个属。其中盐单胞菌属(Halomonas,29.7%)和芽胞杆菌属(Bacillus,12.5%)为优势菌属,并且广泛存在于各个样品中。反硝化功能初筛结果表明,35株菌能在72h内将20mg·L-1 NO-3-N/NO-2-N完全去除;复筛结果表明,21株菌能在72h内将100 mg·L-1 NO-3-N/NO-2-N完全去除,并且盐单胞菌属、卓贝尔氏菌属(Zobellella)、斯塔普氏菌属(Stappia)及节杆菌属(Arthrobactor)反硝化效果较好,其中斯塔普氏属是首次报道具有好氧反硝化功能。本研究结果表明,污水场/养殖池等环境中可培养反硝化细菌多样性丰富,同时高效反硝化菌的获得也为含氮废水的生物处理提供了良好的菌种资源。     

不同氮源下生长的柚树叶片光合参数对高浓度CO2驯化作用的比较

比较研究了在不同形式氮源下生长柚树叶片光合对高浓度 CO2 驯化过程中有关参数变化。植株生长在人工混成土壤中 ,分别浇灌含有 2 mmol L- 1N的 NO- 3 - N,NH+ 4 - N和 NH4 NO3- N溶液。空气 CO2 增高处理时向生长植株的开顶透明罩中通入 74.4Pa CO2 ,以空气 CO2 生长的植株为对照。利用 CI- 30 1 ( CID,Inc) CO2 气体交换系统测定叶片光合速率和通过光合作用相关响应曲线计算光合参数。结果表明 ,在 CO2分压倍增下 ,NO- 3 - N生长植株光饱和光合速率较大气 CO2 分压下的高。而生长在 NH+ 4 - N和 NH4 NO3- N的植株光合速率与大气 CO2 分压下的相近 ,表现对高 CO2 的驯化。在空气 CO2 倍增下无论供给何种形式氮源并不影响Γ* ,但可增高 Rd( P<0 .0 5 )。 CO2 分压倍增下供给 NO- 3 - N植株的 Vcmax和 Jmax较大气分压相应的植株高 ,而 NH+ 4 - N和 NH4 NO3- N植株则与大气 CO2分压的相应植株相似 ( P>0 .0 5 )。无论供给何种形式氮源 ,生长在空气 CO2 分压倍增下不改变叶片单位面积干重 ,叶绿素含量和叶片中氮在 Rubisco、生物能学组分和捕光色素复合体组分的分配系数 ;但能改变叶片中氮含量。植物对高 CO2 的驯化可能受到不同形式氮利用性的影响 ,在对高 CO2 驯化过程亦反映叶片中氮在不同光合功能组分     

不同氮素形态比例对五味子幼苗生长特性的影响

以2年生五味子苗木为试验材料,在田间条件下,施以铵态氮(NH4+-N)和硝态氮(NO3--N)不同比例,分析了叶片可溶性蛋白、叶绿素含量、根系及茎叶中全氮含量、生物量等季节的动态变化规律,探讨了不同氮素形态比例对五味子苗木生长的影响。结果表明,五味子苗木在不同生长时期对不同氮素形态的吸收和利用存在明显差异,NH4+-N和NO3--N对五味子幼苗生长有显著的联合效应。在五味子生长前期,五味子主要以吸收和同化NH4+-N为主,并以铵态氮和硝态氮比例为75∶25时地上部生物量积累较多;而在五味子生长的中后期,五味子主要以NO3--N吸收和同化为主,并以铵态氮和硝态氮比例为25∶75时地上部生物量积累较多。     

一株海水异养硝化-好氧反硝化菌系统发育及脱氮特性

【目的】确定一株分离自海水的异养硝化-好氧反硝化菌的系统发育地位并探索其脱氮特性和机理,以期为解释异养硝化-好氧反硝化机理以及改进海水养殖及废水的生物脱氮工艺提供理论依据。【方法】通过形态观察、生理生化实验和16S rRNA基因序列分析,鉴定该菌株;通过测定菌株在不同无机氮源降解测试液中的生长和脱氮效率,分析其异养硝化和好氧反硝化性能。【结果】经鉴定该菌株属于盐单胞菌属(Halomonas);最适生长条件为盐度3%、pH 8.5、温度28℃、碳氮比10:1,在盐度为15%的培养液中仍能生长;可以同时去除氨氮、亚硝酸氮和硝酸氮,24 h时对NH4+-N、NO2--N、和NO3--N的去除率可分别达到98.29%、99.07%、96.48%,3种形态无机氮同时存在时,会优先利用NH4+-N,且总无机氮去除率较单一存在时更高,说明该菌株可实现同步硝化反硝化。【结论】该分离自海水的异养硝化-好氧反硝化菌属于盐单胞菌属(Halomonas),在高盐环境中仍能生长,同时具有高效的异养硝化和好氧反硝化能力,能够独立完成脱氮的全部过程。