Phaff Collection News 2012
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The 2014 Golden Gate National Parks Bioblitz - Data Management and the Event Species List Achieving a Quality Dataset from a Large Scale Event
National Park Service U.S. Department of the Interior Natural Resource Stewardship and Science The 2014 Golden Gate National Parks BioBlitz - Data Management and the Event Species List Achieving a Quality Dataset from a Large Scale Event Natural Resource Report NPS/GOGA/NRR—2016/1147 ON THIS PAGE Photograph of BioBlitz participants conducting data entry into iNaturalist. Photograph courtesy of the National Park Service. ON THE COVER Photograph of BioBlitz participants collecting aquatic species data in the Presidio of San Francisco. Photograph courtesy of National Park Service. The 2014 Golden Gate National Parks BioBlitz - Data Management and the Event Species List Achieving a Quality Dataset from a Large Scale Event Natural Resource Report NPS/GOGA/NRR—2016/1147 Elizabeth Edson1, Michelle O’Herron1, Alison Forrestel2, Daniel George3 1Golden Gate Parks Conservancy Building 201 Fort Mason San Francisco, CA 94129 2National Park Service. Golden Gate National Recreation Area Fort Cronkhite, Bldg. 1061 Sausalito, CA 94965 3National Park Service. San Francisco Bay Area Network Inventory & Monitoring Program Manager Fort Cronkhite, Bldg. 1063 Sausalito, CA 94965 March 2016 U.S. Department of the Interior National Park Service Natural Resource Stewardship and Science Fort Collins, Colorado The National Park Service, Natural Resource Stewardship and Science office in Fort Collins, Colorado, publishes a range of reports that address natural resource topics. These reports are of interest and applicability to a broad audience in the National Park Service and others in natural resource management, including scientists, conservation and environmental constituencies, and the public. The Natural Resource Report Series is used to disseminate comprehensive information and analysis about natural resources and related topics concerning lands managed by the National Park Service. -
42 Genome Scale Model Reconstruction of the Methylotrophic
GENOME SCALE MODEL RECONSTRUCTION OF THE METHYLOTROPHIC YEAST OGATAEA POLYMORPHA Simone Schmitz, RWTH Aachen University, Germany [email protected] Ulf W. Liebal, RWTH Aachen University, Germany Aarthi Ravikrishnan, Department of Biotechnology, Bhupat and Jyoti Mehta School of Biosciences; Institute of Technology Madras, India Constantin V.L. Schedel, RWTH Aachen University, Germany Lars M. Blank, RWTH Aachen University, Germany Birgitta E. Ebert, RWTH Aachen University, Germany Key words: Ogataea (Hansenula) polymorpha, metabolic model, phenotype microarray experiments, methylotrophic yeast Ogataea polymorpha is a thermotolerant, methylotrophic yeast with significant industrial applications. It is a promising host to generate platform chemicals from methanol, derived e.g. from carbon capture and utilization streams. Full development of the organism into a production strain requires additional strain design, supported by metabolic modeling on the basis of a genome-scale metabolic model. However, to date, no genome-scale metabolic model is available for O. polymorpha. To overcome this limitation, we used a published reconstruction of the closely related yeast Pichia pastoris as reference and corrected reactions based on KEGG annotations. Additionally, we conducted phenotype microarray experiments to test O. polymorpha’s metabolic capabilities to grown on or respire 192 different carbon sources. Over three-quarter of the substrate usage was correctly reproduced by the model. However, O. polymorpha failed to metabolize eight substrates and gained 38 new substrates compared to the P. pastoris reference model. To enable the usage of these compounds, metabolic pathways were inferred from literature and database searches and potential enzymes and genes assigned by conducting BLAST searches. To facilitate strain engineering and identify beneficial mutants, gene-protein-reaction relationships need to be included in the model. -
Pathogenicity Classification of Fungi Status December 2014 (CGM/141218-03)
Classification of Organisms: Pathogenicity classification of fungi Status December 2014 (CGM/141218-03) COGEM advice CGM/141218-03 Pathogenicity classification of fungi COGEM advice CGM/141218-03 Dutch Regulations Genetically Modified Organisms In the Decree on Genetically Modified Organisms (GMO Decree) and its accompanying more detailed Regulations (GMO Regulations) genetically modified micro-organisms are grouped in four pathogenicity classes, ranging from the lowest pathogenicity Class 1 to the highest Class 4.1 The pathogenicity classifications are used to determine the containment level for working in laboratories with GMOs. A micro-organism of Class 1 should at least comply with one of the following conditions: a) the micro-organism does not belong to a species of which representatives are known to be pathogenic for humans, animals or plants, b) the micro-organism has a long history of safe use under conditions without specific containment measures, c) the micro-organism belongs to a species that includes representatives of class 2, 3 or 4, but the particular strain does not contain genetic material that is responsible for the virulence, d) the micro-organism has been shown to be non-virulent through adequate tests. A micro-organism is grouped in Class 2 when it can cause a disease in humans or animals whereby it is unlikely to spread within the population while an effective prophylaxis, treatment or control strategy exists, as well as an organism that can cause a disease in plants. A micro-organism is grouped in Class 3 when it can cause a serious disease in humans or animals whereby it is likely to spread within the population while an effective prophylaxis, treatment or control strategy exists. -
Evaluation of the Chitin-Binding Dye Congo Red As a Selection Agent for the Isolation, Classification, and Enumeration of Ascomycete Yeasts
Archives of Microbiology (2018) 200:671–675 https://doi.org/10.1007/s00203-018-1498-y SHORT COMMUNICATION Evaluation of the chitin-binding dye Congo red as a selection agent for the isolation, classification, and enumeration of ascomycete yeasts Tomas Linder1 Received: 3 February 2018 / Revised: 19 February 2018 / Accepted: 21 February 2018 / Published online: 23 February 2018 © The Author(s) 2018. This article is an open access publication Abstract Thirty-nine strains of ascomycete yeasts representing 35 species and 33 genera were tested for their ability to grow on solid agar medium containing increasing concentrations of the chitin-binding dye Congo red. Six strains were classified as hyper- sensitive (weak or no growth at 10 mg/l Congo red), five were moderately sensitive (weak or no growth at 50 mg/l), three were moderately tolerant (weak or no growth at 100 mg/l), while the remaining 25 strains were classified as resistant (robust growth at ≥ 100 mg/l) with 20 of these strains classified as hyper-resistant (robust growth at 200 mg/l). Congo red growth phenotypes were consistent within some families but not others. The frequency of Congo red resistance among ascomycete yeasts was deemed too high for the practical use of Congo red as a selection agent for targeted isolation, but can be useful for identification and enumeration of yeasts. Keywords Antifungal · Cell wall · Phenotype · Yeast Introduction groups of yeasts. For example, chemically defined growth medium containing methanol as the sole carbon source is The development of genome sequencing over the past four commonly used to isolate species of methylotrophic yeasts decades has revolutionized yeast taxonomy and now enables (van Dijken and Harder 1974). -
Clasificación Del Clado De Ogataea, Un Punto De Vista Integral
INSTITUTO POLITÉCNICO NACIONAL ESCUELA NACIONAL DE CIENCIAS BIOLÓGICAS Clasificación del clado de Ogataea, un punto de vista integral. PROYECTO DE INVESTIGACIÓN (TESIS) QUE PARA OBTENER EL TÍTULO DE QUÍMICO BACTERIÓLOGO PARASITÓLOGO PRESENTA: ERIKA BERENICE MARTÍNEZ RUIZ MÉXICO, DF. 2013 El presente trabajo se realizó en el Laboratorio de Micología Médica del Departamento de Microbiología de la Escuela Nacional de Ciencias Biológicas, del IPN. Se llevó a cabo bajo la dirección de la Dra. Aída Verónica Rodríguez Tovar y el Dr. Néstor Octavio Pérez Ramírez. Se contó con la colaboración de la Dra. Paulina Estrada de los Santos del Laboratorio de Microbiología Industrial del Departamento de Microbiología de la ENCB, del IPN. AGRADECIMIENTOS Gracias al Instituto Politécnico Nacional, porque al ser una de las Instituciones de más alto Reconocimiento a Nivel Nacional y figurar entre las mejores a nivel Internacional, me brindó un lugar en su matrícula, una preparación académica de excelencia y una nueva sangre que con orgullo portaré día con día porque “Soy Politécnico por convicción y no por circunstancia”. Gracias a la Escuela Nacional de Ciencias Biológicas, que más que una escuela se volvió un segundo hogar en estos últimos 5 años para mí, porque me dio las armas para estar a la altura de los mejores, porque con orgullo intentaré seguir dejando en alto el nombre de mi escuela. Además de brindarnos el apoyo en equipos, instalaciones y materiales para llevar a cabo este proyecto. Dra. Aída y Dr. Néstor, mis asesores, ¡gracias! porque confiaron en mí en un momento de incertidumbre, porque me apoyaron, me escucharon, me impulsaron a seguir adelante y me transmitieron una parte de sus amplios conocimientos. -
Comparative Genomics of Biotechnologically Important Yeasts Supplementary Appendix
Comparative genomics of biotechnologically important yeasts Supplementary Appendix Contents Note 1 – Summary of literature on ascomycete yeasts used in this study ............................... 3 CUG-Ser yeasts ................................................................................................................................................................ 3 Other Saccharomycotina ............................................................................................................................................. 5 Taphrinomycotina ....................................................................................................................................................... 10 Note 2 – Genomes overview .................................................................................................11 Yeast culturing, identification, DNA and total RNA extraction ................................................................. 12 Genome sequencing and assembly ....................................................................................................................... 12 Transcriptome sequencing and assembly ......................................................................................................... 13 Table S1. Genome statistics ..................................................................................................................................... 14 Table S2. Annotation statistics .............................................................................................................................. -
Orthologous Promoters from Related Methylotrophic Yeasts Surpass
Vogl et al. AMB Expr (2020) 10:38 https://doi.org/10.1186/s13568-020-00972-1 ORIGINAL ARTICLE Open Access Orthologous promoters from related methylotrophic yeasts surpass expression of endogenous promoters of Pichia pastoris Thomas Vogl1,2 , Jasmin Elgin Fischer1†, Patrick Hyden1†, Richard Wasmayer1†, Lukas Sturmberger1 and Anton Glieder1* Abstract Methylotrophic yeasts such as Komagataella phafi (syn. Pichia pastoris, Pp), Hansenula polymorpha (Hp), Candida boidinii (Cb) and Pichia methanolica (Pm) are widely used protein production platforms. Typically, strong, tightly regulated promoters of genes coding for their methanol utilization (MUT) pathways are used to drive heterologous gene expression. Despite highly similar open reading frames in the MUT pathways of the four yeasts, the regulation of the respective promoters varies strongly between species. While most endogenous Pp MUT promoters remain tightly repressed after depletion of a repressing carbon, Hp, Cb and Pm MUT promoters are derepressed to up to 70% of methanol induced levels, enabling methanol free production processes in their respective host background. Here, we have tested a series of orthologous promoters from Hp, Cb and Pm in Pp. Unexpectedly, when induced with metha- nol, the promoter of the HpMOX gene reached very similar expression levels as the strong methanol, inducible, and most frequently used promoter of the Pp alcohol oxidase 1 gene (PPpAOX1). The HpFMD promoter even surpassed PPpAOX1 up to three-fold, when induced with methanol, and reached under methanol-free/derepressed conditions similar expression as the methanol induced PPpAOX1. These results demonstrate that orthologous promoters from related yeast species can give access to otherwise unobtainable regulatory profles and may even considerably surpass endogenous promoters in P. -
Towards an Integrated Phylogenetic Classification of the Tremellomycetes
http://www.diva-portal.org This is the published version of a paper published in Studies in mycology. Citation for the original published paper (version of record): Liu, X., Wang, Q., Göker, M., Groenewald, M., Kachalkin, A. et al. (2016) Towards an integrated phylogenetic classification of the Tremellomycetes. Studies in mycology, 81: 85 http://dx.doi.org/10.1016/j.simyco.2015.12.001 Access to the published version may require subscription. N.B. When citing this work, cite the original published paper. Permanent link to this version: http://urn.kb.se/resolve?urn=urn:nbn:se:nrm:diva-1703 available online at www.studiesinmycology.org STUDIES IN MYCOLOGY 81: 85–147. Towards an integrated phylogenetic classification of the Tremellomycetes X.-Z. Liu1,2, Q.-M. Wang1,2, M. Göker3, M. Groenewald2, A.V. Kachalkin4, H.T. Lumbsch5, A.M. Millanes6, M. Wedin7, A.M. Yurkov3, T. Boekhout1,2,8*, and F.-Y. Bai1,2* 1State Key Laboratory for Mycology, Institute of Microbiology, Chinese Academy of Sciences, Beijing 100101, PR China; 2CBS Fungal Biodiversity Centre (CBS-KNAW), Uppsalalaan 8, Utrecht, The Netherlands; 3Leibniz Institute DSMZ-German Collection of Microorganisms and Cell Cultures, Braunschweig 38124, Germany; 4Faculty of Soil Science, Lomonosov Moscow State University, Moscow 119991, Russia; 5Science & Education, The Field Museum, 1400 S. Lake Shore Drive, Chicago, IL 60605, USA; 6Departamento de Biología y Geología, Física y Química Inorganica, Universidad Rey Juan Carlos, E-28933 Mostoles, Spain; 7Department of Botany, Swedish Museum of Natural History, P.O. Box 50007, SE-10405 Stockholm, Sweden; 8Shanghai Key Laboratory of Molecular Medical Mycology, Changzheng Hospital, Second Military Medical University, Shanghai, PR China *Correspondence: F.-Y. -
Downloaded from by Lawrence Berkeley National Laboratory User on 13 May 2019
Lawrence Berkeley National Laboratory Recent Work Title Physiological and comparative genomic analysis of new isolated yeasts Spathaspora sp. JA1 and Meyerozyma caribbica JA9 reveal insights into xylitol production. Permalink https://escholarship.org/uc/item/1r9258f1 Journal FEMS yeast research, 19(4) ISSN 1567-1356 Authors Trichez, Débora Steindorff, Andrei S Soares, Carlos EVF et al. Publication Date 2019-06-01 DOI 10.1093/femsyr/foz034 Peer reviewed eScholarship.org Powered by the California Digital Library University of California FEMS Yeast Research, 19, 2019, foz034 doi: 10.1093/femsyr/foz034 Advance Access Publication Date: 26 April 2019 Research Article Downloaded from https://academic.oup.com/femsyr/article-abstract/19/4/foz034/5480466 by Lawrence Berkeley National Laboratory user on 13 May 2019 RESEARCH ARTICLE Physiological and comparative genomic analysis of new isolated yeasts Spathaspora sp. JA1 and Meyerozyma caribbica JA9 reveal insights into xylitol production Debora´ Trichez1,AndreiS.Steindorff1,†,CarlosE.V.F.Soares1,2, Eduardo F. Formighieri 1 and Joao˜ R. M. Almeida1,2,* 1Embrapa Agroenergia. Parque Estac¸ao˜ Biologica,´ PqEB – W3 Norte Final, Postal code 70.770–901, Bras´ılia-DF, Brazil and 2Graduate Program in Chemical and Biological Technologies, Institute of Chemistry, University of Bras´ılia, Campus Darcy Ribeiro, Postal code 70.910-900, Bras´ılia-DF, Brazil ∗Corresponding author: Embrapa Agroenergia, Parque Estac¸ao˜ Biologica,´ PqEB – W3 Norte Final - s/n◦, 70.770-901 - Bras´ılia, DF – Brasil. Tel: +55 61 3448-2337; E-mail: [email protected] †Present address: U.S. Department of Energy (DOE) Joint Genome Institute, 2800 Mitchell Drive, Walnut Creek, CA 94598, US. -
Hansenula Polymorpha
Inversion of the Chromosomal Region between Two Mating Type Loci Switches the Mating Type in Hansenula polymorpha Hiromi Maekawa*, Yoshinobu Kaneko Yeast Genetic Resources Laboratory, Graduate School of Engineering, Osaka University, Osaka, Japan Abstract Yeast mating type is determined by the genotype at the mating type locus (MAT). In homothallic (self-fertile) Saccharomycotina such as Saccharomyces cerevisiae and Kluveromyces lactis, high-efficiency switching between a and a mating types enables mating. Two silent mating type cassettes, in addition to an active MAT locus, are essential components of the mating type switching mechanism. In this study, we investigated the structure and functions of mating type genes in H. polymorpha (also designated as Ogataea polymorpha). The H. polymorpha genome was found to harbor two MAT loci, MAT1 and MAT2, that are ,18 kb apart on the same chromosome. MAT1-encoded a1 specifies a cell identity, whereas none of the mating type genes were required for a identity and mating. MAT1-encoded a2 and MAT2-encoded a1 were, however, essential for meiosis. When present in the location next to SLA2 and SUI1 genes, MAT1 or MAT2 was transcriptionally active, while the other was repressed. An inversion of the MAT intervening region was induced by nutrient limitation, resulting in the swapping of the chromosomal locations of two MAT loci, and hence switching of mating type identity. Inversion-deficient mutants exhibited severe defects only in mating with each other, suggesting that this inversion is the mechanism of mating type switching and homothallism. This chromosomal inversion-based mechanism represents a novel form of mating type switching that requires only two MAT loci. -
12 Tremellomycetes and Related Groups
12 Tremellomycetes and Related Groups 1 1 2 1 MICHAEL WEIß ,ROBERT BAUER ,JOSE´ PAULO SAMPAIO ,FRANZ OBERWINKLER CONTENTS I. Introduction I. Introduction ................................ 00 A. Historical Concepts. ................. 00 Tremellomycetes is a fungal group full of con- B. Modern View . ........................... 00 II. Morphology and Anatomy ................. 00 trasts. It includes jelly fungi with conspicuous A. Basidiocarps . ........................... 00 macroscopic basidiomes, such as some species B. Micromorphology . ................. 00 of Tremella, as well as macroscopically invisible C. Ultrastructure. ........................... 00 inhabitants of other fungal fruiting bodies and III. Life Cycles................................... 00 a plethora of species known so far only as A. Dimorphism . ........................... 00 B. Deviance from Dimorphism . ....... 00 asexual yeasts. Tremellomycetes may be benefi- IV. Ecology ...................................... 00 cial to humans, as exemplified by the produc- A. Mycoparasitism. ................. 00 tion of edible Tremella fruiting bodies whose B. Tremellomycetous Yeasts . ....... 00 production increased in China alone from 100 C. Animal and Human Pathogens . ....... 00 MT in 1998 to more than 250,000 MT in 2007 V. Biotechnological Applications ............. 00 VI. Phylogenetic Relationships ................ 00 (Chang and Wasser 2012), or extremely harm- VII. Taxonomy................................... 00 ful, such as the systemic human pathogen Cryp- A. Taxonomy in Flow -
Taxonomy and Physiological Characterisation of Scheffersomyces Titanus Sp
www.nature.com/scientificreports OPEN Taxonomy and physiological characterisation of Scheffersomyces titanus sp. nov., a new D-xylose- Received: 28 January 2016 Accepted: 03 August 2016 fermenting yeast species from Published: 25 August 2016 China Xiao-Jing Liu1, Wan-Nan Cao1, Yong-Cheng Ren1, Long-Long Xu1, Ze-Hao Yi1, Zheng Liu1 & Feng-Li Hui1,2 Three strains of a d-xylose-fermenting yeast species were isolated from the host beetle Dorcus titanus collected from two different localities in Henan Province, Central China. These strains formed two hat-shaped ascospores in conjugated and deliquescent asci. Multilocus phylogenetic analysis that included the nearly complete small subunit (SSU), the internal transcribed spacer (ITS) region and the D1/D2 domains of the large subunit (LSU) rDNAs, as well as RNA polymerase II largest subunit (RPB1) gene demonstrated that these strains represent a novel yeast species belonging to the genus Scheffersomyces. The phylogenetic analysis based on the nucleotide sequences of the xylose reductase (XYL1) gene supported the view that the new strains could be grouped as a unique species. Although this new species is highly similar to Scheffersomyces stipitis-like yeasts in terms of nrDNA sequences and morphological and physiological characteristics, the species can be clearly differentiated from its close relatives on the basis of the sequences of XYL1 and RPB1. Therefore, a novel yeast species, Scheffersomyces titanus sp. nov., is proposed to accommodate these strains. The type strain is NYNU 14712T ( CICC 33061T = CBS 13926T). The genus Scheffersomyces was first proposed by Kurtzman and Suzuki (2010) with the description of Scheffersomyces stipitis, S.