晶圆盘菌属的一个中国新记录种

Orbilia Fr. and Hyalorbilia Baral ＆ G Marson are the only genera currently accepted in the family Orbiliaceae which was established by Nannfeldt （Baral, 1994; Kirk et al., 2001）. Hyalorbilia was erected by Baral and Marson （2001） based on unstalked asci arising from crosiers, with hemispherical apices without wall thickenings, some bipolar-symmetrical globose inclusion bodies in ascospores （living state）,     

晶圆盘菌属中国新记录种

<正>晶圆盘菌属Hyalorbilia Baral & G.Marson是圆盘菌科中的一个小属,包括O.inflatula(P.Karst.)P.Karst.等5个种(Baral & Marson,2001)。该属子实层组织胶化,子囊产自产囊丝钩,顶部半球形,壁不     

晶圆盘菌属中国新记录种

晶圆盘菌属Hyalorbilia Baral ＆ G.Marson是圆盘菌科中的一个小属,包括O.inflatula（P.Karst.）P.Karst.等5个种（Baral ＆ Marson,2001）。该属子实层组织胶化,子囊产自产囊丝钩,顶部半球形,壁不 加厚,子囊孢子内通常具有两极对称排列的孢子体或孢子内含物,外囊盘被为角胞组织,侧丝顶端一般不膨大。作者在对中国圆盘菌科的资源调查中,     

Genetic transformation of gentian using wild-type Agrobacterium rhizogenes

Leaf sections of greenhouse-grown Miscanthus x ogiformis Honda 'Giganteus' plants and leaf sections or shoot apices of in vitro shoot cultures were grown on Murashige and Skoog medium containing various concentrations of benzyladenine (BA) and 2,4-dichlorophenoxyacetic acid. On leaf sections, the callus induction decreased with increasing BA concentration. The percentage of embryogenic callus was increased, the percentage of root-forming callus decreased, and a new shoot-forming callus type was formed by inclusion of BA during callus induction. A higher percentage of shoot-forming callus was formed on shoot apices compared with leaf sections of in vitro-grown shoots when cultured on 0.4 μM BA. The largest number of plants per callus piece was regenerated from shoot-forming callus, but maintenance of the high regeneration capacity proved difficult. This revised version was published online in June 2006 with corrections to the Cover Date.     

Monovalent cation transporters; establishing a link between bioinformatics and physiology

Toxic aluminum (Al) ion is a major constraint to plant growth in acid soils. Aluminum tolerance in wheat (Triticum aestivum L.) is strongly related to the Al-triggered efflux of malate from root apices. A role of the secreted malate has been postulated to be in chelating Al and thus excluding it from root apices (malate hypothesis), but the actual process has yet to be fully elucidated. We measured Al content and root growth during and after Al exposure using seedlings of near-isogenic lines [ET8 (Al tolerant) and ES8 (Al sensitive)] differing in the capacity to induce Al-triggered malate efflux. Aluminum doses that caused 50% root growth inhibition during 24-h exposure to Al in calcium (Ca) solution (0.5 mM CaCl₂, pH 4.5) were 50 μM in ET8 and 5 μM in ES8. Under such conditions, the amount of Al accumulated in root apices was approximately 2-fold higher in ET8 than ES8. Al-treated seedlings were then transferred to the Al-free Ca solution for 24 h. Compared to control roots (no Al pretreatment), root regrowth of Al-treated roots was about 100% in ET8 and about 25% in ES8. The impaired regrowth in ES8 was observed even after 24-h exposure to 2.5 μM Al which had caused only 20% root growth inhibition. The addition of malate (100 μM) during exposure to 50 μM Al in ES8 enhanced root growth 1.6 times and regrowth in Al-free solution 7 times, resulting in similar root growth and regrowth as in ET8. Short-term Al treatments of ES8 for up to 5 h indicated that the Al-caused inhibition of root regrowth started after 1-h exposure to Al. The stimulating effect of malate on root regrowth was observed when malate was present during Al exposure, but not when roots previously exposed to Al were rinsed with malate, although Al accumulation in root apices was similar under these malate treatments. We conclude that the malate secreted from root apices under Al exposure is essential for the apices to commence regrowth in Al-free medium, the trait that is not related to the exclusion of Al from the apices.     

Embryogenic callus formation,growth and regeneration in callus and suspension cultures of Miscanthus x ogiformis Honda Giganteus' as affected by proline

The effects of proline additions to culture systems of Miscanthus x ogiformis Honda Giganteus' were investigated. Proline was added in concentrations of 0, 12.5, 25, 50, 100 or 300 mM to the callus induction and suspension culture media containing either Murashige and Skoog or N6 basal salts and 22.6 μM 2,4-dichlorophenoxyacetic acid. Shoot apices and leaves from in vitro-propagated shoots, and immature inflorescences from greenhouse-grown plants were used as explants for callus induction and formation. Suspension cultures initiated from embryogenic callus of immature inflorescences were used to test the effect of proline in suspension cultures. The proline additions affected the formation of embryogenic callus and the growth of suspension cultures. Improvements depended on the proline concentration and the basal salts of the medium. Addition of 12.5 to 50 mM proline to callus induction medium with Murashige and Skoog salts increased embryogenic callus formation on shoot apices and leaf explants while proline had no effect on embryogenic callus formation in medium with N6 salts. Increased growth with increasing proline concentration was obtained in suspension aggregates grown in medium with N6 salts, whereas proline only increased growth of suspension aggregates grown in medium with Murashige and Skoog salts at concentrations of 12.5 or 25 mM. A stimulating effect of proline on plant regeneration was observed in short-term cultures of callus as well as in long-term cultures of suspension aggregates. An optimum proline concentration for plant regeneration was found at 12.5 mM. This revised version was published online in June 2006 with corrections to the Cover Date.     

Noncoding RNA: from dark matter to bright star

正The central dogma states that genes encoded in the DNA should be first transcribed into messenger RNA (mRNA) and then translated into functional proteins (Crick, 1970). This dogma has been written in numerous textbooks and learned by myriad students. However, along with the completion of the human genome project in June 2000, an astonishing fact was revealed:only 1.5%of the human genome encodes for proteins (Lander et al., 2001; Venter et al., 2001). This fact     

THE ROLES OF DETOXIFYING ENZYMES AND AChE INSENSITIVITY IN METHAMIDOPHOS RESISTANCE DEVELOPMENT AND DECLINE IN NILAPARVATA LUGENS

Methamidophos resistance of brown planthopper (Nilaparvata lugens Stal, BPH) was selected in laboratory. After successive selection for 9 generations, the selection was ceased by rearing BPH without contact with any insecticide for 9 generations. In the full course, the successive changes of esterase activity, MFO activity, GSTs activity and AChE insensitivity were analyzed. The results showed that the change of esterase activity was high correlated with that of methamidophos in the full course, which indicated that esterase played very important role both in the resistance development and in the resistance decline. However, the change of AChE insensitivity only significantly correlated with that of resistance in the development stage, and the change of MFO activity or GSTs activity only significantly correlated with that of the resistance in the decline stage, which indicated the changes of AChE insensitivity, MFO activity or GSTs activity only played some roles in different stages of the resistance change.     

Binding of rhodopsin and rhodopsin analogues to transducin,rhodopsin kinase and arrestin-1

AIM: To investigate the interaction of reconstituted rhodopsin, 9-cis-retinal-rhodopsin and 13-cis-retinal-rhodopsin with transducin, rhodopsin kinase and arrestin-1. METHODS: Rod outer segments(ROS) were isolated from bovine retinas. Following bleaching of ROS membranes with hydroxylamine, rhodopsin and rhodopsin analogues were generated with the different retinal isomers and the concentration of the reconstituted pigments was calculated from their UV/visible absorption spectra. Transducin and arrestin-1 were purified to homogeneity by column chromatography, and an enriched-fraction of rhodopsin kinase was obtainedby extracting freshly prepared ROS in the dark. The guanine nucleotide binding activity of transducin was determined by Millipore filtration using β,γ-imido-(3H)-guanosine 5'-triphosphate. Recognition of the reconstituted pigments by rhodopsin kinase was determined by autoradiography following incubation of ROS membranes containing the various regenerated pigments with partially purified rhodopsin kinase in the presence of(γ-32P) ATP. Binding of arrestin-1 to the various pigments in ROS membranes was determined by a sedimentation assay analyzed by sodium dodecyl sulphatepolyacrylamide gel electrophoresis. RESULTS: Reconstituted rhodopsin and rhodopsin analogues containing 9-cis-retinal and 13-cis-retinal rendered an absorption spectrum showing a maximum peak at 498 nm, 486 nm and about 467 nm, respectively, in the dark; which was shifted to 380 nm, 404 nm and about 425 nm, respectively, after illumination. The percentage of reconstitution of rhodopsin and the rhodopsin analogues containing 9-cis-retinal and 13-cis-retinal was estimated to be 88%, 81% and 24%, respectively. Although only residual activation of transducin was observed in the dark when reconstituted rhodopsin and 9-cis-retinal-rhodopsin was used, the rhodopsin analogue containing the 13-cis isomer of retinal was capable of activating transducin independently of light. Moreover, only a basal amount of the reconstituted rhodopsin and 9-cis-retinal-rhodopsin was phosphorylated by rhodopsin kinase in the dark, whereas the pigment containing the 13-cis-retinal was highly phosphorylated by rhodopsin kinase even in the dark. In addition, arrestin-1 was incubated with rhodopsin, 9-cis-retinal-rhodopsin or 13-cis-retinal-rhodopsin. Experiments were performed using both phosphorylated and non-phosphorylated regenerated pigments. Basal amounts of arrestin-1 interacted with rhodopsin, 9-cis-retinal-rhodopsin and 13-cis-retinal-rhodopsin under dark and light conditions. Residual arrestin-1 was also recognized by the phosphorylated rhodopsin and phosphorylated 9-cis-retinal-rhodopsin in the dark. However, arrestin-1 was recognized by phosphorylated 13-cis-retinal-rhodopsin in the dark. As expected, all reformed pigments were capable of activating transducin and being phosphorylated by rhodopsin kinase in a lightdependent manner. Additionally, all reconstituted photolyzed and phosphorylated pigments were capable of interacting with arrestin-1. CONCLUSION: In the dark, the rhodopsin analogue containing the 13-cis isomer of retinal appears to fold in a pseudo-active conformation that mimics the active photointermediate of rhodopsin.     

Striving for the development of biology——The celebration of Biomagnelism formally changed into Progress in Modem Biomedicine

ime flies!Biomagnetism magazine has been gradually growing up since it was started publication,which was firstly sponsored by China Biomagnetism Society in 1987 as a restricted publication.The publication was given official number by Ministry of Science and Technology in April,2001,issued by post office in 2003;it was chosen as one of the core periodicals of science and technology in 2004,with influence factor(0.734)and being classified as ninth-rale in periodicals of biology.Upon the approv…     

Perithecial ontogeny in erithecial ontogeny in the fungal genus Epichloe: An examination of the claviciptalean centrum

The structure and development of perithecia in five collections of Epichloe from Europe and North America were studied. Perithecia in early stages of development are oblong to ovate in overall shape. Dichotomously branched paraphyses form on the bottom and sides of the inner walls of the perithecial primordium. As the ovate primordium expands, a mound of ascogenous mycelium develops in its base. As asci develop from the ascogenous mound, paraphyses proximal to asci evanesce and no paraphyses are observable within the cluster of asci. In E. amarillans and E. baconii paraphyses are converted into pseudoparenchyma-like tissues, while in E. typhina paraphyses remain filamentous until they evanesce. Ascospore development is seen to differ among all three species of Epichloe. The development and structure of the Epichloe centrum are compared to those of the Nectria and Xylaria types. It is apparent that a distinct type of centrum is present in Epichloe, and perhaps all of the Clavicipitaceae. It is proposed that the Epichloe type centrum may represent a key feature for distinguishing the Clavicipitaceae from the Hypocreaceae or other groups of pyrenomycetes.     

MORPHOLOGY OF HYPOMYCES TRICHOTHECOIDES

Large, spirally coiled initials embedded in a subiculum develop into multicellular, multinucleate ascogonia. Hyphae grow up around them to form a prosenchymatous perithecial wall. The ascogonia give rise to multinucleate ascogenous cells from which croziers and asci form. As the ascocarp develops, an apical meristem produces uninucleate cells that elongate downward into long, slender filaments, the apical paraphyses. From a basal layer of ascogenous cells, asci grow up among the apical paraphyses, which disintegrate as the ascocarp matures. Ascospores are verrucose, with obtuse apiculi. This pattern of development is typical of the Nectria-type of Luttrell.     

Rimularia fuscosora, a new corticolous sorediate lichen from north western Europe

Rimularia fuscosora is described on the basis of material from Sweden, Norway. and Scotland. This new species is characterized by a sorediate thallus containing norstictic acid, apothecia with a well developed excipulum, asci of Rimularia-type . branched paraphyses and a corticolous habit.     

Formation of spore ornamentation in two Sphaerophorus species

Two different ways of achieving a spore ornamentation have been demonstrated in Sphaereophorus , belonging to the Caliciales. In S. globosus the ornamentation is formed within the ascus by an external secondary spore wall in an ontogenetic process with several unique features. In S. murrayi the ornamentation is formed at a late stage, when the spores have been released from the asci. Carbonaceous material formed among the asci and paraphyses is added to the surface of the primary wall, and a very irregular ornamentation is formed. The name Sphaerophorus murrayi Ohlsson is validated.     

DEVELOPMENT OF THE PERITHECIUM IN GNOMONIA COMARI (DIAPORTHACEAE)

Perithecia of Gnomonia comari (Ascomycetes) mature within 14 days on cornmeal agar under continuous fluorescent light at 25 C. The perithecium is initiated by a coiled, multicellular ascogonium. Branches from somatic hyphae surround the ascogonium. This hyphal envelope early differentiates into two regions: a centrum of pseudoparenchymatous cells and a peripheral wall of more elongated, flattened cells. The wall produces a long, ostiolate beak by eruption of a column of hyphae from the inner layers at the apex; the cells gradually become thick-walled and brown from the peripheral layers inward. Proliferations from the ascogonial cells near the center of the perithecium form a bowl-shaped mass of ascogenous hyphae which expands centrifugally until it appears in section as a crescentic layer across the middle of the centrum. The centrum pseudoparenchyma above this incipient hymenium disintegrates, and short abortive paraphyses extend upward from the subhymenial pseudoparenchyma into the resulting cavity. The paraphyses disintegrate as the asci develop among them. The hymenium gradually pushes downward into the disintegrating subhymenial pseudoparenchyma until it rests on the perithecial wall. Maturing asci become detached from the hymenium, fill the perithecial cavity, and pass through the ostiole. At the tip of the beak they discharge their ascospores forcibly. Diaporthaceae with abortive paraphyses may occupy an intermediate position in a series leading from forms (Gaeumannomyces graminis) with long delicate paraphyses resembling those in the Sordariaceae to forms (Stegophora ulmea) in which the centrum is entirely pseudoparenchymatous.     

Poroleprieuria, a new xylariaceous genus from Mexico

Poroleprieuria gen. nov. is described and illustrated to accommodate P. rogersii in the Xylariaceae, Xylariales. This ascomycete, known only from the type collection, is characterized by reniform, light brown, smooth ascospores with a germ pore; cylindrical, persistent asci lacking an apical apparatus, septate persistent paraphyses, and erumpent, erect, dark brown, fragile, subcylindrical stromata. The characteristics of this xylariaceous fungus were compared with those of some other ascomycetes having superficially similar cylindrical stromata or ascospores with germ pores.     

MORPHOLOGY OF NECTRIA HAEMATOCOCCA

Ascocarp development in Nectria haematoccocca begins with the formation of deeply staining coils as lateral branches of the vegetative hyphae. As these coils develop into multicellular, multi-nucleate ascogonia, they are surrounded by a pseudoparenchymatous envelope. During ascocarp development an apical meristem produces cells that elongate downward into the centrum, forming long, filamentous, apical paraphyses. When fully developed the cells of the apical paraphyses swell, producing a tissue that is pseudoparenchymatous in appearance. The ascogonium proliferates to form a layer of multinucleate ascogenous cells across the base of the ascocarp. Asci form from the ascogenous cells by means of croziers. The asci grow up among the apical paraphyses, which disintegrate as the ascocarp matures. This pattern is typical of the Nectria-type of development, indicating that this species belongs in the Hypocreales.     

Hyaloscyphaceae in Japan (6): the genus Hyphodiscus in Japan and its anamorph Catenulifera gen. nov.

Three Hyphodiscus species are described and illustrated: Hyphodiscus otanii sp. nov., Hyphodiscus hymeniophilus, and H. theiodeus, which is new to Japan. Culture studies revealed Phialophora-like anamorphs. Catenulifera gen. nov. is proposed for the anamorph of Hyphodiscus. The history of the genus is reviewed. Hyphodiscus can be delimited to members with gelatinized excipulum, Cistella-like hairs with more coarse granulation, small asci, ascospores with conspicuous globules, cylindrical, flexuous paraphyses, and a Catenulifera anamorph. Received: September 6, 2001 / Accepted: October 4, 2001     

The morphology of Cercophora palmicola (Lasiosphaeriaceae)

A detailed study of ascomal morphology and development in Cercophora palmicola showed that ontogeny is ascohymeniaceous, giving rise to an ostiolate perithecium. Ascomal initials consist of a coiled ascogonium surrounded by several layers of hyphae whose cells become pseudoparenchymatous. The centrum of the young ascoma is composed of a few rows of large, thin-walled pseudoparenchymatous cells that line the ascomal wall, with the central region filled by tightly packed, filamentous paraphyses. The ascogenous system forms along the inside of the layer of pseudoparenchymatous cells at the base of the paraphyses and gives rise to unitunicate asci that grow up among the paraphyses. The wall of the mature perithecium is greatly thickened. It is composed of three regions: a thin outer region of darkly pigmented, angular cells with thickened walls; a broad central region of cells with gelatinized walls; and a thin inner region of flattened cells. Ascomal ontogeny in C. palmicola conforms well to the Sordaria type of development, as defined by Huang.