Basidiomycota and Deuteromycotina
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Ustilago: Habitat, Symptoms and Reproduction | Teliomycetes
Ustilago: Habitat, Symptoms and Reproduction | Teliomycetes For B.Sc. Botany 1st By Dr. Meenu Gupta Assistant Professor Botany J.D.W.C. Patna 1. Habit and Habitat of Ustilago: Ustilago, the largest genus of the family Ustilaginaceae is represented by more than 400 cosmopolitan species. Butler and Bisby (1958) reported 108 species from India. All species are parasitic and infect the floral parts of wheat, barley, oat, maize, sugarcane, Bajra, rye and wild grasses. The name Ustilago has been derived from a Latin word ustus meaning ‘burnt’ because the members of the genus produce black, sooty powdery mass of spores on the host plant parts imparting them a ‘burnt’ appearance. This black dusty mass of spores resembles soot or smut, therefore, commonly it is also known as smut fungus. The fungus is of much economic importance, because it causes heavy loss to various economically important plants. This genus is very common in U.P., Bihar, Punjab and Madhya Pradesh. 2. Symptoms of Ustilago: The symptoms appear only on the floral parts. The floral spikes turn black and remain filled with the smut spores. Ustilago produces two main types of symptoms: 1. The blackish powder of spores is easily blown away by the wind, leaving a bare stalk of inflorescence (Fig. 1 B). Species showing such symptoms are called loose smuts e.g., (a) Loose smut of oat caused by U. avenae (b) Loose smut of barley caused by U. nuda (c) Loose smut of wheat caused by U. nuda var. tritici. (Fig. 13A, B). (d) Loose smut of doob grass caused by U. -
Why Mushrooms Have Evolved to Be So Promiscuous: Insights from Evolutionary and Ecological Patterns
fungal biology reviews 29 (2015) 167e178 journal homepage: www.elsevier.com/locate/fbr Review Why mushrooms have evolved to be so promiscuous: Insights from evolutionary and ecological patterns Timothy Y. JAMES* Department of Ecology and Evolutionary Biology, University of Michigan, Ann Arbor, MI 48109, USA article info abstract Article history: Agaricomycetes, the mushrooms, are considered to have a promiscuous mating system, Received 27 May 2015 because most populations have a large number of mating types. This diversity of mating Received in revised form types ensures a high outcrossing efficiency, the probability of encountering a compatible 17 October 2015 mate when mating at random, because nearly every homokaryotic genotype is compatible Accepted 23 October 2015 with every other. Here I summarize the data from mating type surveys and genetic analysis of mating type loci and ask what evolutionary and ecological factors have promoted pro- Keywords: miscuity. Outcrossing efficiency is equally high in both bipolar and tetrapolar species Genomic conflict with a median value of 0.967 in Agaricomycetes. The sessile nature of the homokaryotic Homeodomain mycelium coupled with frequent long distance dispersal could account for selection favor- Outbreeding potential ing a high outcrossing efficiency as opportunities for choosing mates may be minimal. Pheromone receptor Consistent with a role of mating type in mediating cytoplasmic-nuclear genomic conflict, Agaricomycetes have evolved away from a haploid yeast phase towards hyphal fusions that display reciprocal nuclear migration after mating rather than cytoplasmic fusion. Importantly, the evolution of this mating behavior is precisely timed with the onset of diversification of mating type alleles at the pheromone/receptor mating type loci that are known to control reciprocal nuclear migration during mating. -
Evolution of Isoprenyl Diphosphate Synthase-Like Terpene
www.nature.com/scientificreports OPEN Evolution of isoprenyl diphosphate synthase‑like terpene synthases in fungi Guo Wei1, Franziska Eberl2, Xinlu Chen1, Chi Zhang1, Sybille B. Unsicker2, Tobias G. Köllner2, Jonathan Gershenzon2 & Feng Chen1* Terpene synthases (TPSs) and trans‑isoprenyl diphosphate synthases (IDSs) are among the core enzymes for creating the enormous diversity of terpenoids. Despite having no sequence homology, TPSs and IDSs share a conserved “α terpenoid synthase fold” and a trinuclear metal cluster for catalysis, implying a common ancestry with TPSs hypothesized to evolve from IDSs anciently. Here we report on the identifcation and functional characterization of novel IDS-like TPSs (ILTPSs) in fungi that evolved from IDS relatively recently, indicating recurrent evolution of TPSs from IDSs. Through large-scale bioinformatic analyses of fungal IDSs, putative ILTPSs that belong to the geranylgeranyl diphosphate synthase (GGDPS) family of IDSs were identifed in three species of Melampsora. Among the GGDPS family of the two Melampsora species experimentally characterized, one enzyme was verifed to be bona fde GGDPS and all others were demonstrated to function as TPSs. Melampsora ILTPSs displayed kinetic parameters similar to those of classic TPSs. Key residues underlying the determination of GGDPS versus ILTPS activity and functional divergence of ILTPSs were identifed. Phylogenetic analysis implies a recent origination of these ILTPSs from a GGDPS progenitor in fungi, after the split of Melampsora from other genera within the class of Pucciniomycetes. For the poplar leaf rust fungus Melampsora larici-populina, the transcripts of its ILTPS genes were detected in infected poplar leaves, suggesting possible involvement of these recently evolved ILTPS genes in the infection process. -
Flax Rust and Its Control
-1 I , r TECHNICAL BULLETIN 36 MARCH 1926 University of Minnesota Agricultural Experiment Station IN CO-OPERATION WITH UNITED STATES DEPARTMENT OF AGRICULTURE, BUREAU OF PLANT INDUSTRY Flax Rust and its Control A. W. Henry Division of Plant Pathology and Botany UNIVERSITY FARM, ST. PAUL AGRICULTURAL EXPERIMENT STATION ADMINISTRATIVE OFFICERS W. C. COFFEY, M.S., Director ANDREW Boss, Vice-Director F. W. PECK, M.S., Director of Agricultural Extension and Farmers' Institutes C. G. SELVIG, M.A., Superintendent, Northwest Substation, Crookston P. E. MILLER, M.Agr., Superintendent, West Central Substation, AIorris 0. I. BERGH, B.S.Agr., Superintendent, North Central Substation, Grand Rapids M. J. THOMPSON, Superintendent, Northeast Substation, Duluth R E. HODGSON, B.S. in Agr., Superintendent, Southeast Substation, Waseca RAPHAEL ZON, F.E., Director, Forest Experiment Station, Cloquet F. E. HARALSON, Assistant Superintendent, Fruit Breeding Farm, Zumbra Heights, (P.O. Excelsior) W. P. KIRKWOOD, M.A., Editor, and Chief, Division of Publications ALICE MCFEELY, Assistant Editor of Bulletins HARRIET W. SEWALL, B.A., Librarian T. J. HORTON, Photographer R. A. GORTNER, Ph.D., Chief, Division of Agricultural Biochemistry J. D. BLACK, Ph.D., Chief, Division of Agricultural Economics WILLIAM Boss, Chief, Division of Agricultural Engineering ANDREW Boss, Chief, Division of Agronomy and Farm Management W. H. PETERS, M.Agr., Chief, Division of Animal Husbandry FRANCIS JAGER, Chief, Division of Bee Culture C. H. EcKLEs, M.S., D.Sc., Chief, Division of Dairy Husbandry R. N. CHAPMAN, Ph.D., Chief Division of Entomology and Economic Zoology HENRY ScH/Arrz, Ph.D., Chief, Division of Forestry W. H. ALDERMAN, B.S.A., Chief, Division of Horticulture E. -
Classifications of Fungi
Chapter 24 | Fungi 675 Sexual Reproduction Sexual reproduction introduces genetic variation into a population of fungi. In fungi, sexual reproduction often occurs in response to adverse environmental conditions. During sexual reproduction, two mating types are produced. When both mating types are present in the same mycelium, it is called homothallic, or self-fertile. Heterothallic mycelia require two different, but compatible, mycelia to reproduce sexually. Although there are many variations in fungal sexual reproduction, all include the following three stages (Figure 24.8). First, during plasmogamy (literally, “marriage or union of cytoplasm”), two haploid cells fuse, leading to a dikaryotic stage where two haploid nuclei coexist in a single cell. During karyogamy (“nuclear marriage”), the haploid nuclei fuse to form a diploid zygote nucleus. Finally, meiosis takes place in the gametangia (singular, gametangium) organs, in which gametes of different mating types are generated. At this stage, spores are disseminated into the environment. Review the characteristics of fungi by visiting this interactive site (http://openstaxcollege.org/l/ fungi_kingdom) from Wisconsin-online. 24.2 | Classifications of Fungi By the end of this section, you will be able to do the following: • Identify fungi and place them into the five major phyla according to current classification • Describe each phylum in terms of major representative species and patterns of reproduction The kingdom Fungi contains five major phyla that were established according to their mode of sexual reproduction or using molecular data. Polyphyletic, unrelated fungi that reproduce without a sexual cycle, were once placed for convenience in a sixth group, the Deuteromycota, called a “form phylum,” because superficially they appeared to be similar. -
Structural Genomics Applied to the Rust Fungus Melampsora Larici-Populina
www.nature.com/scientificreports OPEN Structural genomics applied to the rust fungus Melampsora larici- populina reveals two candidate efector proteins adopting cystine knot and NTF2-like protein folds Karine de Guillen1, Cécile Lorrain2, Pascale Tsan3, Philippe Barthe1, Benjamin Petre2, Natalya Saveleva2, Nicolas Rouhier2, Sébastien Duplessis2, André Padilla1 & Arnaud Hecker2* Rust fungi are plant pathogens that secrete an arsenal of efector proteins interfering with plant functions and promoting parasitic infection. Efectors are often species-specifc, evolve rapidly, and display low sequence similarities with known proteins. How rust fungal efectors function in host cells remains elusive, and biochemical and structural approaches have been scarcely used to tackle this question. In this study, we produced recombinant proteins of eleven candidate efectors of the leaf rust fungus Melampsora larici-populina in Escherichia coli. We successfully purifed and solved the three- dimensional structure of two proteins, MLP124266 and MLP124017, using NMR spectroscopy. Although both MLP124266 and MLP124017 show no sequence similarity with known proteins, they exhibit structural similarities to knottins, which are disulfde-rich small proteins characterized by intricate disulfde bridges, and to nuclear transport factor 2-like proteins, which are molecular containers involved in a wide range of functions, respectively. Interestingly, such structural folds have not been reported so far in pathogen efectors, indicating that MLP124266 and MLP124017 may bear novel functions related to pathogenicity. Our fndings show that sequence-unrelated efectors can adopt folds similar to known proteins, and encourage the use of biochemical and structural approaches to functionally characterize efector candidates. To infect their host, flamentous pathogens secrete efector proteins that interfere with plant physiology and immunity to promote parasitic growth1. -
CONTROL of SMUT in WHEAT and OTHER SMALL GRAINS by H
Bulletin No. 116 June, 1931 Montana State College, Extension Service, J. C. Taylor, Director, Cooperative Extension Work in Agriculture and Home Economics. Montana State College and Uni~ed States Department of Agriculture, co-operating. Distributed in furtherance of the Acts of Congress ~ay 8 and June 30, 1.914. ~ CONTROL OF SMUT IN WHEAT AND OTHER SMALL GRAINS By H. E. Morris, Extension Plant Pathologist Waldo Kidder, Extension Agronomist Smuts cost the farmers of Montana many thousands of dollars each year. In 1930, stinking smut of wheat alone caused a loss of approximately $750;000, due to decreased yields and to a lower price per bushel. This loss and also that due to the smuts {..:Fig. 1. Smutted and normal heads of wheat. The head at the left ,is a typi:cal head affected with covered or stinking smut, The next, head IS a he'althy head. The two heads on the right show two stages of the loose smut in wheat. (-Courtesy,D. S. Dept. of Agr.) . ,( 2 MONTANA EXTENSION SERVICE of oats, barley and rye may be largely prevented by adopting the methods of seed treatment described in this bulletin. What Is Smut Smut is produced by a small parasitic plant, mould-like in appearance, belonging to a group called fungi (Fig. 2). Smut lives most of its life within and at the expense of the wheat plant. The smut powder, so familiar to all, is composed of myriads of spores which correspond to seeds in the higher plants. In the process of harvesting and threshing, these spores are dis· I Fig'. -
Physiologic Specialization of Melampsora Lini on Linum Usitatissimum '
PHYSIOLOGIC SPECIALIZATION OF MELAMPSORA LINI ON LINUM USITATISSIMUM ' By H. H. FLOR 2 Associate 'pathologist^ Division of Cereal Crops and Diseases^ Bureau of Plant Industry y United States Department of Agriculture INTRODUCTION Melampsora Uni (Pers.) Lev., the fungus that causes rust of culti- vated flax, Linum usitatissimum L., occurs in all the major seed flax- and fiber-flax-producing areas of the world. Injury to the seed crop results from a reduction in the amount of foliage and from the utili- zation by the fungus of some of the food of the host plant. In addition to interfering with the normal photosynthetic metaboUsm of the host plant, rust on fiber flax injures the quality by causing breakage of fibers and preventing normal retting, thus producing what is known as ''measly'' fibers (23)} Consequently a small amount of infection may injure the quality of a fiber-flax crop, while it is only under epidemic conditions that the rust may be destructive to seed flax. Only occasionally is flax rust very destructive in Minnesota and the Dakotas, where most of the domestic flaxseed is grown. However, it sometimes occurs in epidemic form in these areas, and Brentzel ^ and Hart (9) have reported losses ranging from a trace to 100 percent. Measures that have been recommended for the control of flax rust include early sowing, thorough cleaning of the seed, crop rotation, use of high, well-drained land, destruction or removal of infected straw, and the use of resistant varieties. Henry (10) considered the last- named method the most promising and found rust immunity to be inherited independently of morphologic type or wilt resistance. -
Redalyc.CIENTO CINCUENTA AÑOS DE PENSAMIENTO
Acta Biológica Colombiana ISSN: 0120-548X [email protected] Universidad Nacional de Colombia Sede Bogotá Colombia TORRES, ENRIQUE CIENTO CINCUENTA AÑOS DE PENSAMIENTO COEVOLUTIVO: LA VIDA ES UNA MARAÑA DE INTERACCIONES Acta Biológica Colombiana, vol. 14, 2009, pp. 231-245 Universidad Nacional de Colombia Sede Bogotá Bogotá, Colombia Disponible en: http://www.redalyc.org/articulo.oa?id=319028030004 Cómo citar el artículo Número completo Sistema de Información Científica Más información del artículo Red de Revistas Científicas de América Latina, el Caribe, España y Portugal Página de la revista en redalyc.org Proyecto académico sin fines de lucro, desarrollado bajo la iniciativa de acceso abierto Acta biol. Colomb., Vol. 14 S, 2009 231 - 246 CIENTO CINCUENTA AÑOS DE PENSAMIENTO COEVOLUTIVO: LA VIDA ES UNA MARAÑA DE INTERACCIONES One Hundred and Fifty Years of Coevolutionary Thinking: Life is a Web of Interactions ENRIQUE TORRES1, Ph. D. 1Profesor Asociado Emérito, Universidad Nacional de Colombia. Bogotá D.C., Colombia. [email protected] Presentado 16 de septiembre de 2009, aceptado 22 de octubre de 2009, correcciones 25 de mayo de 2010. RESUMEN La supervivencia y reproducción de la inmensa mayoría de organismos multicelulares dependen de interacciones ecológicas, frecuentemente especializadas, con organismos de otras especies. La coevolución, entendida como el conjunto de cambios evolutivos recíprocos entre especies que ejercen estas interacciones, se reconoce como un proceso continuo que organiza la variabilidad darviniana en complejas redes biológicas. Esta visión dinámica suaviza el conflicto entre la natu- raleza armónica de Humboldt y la naturaleza en guerra de Darwin y otros naturalistas del siglo 19. Los cimientos conceptuales de la biología coevolutiva incluyen el papel causal de los microor- ganismos en las enfermedades, la ubicuidad de las simbiosis, su frecuente caracter especialista y la determinación mendeliana de los desenlaces de tales interacciones. -
Archaeobotanical Evidence of the Fungus Covered Smut (Ustilago Hordei) in Jordan and Egypt
ANALECTA Thijs van Kolfschoten, Wil Roebroeks, Dimitri De Loecker, Michael H. Field, Pál Sümegi, Kay C.J. Beets, Simon R. Troelstra, Alexander Verpoorte, Bleda S. Düring, Eva Visser, Sophie Tews, Sofia Taipale, Corijanne Slappendel, Esther Rogmans, Andrea Raat, Olivier Nieuwen- huyse, Anna Meens, Lennart Kruijer, Harmen Huigens, Neeke Hammers, Merel Brüning, Peter M.M.G. Akkermans, Pieter van de Velde, Hans van der Plicht, Annelou van Gijn, Miranda de Kreek, Eric Dullaart, Joanne Mol, Hans Kamermans, Walter Laan, Milco Wansleeben, Alexander Verpoorte, Ilona Bausch, Diederik J.W. Meijer, Luc Amkreutz, Bertil van Os, Liesbeth Theunissen, David R. Fontijn, Patrick Valentijn, Richard Jansen, Simone A.M. Lemmers, David R. Fontijn, Sasja A. van der Vaart, Harry Fokkens, Corrie Bakels, L. Bouke van der Meer, Clasina J.G. van Doorn, Reinder Neef, Federica Fantone, René T.J. Cappers, Jasper de Bruin, Eric M. Moormann, Paul G.P. PRAEHISTORICA Meyboom, Lisa C. Götz, Léon J. Coret, Natascha Sojc, Stijn van As, Richard Jansen, Maarten E.R.G.N. Jansen, Menno L.P. Hoogland, Corinne L. Hofman, Alexander Geurds, Laura N.K. van Broekhoven, Arie Boomert, John Bintliff, Sjoerd van der Linde, Monique van den Dries, Willem J.H. Willems, Thijs van Kolfschoten, Wil Roebroeks, Dimitri De Loecker, Michael H. Field, Pál Sümegi, Kay C.J. Beets, Simon R. Troelstra, Alexander Verpoorte, Bleda S. Düring, Eva Visser, Sophie Tews, Sofia Taipale, Corijanne Slappendel, Esther Rogmans, Andrea Raat, Olivier Nieuwenhuyse, Anna Meens, Lennart Kruijer, Harmen Huigens, Neeke Hammers, Merel Brüning, Peter M.M.G. Akkermans, Pieter van de Velde, Hans van der Plicht, Annelou van Gijn, Miranda de Kreek, Eric Dullaart, Joanne Mol, Hans Kamermans, Walter Laan, Milco Wansleeben, Alexander Verpoorte, Ilona Bausch, Diederik J.W. -
Color Plates
Color Plates Plate 1 (a) Lethal Yellowing on Coconut Palm caused by a Phytoplasma Pathogen. (b, c) Tulip Break on Tulip caused by Lily Latent Mosaic Virus. (d, e) Ringspot on Vanda Orchid caused by Vanda Ringspot Virus R.K. Horst, Westcott’s Plant Disease Handbook, DOI 10.1007/978-94-007-2141-8, 701 # Springer Science+Business Media Dordrecht 2013 702 Color Plates Plate 2 (a, b) Rust on Rose caused by Phragmidium mucronatum.(c) Cedar-Apple Rust on Apple caused by Gymnosporangium juniperi-virginianae Color Plates 703 Plate 3 (a) Cedar-Apple Rust on Cedar caused by Gymnosporangium juniperi.(b) Stunt on Chrysanthemum caused by Chrysanthemum Stunt Viroid. Var. Dark Pink Orchid Queen 704 Color Plates Plate 4 (a) Green Flowers on Chrysanthemum caused by Aster Yellows Phytoplasma. (b) Phyllody on Hydrangea caused by a Phytoplasma Pathogen Color Plates 705 Plate 5 (a, b) Mosaic on Rose caused by Prunus Necrotic Ringspot Virus. (c) Foliar Symptoms on Chrysanthemum (Variety Bonnie Jean) caused by (clockwise from upper left) Chrysanthemum Chlorotic Mottle Viroid, Healthy Leaf, Potato Spindle Tuber Viroid, Chrysanthemum Stunt Viroid, and Potato Spindle Tuber Viroid (Mild Strain) 706 Color Plates Plate 6 (a) Bacterial Leaf Rot on Dieffenbachia caused by Erwinia chrysanthemi.(b) Bacterial Leaf Rot on Philodendron caused by Erwinia chrysanthemi Color Plates 707 Plate 7 (a) Common Leafspot on Boston Ivy caused by Guignardia bidwellii.(b) Crown Gall on Chrysanthemum caused by Agrobacterium tumefaciens 708 Color Plates Plate 8 (a) Ringspot on Tomato Fruit caused by Cucumber Mosaic Virus. (b, c) Powdery Mildew on Rose caused by Podosphaera pannosa Color Plates 709 Plate 9 (a) Late Blight on Potato caused by Phytophthora infestans.(b) Powdery Mildew on Begonia caused by Erysiphe cichoracearum.(c) Mosaic on Squash caused by Cucumber Mosaic Virus 710 Color Plates Plate 10 (a) Dollar Spot on Turf caused by Sclerotinia homeocarpa.(b) Copper Injury on Rose caused by sprays containing Copper. -
Iodiversity of Australian Smut Fungi
Fungal Diversity iodiversity of Australian smut fungi R.G. Shivas'* and K. Vanky2 'Queensland Department of Primary Industries, Plant Pathology Herbarium, 80 Meiers Road, Indooroopilly, Queensland 4068, Australia 2 Herbarium Ustilaginales Vanky, Gabriel-Biel-Str. 5, D-72076 Tiibingen, Germany Shivas, R.G. and Vanky, K. (2003). Biodiversity of Australian smut fungi. Fungal Diversity 13 :137-152. There are about 250 species of smut fungi known from Australia of which 95 are endemic. Fourteen of these endemic species were first collected in the period culminating with the publication of Daniel McAlpine's revision of Australian smut fungi in 1910. Of the 68 species treated by McAlpine, 10 were considered to be endemic to Australia at that time. Only 23 of the species treated by McAlpine have names that are currently accepted. During the following eighty years until 1990, a further 31 endemic species were collected and just 11 of these were named and described in that period. Since 1990, 50 further species of endemic smut fungi have been collected and named in Australia. There are 115 species that are restricted to either Australia or to Australia and the neighbouring countries of Indonesia, New Zealand, Papua New Guinea and the Philippines . These 115 endemic species occur in 24 genera, namely Anthracoidea (1 species), Bauerago (1), Cintractia (3), Dermatosorus (1), Entyloma (3), Farysporium (1), Fulvisporium (1), Heterotolyposporium (1), Lundquistia (1), Macalpinomyces (4), Microbotryum (2), Moreaua (20), Pseudotracya (1), Restiosporium (5), Sporisorium (26), Thecaphora (2), Tilletia (12), Tolyposporella (1), Tranzscheliella (1), Urocystis (2), Ustanciosporium (1), Ustilago (22), Websdanea (1) and Yelsemia (2). About a half of these local and regional endemic species occur on grasses and a quarter on sedges.