Evaluation of the Population Dynamics of Microalgae Isolated from the State of Chiapas, Mexico with Respect to the Nutritional Quality of Water
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植物研究雑誌 J. J. Jpn. Bo t. 79:255-261 79:255-261 (2004) Phylogenetic Phylogenetic Analysis of the Tetrasporalean Genus Asterococcus Asterococcus (Chlorophyceae) sased on 18S 18S Ribosomal RNA Gene Sequences Atsushi Atsushi NAKAZA WA and Hisayoshi NOZAKI Department Department of Biological Sciences ,Graduate School of Science ,University of Tokyo , Hongo Hongo 7-3-1 ,Bunkyo-ku ,Tokyo ,113 ・0033 JAPAN (Received (Received on October 30 ,2003) Nucleotide Nucleotide sequences (1642 bp) from 18S ribosomal RNA genes were analyzed for 100 100 strains of the clockwise (CW) group of Chlorophyceae to deduce the phylogenetic position position of the immotile colonial genus Asterococcus Scherffel , which is classified in the Palmellopsidaceae Palmellopsidaceae of Tetrasporales. We found that the genus Asterococcus and two uni- cellular , volvocalean genera , Lobochlamys Proschold & al. and Oogamochlamys Proschold Proschold & al., formed a robust monophyletic group , which was separated from two te 位asporalean clades , one composed of Tetraspora Link and Paulschulzia Sk 吋a and the other other containing the other palme l1 0psidacean genus Chlamydocaps αFot t. Therefore , the Tetrasporales Tetrasporales in the CW group is clearly polyphyletic and taxonomic revision of the order order and the Palmellopsidaceae is needed. Key words: 18S rRNA gene ,Asterococcus ,Palmellopsidaceae ,phylogeny ,Tetraspor- ales. ales. Asterococcus Asterococcus Scherffel (1908) is a colo- Recently , Ettl and Gartner (1 988) included nial nial green algal genus that is characterized Asterococcus in the family Palmello- by an asteroid chloroplast in the cell and psidaceae , because cells of this genus have swollen swollen gelatinous layers surrounding the contractile vacuoles and lack pseudoflagella immotile immotile colony (e. g. -
Abstract Evaluation of the Green Microalga
ABSTRACT EVALUATION OF THE GREEN MICROALGA MONORAPHIDIUM SP. DEK19 GROWTH UTILIZING ETHANOL PLANT SIDE STREAMS AND POTENTIAL FOR BIOFUEL PRODUCTION David Michael Colson, MS Department of Biological Sciences Northern Illinois University, 2017 Gabriel Holbrook, Director This research was conducted to evaluate the potential for growth of Monoraphidium sp. Dek19 using side streams from an ethanol plant for culture medium. Additionally, the potential of using enzymes to break down the cell wall material to release fermentable sugars and oil was examined. The ethanol streams selected were methanator influent, methanator effluent, and thin stillage. This species of microalgae has been previously studied and found to have the ability to grow in and remediate the effluent water from the DeKalb Sanitary District (DSD). The Monoraphidium sp. Dek19 was grown in various concentrations of the ethanol plant side streams concurrently with algae cultures grown in the DSD effluent. The algae cultures were grown in 250ml flasks to determine the optimal concentrations of the ethanol streams. The concentrations with the growth rate and cell counts closest to or higher than the DSD effluents were selected for further examination. These concentrations were repeated to evaluate the most optimal growth conditions using the ethanol streams in comparison to the DSD effluent grown algae. The selected growth condition for the ethanol streams was determined to be using the methanator effluent as the base water component with the thin stillage added to a 2% concentration. The 2% concentration showed an average increase in cell count to be 8.49% higher than the control cell count. The methanator influent was discarded as a base water component, as the growth of the algae was 40.18% less than that of the control. -
Distribution of the Water-Soluble Astaxanthin Binding Carotenoprotein (Astap) in Scenedesmaceae
marine drugs Article Distribution of the Water-Soluble Astaxanthin Binding Carotenoprotein (AstaP) in Scenedesmaceae Hiroki Toyoshima 1, Ami Miyata 1, Risako Yoshida 1, Taichiro Ishige 2, Shinichi Takaichi 3 and Shinji Kawasaki 1,3,* 1 Department of Bioscience, Tokyo University of Agriculture, 1-1-1 Sakuragaoka, Setagaya-ku, Tokyo 156-8502, Japan; [email protected] (H.T.); [email protected] (A.M.); [email protected] (R.Y.) 2 NODAI Genome Research Centre, Tokyo University of Agriculture, 1-1-1 Sakuragaoka, Setagaya-ku, Tokyo 156-8502, Japan; [email protected] 3 Department of Molecular Microbiology, Tokyo University of Agriculture, 1-1-1 Sakuragaoka, Setagaya-ku, Tokyo 156-8502, Japan; [email protected] * Correspondence: [email protected]; Tel.: +81-3-5477-2764 Abstract: Photooxidative stress-inducible water-soluble astaxanthin-binding proteins, designated as AstaP,were identified in two Scenedesmaceae strains, Coelastrella astaxanthina Ki-4 and Scenedesmus obtusus Oki-4N; both strains were isolated under high light conditions. These AstaPs are classified as a novel family of carotenoprotein and are useful for providing valuable astaxanthin in water-soluble form; however, the distribution of AstaP orthologs in other microalgae remains unknown. Here, we exam- ined the distribution of AstaP orthologs in the family Scenedesmaceae with two model microalgae, Chlamydomonas reinhardtii and Chlorella variabilis. The expression of AstaP orthologs under photooxida- Citation: Toyoshima, H.; Miyata, A.; tive stress conditions was detected in cell extracts of Scenedesmaceae strains, but not in model algal Yoshida, R.; Ishige, T.; Takaichi, S.; strains. Aqueous orange proteins produced by Scenedesmaceae strains were shown to bind astaxanthin. -
Lateral Gene Transfer of Anion-Conducting Channelrhodopsins Between Green Algae and Giant Viruses
bioRxiv preprint doi: https://doi.org/10.1101/2020.04.15.042127; this version posted April 23, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. 1 5 Lateral gene transfer of anion-conducting channelrhodopsins between green algae and giant viruses Andrey Rozenberg 1,5, Johannes Oppermann 2,5, Jonas Wietek 2,3, Rodrigo Gaston Fernandez Lahore 2, Ruth-Anne Sandaa 4, Gunnar Bratbak 4, Peter Hegemann 2,6, and Oded 10 Béjà 1,6 1Faculty of Biology, Technion - Israel Institute of Technology, Haifa 32000, Israel. 2Institute for Biology, Experimental Biophysics, Humboldt-Universität zu Berlin, Invalidenstraße 42, Berlin 10115, Germany. 3Present address: Department of Neurobiology, Weizmann 15 Institute of Science, Rehovot 7610001, Israel. 4Department of Biological Sciences, University of Bergen, N-5020 Bergen, Norway. 5These authors contributed equally: Andrey Rozenberg, Johannes Oppermann. 6These authors jointly supervised this work: Peter Hegemann, Oded Béjà. e-mail: [email protected] ; [email protected] 20 ABSTRACT Channelrhodopsins (ChRs) are algal light-gated ion channels widely used as optogenetic tools for manipulating neuronal activity 1,2. Four ChR families are currently known. Green algal 3–5 and cryptophyte 6 cation-conducting ChRs (CCRs), cryptophyte anion-conducting ChRs (ACRs) 7, and the MerMAID ChRs 8. Here we 25 report the discovery of a new family of phylogenetically distinct ChRs encoded by marine giant viruses and acquired from their unicellular green algal prasinophyte hosts. -
A Taxonomic Reassessment of Chlamydomonas Meslinii (Volvocales, Chlorophyceae) with a Description of Paludistella Gen.Nov
Phytotaxa 432 (1): 065–080 ISSN 1179-3155 (print edition) https://www.mapress.com/j/pt/ PHYTOTAXA Copyright © 2020 Magnolia Press Article ISSN 1179-3163 (online edition) https://doi.org/10.11646/phytotaxa.432.1.6 A taxonomic reassessment of Chlamydomonas meslinii (Volvocales, Chlorophyceae) with a description of Paludistella gen.nov. HANI SUSANTI1,6, MASAKI YOSHIDA2, TAKESHI NAKAYAMA2, TAKASHI NAKADA3,4 & MAKOTO M. WATANABE5 1Life Science Innovation, School of Integrative and Global Major, University of Tsukuba, 1-1-1 Tennodai, Tsukuba, Ibaraki, 305-8577, Japan. 2Faculty of Life and Environmental Sciences, University of Tsukuba, 1-1-1 Tennodai, Tsukuba 305-8577, Japan. 3Institute for Advanced Biosciences, Keio University, Tsuruoka, Yamagata, 997-0052, Japan. 4Systems Biology Program, Graduate School of Media and Governance, Keio University, Fujisawa, Kanagawa, 252-8520, Japan. 5Algae Biomass Energy System Development and Research Center, University of Tsukuba. 6Research Center for Biotechnology, Indonesian Institute of Sciences, Jl. Raya Bogor KM 46 Cibinong West Java, Indonesia. Corresponding author: [email protected] Abstract Chlamydomonas (Volvocales, Chlorophyceae) is a large polyphyletic genus that includes numerous species that should be classified into independent genera. The present study aimed to examine the authentic strain of Chlamydomonas meslinii and related strains based on morphological and molecular data. All the strains possessed an asteroid chloroplast with a central pyrenoid and hemispherical papilla; however, they were different based on cell and stigmata shapes. Molecular phylogenetic analyses based on 18S rDNA, atpB, and psaB indicated that the strains represented a distinct subclade in the clade Chloromonadinia. The secondary structure of ITS-2 supported the separation of the strains into four species. -
Acidophilic Green Algal Genome Provides Insights Into Adaptation to an Acidic Environment
Acidophilic green algal genome provides insights into adaptation to an acidic environment Shunsuke Hirookaa,b,1, Yuu Hirosec, Yu Kanesakib,d, Sumio Higuchie, Takayuki Fujiwaraa,b,f, Ryo Onumaa, Atsuko Eraa,b, Ryudo Ohbayashia, Akihiro Uzukaa,f, Hisayoshi Nozakig, Hirofumi Yoshikawab,h, and Shin-ya Miyagishimaa,b,f,1 aDepartment of Cell Genetics, National Institute of Genetics, Shizuoka 411-8540, Japan; bCore Research for Evolutional Science and Technology, Japan Science and Technology Agency, Saitama 332-0012, Japan; cDepartment of Environmental and Life Sciences, Toyohashi University of Technology, Aichi 441-8580, Japan; dNODAI Genome Research Center, Tokyo University of Agriculture, Tokyo 156-8502, Japan; eResearch Group for Aquatic Plants Restoration in Lake Nojiri, Nojiriko Museum, Nagano 389-1303, Japan; fDepartment of Genetics, Graduate University for Advanced Studies, Shizuoka 411-8540, Japan; gDepartment of Biological Sciences, Graduate School of Science, University of Tokyo, Tokyo 113-0033, Japan; and hDepartment of Bioscience, Tokyo University of Agriculture, Tokyo 156-8502, Japan Edited by Krishna K. Niyogi, Howard Hughes Medical Institute, University of California, Berkeley, CA, and approved August 16, 2017 (received for review April 28, 2017) Some microalgae are adapted to extremely acidic environments in pumps that biotransform arsenic and archaeal ATPases, which which toxic metals are present at high levels. However, little is known probably contribute to the algal heat tolerance (8). In addition, the about how acidophilic algae evolved from their respective neutrophilic reduction in the number of genes encoding voltage-gated ion ancestors by adapting to particular acidic environments. To gain channels and the expansion of chloride channel and chloride car- insights into this issue, we determined the draft genome sequence rier/channel families in the genome has probably contributed to the of the acidophilic green alga Chlamydomonas eustigma and per- algal acid tolerance (8). -
Abstract Use of the Green Microalga Monoraphidium Sp. Dek19 to Remediate Wastewater
ABSTRACT USE OF THE GREEN MICROALGA MONORAPHIDIUM SP. DEK19 TO REMEDIATE WASTEWATER: SALINITY STRESS AND SCALING TO MESOCOSM CULTURES Anthony Robert Kephart, M.S. Department of Biological Sciences Northern Illinois University, 2016 Gabriel Holbrook, Director The purpose of this thesis was to investigate the growth of the green microalga Monoraphidium sp. Dek19 in the context of phycoremediation under conditions representative of wastewater media of a Midwest wastewater treatment facility. Microalgae were grown in effluent collected from four different wastewater streams at the DeKalb Sanitary District (DSD), DeKalb, Illinois, USA in volumes from 1 L to 380 L. It was determined through preliminary modeling of public data that Monoraphidium sp. Dek19 will likely outcompete local heterospecifics in final effluent wastewaters at the DSD 51.8% of the year. It was also determined that neither nitrogen nor phosphorus should become a limiting nutrient throughout the year. Study of the response of Monoraphidium sp. Dek19 to salinity stress was also completed. Salt stress caused a significant increase in lipid accumulation in salt stressed cultures compared to control cultures (37.0-50.5% increase) with a reduction in biomass productivity. Increases in photosynthetic pigments per cell were seen under salt stress, though the ratio of chlorophyll a and b remained constant. Finally, nitrate uptake was not greatly affected by salinity stress except when biomass accumulation became a corollary for uptake (nitrogen saturation). Luxury uptake of phosphate was significantly affected by wastewater salinity (p<0.001). High sodium potentially interrupts phosphate stress response proteins, slowing internalization of phosphate. Phosphate removal was still possible as some protein binding proteins appear to operate independent of sodium. -
Airborne Microalgae: Insights, Opportunities, and Challenges
crossmark MINIREVIEW Airborne Microalgae: Insights, Opportunities, and Challenges Sylvie V. M. Tesson,a,b Carsten Ambelas Skjøth,c Tina Šantl-Temkiv,d,e Jakob Löndahld Department of Marine Sciences, University of Gothenburg, Gothenburg, Swedena; Department of Biology, Lund University, Lund, Swedenb; National Pollen and Aerobiology Research Unit, Institute of Science and the Environment, University of Worcester, Worcester, United Kingdomc; Department of Design Sciences, Lund University, Lund, Swedend; Stellar Astrophysics Centre, Department of Physics and Astronomy, Aarhus University, Aarhus, Denmarke Airborne dispersal of microalgae has largely been a blind spot in environmental biological studies because of their low concen- tration in the atmosphere and the technical limitations in investigating microalgae from air samples. Recent studies show that airborne microalgae can survive air transportation and interact with the environment, possibly influencing their deposition rates. This minireview presents a summary of these studies and traces the possible route, step by step, from established ecosys- tems to new habitats through air transportation over a variety of geographic scales. Emission, transportation, deposition, and adaptation to atmospheric stress are discussed, as well as the consequences of their dispersal on health and the environment and Downloaded from state-of-the-art techniques to detect and model airborne microalga dispersal. More-detailed studies on the microalga atmo- spheric cycle, including, for instance, ice nucleation activity and transport simulations, are crucial for improving our under- standing of microalga ecology, identifying microalga interactions with the environment, and preventing unwanted contamina- tion events or invasions. he presence of microorganisms in the atmosphere has been phyta and Ochrophyta in the atmosphere (taxonomic classifica- Tdebated over centuries. -
The Draft Genome of the Small, Spineless Green Alga
Protist, Vol. 170, 125697, December 2019 http://www.elsevier.de/protis Published online date 25 October 2019 ORIGINAL PAPER Protist Genome Reports The Draft Genome of the Small, Spineless Green Alga Desmodesmus costato-granulatus (Sphaeropleales, Chlorophyta) a,b,2 a,c,2 d,e f g Sibo Wang , Linzhou Li , Yan Xu , Barbara Melkonian , Maike Lorenz , g b a,e f,1 Thomas Friedl , Morten Petersen , Sunil Kumar Sahu , Michael Melkonian , and a,b,1 Huan Liu a BGI-Shenzhen, Beishan Industrial Zone, Yantian District, Shenzhen 518083, China b Department of Biology, University of Copenhagen, Copenhagen, Denmark c Department of Biotechnology and Biomedicine, Technical University of Denmark, Copenhagen, Denmark d BGI Education Center, University of Chinese Academy of Sciences, Beijing, China e State Key Laboratory of Agricultural Genomics, BGI-Shenzhen, Shenzhen 518083, China f University of Duisburg-Essen, Campus Essen, Faculty of Biology, Universitätsstr. 2, 45141 Essen, Germany g Department ‘Experimentelle Phykologie und Sammlung von Algenkulturen’, University of Göttingen, Nikolausberger Weg 18, 37073 Göttingen, Germany Submitted October 9, 2019; Accepted October 21, 2019 Desmodesmus costato-granulatus (Skuja) Hegewald 2000 (Sphaeropleales, Chlorophyta) is a small, spineless green alga that is abundant in the freshwater phytoplankton of oligo- to eutrophic waters worldwide. It has a high lipid content and is considered for sustainable production of diverse compounds, including biofuels. Here, we report the draft whole-genome shotgun sequencing of D. costato-granulatus strain SAG 18.81. The final assembly comprises 48,879,637 bp with over 4,141 scaffolds. This whole-genome project is publicly available in the CNSA (https://db.cngb.org/cnsa/) of CNGBdb under the accession number CNP0000701. -
TRADITIONAL GENERIC CONCEPTS VERSUS 18S Rrna GENE PHYLOGENY in the GREEN ALGAL FAMILY SELENASTRACEAE (CHLOROPHYCEAE, CHLOROPHYTA) 1
J. Phycol. 37, 852–865 (2001) TRADITIONAL GENERIC CONCEPTS VERSUS 18S rRNA GENE PHYLOGENY IN THE GREEN ALGAL FAMILY SELENASTRACEAE (CHLOROPHYCEAE, CHLOROPHYTA) 1 Lothar Krienitz2 Institut für Gewässerökologie und Binnenfischerei, D-16775 Stechlin, Neuglobsow, Germany Iana Ustinova Institut für Botanik und Pharmazeutische Biologie der Universität, Staudtstrasse 5, D-91058 Erlangen, Germany Thomas Friedl Albrecht-von-Haller-Institut für Pflanzenwissenschaften, Abteilung Experimentelle Phykologie und Sammlung von Algenkulturen, Universität Göttingen, Untere Karspüle 2, D-37037 Göttingen, Germany and Volker A. R. Huss Institut für Botanik und Pharmazeutische Biologie der Universität, Staudtstrasse 5, D-91058 Erlangen, Germany Coccoid green algae of the Selenastraceae were in- few diacritic characteristics and that contain only a vestigated by means of light microscopy, TEM, and small number of species) and to reestablish “large” 18S rRNA analyses to evaluate the generic concept in genera of Selenastraceae such as Ankistrodesmus. this family. Phylogenetic trees inferred from the 18S Key index words: 18S rRNA, Ankistrodesmus, Chloro- rRNA gene sequences showed that the studied spe- phyta, Kirchneriella, Monoraphidium, molecular system- cies of autosporic Selenastraceae formed a well- atics, morphology, Podohedriella, pyrenoid, Quadrigula, resolved monophyletic clade within the DO group of Selenastraceae Chlorophyceae. Several morphological characteris- tics that are traditionally used as generic features Abbreviations: LM, light microscopy -
Freshwater Algae in Britain and Ireland - Bibliography
Freshwater algae in Britain and Ireland - Bibliography Floras, monographs, articles with records and environmental information, together with papers dealing with taxonomic/nomenclatural changes since 2003 (previous update of ‘Coded List’) as well as those helpful for identification purposes. Theses are listed only where available online and include unpublished information. Useful websites are listed at the end of the bibliography. Further links to relevant information (catalogues, websites, photocatalogues) can be found on the site managed by the British Phycological Society (http://www.brphycsoc.org/links.lasso). Abbas A, Godward MBE (1964) Cytology in relation to taxonomy in Chaetophorales. Journal of the Linnean Society, Botany 58: 499–597. Abbott J, Emsley F, Hick T, Stubbins J, Turner WB, West W (1886) Contributions to a fauna and flora of West Yorkshire: algae (exclusive of Diatomaceae). Transactions of the Leeds Naturalists' Club and Scientific Association 1: 69–78, pl.1. Acton E (1909) Coccomyxa subellipsoidea, a new member of the Palmellaceae. Annals of Botany 23: 537–573. Acton E (1916a) On the structure and origin of Cladophora-balls. New Phytologist 15: 1–10. Acton E (1916b) On a new penetrating alga. New Phytologist 15: 97–102. Acton E (1916c) Studies on the nuclear division in desmids. 1. Hyalotheca dissiliens (Smith) Bréb. Annals of Botany 30: 379–382. Adams J (1908) A synopsis of Irish algae, freshwater and marine. Proceedings of the Royal Irish Academy 27B: 11–60. Ahmadjian V (1967) A guide to the algae occurring as lichen symbionts: isolation, culture, cultural physiology and identification. Phycologia 6: 127–166 Allanson BR (1973) The fine structure of the periphyton of Chara sp. -
Multispecies Fresh Water Algae Production for Fish Farming Using Rabbit Manure
fishes Article Multispecies Fresh Water Algae Production for Fish Farming Using Rabbit Manure Adandé Richard 1,*, Liady Mouhamadou Nourou Dine 1, Djidohokpin Gildas 1, Adjahouinou Dogbè Clément 1, Azon Mahuan Tobias Césaire 1, Micha Jean-Claude 2 and Fiogbe Didier Emile 1 1 Laboratory of Research on Wetlands (LRZH), Department of Zoology, Faculty of Sciences and Technology, University of Abomey-Calavi, B.P. 526 Cotonou, Benin; [email protected] (L.M.N.D.); [email protected] (D.G.); [email protected] (A.D.C.); [email protected] (A.M.T.C.); edfi[email protected] (F.D.E.) 2 Department of Biology, Research Unit in Environmental Biology, University of Namur, 5000 Namur, Belgium; [email protected] * Correspondence: [email protected]; Tel.: +229-95583595 Received: 27 July 2020; Accepted: 19 October 2020; Published: 30 November 2020 Abstract: The current study aims at determining the optimal usage conditions of rabbit manure in a multispecies fresh water algae production for fish farming. This purpose, the experimental design is made of six treatments in triplicate including one control T0,T1,T2,T3,T4,T5 corresponding respectively to 0, 300, 600, 900, 1200, 1500 g/m3 of dry rabbit manure put into buckets containing 40 L of demineralized water and then fertilized. The initial average seeding density is made of 4 103 2.5 102 cells/L of Chlorophyceae, 1.5 103 1 102 cells/L of Coscinodiscophyceae, × ± × × ± × 3 103 1.2 102 cells/L of Conjugatophyceae, 2.8 103 1.5 102 cells/L of Bascillariophyceae, × ± × × ± × and 2.5 103 1.4 102 cells/L of Euglenophyceae.