江苏省湿地被子植物新记录

通过野外调查和标本鉴定,发现江苏省湿地被子植物新记录7种1变种,分别为北美黄亚麻Linum medium (Planch.) Britton、毛龙葵Solanum sarrachoides Sendtn.、断节莎Cyperus odoratus L.、疣果飘拂草Fimbristylis dipsacea var. verrucifera (Maxim.) T. Koyama、海边月见草Oenothera drummondii Hook.、细花丁香蓼Ludwigia perennis L.、伞房花耳草Hedyotis corymbosa (L.) Lam.、水茫草Limosella aquatica L.,其中水茫草属Limosella L.为江苏省新记录属,北美黄亚麻、毛龙葵、断节莎和海边月见草4个种为江苏省外来归化植物新记录。凭证标本保存于江苏省中国科学院植物研究所标本馆(NAS)。     

甘肃省被子植物分布新记录

报道了甘肃省分布的玄参科(Scrophulariaceae)水茫草属(Limosella Linn.)1个新记录属,以及玄参科(Scrophulariaceae)、木兰科(Magnoliaceae)、蓼科(Polygonaceae)、胡颓子科(Elaeagnaceae)、百合科(Liliaceae)5个新记录种——水茫草(Limosella aquatica Linn.)、峨眉含笑(Michelia wilsonii Finet et Gagnep.)、叉分蓼(Polygonum divaricatum L.)、棱果沙棘(Hippophae goniocarpa Y.S.Lian et al.ex SwensonBartish)、青海黄精(Polygontum qinghaiense Z.L.Wu et Y.C.Yang)。其中,峨眉含笑是国家二级重点保护野生植物。     

贵州省藜芦科一新记录属——白丝草属

报道贵州省藜芦科一新记录属——白丝草属Chamaelirium Willd.,一新记录种——中国白丝草Chamaelirium chinense (K. Krause) N. Tanaka,并对该种的形态特征、生境、分类变动进行描述及讨论。     

中国禾草一新归化属——皱稃草属

报道了中国一新归属－－皱稃草属,强调了准确记录外来植物的重要性并简要讨论了在我国建立生物安全立法的必要性。     

赖草属资料

禾本科赖草属二新种及一新变种,即芒颖赖草Leymus aristiglumus L.B.Cai,伊吾赖草Leymus yiwuensis L.B.Cai ex N.R.Cui和疏节赖草Leymus secalinus var.laxinodis L.B.Cai。     

中国结缕草属一新变型

发表了辽宁产结缕草属一新变型,大穗日本结缕草Zoysia japonica Steud.f.macrostachya H.D.Doun et L.J.Gong.     

中国舞鹤草属新记录种

报道中国舞鹤草属一新记录种——两色鹿药[Maianthemum bicolor(Nakai)Cubey],经解剖、切片和扫描电镜观察,采自吉林省通化县白鸡峰上的两色鹿药与目前国内的舞鹤草属近缘种存在显著形态差异。     

中国黄金茅属与楔颖草属的新分类等级

本文在黄金茅属Eulalia Kunth下发表2新种,即E.splendensKeng et S.L.Chen与E.yunnanensis Keng et S.L.Chen,在楔颖草属Apocopis Nees下发表一新变种A.wrightii var.macrantha S.L.Chen。     

青海肉果草属一新变型

肉果草属一新变型 .     

云南囊颖草属一新种

发表了云南囊颖草属一新种     

Characterization and analysis of posttranslational modifications of the human large cytoplasmic ribosomal subunit proteins by mass spectrometry and Edman sequencing

The 60S ribosomal proteins were isolated from ribosomes of human placenta and separated by reversed phase HPLC. The fractions obtained were subjected to trypsin and Glu-C digestion and analyzed by mass fingerprinting (MALDI-TOF), MS/MS (ESI), and Edman sequencing. Forty-six large subunit proteins were found, 22 of which showed masses in accordance with the SwissProt database (June 2002) masses (proteins L6, L7, L9, L13, L15, L17, L18, L21, L22, L24, L26, L27, L30, L32, L34, L35, L36, L37, L37A, L38, L39, L41). Eleven (proteins L7, L10A, L11, L12, L13A, L23, L23A, L27A, L28, L29, and P0) resulted in mass changes that are consistent with N-terminal loss of methionine, acetylation, internal methylation, or hydroxylation. A loss of methionine without acetylation was found for protein L8 and L17. For nine proteins (L3, L4, L5, L7A, L10, L14, L19, L31, and L40), the molecular masses could not be determined. Proteins P1 and protein L3-like were not identified by the methods applied.     

Larvae of Leptus (Acarina:Erythraeidae), free-living or ectoparasitic on arachnids and lower insects of Australia and Papua New Guinea, with descriptions of reared post-larval instars

Leptus larvae (Acarina:Erythraeidae) of Australia and New Guinea, collected either free-living or ectoparasitic on Arachnida or lower Insecta, are comprehensively reviewed. For Australia the following new species are described. From Scorpionida: L. barmeedius, L. baudini, L. carduus, L. hitchcocki, L. korematus, L. pistoris, L. stnithi and L. urodaci; from Araneae: L. minno; from Insecta: L. norrisi (Archaeognatha); L.flindersi (Blattodea); L. cheesmanae (Phasmatodea); L. bankensis, L. calcar, L. cultellus, L. foliatus, L. lighti, L. pincheni and L. tindalei (Orthoptera, Acridoidea); L. batjallus, L. clavatus, L. clelandi. L. elderi, L.fisheri (Hemiptera); L. grossi and L. puniceus (free-living only); some of the preceding species were also captured free-living. From Papua New Guinea the following new species are described: L. calcar (Acridoidea); L. cheesmanae (Orthoptera:'cricket') (both of these species also from Australia); L. lorarius, L. scutellatus and L. triacanthus (free-living). Additional host and other records are given for previously described species, originally described as ectoparasites of Insecta:from Australia: L. bathypogonus Womersley (Acridoidea); L. cerambycius Southcott (free-living); L. charon Southcott (Araneae, Scorpionida); L.faini Southcott (Araneae); L. orthrius Southcott (Hemiptera); from Papua New Guinea: L. draco Southcott (Odonata, Acridoidea, Tettiginioidea, Phasmatodea, Hemiptera). Protonymphs are described of L. barmeedius, L. baudini, L. calcar, L. charon, L.flindersi, L. orthrius and L. smithi. Deutonymphs are described of L. calcar, L. charon, L. flindersi and L. smithi. A key is provided for the known larvae, protonymphs and deutonymphs of Leptus of Australia and Papua New Guinea. Teratological abnormalities are recorded for L. cultellus, L. fisheri, L, minno and L. urodaci.     

阴道乳酸杆菌的分子生物学鉴定方法研究

目的鉴定女性生殖道乳杆菌种类及各种乳杆菌在阴道中的分布差异。方法通过扩增和测序乳酸杆菌16S rRNA序列中特异性区段（8f926r）,并利用Vector NTI 8.0序列分析软件对各菌株的基因序列与标准菌株比对进行。结果 26株乳酸菌,L1株、L25株和L46株为乳酸杆菌属中的格氏乳酸杆菌（Lactobacillus gasseri）;L2株、L5株、L6株、L7株、L8株、L11株、L13株、L15株、L19株、L20株、L24株、L26株、L28株、L29株、L31株、L32株、L33株、L34株、L35株、L36株、L40株与L45株均为乳酸杆菌属中的卷曲乳酸杆菌（Lactobacillus crispatus）,而L21株未鉴定为乳酸球菌。结论女性阴道乳酸杆菌的优势菌种是卷曲乳杆菌、格氏乳杆菌。     

丽盲蝽属(丽盲蝽亚属)中国种类修订(半翅目:盲蝽科:盲蝽亚科)(英文)

对丽盲蝽属 (丽盲蝽亚属 )Lygocoris (subg .Lygocoris)的中国种类作了修订。文中共包括 19个种 ,其中有 12新种 ,1个中国新纪录种 ,并包括 1项新等级的认定。即暗胝丽盲蝽L .(L .)calligersp .nov .(正模 :四川峨眉山九老洞 ) ,程氏丽盲蝽L .(L .)chengisp .nov .(正模 :四川峨眉山大乘寺 ) ,晕斑丽盲蝽L .(L .)diffusomaculatussp .nov .(正模 :甘肃榆中兴隆山 ) ,淡色丽盲蝽L .(L .)dilutussp .nov .(正模 :甘肃夏河县合作 ) ,锈褐丽盲蝽L .(L .) ferrugineussp .nov .(正模 :云南哀牢山 ) ,褐盾丽盲蝽L .(L .) fuscoscutel latus (Reuter ,190 6 )stat .nov .[由L .(L .)striicornisvar.fuscoscutellatus升为种级阶元 ],广西丽盲蝽L .(L .) guangxiensissp .nov .(正模 :广西龙胜 ) ,东亚丽盲蝽L .(L .)idoneus(Linnavuori,196 3) (中国新纪录种 ) ,完脊丽盲蝽L .(L .)integricarinatussp .nov .(甘肃榆中麻家寺 ) ,林氏丽盲蝽L .(L .)linnavuoriisp .nov .(云南哀牢山簸箕坝 ) ,长翅丽盲蝽L .(L .)longipennis (Reuter ,190 6 ) ,斑盾丽盲蝽L .(L .)maculis cutellatussp .nov .(四川理县刷经寺 ) ,原丽盲蝽L .(L .) pabulinus (Linnaeus ,176 1) ,红盾丽盲蝽L .(L .)rufiscutellatussp .nov .(甘     

Binding of Escherichia coli ribosomal proteins to 23S RNA under reconstitution conditions for the 50S subunit.

The RNA binding capacity of 50S proteins from E. coli ribosomes has been tested under improved conditions; purified proteins active in reconstitution assays were used, and the binding was studied under the conditions of the total reconstitution procedure for the 50S subunit. The results are: 1) Interaction of 23S RNA was found with 17 proteins, namely L1, L2, L3, L4, L7/L12, L9, L10, L11, L15, L16, L17, L18, L20, L22, L23, L24 and L29. 2) The proteins L1, L2, L3, L4, L9, L23 and L24 bound to 23S RNA at a level of about one copy per RNA molecule, whereas L20 could bind more than one copy (no saturation was observed at 1.8 copies per 23S RNA), and the other proteins bound 0.2--0.6 copies per RNA. 3) L1, L3, L7/L12 showed a slight binding to 16S RNA, L26 (identical with S20) strong binding to 16S RNA. 4) The binding of L2, L7/L12, L10, L11, L15, L16 and L18 was preparation sensitive, i.e. the binding ability changed notably from preparation to preparation. 5) All proteins bound equally well to 23S RNA in presence of 4 and 20 mM Mg2+, respectively, except L2, L3, L4, L7/L12, L9, L10, L15, L16 and L18, which bound less strongly at 20 mM than at 4 mM Mg2+.     

Localization of proteins L4, L5, L20 and L25 on the ribosomal surface by immuno-electron microscopy

Summary Ribosomal proteins L4, L5, L20 and L25 have been localized on the surface of the 50S ribosomal subunit of Escherichia coli by immuno-electron microscopy. The two 5S RNA binding proteins L5 and L25 were both located at the central protuberance extending towards its base, at the interface side of the 50S particle. L5 was localized on the side of the central protuberance that faces the L1 protuberance, whereas L25 was localized on the side that faces the L7/L12 stalk. Proteins L4 and L20 were both located at the back of the 50S subunit; L4 was located in the vicinity of proteins L23 and L29, and protein L20 was localized between proteins L17 and L10 and is thus located below the origin of the L7/L12 stalk.     

Karyotypes in Leucadendron (Proteaceae): evidence of the primitiveness of the genus

Karyotypes of 27 species in Leucadendron are analysed for the first time. New chromosome counts are reported for 15 species, with 2 n  = 26 occurring in all of them. Karyotype analysis indicated that chromosomes of Leucadendron taxa are small in size and have predominantly median to submedian centromeres. The mean sizes of somatic metaphase chromosomes ranged from 1.05 to 2.65 µm. Based on Stebbins' karyotype classification, 1A type was found in L. galpinii , L. muirii , L. orientale , L. platyspermum , L. rubrum , and L. salignum ; 2A type in L. conicum , L. flexuosum , L. laureolum , L. meridianum , L. salicifolium , L. stelligerum , and L. teretifolium ; and 2B type in L. argenteum , L. chamelaea , L. discolor , L. elimense , L. eucalyptifolium , L. floridum , L. gandogeri , L. linifolium , L. loeriense , L. macowanii , L. procerum , L. spissifolium , L. strobilinum , and L. tinctum . These types are the three most symmetrical karyotypes and are considered to be primitive.  © 2006 The Linnean Society of London, Botanical Journal of the Linnean Society , 2006, 151 , 387–394.     

Isolation of eukaryotic ribosomal proteins. Purification and characterization of the 60 S ribosomal subunit proteins L4, L5, L7, L9, L11, L12, L13, L21, L22, L23, L26, L27, L30, L33, L35', L37, and L39.

The proteins of the large subunit of rat liver ribosomes were separated into seven groups by stepwise elution from carboxymethylcellulose with LiCl at pH 6.5. Seventeen proteins (L4, L5, L7, L9, L11, L12, L13, L21, L22, L23, L26, L27, L30, L33, L35', L37, and L39) were isolated from three of the groups (B60, D60, G60) by ion exchange chromatography on carboxymethylcellulose and by filtration through Sephadex. The amount of protein obtained varied from 0.5 to 15 mg. Eight of the proteins (L9, L11, L13, L21, L22, L35', L37 and L39) had no detectable contamination; the impurities in the others were no greater than 9%. The molecular weight of the proteins was estimated by polyacrylamide gel electrophoresis in sodium dodecyl sulfate; the amino acid composition was determined.     

Flow Cytometric Determination of Genome Size in some Old World Lupinus Species (Fabaceae)

Abstract: Genome size determinations using propidium iodide flow cytometry were conducted in Lupinus anatolicus, L. pilosus, L. luteus, L. hispanicus ssp. hispanicus and L. hispanicus ssp. hispa-nicus × L. luteus (a complex hybridization product ofL. hispanicus ssp. hispanicus and L. luteus ). Using Glycine max "Ceresia" (1C = 1.134pg) and an accession of L. pilosus (1C = 0.649pg) as internal standards the following 1C values were obtained: L. anatolicus: 0.606 pg; L. pilosus: 0.620–0.678 pg; L. luteus: 1.173 pg; L. hispanicus: 1.043 pg; L. hispanicus ssp. hispanicus × L luteus: 1.036 pg. Lupinus anatolicus is a newly described taxon with smooth seeds whose genome is approximately as small as the smallest genomes measured in the related L. pilosus , a taxon with rough seeds. The genomes in the related smooth-seeded taxa L. luteus, L. hispanicus and L. hispanicus ssp. hispanicus × L. luteus are considerably larger. There is a 1.13-fold difference between L. luteus (crop) and L. hispanicus (wild). The genome size of L. hispanicus ssp. hispanicus × L. luteus , however, is not intermediate, it is close to L. hispanicus .