寄主植物对B型烟粉虱形态学和生物学特性的影响

为了解B型烟粉虱(Bemisiatabaci)在不同寄主植物上的生物学特性,以制定科学的综合治理措施,作者在271℃的条件下,研究测定了B型烟粉虱在棉花(Gossypiumhirsutum)、一品红(Euphorbiapulcherrima)、甘蓝(Brassicaoleraceavar.capitata)、黄瓜(Cucumissativus)、西葫芦(Cucurbitapepo)、茄子(Solanummelongena)和番茄(Lycopersiconesculentum)上各虫态大小、成活率、发育历期、成虫寿命、平均产卵量等生物学参数。结果表明:取食不同寄主植物的烟粉虱伪蛹在黄瓜和棉花上体型最大,在一品红上最小;烟粉虱从卵到成虫羽化,发育历期以在一品红上最长(22.0d),黄瓜上最短(17.3d);平均单雌产卵量以在番茄上最多(266.5粒/雌),一品红上最少(112.9粒/雌);成虫的寿命在番茄、黄瓜和茄子上显著长于在其他4种寄主植物上。烟粉虱从卵发育到成虫的存活率以在黄瓜上最高(77.8%),西葫芦上最低(55.6%),两者差异显著。综合比较7种寄主植物,黄瓜是烟粉虱种群生长发育和繁殖的最适寄主。     

寄主植物对B型烟粉虱选择行为和生物学参数的影响

通过培养皿内自由扩散观察和生物学观察,对黄瓜、茄子、辣椒、棉花和甘薯上B型烟粉虱的寄主选择性和生物学参数进行了研究.结果表明：B型烟粉虱成虫向寄主植物叶片自由扩散的初始阶段（2 h）,各寄主植物叶片上虫量的差异不大,在随后的4～48 h内黄瓜叶片上的虫量不断增加,茄子、棉花和甘薯叶片上的虫量相对稳定,而辣椒叶片上的虫量却不断下降,说明B型烟粉虱对黄瓜的选择性最强、对辣椒的选择性最弱,且饥饿和吡虫啉预处理均不影响B型烟粉虱的寄主选择性;取食不同寄主植物烟粉虱成虫的蜜露分泌量差异显著,从高到低依次为黄瓜、甘薯、棉花、茄子、辣椒;黄瓜、茄子、甘薯、棉花上烟粉虱成虫的寿命显著长于辣椒,其平均单雌产卵量(分别为224.33粒、182.33粒、191.73粒和172.60粒)也均显著高于辣椒(47.83粒);各寄主植物上烟粉虱卵的孵化率和发育历期差异均不显著;烟粉虱若虫在黄瓜、茄子、甘薯和棉花上的发育历期分别为10.60 d、11.96 d、11.11 d和13.20 d,死亡率分别为5.21%、27.78%、17.24%和37.11%,在辣椒上不能完成正常发育.     

丽蚜小蜂两个品系寄生行为及对不同寄主植物上烟粉虱的选择性

对丽蚜小蜂两个品系(分别来自北京和美国)寄生烟粉虱的行为和在番茄、黄瓜、甘蓝、茄子及棉花烟粉虱上的发育历期和寄生率进行了研究。结果表明,丽蚜小蜂通过寄主定位、寄主检查、产卵、清扫和梳理等过程对烟粉虱进行寄生,北京品系平均产卵寄生时间为5.0 m in,美国品系为4.2 m in,品系间差异显著。北京品系在棉花烟粉虱上发育历期最短,为17.4 d,甘蓝烟粉虱上发育历期最长,为20.0 d;美国品系在棉花烟粉虱上发育历期最短,为16.3 d,在其余4种寄主植物烟粉虱上发育历期较长(17.3~17.9 d)。2个品系的寄生率均表现为番茄烟粉虱上最高,分别为37.3%和39.0%;棉花次之,分别为32.2%和35.5%;黄瓜上最低,分别为30.2%和29.6%。在寄主植物选择性试验中,2个品系亦表现为寄生番茄烟粉虱时寄生率最高,美国品系为62.7%,北京品系为56.3%,寄生黄瓜烟粉虱时寄生率最低,分别为30.8%和29.0%。     

烟粉虱及温室白粉虱为害后对后续粉虱种群的影响

【目的】分析烟粉虱Bemisia tabaci(Gennadius)或温室白粉虱Trialeurodes vaporariorum(Westwood)为害番茄后对后续温室白粉虱和烟粉虱生长、发育、成虫寿命和繁殖等产生的促进或抑制作用,可为明确寄主植物番茄介导的温室白粉虱-烟粉虱的种间互作,开展粉虱的科学防控提供科学依据。【方法】通过在寄主植物番茄叶片上先将B型烟粉虱或温室白粉虱按不同的顺序、时间间隔分开接种,再系统观察后续接上的两种粉虱生长、发育、繁殖等种群参数的变化。【结果】(1)先期接上烟粉虱对后续温室白粉虱的发育、寿命、产卵量有明显的促进作用;这种作用需烟粉虱的持续诱导,若去掉烟粉虱,其对温室白粉虱的促进作用即消失;先期接上温室白粉虱可缩短后续烟粉虱伪蛹期,但温室白粉虱的持续存在不利于烟粉虱的产卵,且明显降低烟粉虱的内禀增长率和净增殖率。(2)先后在番茄上同时接上温室白粉虱可降低后续烟粉虱的单雌产卵量和雌、雄虫的成虫寿命;先后同时接种烟粉虱却显著地增加了温室白粉虱的单雌产卵量;烟粉虱的提前存在降低了后续烟粉虱单雌产卵量。(3)但两种粉虱之间作用存在着一定的时间滞后性。烟粉虱对温室白粉虱的发育、寿命、产卵量产生的促进作用大约在其卵期后的一段时间才能显现出来;温室白粉虱对烟粉虱伪蛹期的缩短作用也需提前诱导;而温室白粉虱对温室白粉虱的促进作用相当滞后,直到成虫期才显现出来。【结论】B型烟粉虱和温室白粉虱之间可通过寄主番茄产生相互影响,前期烟粉虱为害可显著促进后续温室白粉虱卵和若虫的发育,而前期温室白粉虱为害对烟粉虱的发育不利。     

烟粉虱MEAM1和AsiaⅡ7隐种对不同寄主的选择性和生态适应性

广东省感染木尔坦棉花曲叶病毒(CLCuMuV)的朱槿上烟粉虱隐种为MEAM1和AsiaⅡ7混合种群,并且AsiaⅡ7是该病毒有效传毒介体,明确这两个隐种的寄主选择性差异,能够为介体烟粉虱的防治提供依据。本研究选择锦葵科的棉花、黄秋葵和茄科的茄子、番茄4种寄主植物为供试寄主,通过笼内自由扩散、实验室嗅觉测定、发育观察,比较了MEAM1和AsiaⅡ7隐种对不同寄主的选择性和生态适应性。结果表明:烟粉虱MEAM1和AsiaⅡ7对4种寄主存在明显的寄主选择性,MEAM1成虫和产卵选择趋性为棉花>茄子>番茄>黄秋葵;AsiaⅡ7成虫和产卵选择趋性为棉花>黄秋葵>茄子>番茄。MEAM1和AsiaⅡ7在4种寄主上的发育历期、存活率有显著差异,MEAM1的存活率(卵到成虫)在棉花、茄子、黄秋葵上均较高(80%以上),番茄上最低(59%);AsiaⅡ7的存活率(卵到成虫)为棉花(90%)>黄秋葵(71%)>茄子(64%),在番茄上发育至1龄全部死亡。上述结果表明,4种作物均适宜MEAM1生长发育,锦葵科的2种作物适宜AsiaⅡ7隐种生长发育,茄科的2种作物不适宜。应避免棉花与黄秋葵近距离种植,防止传毒介体烟粉虱将黄秋葵作为桥梁寄主将病毒传播至棉花。     

茉莉酸诱导番茄对烟粉虱发育、存活与繁殖的影响

【背景】目前,烟粉虱已成为世界性的入侵害虫,对我国的农业生产造成了严重损失。由于烟粉虱抗药性增长迅速,以非化学防治为主的综合防治措施,成为控制烟粉虱的重要手段。近年来,茉莉酸作为与损伤相关的植物激素和信号分子,已被发现广泛存在于植物体内,外施茉莉酸可激活植物的防御系统,诱导其产生次生防御物质,从而影响包括烟粉虱在内的多种害虫的生长发育、繁殖与存活等。【方法】在温度（26±1）℃、相对湿度（75±5）％、光照L：D=14：10的条件下,通过在番茄根部和叶部外施茉莉酸,研究茉莉酸诱导的番茄上烟粉虱的生长发育和繁殖等生物学特性。【结果】在茉莉酸诱导的番茄上,烟粉虱的发育历期以叶部诱导（shootJA．induced,SJA）的番茄上最长,平均历期为27．3d,与对照组（control,CON）番茄上的25．7d和根部诱导（root JA-induced,RJA）番茄上的25．8d差异显著;在SJA和CON番茄上,烟粉虱的世代存活率分别为47．17％和55．57％,而在RJA番茄上烟粉虱的存活率为81．13％,后者与前两者差异达到显著水平;烟粉虱成虫在CON、RJA和SJA番茄上的平均寿命分别为25．1、23．6和18．7d,即在JA诱导的番茄上烟粉虱成虫的平均寿命明显缩短;在产卵量方面,对照番茄上发育的烟粉虱平均单雌产卵量最大,为132．8粒,SJA番茄上发育的烟粉虱平均单雌产卵量最小,为107．9粒,两者差异显著;RJA番茄上发育的烟粉虱平均单雌产卵量为118．1粒,与前两者无显著差异。【结论与意义】利用茉莉酸诱导番茄可对烟粉虱的发育、繁殖和存活产生不同程度的影响,且诱导部位不同产生的影响也有很大差异。本结果对探索烟粉虱等刺吸式害虫的防治新策略有一定的参考价值。     

不同寄主植物对烟粉虱发育和繁殖的影响

研究了烟粉虱 B型 ( Bemisia tabaci Gennadius)在番茄、茄子、黄瓜和甘蓝上的发育、存活和繁殖情况。在 2 6± 1℃的条件下 ,烟粉虱从卵发育到成虫的存活率以在甘蓝上的最高 ,为 68.5 5 % ,黄瓜上的最低 ,为46.2 8% ;发育时间以在茄子上最短 ,为 1 7.5 d,黄瓜上最长 ,为 1 9.3d,差异显著 ;平均单雌产卵量以在甘蓝上最大 ,为 1 43粒 ,黄瓜上最小 ,为 98.2 5粒 ;成虫的寿命以在甘蓝上最长 ,平均为 2 5 .2 d,黄瓜上为 1 7.2 d;内禀增长率 rm以在茄子上的最大 ,为 0 .1 41 6,黄瓜上最小 ,为 0 .1 1 43。综合比较 4种不同寄主植物 ,茄子是烟粉虱种群生长发育和繁殖最适宜的寄主     

B型烟粉虱在四种葫芦科寄主植物上的发育和繁殖

研究了B型烟粉虱在4种葫芦科寄主植物黄瓜、节瓜、苦瓜和丝瓜上的发育和繁殖特性.结果表明,B型烟粉虱在节瓜上的世代发育历期最短,为19.3 d,在苦瓜上的世代发育历期最长,为29.0 d;世代存活率在黄瓜上最高,为92.85％,在苦瓜上最低,为53.08％;平均单雌产卵量在黄瓜上最多,为187.4粒,苦瓜上最少,为30.0粒;雌成虫寿命以在黄瓜上最长,为25.2 d,在苦瓜上最短,为10.9 d.B型烟粉虱在黄瓜、节瓜、苦瓜和丝瓜上的内禀增长率（r_m）分别为0.1453、0.1429、0.0616和0.1055.综合比较4种葫芦科植物,黄瓜是B型烟粉虱的最适宜寄主.     

烟粉虱在烟株上的垂直分布及寄主选择性

烟粉虱是云南省农业生产上的重要害虫之一。通过田间系统调查和室内观察相结合,研究了烟粉虱在烟株上的垂直分布特性和在8种寄主作物上的取食、产卵趋性。（1）烟粉虱在烟株上的垂直分布特征为上部＞中部＞下部,8月中旬为种群高峰期,上、中、下部叶片的成虫密度分别为15．1、10．9、6．7头？片-1;（2）烟粉虱成虫的取食趋性表现为大豆＞南瓜＞甘薯＞番茄＞一品红＞茄子＞甘蓝＞烟草,各处理间差异不显著（P＞0．05）;（3）产卵趋性表现为一品红＞大豆＞南瓜＞甘薯＞番茄＞茄子＞甘蓝＞烟草,一品红与南瓜、甘蓝、茄子、甘薯、番茄、烟草处理间,以及大豆与烟草处理间存在显著差异（P＜0．05）,其他处理间差异不显著（P＞0．05）。在所测定的8种寄主植物中,烟粉虱成虫对烟草的选择性最差,烟区规划烟田种植范围时,应避免与大豆、南瓜、甘薯、番茄等作物间作或距离太近。     

寄主植物对双斑恩蚜小蜂的发育、存活和繁殖的影响

研究了茄子和扶桑两种不同寄主植物对烟粉虱寄生性天敌双斑恩蚜小蜂Encarsia bimaculata发育、存活和繁殖等特性的影响。在26±0.5℃的条件下,在扶桑上,双斑恩蚜小蜂卵至成虫的发育历期为13.6天,2龄幼虫至成虫的存活率为93.2%;而在茄子上双斑恩蚜小蜂卵至成虫的发育历期和2龄幼虫至成虫的存活率分别为12.1天和91.1％。扶桑上双斑恩蚜小蜂雌性成虫的平均寿命为8.0天,平均单雌产卵量为35.9粒;而在茄子上雌性成虫的平均寿命为6.6天,平均单雌产卵量为27.6粒。双斑恩蚜小蜂在扶桑和茄子植物上的种群内禀增长率分别为0.2081和0.892。两种不同寄主植物对双斑恩蚜小蜂在若虫发育历期和存活率、成虫寿命和平均产卵量以及内禀增长率等方面均存在着显著差异。研究结果表明,寄主植物对双斑恩蚜小蜂的发育、存活和繁殖有较大的影响。     

Metal-organophosphonates: hydrothermal synthesis and structures of [Cu(O3PC10H6CO2H)] and [Cu(bpy)(HO3PC10H6CO2)] (H2O3PC10H6CO2H = 2,6-carboxynaphthalene phosphonic acid)

Hydrothermal methods were used to prepare [Cu(O₃PC₁₀H₆CO₂H)] (1) and [Cu(bpy)(HO₃PC₁₀H₆CO₂)]·2H₂O (2·2H₂O), where H₂O₃PC₁₀H₆CO₂H is 2,6-carboxynaphthalene phosphonic acid (H₃cnp). The two-dimensional structure of 1 consists of layers of edge-sharing {CuO₆} octahedra, producing an AlCl₃- type structure of fused hexagonal rings of copper octahedra, enclosing voids of hexagonal profile. The layer composition is CuO₃ or CuO₆/₂ as each oxygen bridges two copper sites. The Hcnp ligands project from either face of the copper “oxide” layer. Adjacent layers interact through hydrogen bonding interactions between the pendant -CO₂H groups of the ligand. Coordination of the bipyridine ligand in [Cu(HO₃PC₁₀H₆CO₂)] (2) obstructs expansion in two-dimensions, and the material exhibits a chain structure. The chain is constructed of binuclear units of edge-sharing ‘4+1’ {CuO₃N₂} square pyramids linked through the dipodal {HO₃PC₁₀H₆CO₂}²⁻ ligands.     

Spectroscopic and electrochemical properties of a new nitrosyl-complex of Ru(II): trans-[Ru(NO){(CH3CH2)2PCH2CH2P(CH2CH3)2}2Cl](PF6)2

A new ruthenium nitric oxide complex with the bidentate phosphine, 1,2-bis(diethylphosphino)ethane (depe), has been synthesized and characterized by UV-Vis, infrared, EPR, NMR, electrochemical techniques and X-ray structure determination. The electronic spectrum showed a typical band of dπ→pπ* charge-transfer (CT) transition, assigned to Ru(II)NO transition, and the vibrational spectrum exhibited a peak of nitrosyl ligand at (ν_NO=1851 cm⁻¹). A model structure for this complex has been proposed based on ¹H, ¹H{³¹P}, ³¹P{¹H}, ¹³C{¹H}, COSY ¹H¹H{³¹P}, J-Resolved, HSQC, HMBC, HSQC ¹H¹³C{³¹P} and ¹H¹³C HSQC/¹H¹H TOCSY spectral data, and confirmed by X-ray diffraction. The nitrosonium character for the NO ligand become evident through both electron paramagnetic resonance and X-ray data (angle RuNO=177.4(3)°). The reversible monoeletronic process at E_1/2=0.040 V versus SHE was assigned to the ligand NO⁺/NO redox couple. Under treatment with Cd(Hg) solutions containing the [Ru(NO)(depe)₂Cl](PF₆)₂ yields a signal in the EPR spectrum (g_⊥=1.99 and g_//=1.88) which fitted quite well with the simulated spectra of coordinated NO species.     

Synthesis and structure of a lead(II)-citrate: {Na(H2O)3}[Pb5(C6H5O7)3(C6H6O7)(H2O)3]·9.5H2O

The reaction of lead(II) nitrate with trisodium citrate Na₃(C₆H₅O₇) in a 1:22.5 ratio at pH 4.8 provides crystals of {Na(H₂O)₃}[Pb₅(H₂O)₃(C₆H₅O₇)₃(C₆H₆O₇)]·9.5H₂O (1). The structure of 1 is two-dimensional and exhibits five distinct Pb(II) sites and four different modes of citrate bonding. The five lead sites all display hemidirected coordination geometries, that is, irregular distribution of neighboring oxygen atoms resulting in obvious gaps in the coordination spheres. Consequently, the lead coordination geometries exhibit proximal bonding to a number of oxygen donors, as well as distal interactions with nearest neighbors. The coordination numbers vary from 8 to 10, with ‘5+3’, ‘5+4’, ‘6+4’ and ‘7+3’ coordination modes where the first number refers to the proximal ligands and the second to the distal set. The four crystallographically distinct citrate groups include three with deprotonated carboxylate groups (C₆H₅O₇)³⁻ and one with a single protonated carboxyl group (C₆H₆O₇)². The citrate ligands bridge 3, 5, 7 and 7 lead sites. Three of the citrate groups exhibit tridentate chelation coordination to a lead site through two carboxylate oxygen donors and the hydroxyl groups. One citrate group projects an uncoordinated -OH group and a pendant protonated carboxyl group into the interlamellar domain. This latter carboxyl group coordinates to a sodium cation, which exhibits five coordinate geometry defined by three aqua ligands and the carbonyl oxygen of the -CO₂H groups in the basal plane and a citrate -OH donor in the apical position.     

A synthetic combination of mutations, including fs(1)pyr? Su(b) , r? Su(b) and b , causes female sterility and reduces embryonic viability in Drosophila melanogaster

A Drosophila melanogaster mutant, fs(1)pyr ^Su(b) , carrying a mutation that maps to the tip of the X chromosome, has been isolated. The mutation, when present alone, does not confer a detectable phenotype. However, this mutation causes female sterility and reduces embryonic viability when combined with mutations which deregulate the pyrimidine and β-alanine pools. Embryos that are homozygous for the mutations fs(1)pyr ^Su(b) , r ^Su(b) [previously designated as Su(b)] and b, and originate from a female parent homozygous for the three mutations show severely reduced viability. Newly laid eggs begin development normally, but the majority of the embryos die just before the eggs are due to hatch. Received: 15 May 1998 / Accepted: 18 January 1999     

Comparative study of three magnetic nano-particles (FeSO4, FeSO4/SiO2, FeSO4/SiO2/TiO2) in plasmid DNA extraction

Recent updates on Magnetic Nano-Particles (MNPs) based separation of nucleic acids have received more attention due to their easy manipulation, simplicity, ease of automation and cost-effectiveness. It has been indicated that DNA molecules absorb on solid surfaces via hydrogen-bonding, and hydrophobic and electrostatic interactions. These properties highly depend on the surface condition of the solid support. Therefore, surface modification of MNPs may enhance their functionality and specification. In the present study, we functionalized Fe₃O₄ nano-particle surface utilizing SiO₂ and TiO₂ layer as Fe₃O₄/SiO₂ and Fe₃O₄/SiO₂/TiO₂ and then compare their functionality in the adsorption of plasmid DNA molecules with the naked Fe₃O₄ nano-particles. The result obtained showed that the purity and amount of DNA extracted by Fe₃O₄ coated by SiO₂ or SiO₂/TiO₂ were higher than the naked Fe₃O₄ nano-particles. Furthermore, we obtained pH 8 and 1.5 M NaCl as an optimal condition for desorption of DNA from MNPs. The result further showed that, 0.2 mg nano-particle and 10 min at 55 °C are the optimal conditions for DNA desorption from nano-particles. In conclusion, we recommended Fe₃O₄/SiO₂/TiO₂ as a new MNP for separation of DNA molecules from biological sources.     

Versatile coordination behaviour of Ph2AsCH2AsPh2 with Ru(II)

Treatment of ‘RuCl₃ · 3H₂O’ with Ph₂AsCH₂AsPh₂ (dpam) in hot EtOH gives either trans-[RuCl₂(dpam-As,As′)(dpam-As)₂] (1), or cis-[RuCl₂(dpam-As,As′)₂] (2), depending on the mole ratio. On exposure to light, solutions of 2 isomerise to trans-[RuCl₂(dpam-As,As′)₂] (3). Treatment of [RuCl₂(PPh₃)₃] with two equivalents of dpam in CH₂Cl₂ gave a mixture of two products, from which trans-[RuCl₂(PPh₃) (dpam-As,As′)(dpam-As)] (4) was isolated by recrystallisation. The crystal structures of 1-4 are reported. Complexes 1-3 in CH₂Cl₂ undergo electrochemical oxidation to Ru(III), and the Ru(III) form of 2 undergoes isomerisation on the voltammetric timescale to the Ru(III) form of 3.     

A novel unexpected luminescent quarternary coordination polymer {Sm3(C8H4O4)4(C12N2H8)2(NO3)}n with three high asymmetrical central Sm fragments by hydrothermal assembly

A novel chain-like luminescent samarium coordination polymer {Sm₃(C₈H₄O₄)₄(C₁₂N₂H₈)₂(NO₃)}_n (C₈H₄O₄ = phthalate, C₁₂N₂H₈ = 1,10-phenanthroline) has been assembled by hydrothermal process. The title complex crystallizes in the monoclinic system, space group P2(1)/c, with lattice parameters a = 22.56(3) Å, b = 11.155(15) Å, c = 20.32(3) Å, β = 96.70(2)°, V = 5078(12) ų, F(000) = 2964, GOF = 0.857, R₁ = 0.0358, wR₂ = 0.0597, Z = 4. Samarium ions exhibit different coordination modes from each other and lead to the unexpected high asymmetrical structure. To our knowledge, it is the first example of lanthanide coordination polymers comprising the three asymmetrical central Sm³⁺ fragments. The photophysical properties have been studied with excitation and emission spectra.     

Inhibition of reticulocyte iron uptake by NH4Cl and CH3NH2

The aim of this investigation was to test the hypothesis that elevation of intracellular pH would inhibit iron uptake by reticulocytes. The experiments were performed with rabbit reticulocytes and iron bound to rabbit transferrin. Incubation of the cells with NH₄Cl, (NH₄)₂CO₃, CH₃NH₂ and (CH₃)₂NH was used in an attempt to increase intracellular pH. These substances were all found to inhibit iron uptake by reticulocytes. The mechanism of action of NH₄Cl and CH₃NH₂ was investigated in detail. Similar results were found with both reagents. They inhibited iron uptake in a concentration-dependent manner, but produced a small increase in the cellular uptake of transferrin. The onset of action was rapid and the effect was reversible. There was no decrease in the number of transferrin-binding sites per cell and their apparent affinity for transferrin increased slightly, while the efficiency of iron removal from transferrin per binding site diminished greatly. The rate of transferrin release from reticulocytes was unaffected. NH₄Cl did not affect the rate of iron release from transferrin in a cell-free system. Incubation of reticulocytes with 10 mM NH₄Cl or CH₃NH₂ was found to produce an increase in intracellular pH of 0.05—0.15 pH units. The intracellular pH determined by used of the weak acid 5,5-dimethyl-oxazolidine-2,4-dione was significantly higher than that obtained with the weak base (CH₃)₂NH. By transmission electron microscopy it was shown that reticulocytes treated with NH₄Cl or CH₃NH₂ have enlarged intracellular vesicles. The results are considered to support the hypothesis that iron release from transferrin in reticulocytes occurs as a result of protonation of the transferrin within intracellular vesicles. According to this hypothesis, weak bases such as NH₃ and CH₃NH₂ inhibit iron release by neutralizing H⁺ within the vesicles.     

Coordination chemistry of acrylamide 6: Formation and structural characterization of [Fe(O-OC(NH2)CHCH2)6][Fe2OCl6]

The new acrylamide iron(II)/iron(III) complex [Fe(O-OC(NH₂)CHCH₂)₆][Fe₂OCl₆] (1) was obtained by the reaction of a mixture of anhydrous FeCl₂ and anhydrous FeCl₃ with acrylamide (molar ratio 1:2:6) in 98% pure commercial nitromethane under nitrogen atmosphere. According to an X-ray structural analysis, the acrylamide ligands in the cation are coordinated via the amide-oxygen atoms. The formation of the (μ-oxo)bis[trichloroferrate(III)]²⁻ anion presumably resulted from partial hydrolysis of FeCl₃ or [FeCl₄]⁻ by small amounts of water in the nitromethane and/or by the nitromethane itself.     

Regulation of rat brain (Na+ + K+)-ATPase activity by cyclic AMP

The interaction between the $\text{(}\text{Na}{}^{\mathrm{+}}\text{+}\text{K}{}^{\mathrm{+}}\text{)-}\text{ATPase}$ and the adenylate cyclase enzyme systems was examined. Cyclic AMP, but not 5′-AMP, cyclic GMP or 5′-GMP, could inhibit the $\text{(}\text{Na}{}^{\mathrm{+}}\text{+}\text{K}{}^{\mathrm{+}}\text{)-}\text{ATPase}$ enzyme present in crude rat brain plasma membranes. On the other hand, the cyclic AMP inhibition could not be observed with purified preparations of $\text{(}\text{Na}{}^{\mathrm{+}}\text{+}\text{K}{}^{\mathrm{+}}\text{)-}\text{ATPase}$ enzyme. Rat brain synaptosomal membranes were prepared and treated with either NaCl or cyclic AMP plus NaCl as described by Corbin, J., Sugden, P., Lincoln, T. and Keely, S. ((1977) J. Biol. Chem. 252, 3854–3861). This resulted in the dissociation and removal of the catalytic subunit of a membrane-bound cyclic AMP-dependent protein kinase. The decrease in cyclic AMP-dependent protein kinase activity was accompanied by an increase in $\text{(}\text{Na}{}^{\mathrm{+}}\text{+}\text{K}{}^{\mathrm{+}}\text{)-}\text{ATPase}$ activity. Exposure of synaptosomal membranes containing the cyclic AMP-dependent protein kinase holoenzyme to a specific cyclic AMP-dependent protein kinase inhibitor resulted in an increase in $\text{(}\text{Na}{}^{\mathrm{+}}\text{+}\text{K}{}^{\mathrm{+}}\text{)-}\text{ATPase}$ enzyme activity. Synaptosomal membranes lacking the catalytic subunit of the cyclic-AMP-dependent protein kinase did not show this effect. Reconstitution of the solubilized membrane-bound cyclic AMP-dependent protein kinase, in the presence of a neuronal membrane substrate protein for the activated protein kinase, with a purified preparation of $\text{(}\text{Na}{}^{\mathrm{+}}\text{+}\text{K}{}^{\mathrm{+}}\text{)-}\text{ATPase}$, resulted in a decrease in overall $\text{(}\text{Na}{}^{\mathrm{+}}\text{+}\text{K}{}^{\mathrm{+}}\text{)-}\text{ATPase}$ activity in the presence of cyclic AMP. Reconstitution of the protein kinase alone or the substrate protein alone, with the $\text{(}\text{Na}{}^{\mathrm{+}}\text{+}\text{K}{}^{\mathrm{+}}\text{)-}\text{ATPase}$ has no effect on $\text{(}\text{Na}{}^{\mathrm{+}}\text{+}\text{K}{}^{\mathrm{+}}\text{)-}\text{ATPase}$ activity in the absence or presence of cyclic AMP. Preliminary experiments indicate that, when the activated protein kinase and the substrate protein were reconstituted with the $\text{(}\text{Na}{}^{\mathrm{+}}\text{+}\text{K}{}^{\mathrm{+}}\text{)-}\text{ATPase}$ enzyme, there appeared to be a decrease in the Na⁺-dependent phosphorylation of the Na⁺-ATPase enzyme, while the K⁺-dependent dephosphorylation of the $\text{(}\text{Na}{}^{\mathrm{+}}\text{+}\text{K}{}^{\mathrm{+}}\text{)-}\text{ATPase}$ was unaffected.