蚊子花的组织培养与快速繁殖

1植物名称蚊子花（Lopezia cordata Hornem．）。 2材料类别茎段和顶芽。 3培养条件基本培养基为MS。（1）芽诱导培养基：1／2MS（MS大量元素用量减半）;（2）增殖培养基：MS＋6-BA0．2mg·L^-1（单位下同）＋NAA0．2;（3）生根培养基：I／2MS＋NAA0．5。以上培养基中均加入6g·L^-1琼脂和30g·L^-1蔗糖,pH5．9—6．0。培养室中温度为（24＋1）℃,光照时间为16h·d^-1,光照强度约为60μmol·m^-2·s^-1。     

壳寡糖对烟草幼苗生长和光合作用及与其相关生理指标的影响

采用酶解法获得的壳寡糖,处理烟草幼苗的结果显示,0．01mg·L^-1壳寡糖对烟草幼苗生长有促进作用,幼苗株高、叶面积增加;功能叶片中叶绿素含量、净光合速率（Pn）、气孔导度（Gs）、蒸腾速率（Tr）和胞间CO2浓度（Ci）升高;气孔限制值（Ls）下降。而高浓度（100mg·L^-1）壳寡糖处理的则抑制生长。促进烟草幼苗生长最适的壳寡糖浓度为0．01mg·L^-1,施用两次的效果优于一次的。     

欧洲小叶椴的胚培养与快速繁殖

1植物名称欧洲小叶椴（Tilia cordata Mill．）。 2材料类别成熟胚。 3培养条件（1）／3动培养基：MS＋6-BA2．0mg·L^-1（单位下同）＋NAA0．1;（2）增殖培养基：MS＋6．BA1．0＋NAA0．1;（3）壮苗生根培养基：1／2MS＋IBA1．0＋NAA0．3。以上培养基均加入0．55％琼脂和20g·L^-1。蔗精,pH5．8-6．0。培养温度为（25±2）℃;光照培养时间12h·d^-1,光照强度40．50μmol·m^-2·s^-1。     

精胺对荇菜抗氧化酶系汞毒害的缓解作用

研究了外施不同浓度的精胺（Spm）对15μmol·L^-1汞胁迫下,荇菜（Nymphoides pehatum）叶中SOD、CAT、APX、POD保护酶的活性、O2^-产生速率、MDA、叶绿素、可溶性蛋白、游离态多胺含量的影响。结果表明：外施0．05～0．5mmol·L^-1的Spn,显著提高了汞胁迫下荇菜叶内的亚精胺、精胺水平以及叶绿素和可溶性蛋白的含量;并能提高SOD、CAT和APX的活性,降低O2^-的产生速率,减缓MDA的积累;0．05～0．5mmol·L^-1的外源Spm可增强植物抗氧化胁迫的能力,缓解汞对荇菜的毒害作用,其中0．05～0．1mmol·L^-1的外源Spm效果最佳,但当Spm浓度达到5mmol·L^-1时,却加剧了汞的毒害作用。     

低磷和高照度光下两种不同磷效率玉米幼苗的几种光合参数变化

以完全培养液（HP,1000μmol·L^-1KH2PO4）培养15d的玉米自交系KH5（磷高效）和SD502（磷低效）幼苗转入低磷（LP,5μmol·L^-1KH2PO4）条件下培养20d后,检测叶中几种与光合作用有关参数的结果表明,低磷下两自交系玉米叶中无机磷含量、植株生物量和叶片的净光合速率（Pn）均下降,KH5的降幅小于SD502。两自交系玉米叶片以高照度光（1600μmol·m^-2·s^-1）照射1h后,叶片的PSII实际光化学效率（ФPSII）、PSII最大光化学效率（Fv/Fm）和表观光合电子传递速率（ETR）均下降,而初始荧光（F0）、非光化学猝灭（NPQ）和天线热耗散（HDR）均升高。在强光胁迫过程中,玉米幼苗叶片发生光抑制,自交系SD502在低磷下的光抑制比KH5严重。     

外源多胺对铜胁迫下荇菜叶片生物膜的保护作用

研究外源亚精胺和精胺对铜胁迫下荇菜叶片细胞膜透性、膜脂脂肪酸组成、光合、呼吸、铜积累影响的结果表明,50μmol·L^-1CuSO4处理导致膜脂脂肪酸组分中饱和脂肪酸组分增加,不饱和脂肪酸组分及不饱和指数（IUFA）下降,细胞膜透性加大,光合速率下降,呼吸速率迅速上升,铜在叶细胞中大量积累。外施0．1mmol·L^-1亚精胺和精胺可以稳定生物膜的结构和功能,降低铜在细胞中的累积。     

外源一氧化氮对盐胁迫下黑麦草幼苗生长及生理特性的影响

研究了外源一氧化氮（nitric oxide,NO）对盐胁迫下多年生黑麦草幼苗生长及相关生理指标变化的影响。结果表明,与对照相比,50～200μmol·L-1NO供体硝普钠（sodium nitroprusside,SNP）可缓解盐胁迫对黑麦草幼苗生长的抑制作用,其中100μmo·lL-1SNP缓解作用最强。外施SNP显著缓解了盐胁迫导致的叶片相对电导率、K＋与Na＋比率、丙二醛含量和活性氧水平的增加,提高了盐胁迫下幼苗叶子中脯氨酸含量和超氧化物歧化酶、过氧化氢酶、抗坏血酸过氧化物酶和过氧化物酶等抗氧化酶的活性。这些结果说明,NO可能通过降低细胞吸收Na＋的量、增加细胞吸收K＋的量和脯氨酸含量以及激活抗氧化保护酶等减轻了盐对黑麦草的伤害,提高了黑麦草的抗盐性。     

同色兜兰的组织培养与快速繁殖

1植物名称同色兜兰[Paphiopedilum concolor（Bateman）Pfitz．]。 2材料类别种子。 3培养条件种子萌发培养基：（1）MS＋100mL·L^-1香蕉汁;（2）1／2MS＋100mL·L^-1香蕉汁。原球茎继代增殖培养基：（3）1／2MS＋NAA0．2mg·L^-1（单位下同）＋100mL·L^-1香蕉汁;（4）1／2MS＋NAA0．4＋100mL·L^-1香蕉汁;（5）1／2MS＋6-BA0．5＋NAA0．2＋100mL·L^-1。     

林床清理对落叶松(Larix gmelinii)人工林土壤呼吸和物理性质的影响

林下可再生生物质资源的利用是当今森林资源利用的热点,通过林床清理可以获得廉价可再生生物质资源,但其对林分土壤碳收支的影响尚不清楚。运用红外气体分析法（IRGA法）连续两年观测了林床清理对落叶松（Larix gmelinii）人工林土壤呼吸及物理性质的影响,并估算了林床清理生物质资源利用对落叶松人工林碳收支的影响。结果表明：林床清理能够降低落叶松人工林的土壤呼吸,2a的平均值由2．20μmol·m^-2s^-1降低到1．18μmol·m^-2s^-1,平均降低幅度1．02μmol·m^-2s^-1,年呼吸总量由41．2μmol·m^-2a^-1降至22．4μmol·m^-2a^-1,而且,使土壤呼吸Q10值从2．33降低到2．22,R0值从0．61μmol·m^-2s^-1降至0．36μmol·m^-2s^-1;林床清理能够使林床土壤温度冬季低于对照,而夏季则有相反趋势,清理使得林床土壤湿度变化幅度加大,而且秋季和春季较对照低,而夏季偏高;林床清理使得表层土壤容重要比对照未清理样地高53％（P〈0．05）,土壤非毛管孔隙度比未处理样地低49．5％（P〈0．001）,毛管孔隙度较对照未清理降低约15％（P〈0．001）。林床清理导致林下生物质资源所储藏的碳非呼吸性释放约175．0mol·m^-2,当考虑到林床清理导致的土壤呼吸的降低作用时,所测定的2a内土壤净碳支出由175．0mol·m^-2降低至137．4mol·m^-2。林床清理措施增加生物质资源利用和其所导致的土壤呼吸释放减少,能够减少非冉生资源利用导致的碳释放压力。但仍然需要注意到林床清理使得土壤物理结构发生改变,可能不利于落叶松的生长和落叶松林生态系统的稳定。     

大旗瓣凤仙花的组织培养与快速繁殖

1植物名称 大旗瓣风仙花（Impatiens macrovexilla Y．L．Chen）。 2材料类别 茎上侧芽。 3培养条件 增殖培养基：（1）MS＋6-BA1．5mg·L^-1（单位下同）;继代和生根培养基：（2）MS＋6-BA1．0。以上培养基中均加入30g·L^-1蔗糖和5．5g·L^-1琼脂,pH5．8。培养温度（25±3）℃,光照时间12h·d^-1,光照强度40～50gmol·m^-2·s^-1。     

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.     

Synthesis and spectroscopic properties of CpRuCl(R-DAB(4e)) and CpRuCo(CO)3(R-DAB(6e)). Part XVII. X-ray structure determination of CpRuCo(CO)3(t-Bu-DAB(6e))

CpRuCl(PPh₃)₂ reacted with excess R-DAB in refluxing toluene to give CpRuCl(R-DAB(4e)) (1a: R = i-Pr; 1b: R = t-Bu; 1c: R = neo-Pent; 1d: R =p-Tol). ¹H NMR and ¹³C NMR spectroscopic data indicated that in these complexes the R-DAB ligand is bonded in a chelating 4e coordination mode.Reaction of 1a and 1b with one equivalent of [Co(CO)₄]⁻ afforded CpRuCo(CO)₃(R-DAB(6e)) (2a: R = i-Pr; 2b: R = t-Bu). The structure of 2b was determined by a single crystal X-ray structure determination. Crystals of 2b are monoclinic, space group P2₁/n, with four molecules in a unit cell of dimensions: a = 16.812(4), b = 12.233(3), c = 9.938(3) Å and β = 105.47(3)°. The structure was solved via the heavy atom method and refined to R = 0.060 and R_w = 0.065 for the 3706 observed reflections. The molecule contains a RuCo bond of 2.660(3) Å and a cyclopentadienyl group that is η⁵-coordinated to ruthenium [RuC(cyclopentadienyl) = 2.208(3) Å (mean)]. Two carbonyls are terminally coordinated to cobalt (CoC(1) = 1.746(7) and CoC(2) = 1.715(6) Å) while the third is slightly asymmetrically bridging the RuCo bond (RuC(3) = 2.025(6) and CoC(3) = 1.912(6) Å). The RuC(3)O(3) and CoC(3)O(3) angles are 138.4(5)° and 136.5(5)°, respectively. The t-Bu-DAB ligand is in the bridging 6e coordination mode: σ-N coordinated to Ru (RuN(2) = 2.125(4) Å), μ₂-N′ bridging the RuCo bond and η²-CN coordinated to Co (RuN(1) = 2.113(5), CoN(1) = 1.941(4) and CoC(4) = 2.084(5) Å). The η²-CN′ bonded imine group has a bond length of 1.394(7) Å indicating substantial π-backbonding from Co into the anti-bonding orbital of this CN bond.¹H NMR spectroscopy indicated that 2a and 2b are fluxional on the NMR time scale. The fluxionality of 6e bonded R-DAB ligands is rarely observed and may be explained by the reversible interchange of the σ-N and η²-CN′ coordinated imine parts of the R-DAB ligand.     

Structure of Poly (U).poly (A).poly (U)

The molecular structure of poly (U).poly (A).poly (U) has been determined and refined using the continuous x-ray intensity data on layer lines in the diffraction pattern obtained from an oriented fiber of the RNA. The final R-value for the preferred structure is 0.24, far lower than that for the plausible alternatives. The polymer forms an 11-fold right-handed triple-helix of pitch 33.5A and each base triplet is stabilized by Crick-Watson-Hoogsteen hydrogen bonds. The ribose rings in the three strands have C3'-endo, C2'-endo and C2'-endo conformations, respectively. The helix derives additional stability through systematic interchain hydrogen bonds involving ribose hydroxyls and uracil bases. The relatively grooveless cylindrical shape of the triple-helix is consistent with the lack of lateral organization.     

Structure of poly (I).poly (A).poly (I)

The molecular structure of poly (I).poly (A).poly (I) has been determined and refined using the continuous intensity data on layer lines in the x-ray diffraction pattern obtained from an oriented fiber of this polymorphic RNA complex. The polymer forms a 12-fold right-handed triple-helix of pitch 39.7A and each base-triplet is stabilized by quasi Crick-Watson-Hoogsteen hydrogen bonds. The ribose rings in all the three strands have C3'-endo conformations. The final R-value for this best structure is 0.24 and the x-ray fit is significantly superior to all the alternative structures where the different chains might have different furanose conformations. This all-purine triple-helix, counter-intuitively, has a diameter roughly 3A shorter than that of DNA and RNA triple-helices containing a homopurine and two complementary homopyrimidine strands. Its compact, grooveless cylindrical shape is consistent with the lack of lateral organization.     

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.     

Biosynthesis of cobalamin (vitamin B(12))

The biosynthesis of vitamin B(12) is summarized, emphasizing the differences observed between the aerobic and anaerobic pathways. The biosynthetic route to adenosylcobalamin from its five-carbon precursor, 5-aminolaevulinic acid, can be divided into three sections: (1) the biosynthesis of uroporphyrinogen III from 5-aminolaevulinic acid, which is common to both pathways; (2) the conversion of uroporphyrinogen III into the ring-contracted, deacylated intermediate precorrin 6 or cobalt-precorrin 6, which includes the primary differences between the two pathways; and (3) the transformation of this intermediate to form adenosylcobalamin.