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Alloactinosynnema Sp
University of New Mexico UNM Digital Repository Chemistry ETDs Electronic Theses and Dissertations Summer 7-11-2017 AN INTEGRATED BIOINFORMATIC/ EXPERIMENTAL APPROACH FOR DISCOVERING NOVEL TYPE II POLYKETIDES ENCODED IN ACTINOBACTERIAL GENOMES Wubin Gao University of New Mexico Follow this and additional works at: https://digitalrepository.unm.edu/chem_etds Part of the Bioinformatics Commons, Chemistry Commons, and the Other Microbiology Commons Recommended Citation Gao, Wubin. "AN INTEGRATED BIOINFORMATIC/EXPERIMENTAL APPROACH FOR DISCOVERING NOVEL TYPE II POLYKETIDES ENCODED IN ACTINOBACTERIAL GENOMES." (2017). https://digitalrepository.unm.edu/chem_etds/73 This Dissertation is brought to you for free and open access by the Electronic Theses and Dissertations at UNM Digital Repository. It has been accepted for inclusion in Chemistry ETDs by an authorized administrator of UNM Digital Repository. For more information, please contact [email protected]. Wubin Gao Candidate Chemistry and Chemical Biology Department This dissertation is approved, and it is acceptable in quality and form for publication: Approved by the Dissertation Committee: Jeremy S. Edwards, Chairperson Charles E. Melançon III, Advisor Lina Cui Changjian (Jim) Feng i AN INTEGRATED BIOINFORMATIC/EXPERIMENTAL APPROACH FOR DISCOVERING NOVEL TYPE II POLYKETIDES ENCODED IN ACTINOBACTERIAL GENOMES by WUBIN GAO B.S., Bioengineering, China University of Mining and Technology, Beijing, 2012 DISSERTATION Submitted in Partial Fulfillment of the Requirements for the Degree of Doctor of Philosophy Chemistry The University of New Mexico Albuquerque, New Mexico July 2017 ii DEDICATION This dissertation is dedicated to my altruistic parents, Wannian Gao and Saifeng Li, who never stopped encouraging me to learn more and always supported my decisions on study and life. -
[654] Screening and Identification of Rare Actinomycetes Isolated from Soil in Pho Hin
RSU International Research Conference 2020 https://rsucon.rsu.ac.th/proceedings 1 MAY 2020 Screening and Identification of Rare Actinomycetes Isolated from Soil in Pho Hin Dad Waterfall (Namtok Sam Lan National Park, Saraburi Province) for Antimicrobial Activities Nantawan Niemhom1* and Chitti Thawai2,3 1Microbiological and Molecular Biological Laboratory, Scientific Instrument Center, Faculty of Science, King Mongkut’s Institute of Technology Ladkrabang, Bangkok, Thailand 2Department of Biology, Faculty of Science, King Mongkut’s Institute of Technology Ladkrabang, Bangkok, Thailand 3Actinobacterial Research Unit, Faculty of Science, King Mongkut’s Institute of Technology Ladkrabang, Bangkok, Thailand *Corresponding author: E-mail: [email protected] ________________________________________________________________________________________________ Abstract Actinomycetes are common soil microorganisms with antibiotic-producing potential. In this study, three actinomycete strains were isolated from the soil in Pho Hin Dad Waterfall, Namtok Sam Lan National Park, Saraburi province, Thailand. Based on phenotypic characteristics and 16S rRNA gene sequence analysis, these actinomycete strains (P9, P12 and P15) belonged to the genus Dactylosporangium, Nonomuraea, and Actinomadura, while most closely related to Dactylosporangium sucinum RY35-23T (100%), Nonomuraea jiangxiensis CGMCC 4.6533T (99.57%), and Actinomadura barringtoniae GKU 128T (99.35%), respectively. Crude ethyl acetate extracts from strain P9, P12, and P15 showed antimicrobial activities against Gram-positive bacteria (Bacillus subtilis ATCC 6633, Kocuria rhizophila ATCC 9341, Staphylococcus aureus ATCC 25923, and Methicillin-resistant Staphylococcus aureus DMST 20654) and yeast (Candida albicans ATCC 10231), but not against Gram-negative bacteria (Escherichia coli ATCC 25922 and Pseudomonas aeruginosa ATCC 27853). The result in this study demonstrated the antibiotic-producing potential of actinomycetes from the soil in Pho Hin Dad Waterfall. -
Inter-Domain Horizontal Gene Transfer of Nickel-Binding Superoxide Dismutase 2 Kevin M
bioRxiv preprint doi: https://doi.org/10.1101/2021.01.12.426412; this version posted January 13, 2021. 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 Inter-domain Horizontal Gene Transfer of Nickel-binding Superoxide Dismutase 2 Kevin M. Sutherland1,*, Lewis M. Ward1, Chloé-Rose Colombero1, David T. Johnston1 3 4 1Department of Earth and Planetary Science, Harvard University, Cambridge, MA 02138 5 *Correspondence to KMS: [email protected] 6 7 Abstract 8 The ability of aerobic microorganisms to regulate internal and external concentrations of the 9 reactive oxygen species (ROS) superoxide directly influences the health and viability of cells. 10 Superoxide dismutases (SODs) are the primary regulatory enzymes that are used by 11 microorganisms to degrade superoxide. SOD is not one, but three separate, non-homologous 12 enzymes that perform the same function. Thus, the evolutionary history of genes encoding for 13 different SOD enzymes is one of convergent evolution, which reflects environmental selection 14 brought about by an oxygenated atmosphere, changes in metal availability, and opportunistic 15 horizontal gene transfer (HGT). In this study we examine the phylogenetic history of the protein 16 sequence encoding for the nickel-binding metalloform of the SOD enzyme (SodN). A comparison 17 of organismal and SodN protein phylogenetic trees reveals several instances of HGT, including 18 multiple inter-domain transfers of the sodN gene from the bacterial domain to the archaeal domain. -
Systematic Research on Actinomycetes Selected According
Systematic Research on Actinomycetes Selected according to Biological Activities Dissertation Submitted in fulfillment of the requirements for the award of the Doctor (Ph.D.) degree of the Math.-Nat. Fakultät of the Christian-Albrechts-Universität in Kiel By MSci. - Biol. Yi Jiang Leibniz-Institut für Meereswissenschaften, IFM-GEOMAR, Marine Mikrobiologie, Düsternbrooker Weg 20, D-24105 Kiel, Germany Supervised by Prof. Dr. Johannes F. Imhoff Kiel 2009 Referent: Prof. Dr. Johannes F. Imhoff Korreferent: ______________________ Tag der mündlichen Prüfung: Kiel, ____________ Zum Druck genehmigt: Kiel, _____________ Summary Content Chapter 1 Introduction 1 Chapter 2 Habitats, Isolation and Identification 24 Chapter 3 Streptomyces hainanensis sp. nov., a new member of the genus Streptomyces 38 Chapter 4 Actinomycetospora chiangmaiensis gen. nov., sp. nov., a new member of the family Pseudonocardiaceae 52 Chapter 5 A new member of the family Micromonosporaceae, Planosporangium flavogriseum gen nov., sp. nov. 67 Chapter 6 Promicromonospora flava sp. nov., isolated from sediment of the Baltic Sea 87 Chapter 7 Discussion 99 Appendix a Resume, Publication list and Patent 115 Appendix b Medium list 122 Appendix c Abbreviations 126 Appendix d Poster (2007 VAAM, Germany) 127 Appendix e List of research strains 128 Acknowledgements 134 Erklärung 136 Summary Actinomycetes (Actinobacteria) are the group of bacteria producing most of the bioactive metabolites. Approx. 100 out of 150 antibiotics used in human therapy and agriculture are produced by actinomycetes. Finding novel leader compounds from actinomycetes is still one of the promising approaches to develop new pharmaceuticals. The aim of this study was to find new species and genera of actinomycetes as the basis for the discovery of new leader compounds for pharmaceuticals. -
Polar Actinomycetes and Their Secondary Metabolites
Journal of Natural Sciences Research www.iiste.org ISSN 2224-3186 (Paper) ISSN 2225-0921 (Online) Vol.8, No.10, 2018 Polar Actinomycetes and Their Secondary Metabolites Potjanicha Nopnakorn 1* Pichamon Nopnakorn 2 1.Key Laboratory of Combinatorial Biosynthesis and Drug Discovery , School of Pharmaceutical Sciences, Wuhan University, Wuhan 430071, China 2.Department of Applied Biological Chemistry, Faculty of Agriculture, Shizuoka University, Shizuoka 422-8529, Japan Abstract In the past decades, extreme environments have become a popular hot spot for scientists and researchers to find novel microorganisms and natural products with biological potential. Actinomycetes are Gram-positive bacteria. It is one of the most important microorganisms that produce various useful secondary metabolites. The novel species of actinomycetes from 2006–2018 were enormously discovered (2,085 species). Among those novel actinomycetes, 64 novel species were isolated from the Arctic, subarctic, and Antarctic regions (an approximate 3 % of novel actinomycetes since 2006). Over 60 % of polar actinomycetes were isolated from soil, followed by sea sediment, and rock. Ten species of actinomycetes were reported to have the ability to produce potential natural products. Most of compounds show antimicrobial activity. Keywords: polar regions, Arctic, subarctic, Antarctic, actinomycetes, natural product 1. Polar Regions The polar regions of the Earth include the regions surrounding geographical poles; the North and the South Poles. The polar regions are covered by ice and snow; floating pack ice (sea ice) in the North Pole and the Antarctic ice sheet in the South Pole. 1.1 Arctic The Arctic is the region surrounding the North Pole, which includes the Arctic Ocean, adjacent seas, parts of Alaska (United States), Finland, Greenland (Kingdom of Denmark), Iceland, Northern Canada (Canada), Norway, Russia and Sweden. -
A New Member of the Family Micromonosporaceae, Planosporangium Flavigriseum Gen
International Journal of Systematic and Evolutionary Microbiology (2008), 58, 1324–1331 DOI 10.1099/ijs.0.65211-0 A new member of the family Micromonosporaceae, Planosporangium flavigriseum gen. nov., sp. nov. Jutta Wiese,1 Yi Jiang,1,2 Shu-Kun Tang,2 Vera Thiel,1 Rolf Schmaljohann,1 Li-Hua Xu,2 Cheng-Lin Jiang2 and Johannes F. Imhoff1 Correspondence 1Leibniz-Institut fu¨r Meereswissenschaften, IFM-GEOMAR, Du¨sternbrooker Weg 20, D-24105 Johannes F. Imhoff Kiel, Germany [email protected] 2Yunnan Institute of Microbiology, Yunnan University, Kunming 650091, PR China Li-Hua Xu [email protected] A novel actinomycete, designated strain YIM 46034T, was isolated from an evergreen broadleaved forest at Menghai, in southern Yunnan Province, China. Phenotypic characterization and 16S rRNA gene sequence analysis indicated that the strain belonged to the family Micromonosporaceae. Strain YIM 46034T showed more than 3 % 16S rRNA gene sequence divergence from recognized species of genera in the family Micromonosporaceae. Characteristic features of strain YIM 46034T were the production of two types of spores, namely motile spores, which were formed in sporangia produced on substrate mycelia, and single globose spores, which were observed on short sporophores of the substrate mycelia. The cell wall contained meso-diaminopimelic acid, glycine, arabinose and xylose, which are characteristic components of cell-wall chemotype II of actinomycetes. Phosphatidylethanolamine was the major phospholipid (phospholipid type II). Based on morphological, chemotaxonomic, phenotypic and genetic characteristics, strain YIM 46034T is considered to represent a novel species of a new genus in the family Micromonosporaceae, for which the name Planosporangium flavigriseum gen. -
Dactylosporangium and Some Other Filamentous Actinomycetes
Biosystematics of the Genus Dactylosporangium and Some Other Filamentous Actinomycetes Byung-Yong Kim (BSc., MSc. Agricultural Chemistry, Korea University, Korea) Thesis submitted in accordance with the requirements of the Newcastle University for the Degree of Doctor of Philosophy November 2010 School of Biology, Faculty of Science, Agriculture and Engineering, Newcastle University, Newcastle upon Tyne, United Kingdom Dedicated to my mother who devoted her life to our family, and to my brother who led me into science "Whenever I found out anything remarkable, I have thought it my duty to put down my discovery on paper, so that all ingenious people might be informed thereof." - Antonie van Leeuwenhoek, Letter of June 12, 1716 “Freedom of thought is best promoted by the gradual illumination of men’s minds, which follows from the advance of science.”- Charles Darwin, Letter of October 13, 1880 ii Abstract This study tested the hypothesis that a relationship exists between taxonomic diversity and antibiotic resistance patterns of filamentous actinomycetes. To this end, 200 filamentous actinomycetes were selectively isolated from a hay meadow soil and assigned to groups based on pigments formed on oatmeal and peptone-yeast extract-iron agars. Forty-four representatives of the colour-groups were assigned to the genera Dactylosporangium, Micromonospora and Streptomyces based on complete 16S rRNA gene sequence analyses. In general, the position of these isolates in the phylogenetic trees correlated with corresponding antibiotic resistance patterns. A significant correlation was found between phylogenetic trees based on 16S rRNA gene and vanHAX gene cluster sequences of nine vancomycin-resistant Streptomyces isolates. These findings provide tangible evidence that antibiotic resistance patterns of filamentous actinomycetes contain information which can be used to design novel media for the selective isolation of rare and uncommon, commercially significant actinomycetes, such as those belonging to the genus Dactylosporangium, a member of the family Micromonosporaceae. -
Diversity and Antimicrobial Activity of Culturable Endophytic Actinobacteria Associated with Acanthaceae Plants
R ESEARCH ARTICLE doi: 10.2306/scienceasia1513-1874.2020.036 Diversity and antimicrobial activity of culturable endophytic actinobacteria associated with Acanthaceae plants a,b, c a Wongsakorn Phongsopitanun ∗, Paranee Sripreechasak , Kanokorn Rueangsawang , Rungpech Panyawuta, Pattama Pittayakhajonwutd, Somboon Tanasupawatb a Department of Biology, Faculty of Science, Ramkhamhaeng University, Bangkok 10240 Thailand b Department of Biochemistry and Microbiology, Faculty of Pharmaceutical Sciences, Chulalongkorn University, Bangkok 10330 Thailand c Department of Biotechnology, Faculty of Science, Burapha University, Chonburi 20131 Thailand d National Center for Genetic Engineering and Biotechnology (BIOTEC), Thailand Science Park, Pathumthani 12120 Thailand ∗Corresponding author, e-mail: [email protected] Received 20 Oct 2019 Accepted 20 Apr 2020 ABSTRACT: In this study, a total of 52 endophytic actinobacteria were isolated from 6 species of Acanthaceae plants collected in Thailand. Most actinobacteria were obtained from the root part. Based on 16S rRNA gene analysis and phylogenetic tree, these actinobacteria were classified into 4 families (Nocardiaceae, Micromonosporaceae, Streptosporangiaceae and Streptomycetaceae) and 6 genera including Actinomycetospora (1 isolate), Dactylosporangium (1 isolate), Nocardia (3 isolates), Microbispora (5 isolates), Micromonospora (10 isolates) and Streptomyces (32 isolates). The result of antimicrobial activity screening indicated that 8 isolates, including 1 Actinomycetospora and 7 Streptomyces, -
Bioactive Actinobacteria Associated with Two South African Medicinal Plants, Aloe Ferox and Sutherlandia Frutescens
Bioactive actinobacteria associated with two South African medicinal plants, Aloe ferox and Sutherlandia frutescens Maria Catharina King A thesis submitted in partial fulfilment of the requirements for the degree of Doctor Philosophiae in the Department of Biotechnology, University of the Western Cape. Supervisor: Dr Bronwyn Kirby-McCullough August 2021 http://etd.uwc.ac.za/ Keywords Actinobacteria Antibacterial Bioactive compounds Bioactive gene clusters Fynbos Genetic potential Genome mining Medicinal plants Unique environments Whole genome sequencing ii http://etd.uwc.ac.za/ Abstract Bioactive actinobacteria associated with two South African medicinal plants, Aloe ferox and Sutherlandia frutescens MC King PhD Thesis, Department of Biotechnology, University of the Western Cape Actinobacteria, a Gram-positive phylum of bacteria found in both terrestrial and aquatic environments, are well-known producers of antibiotics and other bioactive compounds. The isolation of actinobacteria from unique environments has resulted in the discovery of new antibiotic compounds that can be used by the pharmaceutical industry. In this study, the fynbos biome was identified as one of these unique habitats due to its rich plant diversity that hosts over 8500 different plant species, including many medicinal plants. In this study two medicinal plants from the fynbos biome were identified as unique environments for the discovery of bioactive actinobacteria, Aloe ferox (Cape aloe) and Sutherlandia frutescens (cancer bush). Actinobacteria from the genera Streptomyces, Micromonaspora, Amycolatopsis and Alloactinosynnema were isolated from these two medicinal plants and tested for antibiotic activity. Actinobacterial isolates from soil (248; 188), roots (0; 7), seeds (0; 10) and leaves (0; 6), from A. ferox and S. frutescens, respectively, were tested for activity against a range of Gram-negative and Gram-positive human pathogenic bacteria. -
Genome-Based Taxonomic Classification of the Phylum
ORIGINAL RESEARCH published: 22 August 2018 doi: 10.3389/fmicb.2018.02007 Genome-Based Taxonomic Classification of the Phylum Actinobacteria Imen Nouioui 1†, Lorena Carro 1†, Marina García-López 2†, Jan P. Meier-Kolthoff 2, Tanja Woyke 3, Nikos C. Kyrpides 3, Rüdiger Pukall 2, Hans-Peter Klenk 1, Michael Goodfellow 1 and Markus Göker 2* 1 School of Natural and Environmental Sciences, Newcastle University, Newcastle upon Tyne, United Kingdom, 2 Department Edited by: of Microorganisms, Leibniz Institute DSMZ – German Collection of Microorganisms and Cell Cultures, Braunschweig, Martin G. Klotz, Germany, 3 Department of Energy, Joint Genome Institute, Walnut Creek, CA, United States Washington State University Tri-Cities, United States The application of phylogenetic taxonomic procedures led to improvements in the Reviewed by: Nicola Segata, classification of bacteria assigned to the phylum Actinobacteria but even so there remains University of Trento, Italy a need to further clarify relationships within a taxon that encompasses organisms of Antonio Ventosa, agricultural, biotechnological, clinical, and ecological importance. Classification of the Universidad de Sevilla, Spain David Moreira, morphologically diverse bacteria belonging to this large phylum based on a limited Centre National de la Recherche number of features has proved to be difficult, not least when taxonomic decisions Scientifique (CNRS), France rested heavily on interpretation of poorly resolved 16S rRNA gene trees. Here, draft *Correspondence: Markus Göker genome sequences -
Actinoplanes and Dactylosporangium
Int.J.Curr.Microbiol.App.Sci (2019) 8(4): 920-931 International Journal of Current Microbiology and Applied Sciences ISSN: 2319-7706 Volume 8 Number 04 (2019) Journal homepage: http://www.ijcmas.com Original Research Article https://doi.org/10.20546/ijcmas.2019.804.106 Biocatalytic Reduction of Carbonyl Compounds by Actinobacteria from Two Genera of the Micromonosporaceae Family: Actinoplanes and Dactylosporangium K. Ishihara1*, K. Morita1, Y. Nishimori1, S. Okamoto1, T. Hiramatsu1, A. Ohkawa1, D. Uesugi2, M. Yanagi1, H. Hamada1, N. Masuoka3 and N. Nakajima4 1Department of Life Science, Okayama University of Science, Okayama, Japan 2Department of Research & Development, JO Cosmetics Co., Ltd., Tokyo, Japan 3Department of Research & Development, Institute for Fruit Juice Research in Tsudaka, Co., Ltd., Okayama, Japan 4Department of Nutritional Science, Okayama Prefectural University, Soja, Okayama, Japan *Corresponding author ABSTRACT K e yw or ds We screened 10 Actinoplanes and 14 Dactylosporangium strains to investigate the biocatalytic ability of two genera of the Micromonosporaceae family. Two Actinoplanes Biocatalyst, strains (A. ferrugineus NBRC15555 and A. missouriensis NBRC102363) exhibited good Actinomycete, Stereoselective growth when cultured in 228 and 231 media, as did two Dactylosporangium strains reduction, Chiral (Dactylosporangium sp. NBRC101297 and Dactylosporangium sp. NBRC101730) when hydroxy ester, cultured in 227 and 266 media. The stereoselective reduction of various carbonyl Actinoplanes, compounds using these four strains was therefore investigated. The present study Dactylosporangium discovered that these strains can reduce aliphatic and aromatic α-keto esters and an aromatic α-keto amide. On the basis of the conversion ratio and stereoselectivity of the Article Info alcohols produced, A. ferrugineus NBRC15555 is a potential biocatalyst for the Accepted: stereoselective reduction of α-keto esters and an aromatic α-keto amide to the 10 March 2019 corresponding chiral alcohols when cultured in the 227 medium. -
Isolation and Genus-Level Diversity
The Journal of Antibiotics (2011) 64, 599–606 & 2011 Japan Antibiotics Research Association All rights reserved 0021-8820/11 $32.00 www.nature.com/ja ORIGINAL ARTICLE Taxonomic and ecological studies of actinomycetes from Vietnam: isolation and genus-level diversity Duong Van Hop1, Yayoi Sakiyama2, Chu Thi Thanh Binh1, Misa Otoguro2, Dinh Thuy Hang1, Shinji Miyadoh2, Dao Thi Luong1 and Katsuhiko Ando2 Actinomycetes were isolated from 109 soil and 93 leaf-litter samples collected at five sites in Vietnam between 2005 and 2008 using the rehydration-centrifugation (RC) method, sodium dodecyl sulfate-yeast extract dilution method, dry-heating method and oil-separation method in conjunction with humic acid-vitamin agar as an isolation medium. A total of 1882 strains were identified as Vietnamese (VN)-actinomycetes including 1080 (57%) streptomycetes (the genus Streptomyces isolates) and 802 (43%) non-streptomycetes. The 16S ribosomal RNA gene sequences of the VN-actinomycetes were analyzed using BLAST searches. The results showed that these isolates belonged to 53 genera distributed among 21 families. Approximately 90% of these strains were members of three families: Streptomycetaceae (1087 strains, 58%); Micromonosporaceae (516 strains, 27%); and Streptosporangiaceae (89 strains, 5%). Motile actinomycetes of the genera Actinoplanes, Kineosporia and Cryptosporangium, which have quite common morphological characteristics, were frequently isolated from leaf-litter samples using the RC method. It is possible that these three genera acquired common properties during a process of convergent evolution. By contrast, strains belonging to the suborder Streptosporangineae were exclusively isolated from soils. A comparison of the sampling sites revealed no significant difference in taxonomic diversity between these sites.