取食不同寄主植物小菜蛾对氯虫苯甲酰胺敏感性及体内解毒酶活性的变化

为探明寄主植物影响小菜蛾Plutella xylostella L.抗药性的内在因素,本研究以小菜蛾嗜好性不同的菜心(Brassica parachinensis)、芥菜(B.juncea)、白菜(B.chinensis)和芥蓝(B.alboglabra)4种寄主植物为材料,利用生物测定和解毒酶活力测定的方法,研究了取食不同寄主植物的小菜蛾幼虫对氯虫苯甲酰胺敏感性及体内解毒酶活力变化情况。结果表明,4种寄主植物饲养小菜蛾5代后,其敏感性分别为菜心>芥菜>白菜>芥蓝,且其体内活性酶谷胱甘肽S-转移酶(GSTs)、羧酸酯酶(CarE)比活力差异显著(P<0.05),活性的强弱与其敏感性相一致。以取食芥蓝的小菜蛾体内2种解毒酶活性最强。说明寄主植物能影响小菜蛾药剂敏感性及解毒酶活性。试验结果对小菜蛾的综合防控及抗氯虫苯甲酰胺机理研究具有重要的参考价值。     

黄曲条跳甲为害下十字花科蔬菜可溶性糖含量的动态变化

采用蒽酮比色法测定了十字花科蔬菜上黄曲条跳甲Phyllotreta striolata(Fabricius)不同危害程度下叶片可溶性糖含量的变化.结果表明黄曲条跳甲的为害显著影响十字花科蔬菜的可溶性糖含量.萝卜接虫2d,甘蓝接虫4d、12d,芥蓝接虫2d、8d、12d,白菜、芥菜、菜心接虫2d、4d、6d、8d、10d、12d时,健叶、轻度为害叶、中度为害叶、重度为害叶的可溶性糖含量均低于对照.但萝卜接虫4d、6d时,中度为害叶、重度为害叶的可溶性糖含量高于对照,4d时,重度为害叶升高28.65%,甘蓝接虫2d时,可溶性糖含量分别升高18.70%、24.40%、30.88%、30.50%,芥蓝接虫2d、4d时,轻度为害叶、重度为害叶的可溶性糖含量均高于对照.十字花科蔬菜可溶性糖含量的变化是植株对害虫胁迫的一种响应.     

颗粒体病毒对不同蔬菜上小菜蛾实验种群的控制作用

通过组建施用颗粒体病毒Plutella xylostellagranulosis virus(PxGV)后4种十字花科蔬菜上的小菜蛾Plutella xylostellaL.实验种群生命表发现:小菜蛾颗粒体病毒除了能引起幼虫感病死亡外,还能显著地降低成虫的产卵量,推迟产卵高蜂1~2 d,但对化蛹及雌蛾寿命无显著影响。在种群水平上,病毒对小菜蛾的控制作用综合表现为压低了小菜蛾种群增长趋势指数,在菜心、芥蓝、芥菜和小白菜上小菜蛾实验种群增长趋势指数在分别为13.7,12.3,10.7和22.7,病毒对小菜蛾种群的干扰作用控制指数(IIPC)分别为0.334,0.177,0.280和0.433,表明病毒对小菜蛾种群的控制能力受到寄主植物的影响,在芥蓝上控制能力最强,其次为芥菜和菜心,而小白菜最次。     

黄曲条跳甲为害下十字花科蔬菜可溶性糖含量的动态变化

采用蒽酮比色法测定了十字花科蔬菜上黄曲条跳甲Phyllotreta striolata（Fabricius）不同危害程度下叶片可溶性糖含量的变化。结果表明黄曲条跳甲的为害显著影响十字花科蔬菜的可溶性糖含量。萝卜接虫2d,甘蓝接虫4d、12d,芥蓝接虫2d、8d、12d,白菜、芥菜、菜心接虫2d、4d、6d、8d、10d、12d时,健叶、轻度为害叶、中度为害叶、重度为害叶的可溶性糖含量均低于对照。但萝卜接虫4d、6d时,中度为害叶、重度为害叶的可溶性糖含量高于对照,4d时,重度为害叶升高28．65％,甘蓝接虫2d时,可溶性糖含量分别升高18．70％、24．40％、30．88％、30．50％,芥蓝接虫2d、4d时,轻度为害叶、重度为害叶的可溶性糖含量均高于对照。十字花科蔬菜可溶性糖含量的变化是植株对害虫胁迫的一种响应。     

寄主胁迫下小菜蛾种群的RAPD分析

采用RAPD-PCR技术,研究了取食6种不同十字花科寄主植物第4、9、15代小菜蛾Plutella xylostella(L.)种群的DNA多态性。通过17条引物的重复PCR扩增实验,利用NTsys软件对电泳条带统计分析,构建了遗传距离矩阵和聚类分析图谱。结果表明:取食芥蓝的小菜蛾种群与其它5种寄主种群遗传距离较远(0.6523～0.8246),独立聚为一枝;取食萝卜的小菜蛾种群遗传距离与甘蓝上种群较近(0.3443),聚为一枝,并且与白菜、芥菜和菜心上小菜蛾种群遗传距离较近,逐次聚为一枝,芥蓝、萝卜及甘蓝寄主种群随代次的增多种群分化出现稳定规律性。各寄主种群间遗传距离平均值和范围、多态性条带占总条带数目的比例随代次增多而增大,说明种群分化程度随代次增多而加深。     

黄曲条跳甲危害对不同寄主植物可溶性蛋白质含量的影响

采用考马斯亮蓝G-250染色法对6种十字花科蔬菜不同危害程度叶片的可溶性蛋白质含量进行了测定。结果表明黄曲条跳甲Phyllotreta striolata(F.)对6种十字花科蔬菜叶片的可溶性蛋白质含量存在不同程度的影响。萝卜(Raphanus sativus(L.))、白菜(Brassica chinensis(L.))和菜心(B.parachinensis Bailey)叶片在黄曲条跳甲危害胁迫8、10 d时,甘蓝(B.oleracea(L.))在胁迫10、12 d时,芥菜(B.juncea(L.))和芥蓝(B.alboglabra Bailey)在胁迫12 d时,可溶性蛋白质含量显著高于对照(P<0.05)。芥菜在黄曲条跳甲危害2 d时,可溶性蛋白质含量与对照没有显著差异(P>0.05),可能是因为其承受黄曲条跳甲危害的抗虫性能力较强。随着叶片危害程度的加重,叶片可溶性蛋白质含量下降。这可能是寄主植物本身的保护行为,也是对害虫为害胁迫的一种响应。     

四种十字花科蔬菜上小菜蛾自然种群连续世代生命表

利用作用因子生命表技术,组建芥菜、芥蓝、小白菜和菜心4种十字花科蔬菜上小菜蛾自然种群连续世代生命表,分析寄主植物和生物因子对小菜蛾种群数量的控制作用。结果表明：在4种十字花科蔬菜的一造菜上,小菜蛾均能完成两个世代。虽然小菜蛾在芥菜上的初始卵量最高,但害虫种群总增长倍数在芥蓝上最高,其次为小白菜,菜心和芥菜,分别为17．64、11．90、11．43和3．76。这说明尽管芥菜对小菜蛾成虫的产卵有一定的吸引作用,但不适合小菜蛾生长发育。芥蓝是最适宜小菜蛾种群增长的寄主。生物因子在小菜蛾自然种群控制中起着重要的作用,但是在不同种类十字花科蔬菜上,天敌类群对小菜蛾控制作用存在一定差异。除芥菜之外,寄生性天敌对芥蓝、菜心和小白菜上的小菜蛾种群控制作用最大,其次为“捕食及其它”,病原微生物的控制作用最小。“捕食及其它”对芥菜上小菜蛾种群的作用非常明显,如果排除此因子作用,小菜蛾种群两代后将增长126．03倍。该因子是导致芥菜小菜蛾自然种群增长趋势指数低的主要原因。因此在制定小菜蛾防治策略时,应考虑蔬菜的种类和布局,加大对芥蓝小菜蛾种群的防治力度;芥菜可作为一种诱杀植物种植,以吸引小菜蛾产卵,并集中防治。这些防治策略在小菜蛾综合治理中具有重要的实际意义。     

虫害诱导的植株对小菜蛾取食和生长发育的影响

本文从菜田生态系统的角度出发,就黄曲条跳甲Phyllotreta striolata(Fabricius)取食诱导对小菜蛾Plutella xylostella(L.)造成的影响进行了研究。黄曲条跳甲取食诱导对小菜蛾取食的影响比较明显,一般来说,黄曲条跳甲少量或短时间的取食会刺激小菜蛾幼虫在相应叶片上的取食,反之则会抑制;而且不同的寄主,不同完整度的叶片(即是否被黄曲条跳甲取食过)上的承载能力不同,芥菜、白菜、菜心和萝卜的承载力弱于甘蓝和芥蓝,黄曲条跳甲取食过的叶片弱于未被黄曲条跳甲取食过的叶片;不同数量的黄曲条跳甲取食对小菜蛾的产卵量影响显著,对其余生物学参数影响不显著,少量的黄曲条跳甲取食会刺激小菜蛾的产卵,多数则会抑制。     

小菜蛾幼虫对不同寄主的取食嗜好性及其适宜性

对不同寄主种类、不同寄主形态和不同寄主饲喂的小菜蛾(Plutella xylostella)幼虫之间的取食嗜好性比较试验表明,小菜蛾幼虫优先取食大白菜、萝卜或菜心幼苗,其次为油菜和甘蓝幼苗,在大白菜与油菜幼苗之间的取食选择比例是93.33%和6.67％;在甘蓝与菜心幼苗之间的取食选择比例是16.67%和83.33%.小菜蛾幼虫的取食嗜好性受饲喂寄主种类的影响,偏食大白菜或菜心幼苗.小菜蛾幼虫选择寄主取食的次序与寄主体内可溶性糖或淀粉含量没有明显关系,但与两者的相对量呈一定的负相关.取食大白菜或菜心幼苗的小菜蛾生长良好,单头取食达0.583～0.637 cm², 单头体重达2.07～2.18 mg, 与取食甘蓝或油菜幼苗的幼虫在取食量、个体发育方面有明显差异.小菜蛾幼虫也喜好取食已经被虫危害过的幼苗.     

敌敌畏对不同寄主植物上小菜蛾羧酸酯酶活性的体内抑制

敌敌畏对取食花椰菜、白菜和甘蓝的小菜蛾四龄幼虫β-NA羧酸酯酶的体内抑制动态变化有显的差异。取食不同寄主植物的小菜蛾pNA羧酸酯酶活性在受到敌敌畏的抑制之后,恢复的速度不同,取食花椰菜的小菜蛾pNA羧酸酯酶活性恢复速度最快,取食白菜的次之,而取食甘蓝的最慢。     

Physicochemical and biological properties of 6(1),6(3),6(5)-tri-O-alpha-maltosyl-cyclomaltoheptaose (6(1),6(3),6(5)-tri-O-alpha-maltosyl-beta-cyclodextrin)

A unique multibranched cyclomaltooligosaccharide (cyclodextrin, CD) of 6(1),6(3),6(5)-tri-O-alpha-maltosyl-cyclomaltoheptaose [6(1),6(3),6(5)-tri-O-alpha-maltosyl-beta-cyclodextrin, (G(2))(3)-betaCD] was prepared. The physicochemical and biological properties of (G(2))(3)-betaCD were determined together with those of monobranched CDs (6-O-alpha-D-glucopyranosyl-alpha-cyclodextrin (G(1)-alphaCD), 6-O-alpha-D-glucopyranosyl-beta-cyclodextrin (G(1)-betaCD), and 6-O-alpha-maltosyl-beta-cyclodextrin (G(2)-betaCD)). NMR spectra of (G(2))(3)-betaCD were measured using various 2D NMR techniques. The solubility of (G(2))(3)-betaCD in water and MeOH-water solutions was extremely high in comparison with nonbranched betaCD and was about the same as that of the other monobranched betaCDs. The formation of an inclusion complex of (G(2))(3)-betaCD with stereoisomers (estradiol, retinoic acid, quinine, citral, and glycyrrhetinic acid) depends on the cis-trans isomers of guest compounds. The cis isomers of estradiol, retinoic acid, and glycyrrhetinic acid were included more than their trans isomers, while the trans isomers of citral and quinine fit more tightly than their cis isomers. (G(2))(3)-betaCD was the most effective host compound in the cis-trans resolution of glycyrrhetinic acid. Among the branched betaCDs, (G(2))(3)-betaCD exhibited the weakest hemolytic activity in human erythrocytes and showed negligible cytotoxicity in Caco-2 cells up to 200 microM. These results indicate unique characteristics of (G(2))(3)-betaCD in some biological responses of cultured cells.     

Spectral and thermodynamic properties of Ag(I), Au(III), Cd(II), Co(II), Fe(III), Hg(II), Mn(II), Ni(II), Pb(II), U(IV), and Zn(II) binding by methanobactin from Methylosinus trichosporium OB3b

Methanobactin (mb) is a novel chromopeptide that appears to function as the extracellular component of a copper acquisition system in methanotrophic bacteria. To examine this potential physiological role, and to distinguish it from iron binding siderophores, the spectral (UV–visible absorption, circular dichroism, fluorescence, and X-ray photoelectron) and thermodynamic properties of metal binding by mb were examined. In the absence of Cu(II) or Cu(I), mb will bind Ag(I), Au(III), Co(II), Cd(II), Fe(III), Hg(II), Mn(II), Ni(II), Pb(II), U(VI), or Zn(II), but not Ba(II), Ca(II), La(II), Mg(II), and Sr(II). The results suggest metals such as Ag(I), Au(III), Hg(II), Pb(II) and possibly U(VI) are bound by a mechanism similar to Cu, whereas the coordination of Co(II), Cd(II), Fe(III), Mn(II), Ni(II) and Zn(II) by mb differs from Cu(II). Consistent with its role as a copper-binding compound or chalkophore, the binding constants of all the metals examined were less than those observed with Cu(II) and copper displaced other metals except Ag(I) and Au(III) bound to mb. However, the binding of different metals by mb suggests that methanotrophic activity also may play a role in either the solubilization or immobilization of many metals in situ.     

Circular dichroism spectra of DNA quadruplexes [d(G(5)T(5))](4) as formed with G(4) and T(4) tetrads and [d(G(5)T(5)). d(A(5)C(5))]2 as formed with Watson-Crick-like (G-C)(2) and (T-A)(2) tetrads

We utilize electrophoresis and find that a thermally treated equimolar mixture of the oligonucleotide d(G(5)T(5)) and its complementary oligonucleotide d(A(5)C(5)) exhibits either two bands or a single band in one lane, depending on the conditions of the incubation solutions. The thermally treated d(G(5)T(5)) solution loaded in a different lane exhibits a single band of the parallel quadruplex [d(G(5)T(5))](4), which is composed of homocyclic hydrogen-bonded G(4) and T(4) tetrads previously proposed. For the thermally treated equimolar mixture of d(G(5)T(5)) and d(A(5)C(5)), the fast band is assigned to a Watson-Crick d(G(5)T(5)). d(A(5)C(5)) duplex, so that the slow band with the same low mobility as that of [d(G(5)T(5))](4) may be assigned to either [d(G(5)T(5))](4) itself or a [d(G(5)T(5)). d(A(5)C(5))](2) quadruplex. If the latter compound is true, this may be the antiparallel quadruplex composed of the heterocyclic hydrogen-bonded G-C-G-C and T-A-T-A tetrads proposed previously. After removing these three bands for the duplex and two kinds of hypothetical quadruplexes, we electrophoretically elute the corresponding compounds in the same electrophoresis buffer using an electroeluter. The eluted compounds are ascertained to be stable by electrophoresis. The circular dichroism (CD) and UV absorption spectra measured for the three isolated compounds are found to be clearly different. For the electrophoretic elution of the hypothetical [d(G(5)T(5))](4) quadruplex, the result of the molecularity of n = 4 obtained from the CD melting curve analysis provides further support for the formation of the parallel [d(G(5)T(5))](4) quadruplex already proposed. For the thermally treated equimolar mixture of d(G(5)T(5)) and d(C(5)A(5)), the fast band with a molecularity of n = 2 corresponds to the Watson-Crick duplex, d(G(5)T(5)). d(A(5)C(5)). The slow band with a molecularity of n = 4 indicates the antiparallel quadruplex [d(G(5)T(5)). d(A(5)C(5))](2), whose observed CD and UV spectra are different from those of [d(G(5)T(5))](4). By electrophoresis, after reannealing the eluted compound [d(G(5)T(5)). d(A(5)C(5))](2), a distinct photograph showing the band splitting of this quadruplex band into the lower duplex and upper quadruplex bands is not possible; but by a transilluminator, we occasionally observe this band splitting with the naked eye. The linear response polarizability tensor calculations for the thus determined structures of the [d(G(5)T(5))](4) quadruplex, the McGavin-like [d(G(5)T(5)). d(A(5)C(5))](2) quadruplex, and the Watson-Crick d(G(5)T(5)). d(A(5)C(5)) duplex are found to qualitatively predict the observed CD and UV spectra.     

Synthesis and luminescence properties of a blue-emitting Sr(3.5) Y(6.5) O(2) (PO(4) )(1.5) (SiO(4) )(4.5) :Eu(2+) phosphor

A novel blue‐emitting Sr_3.5Y_6.5O₂(PO₄)_1.5(SiO₄)_4.5:Eu²⁺ phosphor was synthesized via a solid‐state reaction. Powder X‐ray diffraction (XRD) analysis demonstrated that the Sr_3.5Y_6.5O₂(PO₄)_1.5(SiO₄)_4.5 host had a hexagonal crystal structure in the space group P6₃/m and unit cell parameters a = 9.418 Å, c = 6.900 Å. The as‐prepared phosphor showed a blue emission and all the main emission peaks were located at around 466 nm for different excitation wavelengths of 297, 333 and 391 nm. The temperature dependence of the photoluminescence property was investigated in the range 20–250 °C, and the emission intensity decreased to 71% of the initial value at room temperature on increasing the temperature to 150 °C. According to the classical theory of fluorescent thermal quenching, the activation energy (ΔE) for the thermal quenching luminescence of the as‐prepared Sr_3.45Y_6.5O₂(PO₄)_1.5(SiO₄)_4.5:0.05Eu²⁺ phosphor was determined to be 0.20 eV. Copyright © 2011 John Wiley & Sons, Ltd.     

The frequencies of Gm(1), Gm(2), Gm(4), Gm(12), and Inv(1) in Hessen (Germany)

Summary The serum groups Gm(1) [Gm(a)], Gm(2) [Gm(x)], Gm(4) [Gm(f)]. Gm(12) [Gm(b)] and Inv(1) [Inv(1)] of 2000 sera of healthy blood donors from the land Hesse were examined. The results obtained were compared with those known until now. Three persons, not related to each other, possessed the extremely rare phenotype Gm(-1, 2, 4, 12) [Gm (a-x+b+f+)]. In 0.75% of the cases we found a discordant behaviour of the factors Gm(4) and Gm(12) [Gm(f) and Gm(b)].

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Zusammenfassung 2000 Seren von gesunden Blutspendern aus Hessen wurden bezüglich der Gamma-Globulin-Serumgruppen Gm(1) [Gm(a)], Gm(2) [Gm(x)], Gm(4) [Gm(f)]. Gm(12) [Gm(b)] und Inv(1) [Inv(1)] untersucht. Die gefundenen Resultate wurden mit den bisher bekannten verglichen. Drei miteinander nicht verwandte Personen wiesen den äußerst seltenen Phänotyp Gm(-1, 2, 4, 12) [Gm(a-x+b+f+)] auf. In 0.75% der Fälle fanden wir ein diskordantes Verhalten der Faktoren Gm(4) und Gm(12) [Gm(f) und Gm(b)].

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Director: Prof. Dr. W. Wachsmuth

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Director: Prof. Dr. W. Spielmann

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The nomenclature suggested by WHO at a round-table conference over genes, genotypes and allotypes of immunglobulins is used. The conference took place in Geneva on the 1965 31. 5. to the 5. 6. [5].

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With technical assistance of S. Mohs.     

Nature and composition of La(III), Ce(III), Pr(III), Nd(III), Sm(III), Gd(III), Dy(III) and Ho(III) complexes of embelin

The isolation and characterization of nine polymeric complexes of the general formula [M(L)_1.5S₂]_n (where M is the metal ion, L the ligand and S the solvent, C₂H₅OH) of La(III) and Ce(III), Pr(III), Nd(III), Sm(III), Gd(III), Tb(III), Dy(III), Ho(III) with.the biologically active compound embelin using elemental and thermal analysis, infrared and electronic spectral studies is reported.