Complete Genome Sequence of Serinicoccus Sp. JLT9, an Actinomycete Isolated from the Shallow-Sea Hydrothermal System
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Corynebacterium Sp.|NML98-0116
1 Limnochorda_pilosa~GCF_001544015.1@NZ_AP014924=Bacteria-Firmicutes-Limnochordia-Limnochordales-Limnochordaceae-Limnochorda-Limnochorda_pilosa 0,9635 Ammonifex_degensii|KC4~GCF_000024605.1@NC_013385=Bacteria-Firmicutes-Clostridia-Thermoanaerobacterales-Thermoanaerobacteraceae-Ammonifex-Ammonifex_degensii 0,985 Symbiobacterium_thermophilum|IAM14863~GCF_000009905.1@NC_006177=Bacteria-Firmicutes-Clostridia-Clostridiales-Symbiobacteriaceae-Symbiobacterium-Symbiobacterium_thermophilum Varibaculum_timonense~GCF_900169515.1@NZ_LT827020=Bacteria-Actinobacteria-Actinobacteria-Actinomycetales-Actinomycetaceae-Varibaculum-Varibaculum_timonense 1 Rubrobacter_aplysinae~GCF_001029505.1@NZ_LEKH01000003=Bacteria-Actinobacteria-Rubrobacteria-Rubrobacterales-Rubrobacteraceae-Rubrobacter-Rubrobacter_aplysinae 0,975 Rubrobacter_xylanophilus|DSM9941~GCF_000014185.1@NC_008148=Bacteria-Actinobacteria-Rubrobacteria-Rubrobacterales-Rubrobacteraceae-Rubrobacter-Rubrobacter_xylanophilus 1 Rubrobacter_radiotolerans~GCF_000661895.1@NZ_CP007514=Bacteria-Actinobacteria-Rubrobacteria-Rubrobacterales-Rubrobacteraceae-Rubrobacter-Rubrobacter_radiotolerans Actinobacteria_bacterium_rbg_16_64_13~GCA_001768675.1@MELN01000053=Bacteria-Actinobacteria-unknown_class-unknown_order-unknown_family-unknown_genus-Actinobacteria_bacterium_rbg_16_64_13 1 Actinobacteria_bacterium_13_2_20cm_68_14~GCA_001914705.1@MNDB01000040=Bacteria-Actinobacteria-unknown_class-unknown_order-unknown_family-unknown_genus-Actinobacteria_bacterium_13_2_20cm_68_14 1 0,9803 Thermoleophilum_album~GCF_900108055.1@NZ_FNWJ01000001=Bacteria-Actinobacteria-Thermoleophilia-Thermoleophilales-Thermoleophilaceae-Thermoleophilum-Thermoleophilum_album -
Diversity of Micromonospora Strains from the Deep Mediterranean Sea and Their Potential to Produce Bioactive Compounds
AIMS Microbiology, 2(2): 205-221. DOI: 10.3934/microbiol.2016.2.205 Received: 15 February 2016 Accepted: 06 June 2016 Published: 14 June 2016 http://www.aimspress.com/journal/microbiology Research article Diversity of Micromonospora strains from the deep Mediterranean Sea and their potential to produce bioactive compounds Andrea Gärtner 1, Jutta Wiese 1, and Johannes F. Imhoff 1,2,* 1 GEOMAR Helmholtz Center for Ocean Research Kiel, RD3 Marine Microbiology, 24105 Kiel, Germany 2 Christian-Albrechts University of Kiel, 24118 Kiel Germany * Correspondence: Email: [email protected]; Tel: +49-431-600-4450; Fax: +49-431-600-4482. Abstract: During studies on bacteria from the Eastern Mediterranean deep-sea, incubation under in situ conditions (salinity, temperature and pressure) and heat treatment were used to selectively enrich representatives of Micromonospora. From sediments of the Ierapetra Basin (4400 m depth) and the Herodotos Plain (2800 m depth), 21 isolates were identified as members of the genus Micromonospora. According to phylogenetic analysis of 16S rRNA gene sequences, the Micromonospora isolates could be assigned to 14 different phylotypes with an exclusion limit of ≥ 99.5% sequence similarity. They formed 7 phylogenetic clusters. Two of these clusters, which contain isolates obtained after enrichment under pressure incubation and phylogenetically are distinct from representative reference organism, could represent bacteria specifically adapted to the conditions in situ and to life in these deep-sea sediments. The majority of the Micromonospora isolates (90%) contained at least one gene cluster for biosynthesis of secondary metabolites for non-ribosomal polypeptides and polyketides (polyketide synthases type I and type II). The determination of biological activities of culture extracts revealed that almost half of the strains produced substances inhibitory to the growth of Gram-positive bacteria. -
Bioinformatic and Mutational Studies of Related Toxin–Antitoxin Pairs in M
Bioinformatic and mutational studies of related toxin–antitoxin pairs in M. tuberculosis predict and identify key functional residues Running title: Toxin-Antitoxin relationships in M.tuberculosis Himani Tandon1, Arun Sharma2, Saruchi Wadhwa2, Raghavan Varadarajan1, Ramandeep Singh2, Narayanaswamy Srinivasan1*, and Sankaran Sandhya1* 1Molecular Biophysics Unit, Indian Institute of Science, Bangalore- 560012, India. 2Tuberculosis Research Laboratory, Vaccine and Infectious Disease Research Centre, Translational Health Science and Technology Institute, NCR Biotech Science Cluster, 3rd Milestone, PO Box # 4, Faridabad, Haryana- 121001, India. * To whom correspondence should be addressed. Sankaran Sandhya: Molecular Biophysics Unit, Indian Institute of Science, Bangalore- 560012; [email protected]; Tel: +918022932837; Fax: +918023600535. Correspondence may also be addressed to Narayanaswamy Srinivasan. Molecular Biophysics Unit, Indian Institute of Science, Bangalore- 560012; [email protected]; Tel: +918022932837; Fax: +918023600535. Keywords: Toxin-antitoxin, homology, paralogues, structure-function, Mycobacterium tuberculosis, genome analysis, bacteriostasis, VapBC, PIN domain, phylogeny, molecular modelling, protein evolution 1 S1. Trends observed in the distribution of homologues of M.tuberculosis TA systems within MTBC and conservation pattern of Rv0909-Rv0910 and Rv1546 in MTBC and other organisms. Ramage et. al, have earlier probed the spread of M.tuberculosis type II TA in 5 of the 10 genomes in the MTBC complex (1). In addition to these genomes, we have included the genomes of M.orygis, M.caprae and M.mungi that are now available since their study, for our analysis. A search of M.tuberculosis TA in MTBC revealed that not all TAs were found as a pair with the same confidence in M.mungi, M.orygis and M.canetti. -
Accugenx-ID® Identification Report Guide Click to Learn More for Bacseq and Funits Interpretation
MICROBIAL SOLUTIONS AccuGENX-ID® Identification Report Guide Click to learn more for BacSeq and FunITS Interpretation Sample C2913343- 20190325011 has a closest match of Kytococcus sedentarius and links directly to it in the Neighbor Joining Tree. The sample and its closest match have 0.49% difference in sequence in the first 500 base-pair region of the 16S gene. The identification result is Kytococcus sedentarius, with a Species-level of confidence. Processing Lab: ® 614 Interchange Blvd Accugenix 1 Newark, DE 19711 2 www.criver.com/accugenix ® [email protected] AccuGENX-ID Report Phone +1.302.292.8888 NEW-SOP-00071 Customer: 3 Valued Customer Account: 7 110440 (ACC1) Address: 4 614 Interchange Blvd, Newark, DE, 19711, United States Accugenix® C# / Run Date: 5 C2913343-20190325011 / 2019-03-22 13:10:12 ID Request Form#: 8 100000 Customer Sample ID: 6 Sample ABC Due Date: 9 2019-03-25 10 AccuGENX-ID® Database Search Result - Bacterial Library Identification: 11 Kytococcus sedentarius Confidence Level: 12 Species Based on published literature, the above identified species has been described as a Gram-positive, cocci-shaped bacterium. Click HERE for more 13 information on this organism. Neighbor Joining Tree 15 C2913343-20180117011 14 16 Kytococcus sedentarius [0.49%] Kytococcus schroeteri [1.18%] Kytococcus aerolatus [1.58%] Sediminivirga luteola [6.90%] Serinicoccus profundi [4.95%] Serinicoccus chungangensis [5.72%] Serinicoccus marinus [6.90%] Ornithinimicrobium tianjinense [6.51%] Dermacoccus abyssi [5.33%] Dermacoccus barathri -
Phylogenetic Diversity of Gram-Positive Bacteria and Their Secondary Metabolite Genes
UC San Diego Research Theses and Dissertations Title Phylogenetic Diversity of Gram-positive Bacteria and Their Secondary Metabolite Genes Permalink https://escholarship.org/uc/item/06z0868t Author Gontang, Erin A Publication Date 2008 Peer reviewed eScholarship.org Powered by the California Digital Library University of California UNIVERSITY OF CALIFORNIA, SAN DIEGO Phylogenetic Diversity of Gram-positive Bacteria and Their Secondary Metabolite Genes A Dissertation submitted in partial satisfaction of the requirements for the degree Doctor of Philosophy in Oceanography by Erin Ann Gontang Committee in charge: William Fenical, Chair Douglas H. Bartlett Bianca Brahamsha William Gerwick Paul R. Jensen Kit Pogliano 2008 3324374 3324374 2008 The Dissertation of Erin Ann Gontang is approved, and it is acceptable in quality and form for publication on microfilm: ____________________________________ ____________________________________ ____________________________________ ____________________________________ ____________________________________ ____________________________________ Chair University of California, San Diego 2008 iii DEDICATION To John R. Taylor, my incredible partner, my best friend and my love. ***** To my mom, Janet M. Gontang, and my dad, Austin J. Gontang. Your generous support and unconditional love has allowed me to create my future. Thank you. ***** To my sister, Allison C. Gontang, who is as proud of me as I am of her. You are a constant source of inspiration and I am so fortunate to have you in my life. iv TABLE OF CONTENTS -
Report on 31 Unrecorded Bacterial Species in Korea That Belong to the Phylum Actinobacteria
Journal of Species Research 5(1):113, 2016 Report on 31 unrecorded bacterial species in Korea that belong to the phylum Actinobacteria JungHye Choi1, JuHee Cha1, JinWoo Bae2, JangCheon Cho3, Jongsik Chun4, WanTaek Im5, Kwang Yeop Jahng6, Che Ok Jeon7, Kiseong Joh8, Seung Bum Kim9, Chi Nam Seong10, JungHoon Yoon11 and ChangJun Cha1,* 1Department of Systems Biotechnology, Chung-Ang University, Anseong 17546, Korea 2Department of Biology, Kyung Hee University, Seoul 02447, Korea 3Department of Biological Sciences, Inha University, Incheon 22212, Korea 4School of Biological Sciences, Seoul National University, Seoul 08826, Korea 5Department of Biotechnology, Hankyong National University, Anseong 17579, Korea 6Department of Life Sciences, Chonbuk National University, Jeonju-si 54896, Korea 7Department of Life Science, Chung-Ang University, Seoul 06974, Korea 8Department of Bioscience and Biotechnology, Hankuk University of Foreign Studies, Gyeonggi 17035, Korea 9Department of Microbiology, Chungnam National University, Daejeon 34134, Korea 10Department of Biology, Sunchon National University, Suncheon 57922, Korea 11Department of Food Science and Biotechnology, Sungkyunkwan University, Suwon 16419, Korea *Correspondent: [email protected] To discover and characterize indigenous species in Korea, a total of 31 bacterial strains that belong to the phylum Actinobacteria were isolated from various niches in Korea. Each strain showed the high sequence similarity (>99.1%) with the closest bacterial species, forming a robust phylogenetic clade. These strains have not been previously recorded in Korea. According to the recently updated taxonomy of the phylum Actinobacteria based upon 16S rRNA trees, we report 25 genera of 13 families within 5 orders of the class Actinobacteria as actinobacterial species found in Korea. -
Aquatic Microbial Ecology 52:1
Vol. 52: 1–11, 2008 AQUATIC MICROBIAL ECOLOGY Published online June 19, 2008 doi: 10.3354/ame01211 Aquat Microb Ecol Comparative actinomycete diversity in marine sediments Alejandra Prieto-Davó, William Fenical, Paul R. Jensen* Center for Marine Biotechnology and Biomedicine, Scripps Institution of Oceanography, University of California San Diego, La Jolla, California, 92093-0204, USA ABSTRACT: The diversity of cultured actinomycete bacteria was compared between near- and off- shore marine sediments. Strains were tested for the effects of seawater on growth and analyzed for 16S rRNA gene sequence diversity. In total, 623 strains representing 6 families in the order Actino- mycetales were cultured. These strains were binned into 16 to 63 operational taxonomic units (OTUs) over a range of 97 to 100% sequence identity. The majority of the OTUs were closely related (>98% sequence identity) to strains previously reported from non-marine sources, indicating that most are not restricted to the sea. However, new OTUs averaged 96.6% sequence identity with previously cul- tured strains and ca. one-third of the OTUs were marine-specific, suggesting that sediment commu- nities include considerable actinomycete diversity that does not occur on land. Marine specificity did not increase at the off-shore sites, indicating high levels of terrestrial influence out to 125 km from shore. The requirement of seawater for growth was observed among <6% of the strains, while all members of 9 OTUs possessed this trait, revealing a high degree of marine adaptation among some lineages. Statistical analyses predicted greater OTU diversity at the off-shore sites and provided a rationale for expanded exploration of deep-sea samples. -
UNIVERSITY of CALIFORNIA, SAN DIEGO Phylogenetic and Chemical
UNIVERSITY OF CALIFORNIA, SAN DIEGO Phylogenetic and Chemical Diversity of Marine-Derived Actinomycetes from Southern California Sediments A Dissertation submitted in partial satisfaction of the requirements for the degree Doctor of Philosophy in Oceanography by Alejandra Prieto-Davó Committee in charge: William Fenical, Chair Lihini Aluwihare Douglas H. Bartlett Paul R. Jensen Brian Palenik Christopher Wills 2008 The Dissertation of Alejandra Prieto-Davó is approved, and it is acceptable in quality and form for publication on microfilm: ____________________________________ ____________________________________ ____________________________________ ____________________________________ ____________________________________ ____________________________________ Chair University of California, San Diego 2008 iii DEDICATION To my father, who I have admired throughout my life and who has always been an example of strength and perseverance. ***** To my mother, who has taught me that a woman’s place is not in the kitchen and who has always supported all my crazy dreams. ***** To my husband Luis Alfonso, for showing me that love has no borders. Te amo. iv TABLE OF CONTENTS Signature Page………………………………………………………………….…..iii Dedication……………………………………………………………………….….iv Table of Contents……………………………………………………………………v List of Figures ……………………………………………………………………..vii List of Tables………………………………………………………………………..ix Acknowledgements……………………………………………………...……….….x Vita………………………………………………………………………...…....…xiv Abstract………………………………………………...…………...………….…..xv Chapter 1: Introduction: -
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. -
Actinomycetes from the South China Sea Sponges: Isolation, Diversity, and Potential for Aromatic Polyketides Discovery
ORIGINAL RESEARCH published: 01 October 2015 doi: 10.3389/fmicb.2015.01048 Actinomycetes from the South China Sea sponges: isolation, diversity, and potential for aromatic polyketides discovery Wei Sun, Fengli Zhang, Liming He, Loganathan Karthik and Zhiyong Li * Marine Biotechnology Laboratory, State Key Laboratory of Microbial Metabolism, School of Life Sciences and Biotechnology, Shanghai Jiao Tong University, Shanghai, China Marine sponges often harbor dense and diverse microbial communities including actinobacteria. To date no comprehensive investigation has been performed on the culturable diversity of the actinomycetes associated with South China Sea Edited by: Wen-Jun Li, sponges. Structurally novel aromatic polyketides were recently discovered from Sun Yat-Sen University, China marine sponge-derived Streptomyces and Saccharopolyspora strains, suggesting that Reviewed by: sponge-associated actinomycetes can serve as a new source of aromatic polyketides. Julie L. Meyer, In this study, a total of 77 actinomycete strains were isolated from 15 South China University of Florida, USA Virginia Helena Albarracín, Sea sponge species. Phylogenetic characterization of the isolates based on 16S rRNA National Scientific and Technical gene sequencing supported their assignment to 12 families and 20 genera, among Research Council (CONICET), Argentina which three rare genera (Marihabitans, Polymorphospora, and Streptomonospora) were *Correspondence: isolated from marine sponges for the first time. Subsequently, β-ketoacyl synthase Zhiyong Li, (KSα) gene was used as marker for evaluating the potential of the actinomycete Marine Biotechnology Laboratory, strains to produce aromatic polyketides. As a result, KSα gene was detected in 35 State Key Laboratory of Microbial Metabolism, School of Life Sciences isolates related to seven genera (Kocuria, Micromonospora, Nocardia, Nocardiopsis, and Biotechnology, Shanghai Jiao Saccharopolyspora, Salinispora, and Streptomyces). -
Phylogenetic Diversity and Activity Screening of Cultivable Actinobacteria Isolated
bioRxiv preprint doi: https://doi.org/10.1101/2020.01.09.901108; this version posted June 20, 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 Phylogenetic diversity and activity screening of cultivable actinobacteria isolated 2 from marine sponges and associated environments from the western coast of 3 India 4 5 Ulfat Baig1, Neelesh Dahanukar1, Neha Shintre2, Ketki Holkar1, Anagha Pund1, Uttara Lele1, 6 Tejal Gujarathi1, Kajal Patel1, Avantika Jakati1, Ruby Singh1, Harshada Vidwans1, Vaijayanti 7 Tamhane3, Neelima Deshpande2 and Milind Watve4 8 9 1Indian Institute of Science Education and Research, Pune (IISER-P), Dr. Homi Bhabha 10 Road, Pashan, Pune 411008, Maharashtra, India. 11 2Department of Microbiology, M.E.S. Abasaheb Garware College, Karve Road, Pune 12 411004, Maharashtra, India. 13 3Institute of Bioinformatics and Biotechnology, Savitribai Phule Pune University, Pune – 14 411007, Maharashtra, India 15 4Behavioural Intervention for Lifestyle Disorders (BILD) clinic, Deenanath Mangeshkar 16 Hospital and Research Centre, Erandwane, Pune 411004, Maharashtra, India. 17 18 Correspondence and requests for materials should be addressed to N. Dahanukar (email: 19 [email protected]) 20 21 22 23 Keywords: Bacterial predation; Antibiotic production; Secondary metabolites; Enzyme 24 inhibition; Molecular phylogeny. 25 1 bioRxiv preprint doi: https://doi.org/10.1101/2020.01.09.901108; this version posted June 20, 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. -
Of Bergey's Manual
BERGEY’S MANUAL® OF Systematic Bacteriology Second Edition Volume Five The Actinobacteria, Part A and B BERGEY’S MANUAL® OF Systematic Bacteriology Second Edition Volume Five The Actinobacteria, Part A and B Michael Goodfellow, Peter Kämpfer, Hans-Jürgen Busse, Martha E. Trujillo, Ken-ichiro Suzuki, Wolfgang Ludwig and William B. Whitman EDITORS, VOLUME FIVE William B. Whitman DIRECTOR OF THE EDITORIAL OFFICE Aidan C. Parte MANAGING EDITOR EDITORIAL BOARD Fred A. Rainey, Chairman, Peter Kämpfer, Vice Chairman, Paul De Vos, Jongsik Chun, Martha E. Trujillo and William B. Whitman WITH CONTRIBUTIONS FROM 116 COLLEAGUES William B. Whitman Bergey’s Manual Trust Department of Microbiology 527 Biological Sciences Building University of Georgia Athens, GA 30602-2605 USA ISBN 978-0-387-95043-3 ISBN 978-0-387-68233-4 (eBook) DOI 10.1007/978-0-387-68233-4 Springer New York Dordrecht Heidelberg London Library of Congress Control Number: 2012930836 © 2012, 1984–1989 Bergey’s Manual Trust Bergey’s Manual is a registered trademark of Bergey’s Manual Trust. All rights reserved. This work may not be translated or copied in whole or in part without the written permission of the publisher (Springer Science+Business Media, LLC, 233 Spring Street, New York, NY 10013, USA), except for brief excerpts in connection with reviews or scholarly analysis. Use in connection with any form of information storage and retrieval, electronic adaptation, computer software, or by similar or dissimilar methodology now known or hereafter developed is forbidden. The use in this publication of trade names, trademarks, service marks, and similar terms, even if they are not identified as such, is not to be taken as an expression of opinion as to whether or not they are subject to proprietary rights.