榕树隐头花序挥发物组成及其传粉榕小蜂寄主识别行为

榕树(Ficus spp.)通过挥发性化学物质来吸引传粉榕小蜂(Agaonidae),这种特异性的化学信号释放存在着两种模式,一种是释放多种化合物的"泛化"模式,另一种是释放不常见单一化合物的"专化"模式。为揭示榕树(Ficus microcarpa)及其传粉榕小蜂Eupristina verticillata之间的化学通讯机制,该研究采用固相微萃取法提取榕树隐头花序不同发育期(花前期、雌花期传粉前后、间花期、雄花期和花后期)释放的挥发物,并用气相色谱-质谱联用仪鉴定挥发物成分,分析其变化动态,再通过Y型嗅觉仪检测榕树传粉榕小蜂对各发育期隐头花序的行为反应。结果表明:榕树隐头花序释放的挥发性化合物共鉴定出21种,主要是脂肪酸衍生物、萜类化合物和芳香族化合物。不同发育期隐头花序的挥发物组分差异明显,雌花期传粉前后的挥发物差异表现为传粉后萜类化合物含量下降,脂肪酸衍生物含量增加,特别是传粉前含量较高的特征化合物2-庚酮和3-辛酮消失,D-柠檬烯含量下降,而可巴烯、环己烷和2-己烯醛含量上升。行为检测的结果也表明:雌花期隐头花序对传粉榕小蜂的吸引作用最强,而雄花期的隐头花序释放的挥发物对传粉榕小蜂有趋避作用,形成了对传粉榕小蜂"推拉"的互作模式。有多种化合物在榕树传粉榕小蜂的寄主识别过程中发挥作用,表明榕树及其传粉榕小蜂的互惠共生关系是通过多种化合物的"泛化"策略来维系的。     

钝叶榕榕果挥发物成分及其构成特征分析

为揭示钝叶榕与其传粉榕小蜂及两种协同进果的非传粉榕小蜂Diaziella yangi和Lipothymus sp.间的化学联系与分配机制,采用顶空动态法提取钝叶榕(Ficus curtipes Corner)雌花期和传粉后的榕果挥发物,用定性和定量的方法鉴定、分析了挥发物的成分和变化动态。结果表明:从钝叶榕榕果中共鉴定出45种挥发物成分,主要是单萜类和倍半萜类化合物。6-甲基-5-庚烯-2-酮、β-罗勒烯、反-β-金合欢烯、α-金合欢烯、α-派烯、香桧烯、顺-β-罗勒烯、顺-β-香柠檬烯、大香叶烯D和4,8-二甲基-1,3,7-壬三烯可能是构建钝叶榕特异性化学信息的基础。雌花期榕果挥发物释放量明显高于传粉后挥发物的释放量,且两者在时间和空间上存在异质性。这说明榕蜂育幼繁殖系统间存在着化学信息的联系。     

传粉榕小蜂与非传粉小蜂间寄主识别行为的趋同进化

在高度专性传粉的榕树-榕小蜂互惠共生系统中普遍存在着一些非传粉小蜂,它们中的一些种类进入果腔后也能为榕树传粉,且在形态和物候上已与传粉榕小蜂发生了趋同进化。但其寄主识别行为是否也与传粉榕小蜂发生了趋同进化还不得而知。我们在西双版纳选择了钝叶榕(Ficuscurtipes)及其3种进果繁殖小蜂开展了相关的行为实验。3种小蜂中,1种是钝叶榕的专性传粉榕小蜂(Eupristina sp.),另外2种是寄居性非传粉小蜂(杨氏金小蜂Diaziellayangi和Lipothymus sp.),这2种非传粉小蜂进入果腔后也像传粉榕小蜂那样为钝叶榕传粉。我们以钝叶榕不同发育时期的榕果及这3种小蜂为材料,采用Y型嗅觉仪观察了这3种小蜂对各发育时期榕果和信息化学物质6-甲基-5-庚烯-2-醇、6-甲基-5-庚烯-2-酮及这2种化合物的混合物的选择行为。结果表明,当提供雌花期榕果与其他发育时期榕果和空气对照供这3种小蜂选择时,它们均显著地偏向于选择雌花期榕果;当提供雄花期榕果与其他发育时期榕果和空气对照供这3种小蜂选择时,它们均显著地偏向于选择其他发育时期榕果和空气对照,即都会避开雄花期榕果;此外,这3种小蜂均对钝叶榕雌花期果释放的一种主要化合物6-甲基-5-庚烯-2-醇的同一剂量(1μL)表现出显著的偏好。这一结果为传粉榕小蜂与非传粉小蜂间的寄主识别行为趋同进化的假说提供了证据。     

薜荔榕小蜂对薜荔和爱玉子雌花期榕果挥发物的行为反应

薜荔和爱玉子均属雌雄异株桑科榕属植物,两者互为原变种与变种的关系,分别与薜荔传粉小蜂和爱玉子传粉小蜂(二者互为隐存种)建立了专性共生关系,榕树榕果挥发物在维系传粉小蜂与其寄主的共生关系上起着重要作用。利用Y型嗅觉仪测定薜荔榕小蜂(薜荔和爱玉子的传粉小蜂)对薜荔和爱玉子雌花期榕果挥发物的行为反应。结果表明:(1)雌花期果型的大小对薜荔榕小蜂行为反应无显著影响,薜荔大、小果型雌花期雌(雄)榕果挥发物对其传粉小蜂均具有强烈的吸引作用;(2)榕果挥发物浓度影响薜荔榕小蜂行为反应,薜荔、爱玉子雌花期雌(雄)榕果挥发物对其传粉小蜂的吸引作用均可能存在阈值反应,即榕果挥发物浓度未超过阈值时,雌花期榕果挥发物对传粉小蜂的吸引作用与挥发物浓度成正相关关系,而一旦超过阈值,榕果挥发物对传粉蜂的吸引作用显著下降,表明寄主榕果挥发物浓度影响传粉小蜂的寄主定位;(3)薜荔传粉小蜂对低浓度爱玉子雌花期雌(雄)榕果挥发物、爱玉子传粉小蜂对低浓度薜荔雌花期雌(雄)榕果挥发物均既无趋向也无驱避行为;薜荔传粉小蜂对高浓度的爱玉子雌花期雌(雄)榕果挥发物表现为显著的驱避行为,而爱玉子传粉小蜂对高浓度薜荔雌(雄)雌花期榕果挥发物表现为显著的趋向行为,因此,薜荔传粉小蜂与爱玉子传粉小蜂存在寄主专一性不对称现象,爱玉子传粉小蜂进入薜荔雌(雄)果内传粉或产卵的可能性较大,而福州地区的薜荔传粉小蜂可能难以进入爱玉子雌(雄)果内传粉或产卵。本研究结果将为榕-蜂共生体系的化学生态学理论研究以及爱玉子栽培提供科学依据。     

榕果挥发物对传粉榕小蜂的吸引作用

榕树 /榕小蜂专一性共生系统的维持 ,与榕树开花期释放的特殊的挥发性化合物以及榕小蜂对其寄主榕树的化学识别和定位紧密相关。研究选取了西双版纳地区常见的 3种榕树 ,即对叶榕 Ficus hispida、木瓜榕 F.auriculata和鸡嗉子榕F.semicordata的榕果作为实验材料 ,利用野外诱捕实验、室内生物检测实验检测传粉榕小蜂 Hymenoptera:ChalcidoidaeAgaonidae对 12种信息化合物及榕果的二氯甲烷浸提物的趋向性反应 ,研究不同榕属植物的传粉榕小蜂对相同的信息化合物的反应差异 ,以及传粉榕小蜂受不同发育时期榕果浸提物吸引的显著性程度。诱捕实验中对叶榕小蜂 Ceratosolen solmsimarchali对香叶醇的趋向性反应显著 ,大果榕小蜂 C.emarginatus对接受期榕果浸提物和芳樟醇都有明显的趋向性反应 ,而对间花期榕果浸提物则无显著反应。嗅觉仪生物检测实验中 ,鸡嗉果榕小蜂 C.gravelyi对香叶醇和松油醇都表现出显著的趋向性反应。结果表明 ,对叶榕、鸡嗉子榕传粉榕小蜂对 12种信息化合物的反应存在一定的差异 ,木瓜榕传粉榕小蜂对香叶醇和木瓜榕接受期榕果浸提物的趋向性反应比间花期榕果强得多     

六种同域分布雌雄异株榕树挥发物多样性与系统发育一致性

植物花挥发物是维持昆虫-植物传粉互作的重要化学信号,其组成的多样性对于理解传粉昆虫与植物相互作用的形成、维持和进化具有重要意义。榕树与其传粉榕小蜂是一种专性的互惠共生关系,榕树为榕小蜂提供繁殖场所,榕小蜂为榕树传粉。而榕果雌花期（接收期）释放的特异性挥发物是维持双方相互作用的关键媒介。本研究以西双版纳地区同域分布的6种雌雄异株榕树为研究对象,用固相微萃取和气相色谱质谱联用仪对雌花期榕果的挥发物组成进行了分析。共发现77种化合物,包含脂肪酸类衍生物6种、单萜类化合物16种、倍半萜类衍生物50种和芳香族化合物5种,不同化合物对挥发物距离差异性的贡献率依次是：对甲基苯甲醚（4-methylanisole,2.15）、β-罗勒烯（β-Ocimene,0.84）和喜沙木烯（Prezizaene,0.73）。不同物种间挥发物组成有显著的差异,且挥发物的差异与榕树系统发育距离具有正相关性,但同一物种不同性别间的挥发物组成上没有显著的差异。本研究中发现雌雄异株榕树挥发物组成具有多样性高、种内性别间相似、种间差异大,系统发育一致性的特点,上述特点在榕树物种分化以及维持雌雄异株榕树繁殖的化学通讯机制中可能发挥着关键作用。     

雌花期榕小蜂进入榕果的行为及其活动时间

在西双版纳,钝叶榕传粉榕小蜂Eupristina sp.和杨氏榕树金小蜂Diaziella yangi均在雌花期进入钝叶榕果内繁殖和传粉,比较研究它们进入榕果的行为和活动时间。结果显示:在搜寻苞片处进蜂口时,2种榕小蜂的种内均出现打斗行为,并且杨氏榕树金小蜂的打斗更为激烈,但种间没有打斗行为发生,杨氏榕树金小蜂总是等待钝叶榕传粉榕小蜂先期进入榕果,然后才跟随着进入。在搜寻和进入苞片口通道阶段,钝叶榕传粉榕小蜂均比杨氏榕树金小蜂花费较长时间;而在果腔内产卵、传粉的时间,2种榕小蜂均最多不超过3d。相似的进蜂过程和活动时间,可能是2种榕小蜂与寄主榕树长期协同进化的结果。     

爱玉子花序挥发物成分以及对其传粉小蜂的吸引作用

利用动态顶空吸附法和GC-MS分析,研究接受期以及传粉或产卵5d后爱玉子(Ficus awkeotsang)雌、雄隐头花序挥发物成分。研究结果表明:爱玉子隐头花序挥发物的组成成分复杂,种类繁多,主要成分是对传粉小蜂具有显著吸引作用的芳樟醇。组成雌、雄花序的接受期挥发物信号的化合物种类与数量不同,但两者之间的共有化合物却占花序挥发物总量的70%以上,且接受期雌、雄花序挥发物组成比例相似,小蜂无法通过花序挥发物信号的差异,区别雌、雄花序,从而支持"榕树雌、雄花序接受期挥发物存在相互模拟现象"的假说。爱玉子传粉(或产卵)前后花序挥发物信号发生变化,表现在花序在传粉(或产卵)后,一些挥发性化合物在榕果中消失或相对含量减少(如芳樟醇),有些化合物的相对含量增加(如苯甲酸甲酯),并出现新的化合物(如2-乙基己醇);在化合物组成上,萜类化合物相对含量下降,芳香族化合物、脂肪族化合物相对含量上升。嗅觉仪实验表明爱玉子接受期雌、雄花序挥发物对其传粉榕小蜂有极显著的吸引作用,而传粉(或产卵)5d后的雌、雄花序挥发物对传粉榕小蜂有显著的趋避作用。传粉小蜂对雌、雄接受期花序挥发物的选择没有偏向性。榕果通过挥发物的释放量和成分的改变反映出花发育与被授粉(被产卵)状况,传粉小蜂通过接收榕果发出的化学信息,判断选择适合的寄主。研究对于爱玉子的高产栽培以及植物与昆虫专性共生化学生态学机制的理论研究具有重要的意义。     

爱玉子花发育的形态学研究

通过花序标记、形态解剖及放蜂实验方法,观察不同发育时期爱玉子雌、雄花序中花的形态特征,以及花发育与小蜂传粉(或产卵)之间的相关性。结果表明,雌前期、雌花期的瘿花在形态上没有明显变化,而雌花的花柱与柱头连成长鞭状,在雌前期呈直立管状,进入雌花期后呈弯曲的S形;在榕小蜂进入花序传粉或产卵5 d后,雌花和瘿花的柱头变黄,花柱开始脱水;在榕小蜂传粉或产卵10 d后,雌花和瘿花花梗伸长,花明显分层,胚迅速发育,子房饱满,花柱和柱头明显萎蔫。传粉小蜂在花序腔内的存活时长不超过3 d。本研究为揭示榕-蜂共生机制提供科学依据。     

西双版纳热带雨林对叶榕传粉生物学(英)

研究了西双版纳热带雨林地区雌雄异株植物对叶榕 (FicushispidaL .)的生物学、传粉物候学以及榕小蜂(CeratosolensolmsimarchaliMayr)的传粉和繁殖行为。研究结果表明 :雌雄异株的对叶榕与其他雌雄同株的榕属植物不同 ,它的种子形成与传粉者有着更为复杂的相互关系。对叶榕一年结隐花果 6～ 8次 ,结果高峰期 4～ 5次 ,其中雄性植株仅产生花粉和孕育榕小蜂 ,而雌性植株 (无雄蕊 )则需榕小蜂带花粉进入隐花果内 ,进行传粉授精 ,使之发育成种子。对叶榕的成熟花粉不能从花药开裂处自行散发出来 ,必须由榕小蜂采集才能散落。榕小蜂雌蜂羽化、交配后 ,找到雄花区 ,用足、触角、口器在推动中采集花粉。雌蜂飞出熟榕果找寻雌株或雄株榕树上的幼嫩隐花果 ,一般需 3～ 6 7min ;一部分雌蜂在雄株中寻找幼嫩的隐花果 ,进去产卵繁殖 ,另一部分雌蜂则寻找雌株雌花期嫩隐花果进去传粉。雌蜂在雌株榕树的隐花果内传粉时间为 15～ 2 3h ,在雄株榕树的隐花果内产卵时间为 6～ 9h。对叶榕小蜂在雌株上进入单个隐花果的数量多少关系到雌花结实率 ;观察表明 ,每个隐花果最佳进蜂数为 2头 ;榕小蜂传粉后榕树成熟种子形成率在 5 4 .1%～ 82 .5 %之间 ,平均为 73.8% ;而在雄株上雌蜂进蜂数量则关系到榕小蜂在隐花果内的产卵率 ,     

Foreign exploration for Scirtothrips perseae Nakahara (Thysanoptera: Thripidae) and associated natural enemies on avocado (Persea americana Miller)

Scirtothrips perseae Nakahara was discovered attacking avocados in California, USA, in 1996. Host plant surveys in California indicated that S. perseae has a highly restricted host range with larvae being found only on avocados, while adults were collected from 11 different plant species. As part of a management program for this pest, a “classical” biological control program was initiated and foreign exploration was conducted to delineate the home range of S. perseae, to survey for associated natural enemies and inventory other species of phytophagous thrips on avocados grown in Mexico, Guatemala, Costa Rica, the Dominican Republic, Trinidad, and Brazil. Foreign exploration efforts indicate that S. perseae occurs on avocados grown at high altitudes (>1500 m) from Uruapan in Mexico south to areas around Guatemala City in Guatemala. In Costa Rica, S. perseae is replaced by an undescribed congener as the dominant phytophagous thrips on avocados grown at high altitudes (>1300 m). No species of Scirtothrips were found on avocados in the Dominican Republic, Trinidad, or Brazil. In total, 2136 phytophagous thrips were collected and identified, representing over 47 identified species from at least 19 genera. The significance of these species records is discussed. Of collected material 4% were potential thrips biological control agents. Natural enemies were dominated by six genera of predatory thrips (Aeolothrips, Aleurodothrips, Franklinothrips, Leptothrips, Scolothrips, and Karnyothrips). One genus each of parasitoid (Ceranisus) and predatory mite (Balaustium) were found. Based on the results of our sampling techniques, prospects for the importation of thrips natural enemies for use in a “classical” biological control program in California against S. perseae are not promising.     

Characterization of SSEA-1 glycolipids from the brain of a patient with fucosidosis

Neutral glycolipids from the brain of a patient with Fucosidosis were analyzed and two complex glycolipids containing five and eight sugars were isolated from the cortical grey matter. These two glycolipids reacted with antibodies recognizing the SSEA-1 [Le^x(X)] carbohydrate determinant. SSEA-1 glycolipids are normally expressed in human embryonic brain but are found in only small amounts in postnatal human brain. The accumulation of the two SSEA-1 glycolipids in Fucosidosis brain thus represents a defect which affects the normal developmentally regulated decrease in postnatal, expression of these glycolipids, and may be a contributing factor in the abnormal brain development associated with the disease. Chemical characterization of the two isolated glycolipids by gas chromatographic and mass spectrometric analyses has identified the two glycolipids as lacto-N-fucopentaosylceramide (III) and difucosyl-neolactonorhexaosylceramide.Abbreviations DCl direct chemical ionization - FAB tastatiom bombardment - GC gas chromatography - GSLs glycosphingolipids - MS mass spectrometry - SSEA-1 stage specific embryonic antigen-1 - TLC thin layer chromatographys     

1H and13C-NMR analysis of four pentasaccharides from urine of blood-group A and B,Leb adults. Confirmation of the structure of two new oligosaccharides: Fuc(α1–2)[GalNAc(α1–3)]Gal(β1–3)[Fuc(α1–4)]Glc and Fuc(α1–2)[Gal(α1–3)]Gal(β1–3)[Fuc(α1–4)]Glc

The major pentasaccharides Fuc(1-2)[GalNAc(1-3)]Gal(1-4)[Fuc(1-3)]Glc and Fuc(1-2) [Gal(1-3)]Gal(1-4)[Fuc(1-3)]Glc, which are normally present in the urine of bloodgroup A Le^b and B Le^b healthy subjects, were each found to be contaminated by a minor component when analysed by¹H-NMR. The determination of these structures, Fuc(1-2) [GalNAc(1-3)]Gal(1-3)[Fuc(1-4)]Glc and Fuc(1-2) [Gal(1-3)]Gal(1-3)[Fuc(1-4)]Glc, was based on the results of methylation analysis and¹H/¹³C-NMR spectroscopy.Abbreviations HPLC high performance liquid chromatography - GLC gas liquid chromatography - NMR nuclear magnetic resonance - COSY correlation spectroscopy - Gal d-galactopyranose - GalNAc 2-acetamido-2-deoxy-d-galactopyranose - Glc d-glucopyranose - Fuc l-fucopyranose - LNDFH I lacto-N-difucohexaose I (Le^b determinant     

Structural Peculiarities of Na+,K+-ATPase Isozymes from the Calf Brain

Functionally active preparations of Na⁺,K⁺-ATPase isozymes from calf brain that contain catalytic subunits of three types (1, 2, and 3) were obtained using two approaches: a selective removal of contaminating proteins by the Jorgensen method and a selective solubilization of the enzyme with subsequent reconstitution of their membrane structure by the Esmann method. The ouabain inhibition constants were determined for the isozymes. The real isozyme composition of the Na⁺ pump from the grey matter containing glial cells and the brain stem containing neurons was determined. The plasma membranes of glial cells were shown to contain mainly Na⁺,K⁺-ATPase of the 11 type and minor amounts of isozymes of the 22(1) and the 31(2) type. The axolemma contains 21 and 31 isozymes. A carbohydrate analysis indicated that 11 enzyme preparations from the brain grey matter substantially differ from the renal enzymes of the same composition in the glycosylation of the 1 isoform. An enhanced sensitivity of the 3 catalytic subunit of Na⁺,K⁺-ATPase from neurons to endogenous proteolysis was found. A point of specific proteolysis in the amino acid sequence PNDNR⁴⁹² Y⁴⁹³ was localized (residue numbering is that of the human 3 subunit). This sequence corresponds to one of the regions of the greatest variability in 1-, 2-, 3-, and 4-subunits, but at the same time, it is characteristic of the 3 isoforms of various species. The presence of the 3 isoform of tubulin (cytoskeletal protein) was found for the first time in the high-molecular-mass Na⁺,K⁺-ATPase 31 isozyme complex isolated from the axolemma of brain stem neurons, and its binding to the 3 catalytic subunit was shown.     

Phylogeny of cardinalfishes (Teleostei: Gobiiformes: Apogonidae) and the evolution of visceral bioluminescence

The cardinalfishes (Apogonidae) are a diverse clade of small, mostly reef-dwelling fishes, for which a variety of morphological data have not yielded a consistent phylogeny. We use DNA sequence to hypothesize phylogenetic relationships within Apogonidae and among apogonids and other acanthomorph families, to examine patterns of evolution including the distribution of a visceral bioluminescence system. In conformance with previous studies, Apogonidae is placed in a clade with Pempheridae, Kurtidae, Leiognathidae, and Gobioidei. The apogonid genus Pseudamia is recovered outside the remainder of the family, not as sister to the superficially similar genus Gymnapogon. Species sampled from the Caribbean and Western Atlantic (Phaeoptyx, Astrapogon, and some Apogon species) form a clade, as do the larger-bodied Glossamia and Cheilodipterus. Incidence of visceral bioluminescence is found scattered throughout the phylogeny, independently for each group in which it is present. Examination of the fine structure of the visceral bioluminescence system through histology shows that light organs exhibit a range of morphologies, with some composed of complex masses of tubules (Siphamia, Pempheris, Parapriacanthus) and others lacking tubules but containing chambers formed by folds of the visceral epithelium (Acropoma, Archamia, Jaydia, and Rhabdamia). Light organs in Siphamia, Acropoma, Pempheris and Parapriacanthus are distinct from but connected to the gut; those in Archamia, Jaydia, and Rhabdamia are simply portions of the intestinal tract, and are little differentiated from the surrounding tissues. The presence or absence of symbiotic luminescent bacteria does not correlate with light organ structure; the tubular light organs of Siphamia and chambered tubes of Acropoma house bacteria, those in Pempheridae and the other Apogonidae do not.     

Biological control of three floating water weeds,<Emphasis Type="Italic">Eichhornia crassipes,Pistia stratiotes</Emphasis>, and <Emphasis Type="Italic">Salviniamolesta</Emphasis> in the Republic of Congo

Since 1999, four specific weevils (Coleoptera, Curculionidae) were released in the Republic of Congo against three exotic floating water weeds: Neochetina eichhorniae Warner and N. bruchi Hustache against water hyacinth, Neohydronomus affinis Hustache against water lettuce, and Cyrtobagous salviniae Calder and Sands against water fern. Recoveries of exotic weevils were made from all 24 release sites except one, and all four species have established and spread (up to 800 km for water hyacinth weevils). Within a few years of releases, control of water fern and water lettuce was such that fishing and navigation could be resumed, while reductions of water hyacinth populations were only beginning.     

A molecular phylogeny of Hebeloma species from Europe

In order to widen the scope of existing phylogenies of the ectomycorrhizal agaric genus Hebeloma a total of 53 new rDNA ITS sequences from that genus was generated, augmented by sequences retrieved from GenBank, and analysed using Bayesian, strict consensus and neighbour joining methods. The lignicolous Hebelomina neerlandica, Gymnopilus penetrans, and two species of Galerina served as outgroup taxa. Anamika indica, as well as representatives of the genera Hymenogaster and Naucoria, were included to test the monophyly of Hebeloma, which is confirmed by the results. Hebeloma, Naucoria, Hymenogaster and Anamika indica cluster in a strongly supported monophyletic hebelomatoid clade. All trees largely reflect the current infrageneric classification within Hebeloma, and divide the genus into mostly well-supported monophyletic groups surrounding H. crustuliniforme, H. velutipes, H. sacchariolens, H. sinapizans, and H. radicosum, with H. sarcophyllum being shown at an independent position; however this is not well supported. The section Indusiata divides with strong support into three groups, the position of the pleurocystidiate Hebeloma cistophilum suggests the possible existence of a third subsection within sect. Indusiata. Subsection Sacchariolentia is raised to the rank of section.     

The evolution of the Hox cluster: insights from outgroups

Two burgeoning research trends are helping to reconstruct the evolution of the Hox cluster with greater detail and clarity. First, Hox genes are being studied in a broader phylogenetic sampling of taxa: the past year has witnessed important new data from teleost fishes, onychophorans, myriapods, polychaetes, glossiphoniid leeches, ribbon worms, and sea anemones. Second, commonly accepted notions of animal relationships are being challenged by alternative phylogenetic hypotheses that are causing us to rethink the evolutionary relationships of important metazoan lineages, especially arthropods, annelids, nematodes, and platyhelminthes.     

N-andO-glycosylation of glycoprotein C synthesized by Herpes simplex virus type 1-infected ricin resistant cells

The progeny of Herpes simplex virus type 1 (HSV-1) grown in ricin-resistant 14 cells (Ric^R14) lackingN-acetylglucosaminyltransferase I was released in the extracellular medium at a very low rate. By using a monoclonal antibody immobilized on Sepharose we purified from HSV-1-infected Ric^R14 cells a viral glycoprotein (gC), which carries bothN-andO-linked oligosaccharides. Glycopeptides obtained from [³H]mannoselabeled gC by Pronase digestion were entirely susceptible to endo--N-acetylglucosaminidase H, and the major oligosaccharide released was Man₄GlcNAc. The accumulation of this high-mannose species was related to the enzymic defect of the host cells and to the long retention of the viral glycoprotein within the cells. The extent ofO-glycosylation evaluated in [¹⁴C]glucosamine-labeled gC from Ric^R14 cells as compared to that of gC from wild type cells did not appear to be significantly modified.Abbreviations Con A concanavalin A - BHK cells baby hamster kidney cells - HSV Herpes simplex virus